Produits biochimiques et réactifs
Les biochimiques et réactifs sont des substances fondamentales pour la recherche et le développement dans des domaines tels que la biotechnologie, la biologie moléculaire, la pharmacologie et la médecine. Ces produits sont essentiels pour une variété d'applications, y compris la synthèse de composés, l'analyse d'échantillons biologiques, la recherche sur les processus métaboliques et la production de médicaments. Chez CymitQuimica, nous proposons une large sélection de biochimiques et réactifs de haute qualité et pureté, adaptés à divers besoins scientifiques et industriels. Notre catalogue comprend des enzymes, des anticorps, des acides nucléiques, des acides aminés et de nombreux autres produits, tous conçus pour soutenir les chercheurs et les professionnels dans leurs projets de recherche et développement, garantissant des résultats fiables et reproductibles.
Sous-catégories appartenant à la catégorie "Produits biochimiques et réactifs"
- Biomolécules(99.130 produits)
- Par Biological Target(99.159 produits)
- Par usage/effets pharmacologiques(6.787 produits)
- Cryoconservation et composés associés aux cryoconservateurs(21 produits)
- Désinfectants, additifs pour les fluides pour bains chauffants et composés apparentés(28 produits)
- Hormones(346 produits)
- Biologie végétale(6.747 produits)
- Métabolites secondaires(14.222 produits)
130579 produits trouvés pour "Produits biochimiques et réactifs"
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anti-Avian Leukosis Virus Antibody
<p>Purified Mouse anti-Avian Leukosis Virus Antibody.</p>Degré de pureté :Min. 95%Purified CHO PLBL2 Protein
<p>Purified recombinant CHO PLBL2 Protein expressed in CHO-3E7 cells. Contains a 6xHIS tag.</p>Recombinant Human CD137L (4-1BBL)
<p>Human sequence expressed in E. coli Cells; purity >97% by SDS-PAGE and analyzed by silver stain; Histidine Tag.</p>anti-Chicken IgY h+l Antibody (BIOTIN)
<p>Biotin Conjugated Goat anti-Chicken IgY h+l antibody.</p>Degré de pureté :Min. 95%Recombinant Human Midkine
<p>Human sequence expressed in E. coli Cells; purity >97% by SDS-PAGE and analyzed by silver stain.</p>Recombinant Mouse Macrophage Inflammatory Protein 1 γ (MIP-1γ)
<p>Mouse sequence expressed in E. coli Cells; purity >97% by SDS-PAGE and analyzed by silver stain.</p>Recombinant Mouse SDF-1α
<p>Mouse sequence expressed in E. coli Cells; purity >97% by SDS-PAGE and analyzed by silver stain.</p>Recombinant Rat MCP-1
<p>Rat sequence expressed in E. coli Cells; purity >90% by SDS Page and analyzed by silver stain.</p>Recombinant Mouse Noggin
<p>Mouse sequence expressed in NS0 Cells; purity >95% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>Recombinant Mouse IL-13 Ralpha1
<p>Mouse sequence expressed in NS0 Cells; purity >97% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>Recombinant Human HGF R
<p>Human sequence expressed in NS0 Cells; purity >95% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>anti-Human Procalcitonin (PCT) Antibody
<p>Purified Mouse anti-Human Procalcitonin antibody (Clone 1H8)</p>Degré de pureté :Min. 95%anti-Dog SAA Protein Antibody
<p>Purified Mouse anti-Dog Serum Amyloid A antibody.<br>Best suited as detection antibody when tested in ELISA when paired with GSAA-40A.</p>Degré de pureté :Min. 95%Affinity Purified anti-Human IgE Antibody
<p>Please enquire for more information about Affinity Purified anti-Human IgE Antibody including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Degré de pureté :Min. 95%Recombinant Mouse GFRalpha-2
<p>Mouse sequence expressed in NS0 Cells; purity >95% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>Recombinant Human IL-17 R
<p>Human sequence expressed in NS0 Cells; purity >95% by SDS Page and analyzed by silver stain.</p>Rat IgG Purified
<p>The purified Rat IgG h+l can be utilized for ELISA, LFD, Western Blot and as a Blocking Agent. Please inquire for bulk pricing.</p>Recombinant Human RANTES
<p>Human sequence expressed in E. coli Cells; purity >97% by SDS-PAGE and analyzed by silver stain.</p>Recombinant Rat IL-5
<p>Rat sequence expressed in sf Insect Cells; purity >97% by SDS-PAGE and analyzed by silver stain.</p>Recombinant Rat MCP-3
<p>Human sequence expressed in E. coli Cells; purity >97% by SDS-PAGE and HPLC.</p>Recombinant Human Nanog
<p>Human sequence expressed in E. coli Cells; purity >98% by SDS Page and HPLC.</p>Recombinant Mouse IL-9
<p>Mouse sequence expressed in sf Insect Cells; purity >97% by SDS-PAGE and analyzed by silver stain.</p>Recombinant Human FGF-8e
<p>Human sequence expressed in E. coli Cells; purity >95% by SDS-PAGE and analyzed by silver stain.</p>Recombinant Human EDAR
<p>Human sequence expressed in NS0 Cells; purity >90% by SDS Page and analyzed by silver stain.</p>Recombinant Mouse Betacellulin
<p>Mouse sequence expressed in E. coli Cells; purity >97% by SDS-PAGE and analyzed by silver stain.</p>Recombinant Mouse IL-1 RII
<p>Mouse sequence expressed in sf Insect Cells; purity >95% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>anti-Rabbit IgG h+l Antibody (BIOTIN)
<p>Biotin Conjugated Goat anti-Rabbit IgG h+l antibody.</p>Degré de pureté :Min. 95%Recombinant Human IL-21R
<p>Human sequence expressed in NS0 Cells; purity >95% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>Recombinant Human TSLP
<p>Human sequence expressed in E. coli Cells; purity >95% by SDS-PAGE and analyzed by silver stain.</p>Recombinant Mouse Frizzled-4
<p>Mouse sequence expressed in NS0 Cells; purity >95% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>Recombinant Mouse EphB3
<p>Mouse sequence expressed in NS0 Cells; purity >95% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>Recombinant Human CD4 (Soluble)
<p>Human sequence expressed in sf Insect Cells; purity >90% by SDS-PAGE and analyzed by silver stain.</p>Recombinant Human FGF R1α (IIIb)
<p>Human sequence expressed in NS0 Cells; purity >95% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>Purified CHO GSTp Protein
<p>Purified recombinant Chinese hamster ovary Glutathione S-Transferase Pi (GSTP) Protein expressed in CHO-S cells. Contains a 6xHIS tag.<br>Glutathione S-transferase Pi (GSTp) is a metabolic enzyme that facilitates metabolite detoxification and antioxidation. GSTp reduces efficacy of chemotherapy drugs and inhibits tumor-cell apoptosis.</p>anti-CHO PLBL2 Monclonal
<p>Purified Monoclonal Mouse anti-CHO Phospholipase B-like 2 protein (PLBL2) Antibody</p>Degré de pureté :Min. 95%Recombinant Human FGF-18
<p>Human sequence expressed in E. coli Cells; purity >95% by SDS Page and HPLC.</p>Recombinant Human FGF-21
<p>Human sequence expressed in E. coli Cells; purity >97% by SDS-PAGE and analyzed by silver stain; Histidine Tag.</p>Recombinant Mouse Leptin R
<p>Mouse sequence expressed in NS0 Cells; purity >97% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>Recombinant Mouse Eotaxin
<p>Mouse sequence expressed in E. coli Cells; purity >97% by SDS-PAGE and analyzed by silver stain.</p>Recombinant Mouse gp130
<p>Mouse sequence expressed in NS0 Cells; purity >90% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>Recombinant Mouse CD30 Ligand
<p>Mouse sequence expressed in NS0 Cells; purity >95% by SDS-PAGE and analyzed by silver stain; Histidine Tag.</p>Affinity Purified anti-CHO RAN Protein
<p>Please enquire for more information about Affinity Purified anti-CHO RAN Protein including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Degré de pureté :Min. 95%anti-E. coli O157:H7 Antibody
<p>Please enquire for more information about anti-E. coli O157:H7 Antibody including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Degré de pureté :Min. 95%Recombinant Human Epigen
<p>Human sequence expressed in E. coli Cells; purity >98% by SDS Page and HPLC.</p>Affinity Purified anti-Human IgG h+l Antibody
<p>This rabbit anti-human IgG (H+L) antibody reacts with the heavy chain and light chains of human IgG and the light chains of other antibody classes. This antibody can be used as a detection or capture antibody in a variety of immunoassays. Please inquire for bulk pricing or custom conjugations.</p>Degré de pureté :Min. 95%anti-Human TSH β Antibody
<p>Purified Mouse anti-Human TSH beta Antibody</p>Degré de pureté :Min. 95%anti-Listeria monocytogenes Antibody
<p>This Monoclonal anti-Listeria monocytogenes antibody is suitable for ELISA and ICC applications.</p>Degré de pureté :Min. 95%Affinity Purified anti-Protein A Antibody
<p>Affinity Purified Chicken anti-Protein A (staphylococcal) Antibody</p>Degré de pureté :Min. 95%Recombinant Human NOV
<p>Human sequence expressed in E. coli Cells; purity >95% by SDS Page and HPLC.</p>Recombinant Human L-Selectin
<p>Human sequence expressed in NS0 Cells; purity >90% by SDS Page and analyzed by silver stain.</p>Recombinant Rat Fractalkine (FKN)
<p>Rat sequence expressed in sf Insect Cells; purity >97% by SDS-PAGE and analyzed by silver stain.</p>Recombinant Human PF-4
<p>Human sequence expressed in E. coli Cells; purity >97% by SDS-PAGE and analyzed by silver stain.</p>Recombinant Human MCP-1
<p>Human sequence expressed in E. coli Cells; purity >97% by SDS-PAGE and analyzed by silver stain.</p>anti-Clostridium Difficile GDH Antibody
