Compuestos y reactivos bioquímicos

<p>Peptide H-SANSNP^AMAPRERKAGCKNFFWKTFTSC-OH is a Research Peptide with significant interest within the field academic and medical research. This peptide is available for purchase at Cymit Quimica in multiple sizes and with a specification of your choice.</p>

<p>H-WKNDMVDQMHEDVIS-OH is a custom peptide that can be synthesized rapidly by our peptide experts in under 2 weeks. H-WKNDMVDQMHEDVIS-OH is provided at greater that &gt;80% purity (HPLC) from Cymit Quimica for a variety of research applications. We also offer H-WKNDMVDQMHEDVIS-OH in bulk quantities in addition to our standard pack sizes.Please enquire for more information about H-WKNDMVDQMHEDVIS-OH at the technical inquiry form on this page</p>

<p>Inhibitor of FLT3 receptor tyrosine kinases; anti-neoplastic</p>

<p>Alpha1-adrenoceptor antagonist; for treatment of benign prostatic hyperplasia</p>

<p>Agonist of alpha-2-adrenoceptor</p>

<p>Oxcarbazepine metabolite; anticonvulsant; sodium channel blocker</p>

<p>H-WGIKQLQARILAVER-OH is a custom peptide that can be synthesized rapidly by our peptide experts in under 2 weeks. H-WGIKQLQARILAVER-OH is provided at greater that &gt;80% purity (HPLC) from Cymit Quimica for a variety of research applications. We also offer H-WGIKQLQARILAVER-OH in bulk quantities in addition to our standard pack sizes.Please enquire for more information about H-WGIKQLQARILAVER-OH at the technical inquiry form on this page</p>

<p>A potent prostanoid receptor (FP) agonist and PGF2α analog. Its biological activity is mediated by action on prostamide receptors. Has therapeutic potential for glaucoma and ocular hypertension.</p>

<p>H-GASETIANIYTT-OH is a custom peptide that can be synthesized rapidly by our peptide experts in under 2 weeks. H-GASETIANIYTT-OH is provided at greater that &gt;90% purity (HPLC) from Cymit Quimica for a variety of research applications. We also offer H-GASETIANIYTT-OH in bulk quantities in addition to our standard pack sizes.Please enquire for more information about H-GASETIANIYTT-OH at the technical inquiry form on this page</p>

<p>Peptide Ac-QEQLERALNSS-OH is a Research Peptide with significant interest within the field academic and medical research. This peptide is available for purchase at Cymit Quimica in multiple sizes and with a specification of your choice.</p>

<p>H-Arg-Lys-OH acetate salt is a cyclic peptide that has been shown to have antimicrobial activity. It is an immunomodulator that has been shown to reduce the progression of autoimmune diseases by regulating the production of IgG, IgM and IgA. This drug is also a potent inhibitor of 2-adrenergic receptors in neuro2a cells and inhibits the release of IGF-I. H-Arg-Lys-OH acetate salt has been shown to be effective against infectious diseases such as meningitis, bronchitis, and pneumonia. It also inhibits proteolytic enzymes produced by bacteria, which may result in tissue damage.</p>

<p>Custom research peptide; min purity 95%. For different specs please use the Peptide Quote Tool</p>

<p>Peptide H-AKPALEDL^R-OH is a Research Peptide with significant interest within the field academic and medical research. This peptide is available for purchase at Cymit Quimica in multiple sizes and with a specification of your choice.</p>

<p>Rotigaptide is a synthetic peptide that has been shown to inhibit the activity of the cell factor, which is responsible for regulating the heart. This drug may be used in the treatment of congestive heart failure, as well as other cardiac disorders such as atrial and myocardial infarcts. Rotigaptide has been found to have pharmacological properties that are similar to those of angiotensin II or angiotensin converting enzyme (ACE) inhibitors. The drug also exhibits anti-platelet activity and may be useful in treating structural heart disease.</p>

<p>FP receptor ligand; activator of PGF2αR</p>

<p>H-TGEIIGDIRQAHCNL-OH is a custom peptide that can be synthesized rapidly by our peptide experts in under 2 weeks. H-TGEIIGDIRQAHCNL-OH is provided at greater that &gt;80% purity (HPLC) from Cymit Quimica for a variety of research applications. We also offer H-TGEIIGDIRQAHCNL-OH in bulk quantities in addition to our standard pack sizes.Please enquire for more information about H-TGEIIGDIRQAHCNL-OH at the technical inquiry form on this page</p>

<p>H-IEVASSVK-OH is a custom peptide that can be synthesized rapidly by our peptide experts in under 2 weeks. H-IEVASSVK-OH is provided at greater that &gt;95% purity (HPLC) from Cymit Quimica for a variety of research applications. We also offer H-IEVASSVK-OH in bulk quantities in addition to our standard pack sizes.Please enquire for more information about H-IEVASSVK-OH at the technical inquiry form on this page</p>