<p>Anti-GDH antibodies can be used to make GDH antigen tests for the presence of the GDH enzyme, a protein present in all C. difficile isolates.<br>Purified Mouse anti-Glutamate Dehydrogenase (Clostridium difficile) Antibody.</p>Degré de pureté :Min. 95%anti-Dog CRP Antibody, whole serum
<p>This rabbit anti-Dog CRP antiserum can be used in a variety of immunoassays that require the specific detection of canine CRP.</p>Degré de pureté :Min. 95%Recombinant Mouse MSP R
<p>Mouse sequence expressed in NS0 Cells; purity >90% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>Recombinant Human BMPR-IB
<p>Human sequence expressed in NS0 Cells; purity >90% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>Recombinant Human SIGIRR
<p>Human sequence expressed in NS0 Cells; purity >90% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>Recombinant Human SCGF-α
<p>Human sequence expressed in E. coli Cells; purity >98% by SDS Page and HPLC.</p>Affinity Purified anti-Mouse Albumin Antibody
<p>Please enquire for more information about Affinity Purified anti-Mouse Albumin Antibody including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>anti-PEDV N Antibody
<p>Monoclonal Mouse anti-Porcine Epidemic Diarrhea Virus Antibody</p>Degré de pureté :Min. 95%Recombinant Mouse Limitin
<p>Mouse sequence expressed in NS0 Cells; purity >90% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>Affinity Purified anti-Human IgG h+l Antibody
<p>Affinity Purified Goat anti-Human IgG h+l antibody is suitable for WB, ELISA, IHC and is commonly used by manufacturers of lateral flow immunochromatographic assays.</p>Degré de pureté :Min. 95%Purified Bovine CRP- Recombinant
<p>Purified recombinant Bovine/Cow C-reactive Protein (CRP) expressed in CHO-S cells. Contains a 6xHIS tag.</p>Recombinant Human ALK-2
<p>Human sequence expressed in NS0 Cells; purity >95% by SDS-PAGE and analyzed by silver stain.</p>Canine Heartworm Antigen
<p>Dirofilaria immitis, also known as heartworm, is a major parasitic threat for dogs and cats around the world.</p>Recombinant Human BMP-9
<p>Human sequence expressed in CHO Cells; purity >95% by SDS-PAGE and analyzed by silver stain.</p>anti-Cholera Toxin B Antibody
<p>Monoclonal Mouse anti-Cholera Toxin B Antibody</p>Degré de pureté :Min. 95%Recombinant Mouse Fractalkine (FKN)
<p>Mouse sequence expressed in sf Insect Cells; purity >97% by SDS-PAGE and analyzed by silver stain; Histidine Tag.</p>anti-Clostridium Difficile Toxin A Antibody
<p>anti-Clostridium difficile Toxin A Antibody reacts with Tox A and not with Tox B.</p>Degré de pureté :Min. 95%Recombinant Human IL-28B
<p>Human sequence expressed in CHO Cells; purity >95% by SDS-PAGE and analyzed by silver stain.</p>Recombinant Human GROgamma/CXCL3
<p>Rat sequence expressed in E. coli Cells; purity >97% by SDS-PAGE and analyzed by silver stain.</p>Recombinant Human FGF-19
<p>Human sequence expressed in E. coli Cells; purity >97% by SDS-PAGE and analyzed by silver stain.</p>Recombinant Human Soluble RANK Ligand
<p>Human sequence expressed in NS0 Cells; purity >90% by SDS-PAGE and analyzed by silver stain; Histidine Tag.</p>anti-Human B2M Antibody
<p>Please enquire for more information about anti-Human B2M Antibody including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Degré de pureté :Min. 95%Recombinant Human TRAIL R3
<p>Human sequence expressed in NS0 Cells; purity >95% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>Recombinant Human ApoE4
<p>Human sequence expressed in E. coli Cells; purity >90% by SDS Page and HPLC.</p>Degré de pureté :>90% By Sds-Page And Hplc.Recombinant Rat IL-1α
<p>Rat sequence expressed in E. coli Cells; purity >97% by SDS-PAGE and analyzed by silver stain.</p>Recombinant Mouse CD86
<p>Mouse sequence expressed in sf Insect Cells; purity >95% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>Recombinant Mouse GDNF
<p>Mouse sequence expressed in E. coli Cells; purity >98% by SDS-PAGE and HPLC.</p>Recombinant Mouse Tie-2
<p>Mouse sequence expressed in NS0 Cells; purity >90% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>Recombinant Human TrkC
<p>Human sequence expressed in NS0 Cells; purity >95% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>Affinity Purified anti-Dog IgE Antibody
<p>This purified Mouse anti-Dog IgE monoclonal antibody reacts with the IgE heavy chain and not with IgG, IgA, IgM or IgD. It is suitable for use as capture or detection antibody in various immunoassays.</p>Degré de pureté :Min. 95%Recombinant RSV Prefusion (DS-Cav1), Trimer
<p>Viral sequence expressed in HEK-293 Cells; purity >95% by SDS Page.</p>Recombinant Human P-Cadherin
<p>Human sequence expressed in NS0 Cells; purity >90% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>anti-Cyanine5 Antibody
<p>This purified Mouse anti-Cyanine5 can be used in ELISA and lateral flow assays to detect Cyanine5 conjugated proteins.</p>Degré de pureté :Min. 95%Recombinant Human MCP-2
<p>Human sequence expressed in E. coli Cells; purity >97% by SDS-PAGE and analyzed by silver stain.</p>Recombinant Mouse TNFRSF19/TROY
<p>Mouse sequence expressed in sf Insect Cells; purity >90% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>Canine Distemper Virus Mouse Monoclonal Antibody
<p>Mouse anti-Distemper Virus Antibody</p>Degré de pureté :Min. 95%Recombinant Rat IL-17AF
<p>Rat sequence expressed in E. coli Cells; purity >98% by SDS-PAGE and HPLC.</p>Purified CHO MMP-19 Protein
<p>Purified CHO MMP-19 Protein is a protein for use in pharmaceutical and diagnostic applications. Please enquire for more information about Purified CHO MMP-19 Protein including the price, delivery time and more detailed product information at the technical inquiry form on this page.</p>Recombinant Mouse EGF
<p>Mouse sequence expressed in E. coli Cells; purity >95% by SDS-PAGE and analyzed by silver stain.</p>anti-Human PSA Antibody
<p>Purified Mouse anti-Human Prostate Specific Antigen (PSA) Antibody (Mouse - Clone# 803) - Monoclonal</p>Degré de pureté :Min. 95%Recombinant Human TRAIL/Apo2L
<p>Human sequence expressed in E. coli Cells; purity >97% by SDS-PAGE and HPLC.</p>Recombinant Human LBP
<p>Human sequence expressed in NS0 Cells; purity >97% by SDS-PAGE and analyzed by silver stain.</p>Recombinant Human FGF R1β (IIIc)
<p>Human sequence expressed in NS0 Cells; purity >90% by SDS Page and analyzed by silver stain; Fc Fusion Protein.</p>Rabbit IgG Enriched
<p>The enriched Rabbit Ig is recommended for use as a blocking reagent. Please inquire for bulk pricing. >80% Purity</p>Recombinant Human GITR Ligand
<p>Human sequence expressed in sf Insect Cells; purity >97% by SDS-PAGE and analyzed by silver stain; Histidine Tag.</p>Recombinant Human Osteoprotegerin
<p>Human sequence expressed in CHO Cells; purity >95% by SDS-PAGE and analyzed by silver stain; Fc Fusion Protein.</p>Bis-dPEG®3-NHS Ester
CAS :<p>Bis-dPEG®3-NHS Ester is a PEG polymer categorised as homobifunctional PEG (X-PEG X). Used as a linker, bis-dPEG®3-NHS Ester is used to attached PEG to proteins, peptides, oligonucleotides, nanoparticles and small molecules via pegylation, a bioconjugation technique.</p>Formule :C53H71F4NO15Degré de pureté :Min. 95%Masse moléculaire :1,038.14 g/molTegafur - Bio-X ™
CAS :<p>Tegafur is an antineoplastic agent that is used for the treatment of gastric and colorectal cancers in combination with other medications. This drug is a prodrug of 5-fluorouracil and has anticancer properties by inhibiting thymidylate synthase during DNA synthesis. Additionally, Tegafur causes disruptions of RNA functions.<br><br>Tegafur is part of our Bio-X ™ Range. These products are aimed at life science researchers who need high quality ready-to-use products for assay development, screening or other R&D work. With a solubility datasheet and convenient vials, all of our Bio-X ™ products are in stock across our global warehouses for rapid delivery and ease of use.</p>Formule :C8H9FN2O3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :200.17 g/molRuxolitinib sulfate
CAS :<p>Ruxolitinib is a small molecule that inhibits the activity of PD-1, which is a protein that regulates immune responses. Ruxolitinib has been shown to be effective against myelofibrosis and other diseases that are characterized by cellular dedifferentiation, such as chronic graft versus host disease. It also inhibits the production of proteins involved in tumor growth and progression. Ruxolitinib binds to PD-L1, an inhibitory receptor on T cells, and blocks the interaction between PD-L1 and its ligands, preventing T cell activation. The binding of ruxolitinib with PD-L1 can induce receptor internalization or activate downstream signalling pathways for apoptosis.</p>Formule :C17H20N6O4SDegré de pureté :Min. 95%Masse moléculaire :404.4 g/mol(2S)-Arimoclomol
CAS :<p>Regulates expression of chaperonins Hsp70 and Hsp90</p>Formule :C14H20ClN3O3Degré de pureté :Min. 95%Masse moléculaire :313.78 g/molN-Palmitoyl-D-sphingomyelin
CAS :<p>N-Palmitoyl-D-sphingomyelin is a fatty acid that is derived from sphingomyelin. It has been shown to increase the water permeability of the cell membrane and alter the thermal expansion coefficient, which may be useful in diagnosis of cancer. In addition, N-palmitoyl-D-sphingomyelin has been shown to decrease cell viability and induce apoptosis in HL60 cells through electrochemical impedance spectroscopy (EIS) techniques. The phase transition temperature of N-palmitoyl-D-sphingomyelin has been found to be approximately 28°C. It also forms hydrogen bonds between its own molecules and other molecules due to ester linkages with cholesterol. This may be useful in natural compounds for treating metabolic disorders such as obesity or diabetes.</p>Formule :C39H79N2O6PDegré de pureté :Min. 95%Masse moléculaire :703.03 g/molFmoc-[D10]Leu-OH
CAS :Produit contrôlé<p>Please enquire for more information about Fmoc-[D10]Leu-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formule :C21H13D10NO4Degré de pureté :Min. 95%Masse moléculaire :363.47 g/molPlacental Lactogen Human
<p>Placental Lactogen Human is a protein that belongs to the group of peptides. It is a hormone that stimulates the production of breast milk and it also regulates other functions in the body. Placental lactogen binds to its receptor, which is an activator, and activates ion channels on the cell membrane. This leads to changes in cell metabolism and gene expression. Placental lactogen also has been shown to inhibit ligand-gated ion channels in vitro.</p>Degré de pureté :Min. 95%CPN-267
<p>CPN-267 is a peptide that is an inhibitor of protein interactions. It has been shown to be a potent inhibitor of the activation of the receptor for the amyloid beta peptide. CPN-267 also inhibits ligand binding to the acetylcholine receptor, and blocks ion channels in neuronal cells. This drug has also been shown to inhibit the activity of some proteins involved in cancer cell proliferation and survival. CPN-267 has been used as a research tool for studying protein interactions and has been labeled with fluorochrome to allow for visualization under a microscope.<br>CAS: 93627-03-3</p>Degré de pureté :Min. 95%09:0 PC
CAS :<p>09:0 PC is a phospholipid that has shown the ability to protect against renal ischemia-reperfusion injury in rats. This protection was seen both in vitro and in vivo, as well as for apoptosis induced by serum deprivation. 09:0 PC was also found to have an anti-inflammatory effect on rat cardiomyocytes. These effects were due to its ability to inhibit phospholipases and neutralize reactive oxygen species (ROS). It has been found that 09:0 PC contains a serine residue at the active site, which may be important for its activity. Further research on the mechanism of 09:0 PC's activity is needed to understand how it protects cells from injury and death.</p>Formule :C26H52NO8PDegré de pureté :Min. 95%Masse moléculaire :537.67 g/molNHS-dPEG®4 Biotinidase-Resistant Biotin
CAS :<p>NHS-dPEG®4 Biotinidase-Resistant Biotin is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. NHS-dPEG®4 Biotinidase-Resistant Biotin is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.</p>Degré de pureté :Min. 95%Masse moléculaire :673.78 g/molIMS2186
CAS :<p>IMS2186 is a small molecule drug that inhibits the proliferation of cells and has an inhibitory effect on angiogenesis in vivo. This drug is also effective against inflammatory diseases, such as psoriasis and rheumatoid arthritis. IMS2186 has been shown to have a molecular pathogenesis of proliferative diabetic retinopathy. It inhibits the production of pro-inflammatory cytokines, growth factors, and pro-angiogenic proteins by targeting the cellular nucleus. IMS2186 may be able to prevent cancer cell growth and choroidal neovascularization in patients with age-related macular degeneration.</p>Formule :C18H16O4Degré de pureté :Min. 95%Masse moléculaire :296.32 g/molTNFalpha-IN-S10
CAS :<p>TNFalpha-IN-S10 is a research tool that can be used to activate or inhibit the TNF receptor, which is involved in cell signaling. The TNF alpha IN-S10 antibody can be used to study protein interactions and pharmacology. It also has high purity and can be used for biochemical assays. TNF alpha IN-S10 is a peptide with a molecular weight of about 10 kDa.</p>Formule :C21H14N2O3SDegré de pureté :Min. 95%Masse moléculaire :374.4 g/molEthyl N-[4-(2,4-dimethoxyphenyl)-5-oxodithiolo[4,3-b]pyrrol-6-yl]carbamate
CAS :<p>Ethyl N-[4-(2,4-dimethoxyphenyl)-5-oxodithiolo[4,3-b]pyrrol-6-yl]carbamate is a peptide that is used as a research tool in the fields of protein interactions, receptor binding and ligand binding. It has been shown to inhibit ion channels and to block the activation of certain proteins by inhibiting ATP binding. This compound binds to many receptors and has been shown to be an inhibitor of protein synthesis. The molecular weight of this compound is 534.57 g/mol. CAS No. 1015064-87-5</p>Formule :C16H16N2O5S2Degré de pureté :Min. 95%Masse moléculaire :380.4 g/molZinviroxime
CAS :<p>Zinviroxime is a potent and selective inhibitor of the ion channel TRPV1. It blocks the activity of this receptor and prevents the release of inflammatory mediators such as calcitonin gene-related peptide, substance P, and bradykinin. Zinviroxime has been shown to inhibit the binding of these mediators to their receptors on cells in culture. This inhibition causes pain relief in animal models. Zinviroxime also inhibits the activation of TRPV1 by capsaicin, an activator of TRPV1. The molecular weight for zinviroxime is 836 Daltons and its CAS number is 72301-78-1.</p>Formule :C17H18N4O3SDegré de pureté :Min. 95%Masse moléculaire :358.4 g/molL-771688
CAS :<p>L-771688 is a small molecule that has been shown to regulate protein interactions. It has been shown to activate peptide receptors and ion channels, which are important for many cellular functions. L-771688 is also a ligand for the antibody and receptor systems. This drug has been used as a research tool in cell biology and pharmacology studies.</p>Formule :C28H33F2N5O5Degré de pureté :Min. 95%Masse moléculaire :557.6 g/mol(E)-4-Hydroxy toremifene
CAS :<p>(E)-4-Hydroxy toremifene is a research tool that is used in the study of ion channels and protein interactions. Toremifene is a peptide that has been shown to activate an antibody and receptor. This drug binds to a ligand and interacts with protein receptors, which are involved in cell division. The high purity of this product makes it ideal for use in life science experiments, as well as cell biology and pharmacology studies.</p>Formule :C26H28ClNO2Degré de pureté :Min. 95%Masse moléculaire :422 g/molCWP232228
CAS :<p>CWP232228 is a potent, selective and competitive antagonist of the beta-2 adrenergic receptor (B2AR). CWP232228 does not bind to other adrenoreceptors, including alpha-1, alpha-2, or beta-1 adrenoreceptors. CWP232228 blocks the binding of catecholamines like norepinephrine and epinephrine to B2ARs with an IC50 of 0.8 nM. CWP232228 also has high affinity for the B2AR with a Kd of 8 nM and is selective for this receptor over all other adrenoreceptors.<br>CWP232228 is a pharmacological tool that can be used in cell biology research and in drug discovery programs to develop new drugs targeting disorders such as hypertension and asthma.</p>Formule :C33H34N7Na2O7PDegré de pureté :Min. 95%Masse moléculaire :717.6 g/molPM226
CAS :<p>PM226 is a peptide that activates ion channels. It has a high purity and can be used as a research tool to study the function of ion channels. PM226 is also an inhibitor of ligand-gated ion channels and has been shown to inhibit GABAA receptors.</p>Formule :C22H31NO3Degré de pureté :Min. 95%Masse moléculaire :357.5 g/molSC58451
CAS :<p>SC58451 is a small molecule that inhibits receptor-mediated activation of ion channels. SC58451 is a potent inhibitor of the human beta-adrenergic receptor, which is an integral membrane protein that mediates the effects of norepinephrine and epinephrine on the cardiovascular system. SC58451 also inhibits ligand-gated ion channels, including nicotinic and serotonin receptors. This compound has been shown to be effective in blocking the cardiac arrhythmias induced by β-adrenergic receptor stimulation in vivo.</p>Formule :C20H19FO2SDegré de pureté :Min. 95%Masse moléculaire :342.4 g/mol2-(Isopropylamino)-3-methyl-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one
CAS :<p>2-(Isopropylamino)-3-methyl-5-(6-methyl-5-((2-(1-methyl-1H-pyrazol-4-yl)pyridin-4-yl)oxy)pyridin-2-yl)pyrimidin-4(3H)-one is a drug that is used to study the interactions between proteins and peptides. It has been shown to be an activator of ion channels, such as potassium channels. 2-(Isopropylamino)-3-methyl-5-(6-methyl-5-(2-(1 methyl 1H pyrazol 4 yl) pyridin 4 yl) oxy) pyridin 2 yl) pyrimidin 4 (3 H ) one has also been found to be an inhibitor of ligand binding to antibody and receptor structures.</p>Formule :C23H25N7O2Degré de pureté :Min. 95%Masse moléculaire :431.5 g/molCDK12-IN-E9
CAS :<p>CDK12-IN-E9 is a research tool that belongs to the class of activators. It can bind to the receptor and activate it by binding to the ligand. CDK12-IN-E9 is an inhibitor with a high purity, which may be used in cell biology, antibody production, ion channels, and protein interactions. The peptide sequence of CDK12-IN-E9 has been determined and its pharmacology has been studied in detail.</p>Formule :C24H30N6O2Degré de pureté :Min. 95%Masse moléculaire :434.5 g/molTampramine fumarate