<p>Ac-CKGPNVAAIVGGTVV-NH2 is a custom peptide that can be synthesized rapidly by our peptide experts in under 2 weeks. Ac-CKGPNVAAIVGGTVV-NH2 is provided at greater that &gt;90% purity (HPLC) from Cymit Quimica for a variety of research applications. We also offer Ac-CKGPNVAAIVGGTVV-NH2 in bulk quantities in addition to our standard pack sizes.Please enquire for more information about Ac-CKGPNVAAIVGGTVV-NH2 at the technical inquiry form on this page</p>

<p>Imiquimod is a toll-like receptor 7 agonist drug that is used for the treatment of genital warts, basal cell carcinoma and condyloma acuminata. This drug works by relieving and controlling wart production. Studies in mice have shown that this drug may induce cytokines such as interleukins. Imiquimod helps to increase apoptosis of diseased tissues and an infiltration of lymphocytes into tumor lesions.</p>

<p>Cardiac Troponin Complex Chimeric Mouse Monoclonal Antibody, Recombinant</p>

<p>Elesclomol is an investigational anticancer agent, which is a small-molecule compound. It functions by targeting the cellular oxidative stress pathway; specifically, it enhances the production of reactive oxygen species (ROS) within cancer cells. By elevating ROS levels beyond the threshold tolerable by cancer cells, Elesclomol induces apoptosis through the disruption of mitochondrial function, making it selective for environments with heightened oxidative stress.</p>

<p>Potent inhibitor of dual specificity tyrosine-phosphorylation-regulated kinase 3 (DYRK3) with IC50 value of 0.7 nM. Elevates hemoglobin and platelet levels in anemic mice.</p>

<p>Modifier of the SMN2 gene splicing</p>

<p>Ac-GTLTVTSTLPC-NH2 is a custom peptide that can be synthesized rapidly by our peptide experts in under 2 weeks. Ac-GTLTVTSTLPC-NH2 is provided at greater that &gt;95% purity (HPLC) from Cymit Quimica for a variety of research applications. We also offer Ac-GTLTVTSTLPC-NH2 in bulk quantities in addition to our standard pack sizes.Please enquire for more information about Ac-GTLTVTSTLPC-NH2 at the technical inquiry form on this page</p>

<p>Prasugrel is a thienopyridine prodrug that inhibits the enzyme ADP-dependent P2Y purinergic receptor. Prasugrel inhibits platelet aggregation and the formation of blood clots by blocking the conversion of ADP to ATP on the surface of platelets, thus preventing the release of serotonin from platelets. The reaction products formed by prasugrel are similar to those formed by clopidogrel and include hydrogen sulfate ions and a thiol-containing metabolite. It has also been shown to have potent cytotoxic activity against melanoma cells and anti-inflammatory properties. <br>Prasugrel 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&amp;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>

<p>H-CNEKGMSSRRKESSD-OH is a custom peptide that can be synthesized rapidly by our peptide experts in under 2 weeks. H-CNEKGMSSRRKESSD-OH is provided at greater that &gt;95% purity (HPLC) from Cymit Quimica for a variety of research applications. We also offer H-CNEKGMSSRRKESSD-OH in bulk quantities in addition to our standard pack sizes.Please enquire for more information about H-CNEKGMSSRRKESSD-OH at the technical inquiry form on this page</p>

<p>Inhibitor of 5-lipoxygenase activating protein_x000D_</p>

<p>GLP-1 (9-36) amide trifluoroacetate is a bioactive peptide fragment derived from the full-length glucagon-like peptide-1 (GLP-1), an incretin hormone. It is typically obtained through enzymatic cleavage or synthetic processes involving solid-phase peptide synthesis. The mode of action of GLP-1 (9-36) amide involves binding to and modulating GLP-1 receptors, although it lacks the insulinotropic activity of its precursor GLP-1 (7-36) amide, making it a valuable tool for studying distinct signaling pathways and metabolic effects.</p>

<p>Peptide H-YML^DLQPETT-OH is a Research Peptide with significant interest within the field academic and medical research. This peptide is available for purchase at Cymit Quimica in multiple sizes and with a specification of your choice.</p>

<p>Ac-CDADLKDVNVIPATA-OH is a custom peptide that can be synthesized rapidly by our peptide experts in under 2 weeks. Ac-CDADLKDVNVIPATA-OH is provided at greater that &gt;90% purity (HPLC) from Cymit Quimica for a variety of research applications. We also offer Ac-CDADLKDVNVIPATA-OH in bulk quantities in addition to our standard pack sizes.Please enquire for more information about Ac-CDADLKDVNVIPATA-OH at the technical inquiry form on this page</p>

<p>Inhibitor of ataxia telangiectasia mutated (ATM) kinase and AKT kinase with anti-cancer activity. ATM is a nuclear protein kinase and a signal transducer sensing DNA damage as well as controlling double strand DNA break (DSB) repair. It is a radiotherapy and chemotherapy sensitizer, especially in tumors sensitive to DNA alkylating agents (such as temozolomide). Moreover, KU 55933 inhibits phosphorylation of cytoplasmic AKT kinase, downregulates synthesis of cyclin D1 and induces cell cycle arrest in G1 phase.</p>