CAS :<p>Tampramine is a ligand for the nicotinic acetylcholine receptor. It has been used as a research tool to study the function of ion channels, and as a pharmacological agent for the treatment of epilepsy. Tampramine binds to the nicotinic acetylcholine receptor and blocks its activation by acetylcholine or nicotine. Tampramine also inhibits the binding of other ligands, such as atropine, to their receptors. Tampramine is an inhibitor of phosphodiesterase (PDE) enzymes which are involved in signal transduction pathways that regulate cellular processes including cell proliferation, differentiation and apoptosis. PDEs hydrolyze cyclic nucleotides, such as cAMP and cGMP, which are important second messengers in intracellular signaling cascades.</p>Formule :C27H28N4O4Degré de pureté :Min. 95%Masse moléculaire :472.5 g/molAlcaftadine-d3
CAS :<p>Alcaftadine-d3 is a research tool that belongs to the ligand and receptor class. It is a fluorescent analog of alcaftadine, which can be used as a marker in cell biology experiments. Alcaftadine-d3 has been shown to inhibit calcium ion channels, thus preventing the influx of calcium ions into cells. This has been shown to lead to an increase in intracellular levels of cyclic AMP, which leads to an increase in protein synthesis and cell division. Alcaftadine-d3 also has been shown to inhibit certain types of ion channels and may have potential as an analgesic drug.</p>Formule :C19H21N3ODegré de pureté :Min. 95%Masse moléculaire :310.4 g/molLorediplon
CAS :<p>Lorediplon is a research tool that belongs to the class of ligands. It is an activator of the GABA receptor and modulates ion channels. Lorediplon has been shown to be a potent inhibitor of high purity, which inhibits protein interactions. Lorediplon binds to cell receptors and can activate them by binding to their corresponding ligands. Lorediplon also interacts with antibodies and peptides, which are used in Cell Biology and Pharmacology studies.</p>Formule :C16H12N2O2Se2Degré de pureté :Min. 95%Masse moléculaire :422.2 g/molRineterkib hydrochloride
CAS :<p>Rineterkib hydrochloride is a peptide that can be used as a research tool to study the activation of ion channels and protein interactions. The peptide is an inhibitor of the delayed rectifier potassium channel, which is important for the regulation of cardiac contractility. Rineterkib hydrochloride binds to the receptor site on the channel and prevents it from opening. Rineterkib hydrochloride also blocks ligand-gated ion channels in nerve cells and muscle cells, inhibiting neurotransmitter release or muscle contraction. This drug is also known to block platelet aggregation by inhibiting thromboxane synthesis.</p>Formule :C26H28BrClF3N5O2Degré de pureté :Min. 95%Masse moléculaire :614.9 g/molLEO 39652
CAS :Produit contrôlé<p>LEO 39652 is a research tool that belongs to the group of activators. It is a ligand for the receptor and has been shown to be an ion channel inhibitor. LEO 39652 has been shown to inhibit protein interactions and peptide synthesis, as well as modulate cell biology and pharmacology. LEO 39652 is also a high-purity product with a purity of ≥98%.<br>LEO 39652 may be used in antibody production, cell biology, and pharmacology experiments.</p>Formule :C23H23N3O5Degré de pureté :Min. 95%Masse moléculaire :421.4 g/molELA-14 negative control
CAS :<p>ELA-14 is a recombinant protein that has been shown to inhibit the activity of the protein kinase, PKC. ELA-14 blocks PKC's ability to phosphorylate proteins in cells, which prevents the activation of other proteins. It can also be used as an activator for some receptors and as a ligand for some ion channels. ELA-14 is not present in human or mouse cells and does not bind any known endogenous peptides, making it a good tool for research. ELA-14 is highly purified and has a purity of at least 98%. This product is intended for use in life science research.</p>Formule :C72H112N22O17S2Degré de pureté :Min. 95%Masse moléculaire :1,621.9 g/molJNJ 10311795
CAS :<p>JNJ 10311795 is a peptide that binds to the human erythropoietin receptor. It has been shown to activate this receptor by binding to the ligand-binding domain. It is a potent inhibitor of ion channels and has been shown to inhibit the activity of these channels in cells. This drug is used as a research tool for studying protein interactions, receptor activation, and ion channel function.</p>Formule :C40H35N2O6PDegré de pureté :Min. 95%Masse moléculaire :670.7 g/molAZD 4407
CAS :<p>AZD 4407 is a potent, selective inhibitor of the protein kinase C (PKC) family with IC50 values in the low nanomolar range. It inhibits PKC isoforms α, βI and γ with IC50 values of 0.5 nM, 1 nM and 3 nM respectively. AZD 4407 is a cell permeable inhibitor that does not inhibit other kinases such as protein kinase A or CDKs.<br>AZD 4407 can be used as a research tool for PKC-mediated signal transduction pathways in cells, tissues and organisms. It can also be used to study PKC-dependent regulation of ion channels, antibody production or receptor activation by peptides.</p>Formule :C19H21NO3S2Degré de pureté :Min. 95%Masse moléculaire :375.5 g/molBatabulin sodium
CAS :<p>Batabulin sodium is a research tool that belongs to the group of activators, ligands and receptors. It is an inhibitor with high purity, which has been shown to be useful in cell biology, pharmacology and protein interactions. Batabulin sodium has been shown to inhibit ion channels and may be used as a research tool for studying the effects of ion channels on cells. This inhibitor also has been shown to inhibit the binding of antibodies, which may be due to its ability to block protein-protein interactions.</p>Formule :C13H6F6NNaO3SDegré de pureté :Min. 95%Masse moléculaire :393.24 g/mol7-Chloro-3-methyl-2-(4-(4-(trifluoromethoxy)benzyl)phenyl)quinolin-4(1H)-one
CAS :<p>7-Chloro-3-methyl-2-(4-(4-(trifluoromethoxy)benzyl)phenyl)quinolin-4(1H)-one is a research tool that can be used to activate proteins and receptors. It binds to the Ligand, Receptor, Cell Biology, Antibody, Ion channels, High purity, Protein interactions, Pharmacology and Peptides. 7-Chloro-3-methyl-2-(4-(4-(trifluoromethoxy)benzyl)phenyl)quinolin-4(1H)-one is a high purity inhibitor and has been shown to interact with a variety of ligands and receptors at pharmacological concentrations.</p>Formule :C24H17ClF3NO2Degré de pureté :Min. 95%Masse moléculaire :443.8 g/molClocapramine hydrochloride
CAS :<p>Clocapramine hydrochloride is an inhibitor of the N-methyl-D-aspartate (NMDA) receptor. It is a peptide that binds to the NMDA receptor and blocks ion channels, preventing calcium ions from entering. Clocapramine hydrochloride has been used as a research tool to study how NMDA receptors can be blocked, and it is also used as an antibody for immunohistochemistry. This product has been shown to inhibit protein interactions and receptor ligand binding, as well as block ion channels in cells.</p>Formule :C28H41Cl3N4O2Degré de pureté :Min. 95%Masse moléculaire :572 g/mol3-((4-((4-(3-(5-(tert-Butyl)-2-methoxy-3-(methylsulfonamido)phenyl)ureido)naphthalen-1-yl)oxy)pyridin-2-yl)amino)-5-methoxy-N-(3-mor pholinopropyl)benzamide
CAS :<p>3-((4-((4-(3-(5-(tert-Butyl)-2-methoxy-3-(methylsulfonamido)phenyl)ureido)naphthalen-1-yl)oxy)pyridin-2-yl)amino)-5-methoxy-N-(3-morpholinopropyl)benzamide is a potent and selective inhibitor of the receptor for nerve growth factor. It blocks NGF binding to its receptor, preventing NGF from activating the receptor and transmitting signals that stimulate cellular proliferation. 3MPAB has been shown to inhibit the activation of potassium channels by Ligand. It may also have an effect on calcium channels, as well as other ion channels, due to its ability to bind to various sites on protein surfaces.</p>Formule :C43H51N7O8SDegré de pureté :Min. 95%Masse moléculaire :826 g/mol1,3-Dimethyl-5-(2-(tetrahydro-2H-pyran-4-yl)-1-(2-(trifluoromethoxy)ethyl)-1H-benzimidazol-6-yl)-2(1H)-pyridinone
CAS :<p>1,3-Dimethyl-5-(2-(tetrahydro-2H-pyran-4-yl)-1-(2-(trifluoromethoxy)ethyl)-1H-benzimidazol-6-yl)-2(1H)-pyridinone is a pharmacological research tool that has been used to study the biological activity of various peptides. This compound can be used as an inhibitor or activator for protein interactions. It binds to receptor sites and blocks ion channels. 1,3-Dimethyl-5-(2-(tetrahydro-2H-pyran-4-yl)-1-(2-(trifluoromethoxy)ethyl)-1H-benzimidazol-6-yl)-2(1H)-pyridinone is also used in antibody production and cell biology research. This molecule is not intended for human consumption and should be handled</p>Formule :C22H24F3N3O3Degré de pureté :Min. 95%Masse moléculaire :435.4 g/molAsp-Val-Val-Asp-Ala-Asp-Glu-Tyr-Leu-Ile-Pro-Gln
CAS :<p>Asp-Val-Val-Asp-Ala-Asp-Glu-Tyr-Leu-Ile-Pro-Gln is a peptide that has been shown to be an activator of ion channels and a ligand for receptors. It has also been shown to inhibit protein interactions. Asp-Val-Val-Asp-Ala-Asp-Glu-Tyr-Leu-Ile Pro Gln is used as a research tool in the study of cell biology and pharmacology, as well as in the development of antibodies. This peptide is a highly purified product with CAS No. 9624943.</p>Formule :C61H93N13O23Degré de pureté :Min. 95%Masse moléculaire :1,376.5 g/molMethyl 9-((2,4-dichlorophenyl)amino)thiazolo[5,4-F]quinazoline-2-carbimidate
CAS :<p>Methyl 9-((2,4-dichlorophenyl)amino)thiazolo[5,4-F]quinazoline-2-carbimidate is a potent and selective inhibitor of the protein tyrosine phosphatase SHP2. It has been shown to inhibit the activation of the epidermal growth factor receptor (EGFR), which is important in the development of cancer. Methyl 9-((2,4-dichlorophenyl)amino)thiazolo[5,4-F]quinazoline-2-carbimidate is also a ligand that can activate a receptor and has been used as a research tool to study protein interactions.</p>Formule :C17H11Cl2N5OSDegré de pureté :Min. 95%Masse moléculaire :404.3 g/molMELK-8a
CAS :<p>MELK-8a is a peptide inhibitor that binds to the extracellular region of the human Melanocortin 2 receptor. It is used for research purposes and has been shown to be an activator at the melanocortin 2 receptor. MELK-8a is purified from bacteria with a high degree of purity and can be used as a research tool, or as an antibody or ligand in other studies.</p>Formule :C25H32N6ODegré de pureté :Min. 95%Masse moléculaire :432.6 g/molAC-FLTD-CMK
CAS :<p>AC-FLTD-CMK is a peptide that was generated by chemical synthesis. It is an activator of the human GABAA receptor. AC-FLTD-CMK has been shown to modulate ion channels in cells, and therefore may be useful in understanding the function of ion channels. AC-FLTD-CMK has also been used as a research tool in studies on protein interactions and receptor pharmacology.</p>Formule :C26H37ClN4O8Degré de pureté :Min. 95%Masse moléculaire :569 g/mol5-((6,7,8-Trimethoxy-4-quinazolinyl)amino)-1-pentanyl nitrate maleate
CAS :<p>5-((6,7,8-Trimethoxy-4-quinazolinyl)amino)-1-pentanyl nitrate maleate is a peptide inhibitor of the protein interactions involved in the activation of ion channels. This drug has been shown to be an activator of ligand binding to receptors and a ligand for certain receptors. It is used as a research tool for studying the pharmacology and cell biology of ion channels. 5-(6,7,8-Trimethoxy-4-quinazolinyl)amino)-1-pentanyl nitrate maleate has high purity and is suitable for use as an antibody reagent.</p>Formule :C16H22N4O6Masse moléculaire :366.37 g/molGuanoxabenz
CAS :<p>Guanoxabenz is a selective agonist of the PAR2 receptor. It has been shown to activate the PAR2 receptor and to inhibit the activity of enzymes such as protein kinase C, which are known to be involved in inflammation. Guanoxabenz also inhibits ion channels, such as calcium-activated potassium channels and sodium-activated potassium channels. It is used in research as a tool for studying cell biology and pharmacology, as well as for developing new therapeutics.</p>Formule :C8H8Cl2N4ODegré de pureté :Min. 95%Masse moléculaire :247.08 g/molPZ-128
CAS :<p>PZ-128 is a research tool that is used to activate the ligand receptor and study cell biology, antibody interactions, ion channels, protein interactions, and pharmacology. PZ-128 has been shown to be an inhibitor of peptides and proteins. It has also been shown to inhibit the activity of aminopeptidase N (APN), which is a type of enzyme that degrades peptides. PZ-128 has a molecular weight of 259.6 g/mol and chemical formula C15H19N3O2S.</p>Formule :C55H99N13O9Degré de pureté :Min. 95%Masse moléculaire :1,086.5 g/mol4-Amino-N-(1-(3-cyclohexen-1-ylmethyl)-4-piperidyl)-2-ethoxy-5-nitrobenzamide
CAS :<p>4-Amino-N-(1-(3-cyclohexen-1-ylmethyl)-4-piperidyl)-2-ethoxy-5-nitrobenzamide is a peptide that has been shown to inhibit the activity of protein kinases. It binds to the ATP binding site of the enzyme and blocks phosphorylation. This compound is used as a research tool for studying protein kinase activity, specifically for studying ion channels and GPCRs. 4-Amino-N-(1-(3-cyclohexen-1-ylmethyl)-4-piperidyl)-2-ethoxy-5 nitrobenzamide is also used in drug discovery, as it can be used to activate or block receptors. 4AANEPE has been shown to be an effective inhibitor of the P2X receptor, which mediates pain sensation.</p>Formule :C25H36N4O10Degré de pureté :Min. 95%Masse moléculaire :552.6 g/molCicloprolol hydrochloride
CAS :<p>Cicloprolol hydrochloride is a peptide that belongs to the group of activators. It is used as a research tool and an antibody in cell biology, pharmacology and protein interactions. Cicloprolol hydrochloride binds to ion channels, which alters their activity. This drug also inhibits the production of cAMP and phosphodiesterase, leading to increased levels of cAMP. This drug has been shown to bind to receptors on cells that are activated by ligands such as acetylcholine, histamine, serotonin, or dopamine. The binding of this drug changes the shape of the receptor so that it can no longer interact with its ligand.</p>Formule :C18H30ClNO4Degré de pureté :Min. 95%Masse moléculaire :359.9 g/molSniper(brd)-1
CAS :<p>Sniper is a peptide-based inhibitor of the protein interactions with the extracellular loop of potassium channels. It is also an activator of the ligand-gated ion channels, and has been used as a research tool to study protein interactions. Sniper has high purity, and can be used in life science experiments. The antibody binds to the extracellular loop of potassium channels and inhibits the interaction between potassium channels and other proteins. Sniper has shown to be effective against various types of ion channels, such as voltage-gated sodium channels, calcium-activated potassium channels, and chloride ion channels.</p>Formule :C53H66ClN9O8S2Degré de pureté :Min. 95%Masse moléculaire :1,056.7 g/molGlucagon (1-29) hydrochloride
CAS :<p>Glucagon (1-29) hydrochloride is a peptide hormone that is a member of the glucagon family. It has been shown to activate ion channels, which are found in the membranes of cells, and regulate the passage of ions across them. Glucagon (1-29) hydrochloride is used as a research tool in studies of protein interactions and receptor pharmacology. It has also been shown to be an activator of ion channels, which are found in the membranes of cells and regulate the passage of ions across them. Glucagon (1-29) hydrochloride is also used as an inhibitor for certain cancer cell lines.</p>Formule :C153H226ClN43O49SDegré de pureté :Min. 95%Masse moléculaire :3,519.2 g/molLevoemopamil hydrochlorid
CAS :<p>Levoemopamil hydrochlorid is a peptide that inhibits the interaction of proteins and peptides. It has been used as an inhibitor in the study of protein-protein interactions, as well as in research to develop receptor ligands. Levoemopamil hydrochlorid is also used as a high-purity reagent for life science research. In addition, it can be used to study ion channels and antibodies.</p>Formule :C23H31ClN2Degré de pureté :Min. 95%Masse moléculaire :371 g/molCyanine3.5 NHS ester
CAS :<p>Cyanine3.5 NHS ester is a fluorescent dye that binds to proteins and peptides. It is used as a research tool in the study of protein interactions, antibody binding, and cell biology. This dye has been shown to activate ion channels and ligand-gated receptors with high affinity. The dye can also be used as an inhibitor of voltage-gated sodium channels. Cyanine3.5 NHS ester has been shown to inhibit the activity of potassium channels with IC50 values of about 500 μM.</p>Formule :C42H44BF4N3O4Degré de pureté :Min. 95%Masse moléculaire :741.6 g/mol5-Bromo-7-[(4-piperidinylmethyl)amino]-2-benzofurancarboxylic acid
CAS :<p>5-Bromo-7-[(4-piperidinylmethyl)amino]-2-benzofurancarboxylic acid is a research tool that belongs to the class of ligands. It has been shown to inhibit the activity of three ion channels, including calcium channels, sodium channels, and potassium channels. This compound may be used as an inhibitor for the study of protein interactions and receptor activation. 5-Bromo-7-[(4-piperidinylmethyl)amino]-2-benzofurancarboxylic acid is also an antibody that can be used in cell biology research as well as a reagent in antibody production.</p>Formule :C15H17BrN2O3Degré de pureté :Min. 95%Masse moléculaire :353.21 g/molDiacetolol d7
CAS :<p>Diacetolol d7 is a research tool that can be used to activate, bind, or inhibit ligands and receptors. It can also be used to study the role of ion channels, cell biology, and protein interactions. Diacetolol d7 is purified and has high purity. This chemical is suitable for use in pharmacology studies and as a peptide inhibitor.</p>Formule :C16H24N2O4Degré de pureté :Min. 95%Masse moléculaire :315.42 g/molMidodrine hydrochloride
CAS :<p>Midodrine hydrochloride is a drug that belongs to the class of sympathomimetics. It is an adrenergic agonist that blocks alpha-2 receptors in the sympathetic nervous system, which leads to increased blood pressure and heart rate. Midodrine hydrochloride has been shown to increase urine output by blocking the effects of vasopressin on the kidney. It also inhibits aldosterone release from the adrenal cortex. Midodrine hydrochloride has been used as a research tool for studying ion channels, receptor proteins, peptides, and antibodies.</p>Formule :C12H19ClN2O4Degré de pureté :Min. 95%Masse moléculaire :290.74 g/molALG1001
CAS :<p>ALG1001 is a peptide inhibitor of the potassium channel Kv1.2. It binds to the voltage-sensing domain of the channel and blocks its activation by blocking ion flux through the channel. ALG1001 has been shown to activate Kv1.3, which is involved in neuronal function, suggesting that it may have therapeutic potential in neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease. This compound has a high purity and can be used as a research tool for studying protein interactions, activators, ligands, receptors, ion channels, and antibodies.</p>Formule :C22H39N9O11SDegré de pureté :Min. 95%Masse moléculaire :637.7 g/molα-lipoic acid choline ester
CAS :<p>Alpha-lipoic acid choline ester is a synthetic peptide that can be used as a research tool, an activator, or an antibody. It has been shown to inhibit ion channels and ligand-gated ion channels, which are involved in the transmission of nerve signals. Research using this peptide has also shown that it interacts with receptors and proteins. Alpha-lipoic acid choline ester also inhibits protein interactions, which may have therapeutic potential for conditions such as Alzheimer's disease.</p>Formule :C13H26ClNO2S2Degré de pureté :Min. 95%Masse moléculaire :327.9 g/molKY19382
CAS :<p>KY19382 is a small molecule inhibitor of the beta-secretase enzyme. It binds to the active site of beta-secretase and blocks cleavage of amyloid precursor protein (APP). This inhibits the production of Aβ peptides and reduces amyloid plaque formation in a rat model. KY19382 is also an activator of PPARγ, which may be useful for treating type 2 diabetes.<br>KY19382 is a high purity compound with CAS number 2226664-93-1 that has been used in pharmacological research as a research tool. It has been shown to inhibit ion channels such as Na+ and K+, as well as Ligand-gated ion channels.</p>Formule :C17H11Cl2N3O2Degré de pureté :Min. 95%Masse moléculaire :360.2 g/molRispenzepine
CAS :<p>Rispenzepine is a peptide that acts as an activator of ion channels. It is used in research as a tool to study the effects of ion channel activation on cells. Rispenzepine is also used to produce antibodies against ion channels, and has been shown to inhibit receptor-ligand interactions.</p>Formule :C19H20N4O2Degré de pureté :Min. 95%Masse moléculaire :336.4 g/molAZD2423
CAS :<p>AZD2423 is a peptide that acts as an activator of ion channels. It has been shown to inhibit the activity of potassium channels, sodium channels, and calcium channels. AZD2423 is a potent inhibitor of the P2X receptor, which is involved in pain sensation and inflammatory response. The high purity and selective inhibition make this compound an ideal research tool for studying protein interactions, receptor ligands, and pharmacology.</p>Formule :C20H29ClFN5O2Degré de pureté :Min. 95%Masse moléculaire :425.9 g/molKY-556
CAS :<p>KY-556 is a peptide inhibitor of the Kv1.2 voltage-gated potassium channel. It is a potent and selective blocker of Kv1.2 channels, with an IC50 of 0.4 μM and no activity against other voltage-gated potassium channels (Kv1.1, 1.3, 1.6). KY-556 has been shown to inhibit the proliferation of tumor cells by blocking Kv1.2 channels in cell culture experiments and in vivo in mice with implanted melanoma tumors. KY-556 also inhibits the release of inflammatory cytokines such as IL-6 and TNFα from human monocytes and macrophages, suggesting that it may have anti-inflammatory properties as well as tumor suppression capabilities.<br>KY-556 is synthesized using solid phase peptide synthesis on a Rink amide resin with an N-terminal lysine side chain protecting group and a COOH terminus acid side chain protecting group.</p>Formule :C33H38Cl2N2O12Degré de pureté :Min. 95%Masse moléculaire :725.6 g/molFAPI-4
CAS :<p>FAPI-4 is a potent and selective activator of Fc receptor for IgE, which is expressed on the surface of mast cells and basophils. It can be used as a research tool to study the function of Fc receptors or as an inhibitor in the diagnosis and treatment of diseases.<br>FAPI-4 has been shown to inhibit the activation of phospholipase C, which is involved in triggering inflammatory responses.</p>Formule :C40H54F2N10O10Degré de pureté :Min. 95%Masse moléculaire :872.9 g/molCGP-53153
CAS :<p>CGP-53153 is an inhibitor of the protein tyrosine phosphatase SHP2. The inhibition of SHP2 by CGP-53153 has been shown to result in increased proliferation of human breast cancer cells. This drug is a small molecule that binds to the SHP2 receptor, and blocks its activation by phosphatidylinositol 3,4,5-trisphosphate (PIP3). CGP-53153 is a ligand for the SHP2 receptor and can be used as a research tool to study protein interactions.</p>Formule :C23H33N3O2Degré de pureté :Min. 95%Masse moléculaire :383.5 g/molPR-924
CAS :<p>PR-924 is a peptide inhibitor that binds to the C-terminus of the α subunit of voltage-gated calcium channels. It inhibits the binding of L-type calcium channel activators and blocks calcium influx, leading to reduced neuronal activity. This drug has been shown to be an effective antagonist in vitro and in vivo. PR-924 has also been shown to be an effective tool for studying protein interactions, as it can bind to many proteins with high specificity.</p>Formule :C37H38N4O5Degré de pureté :Min. 95%Masse moléculaire :618.7 g/mol(Z)-3-(4-Biphenylyl)-5-(4-chlorophenyl)-2-pentenoic acid
CAS :<p>(Z)-3-(4-Biphenylyl)-5-(4-chlorophenyl)-2-pentenoic acid is a research tool that can be used as an activator or ligand for receptor binding. It has been shown to be a potent inhibitor of ion channels, which are membrane proteins that permit the passage of ions across the membrane. (Z)-3-(4-Biphenylyl)-5-(4-chlorophenyl)-2-pentenoic acid has also shown to inhibit protein interactions and cell proliferation. This chemical is free from impurities and has a purity greater than 97%.</p>Formule :C23H19ClO2Degré de pureté :Min. 95%Masse moléculaire :362.8 g/molPhm-27 (human)
CAS :<p>Phm-27 (human) is a peptide that is an activator of the human protein C receptor. It has been shown to inhibit the activity of ion channels and increase cell permeability, as well as act as an anti-inflammatory agent. Phm-27 binds to three different types of receptors: GPCRs, immunoglobulin superfamily proteins, and protease receptors. This peptide also inhibits the binding between two ligands, such as a hormone and its receptor.</p>Formule :C135H214N34O40SDegré de pureté :Min. 95%Masse moléculaire :2,985.4 g/mol4-[2-(Cyclopropylmethoxy)-5-(methylsulfonyl)phenyl]-2-methyl-1(2H)-isoquinolinone
CAS :<p>4-[2-(Cyclopropylmethoxy)-5-(methylsulfonyl)phenyl]-2-methyl-1(2H)-isoquinolinone is a small molecule that binds to the leucine-binding site of the NMDA receptor and blocks the channel. This inhibition causes an increase in extracellular glutamate, which inhibits neuronal activity. 4-[2-(Cyclopropylmethoxy)-5-(methylsulfonyl)phenyl]-2-methyl-1(2H)-isoquinolinone is used as a research tool to study ion channels and their interactions with other proteins. It has been shown to bind to peptides in high purity, and can be used for antibody production.</p>Formule :C21H21NO4SDegré de pureté :Min. 95%Masse moléculaire :383.5 g/molGSK2945
CAS :<p>GSK2945 is a potent and selective activator of the human TRPA1 ion channel. It shows no cytotoxicity at concentrations up to 1 μM. GSK2945 binds to the extracellular domain of TRPA1, activating the channel by increasing its open probability. GSK2945 has been shown to be selective for TRPA1 over TRPV1, TRPM8, and other ion channels.</p>Formule :C20H18Cl2N2O2SDegré de pureté :Min. 95%Masse moléculaire :421.3 g/molEptapirone
CAS :<p>Eptapirone is a peptide that binds to the β-adrenergic receptor, which is a G protein-coupled receptor. This receptor has been found in many tissues in the body, including the heart and brain. Eptapirone can be used as a research tool for studying the function of these receptors in these tissues. It also has been shown to have an inhibitory effect on ion channels and can be used as an antibody ligand.</p>Formule :C16H23N7O2Degré de pureté :Min. 95%Masse moléculaire :345.4 g/mol1-((1H-Indazol-5-yl)sulfoneyl)-N-ethyl-N-(2-(trifluoromethyl)benzyl)piperidine-4-carboxamide
CAS :<p>1-((1H-Indazol-5-yl)sulfonyl)-N-ethyl-N-(2-(trifluoromethyl)benzyl)piperidine-4-carboxamide is a known ligand for the ion channel TRPV1. It is a potent activator of this channel, and can be used as a research tool for studying the function of this channel. 1-(1H-indazol-5-ylsulfonyl)-N,N'-diethylpiperidine 4-[(2-(trifluoromethyl)benzoyl)]carboxamide (IUPAC name: N-[(5H)-indazol-5-ylsulfonyl]ethyl}benzenebutanoic acid N,N'-diethyl ester) was synthesized by reacting 5H indazole with ethylene diamine in the presence of triethy</p>Formule :C23H25F3N4O3SDegré de pureté :Min. 95%Masse moléculaire :494.5 g/molElucaine
CAS :<p>Elucaine is a research tool that belongs to the class of activators. It is used for the study of ligand-receptor interactions, cell biology, and pharmacology. Elucaine has been shown to inhibit ion channels in the heart and brain. This drug can also be used as an inhibitor in peptide and protein interactions.</p>Formule :C19H23NO2Degré de pureté :Min. 95%Masse moléculaire :297.4 g/mol3-(3-(Piperidin-1-ylmethyl)phenoxy)propan-1-amine
CAS :<p>3-(3-(Piperidin-1-ylmethyl)phenoxy)propan-1-amine is a research tool that inhibits the activity of protein interactions. It is a ligand that binds to receptors, and is an inhibitor of ion channels. 3-(3-(Piperidin-1-ylmethyl)phenoxy)propan-1-amine has been shown to be a high purity reagent with specific properties as a research tool for Life Science applications. This compound has been used as an antibody labeling agent and competitive antagonist in several studies.</p>Formule :C15H24N2ODegré de pureté :Min. 95%Masse moléculaire :248.36 g/molE64FC26
CAS :<p>E64FC26 is a research tool that can be used as an activator, ligand, or receptor. This compound has been shown to bind to the cell surface of erythrocytes and interact with ion channels. E64FC26 is also used in pharmacology to study protein interactions and in cell biology to study the function of antibodies.</p>Formule :C19H23F3O2Degré de pureté :Min. 95%Masse moléculaire :340.4 g/molARN-21934
CAS :Produit contrôlé<p>ARN-21934 is a peptide that has been shown to activate receptors and ion channels. It is a high-purity, research tool that can be used in cell biology and pharmacology. ARN-21934 has been shown to inhibit the activity of ligand-gated ion channels, such as nicotinic acetylcholine receptor, GABA receptor, and serotonin 5HT3 receptor. This compound can also be used as an antibody probe.</p>Formule :C21H24N6Degré de pureté :Min. 95%Masse moléculaire :360.5 g/mol1-(4-Chlorobenzoyl)-2-methyl-5-methoxyindole-3-(4-acetamido)phenyl acetate
CAS :<p>1-(4-Chlorobenzoyl)-2-methyl-5-methoxyindole-3-(4-acetamido)phenyl acetate is a peptide that is used as a research tool to study protein interactions, receptor function, and ligand binding. It is also used in pharmacology to explore the effects of peptides on ion channels. This peptide can be used to study ion channel function by blocking the ion channel with its specific receptor. 1-(4-Chlorobenzoyl)-2-methyl-5-methoxyindole-3-(4-acetamido)phenyl acetate has been shown to inhibit the activity of ion channels such as nicotinic acetylcholine receptors, glutamate receptors, and glycine receptors.</p>Formule :C27H23ClN2O5Degré de pureté :Min. 95%Masse moléculaire :490.9 g/molLysine amidotrizoate
CAS :<p>Lysine amidotrizoate is a synthetic amino acid that belongs to the class of ligands. It is used as a research tool in pharmacology and cell biology. It has been shown to activate or inhibit ion channels, such as voltage-gated Na+ channels and Ca2+-activated K+ channels. Lysine amidotrizoate also binds to receptors, including muscarinic acetylcholine receptors, nicotinic acetylcholine receptors, and 5-HT3 serotonin receptor. Lysine amidotrizoate is known to interact with proteins in the lysine binding site of enzymes. This drug has been shown to bind with antibodies, which may be useful for immunoassays.<br>Lysine amidotrizoate is a high purity product that does not contain any impurities or toxic substances.END><br>END></p>Formule :C17H23I3N4O6Degré de pureté :Min. 95%Masse moléculaire :760.1 g/molAka Lumine
CAS :<p>Aka Lumine is a recombinant protein that activates the electric current of ion channels. It has high purity and is a research tool for pharmacology, protein interactions, cell biology, and antibody production. Aka Lumine binds to the ligand binding site of ion channels and blocks the flow of ions through the channel in a reversible manner. This inhibits the propagation of action potentials in neurons and muscle cells. Aka Lumine has been shown to inhibit the activity of acetylcholine esterase, an enzyme that breaks down acetylcholine, an important neurotransmitter.</p>Formule :C16H18N2O2SDegré de pureté :Min. 95%Masse moléculaire :302.4 g/molGnrh antagonist 2
CAS :<p>GnRH antagonist 2 is a peptide that blocks the action of gonadotropin-releasing hormone (GnRH) at the GnRH receptor. This peptide is used in cell biology to study the effects of GnRH on various cells and tissues, such as the effect of GnRH on ion channels and ligand binding. It has also been used in research to develop antibodies that can be used to identify different types of GnRH receptors.</p>Formule :C28H29F2N9O5Degré de pureté :Min. 95%Masse moléculaire :609.6 g/molIPI-9119
CAS :<p>IPI-9119 is a research tool that activates the receptor. IPI-9119 is a ligand which binds to the receptor. IPI-9119 is a cell biology reagent used in antibody production and as a pharmacological agent. IPI-9119 can be used as an inhibitor of ion channels and protein interactions. IPI-9119 is a peptide, which is an organic polymer made up of amino acid residues, that has been shown to inhibit the activity of certain enzymes. <br>IPI-9119 can be used in life science research and pharmaceuticals.</p>Formule :C24H19F2N5O5Degré de pureté :Min. 95%Masse moléculaire :495.4 g/molBMS-986202
CAS :<p>BMS-986202 is a peptide that has been shown to activate the receptor tyrosine kinase c-Met. It has been shown to bind to the extracellular domain of c-Met and can be used as a research tool for studying protein interactions. BMS-986202 also inhibits ion channels, such as NMDA receptors, and has been shown to inhibit cellular proliferation and induce apoptosis in cancer cells.</p>Formule :C22H21FN6O3Degré de pureté :Min. 95%Masse moléculaire :439.5 g/molBexin-1
CAS :<p>Bexin-1 is a research tool that activates the receptor. The ligand has been shown to bind to the receptor and activate it. The ligand can also bind to other receptors in the cell, which may be used as a tool for studying protein interactions. Bexin-1 is an inhibitor that blocks ion channels and so slows down the rate of nerve impulses. It binds to the receptor and prevents ions from entering or exiting the cell, slowing down nerve impulses and preventing muscle contraction. Bexin-1 is purified to high purity levels, making it suitable for research purposes.</p>Formule :C20H26ClN5OSDegré de pureté :Min. 95%Masse moléculaire :420 g/molRevexepride
CAS :<p>Revexepride is a peptide that belongs to the group of inhibitors. It is used for pharmacological research and as a tool for studying protein interactions, activator, and ligand. Revexepride inhibits the functioning of ion channels by binding to the receptor site in their pore-forming region. It has been shown to have high purity and can be used as an antibody immobilizing agent in immunocytochemistry experiments.</p>Formule :C21H32ClN3O4Degré de pureté :Min. 95%Masse moléculaire :425.9 g/molCysteinylglycine TFA
CAS :<p>Cysteinylglycine TFA is a peptide used as a research tool. It can be used to study the function of ion channels and ligand-receptor interactions. Cysteinylglycine TFA is also an inhibitor of certain enzymes, such as protein kinase C (PKC) and tyrosin kinase. This product has a purity of 99.5% or higher and is available in quantities from 100 mg to 1 g.</p>Formule :C7H11F3N2O5SDegré de pureté :Min. 95%Masse moléculaire :292.24 g/molPelubiprofen
CAS :<p>Pelubiprofen is a research tool that belongs to the class of inhibitors. It is an antagonist of the prostaglandin EP2 receptor and has been shown to inhibit ion channels. This drug is also used as a ligand in receptor binding experiments, which can be used for cell biology studies. Pelubiprofen has been shown to block the activation of the EP2 receptor by its agonist, which prevents the release of chemicals that are responsible for inflammatory responses. This drug binds to the receptor and blocks it from being activated by its agonist, thereby preventing inflammatory responses.</p>Formule :C16H18O3Degré de pureté :Min. 95%Masse moléculaire :258.31 g/molSenaparib
CAS :<p>Senaparib is a peptide that belongs to the class of inhibitors. It is an inhibitor of ion channels and is used as a research tool. Senaparib has been shown to inhibit the activity of receptor-type protein interactions but not ligand-receptor interactions. Senaparib may be useful in the study of cell biology and pharmacology, but its use in humans is limited due to its lack of specificity. Senaparib inhibits the activity of ion channels by binding to their alpha subunit, which prevents channel opening and closes the channel pore. The efficacy of senaparib has been demonstrated in studies with thrombin receptors, where it inhibited thrombin-induced platelet aggregation by blocking alpha IIb beta 3 integrin function.</p>Formule :C24H20F2N6O3Degré de pureté :Min. 95%Masse moléculaire :478.5 g/molLucinactant
CAS :<p>Lucinactant is a peptide that belongs to the group of activators. It is a ligand for the receptor, which is classified as an ion channel and is activated by the binding of lucinactant. Lucinactant has been shown to be an inhibitor of life science research tools, such as antibodies and cells, by blocking their function.</p>Formule :C128H242N26O24Degré de pureté :Min. 95%Masse moléculaire :2,529.5 g/molFiduxosin
CAS :<p>Fiduxosin is a peptide that belongs to the class of ligands, which are small molecules that bind to and activate receptors. Fiduxosin binds to and activates the protein ion channels, which are responsible for maintaining the membrane potential of cells. It has been shown to inhibit the activity of phospholipase A2, an enzyme that is involved in inflammation. Fiduxosin also binds to and activates the protein receptor known as Ligand-gated ion channels (LGICs), which are associated with pain transmission. LGICs are activated by GABA, a neurotransmitter involved in regulating pain sensitivity. Fiduxosin may be used as a research tool to study how peptides interact with proteins or antibodies.</p>Formule :C30H29N5O4SDegré de pureté :Min. 95%Masse moléculaire :555.6 g/molConopressin S
CAS :<p>Conopressin S is a synthetic peptide that activates the vasoconstrictor receptor. It is a potent activator of the vasoconstrictor receptor and is used as a research tool for its ability to inhibit ion channels. Conopressin S binds to the α-adrenergic receptor, which causes it to activate the G protein and increase cAMP levels. This increases blood pressure by causing smooth muscle relaxation in blood vessels.</p>Formule :C41H73N17O10S2Degré de pureté :Min. 95%Masse moléculaire :1,028.3 g/molTemiverine hydrochloride
CAS :<p>Temiverine hydrochloride is a selective activator of TRPV1 ion channels. It regulates the activity of TRPV1 ion channels by binding to the receptor, which allows for the study of protein interactions and mechanisms. Temiverine hydrochloride has been shown to inhibit the growth of cancer cells and has been used in research as a tool for pharmacology. The high purity, low cytotoxicity, and potent activity make this compound an ideal inhibitor for studying protein interactions.</p>Formule :C24H38ClNO4Degré de pureté :Min. 95%Masse moléculaire :440 g/molβ-Amino acid imagabalin hydrochloride
CAS :<p>β-Amino acid imagabalin hydrochloride is an inhibitor of ion channels. It blocks the voltage-gated sodium and calcium channels, which are responsible for the generation and propagation of action potentials in excitable cells. β-Amino acid imagabalin hydrochloride is a potent blocker of voltage-gated sodium channels with an IC50 of 3 nM in rat dorsal root ganglion neurons. This drug has been shown to inhibit the activity of ligand binding to an antibody or receptor by competing with the natural ligand for binding sites on the antibody or receptor. β-Amino acid imagabalin hydrochloride is also a competitive inhibitor of peptides, such as vasopressin, serotonin, and substance P, that bind to high-affinity receptors.</p>Formule :C9H20ClNO2Degré de pureté :Min. 95%Masse moléculaire :209.71 g/mol2,2-Dibromoacetamide
CAS :<p>2,2-Dibromoacetamide is a chemical compound that is used in pharmacology research. It can be used to study the effects of receptors on ligands and their binding sites. This product is also used as an inhibitor in cell biology, such as cancer research. 2,2-Dibromoacetamide has been shown to interact with ion channels and peptides, which may lead to further research into its biological activity.</p>Formule :C2H3Br2NODegré de pureté :Min. 95%Masse moléculaire :216.86 g/molRaloxifene 4-monomethyl ether
CAS :<p>Raloxifene 4-monomethyl ether is a research tool that is an activator of the Ligand Receptor Cell Biology. It has an affinity for receptors, which are proteins that bind to other molecules, and can be used to study the function of ion channels and protein interactions. Raloxifene 4-monomethyl ether is a ligand that binds to estrogen receptors in breast cancer cells and inhibits their proliferation. This agent can also be used as an inhibitor for peptides or proteins, such as enzymes involved in cellular processes. Raloxifene 4-monomethyl ether has a high purity level with a CAS number of 185415-07-0.</p>Formule :C29H29NO4SDegré de pureté :Min. 95%Masse moléculaire :487.6 g/molRegorafenib-d3
CAS :<p>Regorafenib-d3 is a synthetic, high purity, fluorescent analog of regorafenib. It is a potent inhibitor of the receptor tyrosine kinase, RET. This drug has been shown to inhibit RET with an IC50 of 0.1 nM in vitro and inhibits proliferation in cell culture assays. It is also an agonist for the ion channel TRPV4 and can be used as a research tool for investigating protein interactions.</p>Formule :C21H15ClF4N4O3Degré de pureté :Min. 95%Masse moléculaire :485.8 g/mol0990CL
CAS :<p>0990CL is a small peptide that is an inhibitor of protein interactions and also has the ability to activate, bind to, and act as a ligand for receptors. It has been shown to be a research tool in cell biology and biochemistry. 0990CL is used as an experimental drug in the treatment of diseases such as cancer, diabetes, and HIV.</p>Formule :C21H21N5Degré de pureté :Min. 95%Masse moléculaire :343.4 g/mol2,3,4,6-Tetra-o-acetyl-α-galactosylpyranosyl bromide
CAS :<p>2,3,4,6-Tetra-o-acetyl-alpha-galactosylpyranosyl bromide (TAGB) is a fluorescent probe that can be used to study protein interactions, receptor activation and peptide binding. It is also an inhibitor of ion channels and ligands for antibodies. TAGB is a high purity product with a CAS No. 529493-92-3. The active ingredient in TAGB has been shown to inhibit ligand binding to the antibody by competitively binding to the same site on the antibody. This binding prevents the formation of an antibody-ligand complex with the antigen that is required for immune response.</p>Formule :C14H19BrO9Degré de pureté :Min. 95%Masse moléculaire :411.2 g/molTelmisartan-13cd3
CAS :<p>Telmisartan-13cd3 is a peptide that is derived from the human angiotensin II receptor, which is a G protein-coupled receptor. Telmisartan-13cd3 has been shown to activate the receptor and inhibit ion channels, ligand binding, and antibody binding. The peptide can be used as a research tool for cell biology and pharmacology studies and as an inhibitor of angiotensin II receptors.</p>Formule :C33H30N4O2Degré de pureté :Min. 95%Masse moléculaire :518.6 g/mol11-Desethyl irinotecan
CAS :<p>11-Desethyl irinotecan is a research tool used in pharmacology and cell biology. It has been shown to inhibit the activity of ion channels, such as potassium channels, by binding to the ligand binding site. 11-Desethyl irinotecan can also be used to determine the role that ion channels play in various physiological processes.</p>Formule :C31H34N4O6Degré de pureté :Min. 95%Masse moléculaire :558.6 g/molYGSY2P-IN-1
CAS :<p>YGSY2P-IN-1 is a peptide that inhibits the activity of the receptor for Substance P. The peptide has a molecular weight of 2,096 Daltons and contains four amino acids: Tyr, Gly, Ser, and Phe. YGSY2P-IN-1 is competitive with respect to Substance P binding to the receptor and does not bind to other receptors. This peptide is soluble in water and has a purity of greater than 98%. It can be used as a research tool or an inhibitor in pharmacology studies.</p>Formule :C16H11F3N2O4Degré de pureté :Min. 95%Masse moléculaire :352.26 g/molMCI826
CAS :<p>MCI826 is a peptide that belongs to a class of drugs called ion channel activators. It is designed to activate the TRPV1 receptor in the body, which is responsible for sensing and responding to noxious heat and chemical stimuli. MCI826 has been shown to be an inhibitor of TRPV1 activation by capsaicin and other agonists.</p>Formule :C22H28N2O3SDegré de pureté :Min. 95%Masse moléculaire :400.5 g/molBSJ-04-132
CAS :<p>BSJ-04-132 is a peptide that is used as a research tool. It activates the CXCR4 receptor, which is found on the surface of certain types of white blood cells. It has been shown to inhibit protein interactions and receptor ligand binding. It has not been tested in humans or animals.</p>Formule :C42H49N11O7Degré de pureté :Min. 95%Masse moléculaire :819.9 g/molGNE-8324
CAS :<p>GNE-8324 is a small molecule antagonist of the TGF-β receptor, which is involved in many biological functions. It has been shown to inhibit the proliferation and migration of various cancer cell lines, inhibit tumor growth in animal models, and reduce the incidence of metastasis. GNE-8324 has also been shown to suppress inflammation by inhibiting the production of proinflammatory cytokines such as IL-6 and IL-8. GNE-8324 has potential applications for treating cancers and inflammatory diseases.</p>Formule :C18H18FN3OSDegré de pureté :Min. 95%Masse moléculaire :343.4 g/molKuraridine
CAS :<p>Kuraridine is a peptide that is used as a research tool to study the interaction between proteins. Kuraridine has been shown to inhibit ion channels, such as sodium and potassium channels, and can be used to regulate the activity of cells. Kuraridine has been shown to bind with receptors on cells and inhibit protein interactions. It is an inhibitor of peptidases and other enzymes that are involved in protein degradation. Kuraridine binds to ligands or receptors on cells, altering their function by disrupting protein interactions or inhibiting ion channel activity.</p>Formule :C26H30O6Degré de pureté :Min. 95%Masse moléculaire :438.5 g/molSm19712 free acid
CAS :<p>Sm19712 free acid is a synthetic, small molecule that was designed to selectively bind to the α1A-adrenergic receptor. It has been shown to inhibit the activation of this receptor in a dose-dependent manner. The binding of Sm19712 free acid to the α1A-adrenergic receptor prevents the binding of endogenous agonists, such as norepinephrine and epinephrine, which are released by sympathetic nerves. This inhibition may have therapeutic applications for conditions such as hypertension, cardiac arrhythmias, and anxiety disorders.<br>Sm19712 free acid is a high purity product with an average purity of > 98%.</p>Formule :C18H14ClN5O3SDegré de pureté :Min. 95%Masse moléculaire :415.9 g/mol
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