<p>An agonist of 5-HT1A serotonin receptors. Neurotrophic and neuroprotective activities have been demonstrated in neurodegenerative models in vivo. This is mediated by increasing the secretion of nerve growth factor (NGF), when tested in astrocytes in vitro. Anti-nociceptive activity was displayed in a model of acute tonic nociceptive and inflammatory pain.</p>

<p>Suc-Ala-Ala-Pro-Trp-pNA is a peptide that is used as a substrate for elastase. This peptide has been shown to be an effective substrate for this enzyme, with a Km of 0.8 mM and an kcat of 2.6 x 10 M/s. Suc-Ala-Ala-Pro-Trp-pNA is also used as a substrate for pancreatic enzymes such as trypsin and chymotrypsin, with Km values of 1.1 and 0.5 mM respectively. It has been shown to inhibit the activity of these enzymes by forming inactive complexes with them.</p>

<p>Antagonist of α-adrenoceptors; vasoactive agent</p>

<p>Ac-Asp-Glu-Val-Asp-AMC ammonium salt is a small molecule that is used as a tool to study apoptosis in vitro. Ac-Asp-Glu-Val-Asp-AMC ammonium salt induces apoptosis by blocking the mitochondrial membrane potential and inducing the release of cytochrome c from mitochondria into the cytoplasm. This drug also induces activation of caspase 3, which initiates the cascade of events leading to cell death. Ac-Asp-Glu-Val-Asp-AMC ammonium salt has been shown to have an antiangiogenic effect on hl60 cells. This effect may be due to its ability to inhibit expression of survivin, a protein that protects cells from apoptosis. The efficacy of this drug in an experimental model has been shown to be dependent on toll like receptor (TLR) signaling pathways and mitochondrial function.br&gt;</p>

<p>Peptide LCBiot-GSTSGSGKPGSGEGSTKG-NH2 is a Research Peptide with significant interest within the field academic and medical research. This peptide is available for purchase at Cymit Quimica in multiple sizes and with a specification of your choice.</p>

<p>Fmoc-Trp(Boc)-Ser(Psi(Me,Me)pro)-OH is a versatile building block that can be used in the synthesis of complex compounds. Fmoc-Trp(Boc)-Ser(Psi(Me,Me)pro)-OH is a high quality compound with a CAS No. 908601-15-0. This compound is useful as an intermediate or research chemical and can be used as a useful scaffold for making new compounds.</p>

<p>Pomalidomide is an immunomodulatory agent that inhibits transcriptional regulation by interacting with the pomalidomide-binding protein, which prevents its interaction with RNA polymerase II and thereby prevents DNA transcription. The study with U266 cells demonstrated that pomalidomide targets CRBN, part of an E3 ligase complex, and inhibits its autoubiquinitation and supresses a critical gene (IRF4, interferon regulatory factor 4) for myeloma cell growth with concentrations up to 10 μM. In vitro assays have shown that pomalidomide has inhibitory effects on cell signaling pathways, such as the NF-κB pathway. Pomalidomide also decreases the production of proinflammatory cytokines, such as TNFα and IL-1β, by inhibiting their synthesis or their release from activated monocytes. Recently, the promoting effect of pomalidomide, as its analog lenalidomide, on erythropoiesis (production of red blood cells) has been investigated, demonstrating positive results for its use as a potential new therapy agent for β-hemoglobinopathies.<br>Pomalidomide 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&amp;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>

<p>Orexin A (human) TFA is a high quality reagent that can be used as an intermediate in the synthesis of complex compounds, useful for research and development. It has many potential uses, including as a fine chemical, speciality chemical and reaction component. Orexin A (human) TFA is a versatile building block with many applications, such as being a useful scaffold or building block in reactions where it can be used in the synthesis of other compounds. It is also a valuable research chemical that can be used to study orexin receptors and their ligands.</p>

<p>Protein found in egg white</p>

<p>Alpha-conotoxin ImI is a peptide that belongs to the class of alpha-conotoxins. It is an activator of nicotinic acetylcholine receptors, which inhibit voltage-gated calcium channels. The high purity of this product allows for its use in research and development. Alpha-conotoxin ImI has been used to study protein interactions and receptor pharmacology.</p>

<p>Serotonin 5-HT4 receptor agonist</p>

<p>Please enquire for more information about (Asn(4-aminobutyl)1·7·23,Gln(4-aminobutyl)3·11·22)-Amyloid b-Protein (1-40) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>C.I.Mordant green 4 is a dye that is used in the textile industry for dyeing wool and silk. It is an organic compound classified as an azo dye. C.I. Mordant green 4 is used to dye wool, cotton, and other natural fibers in shades of green or blue-green depending on the pH of the solution. The color can also be changed by adding different chemicals such as potassium bichromate or hydrogen peroxide. This product has a particle size of less than 0.1 microns and its color varies depending on the pH of the solution it is added to.br&gt;<br>br&gt;<br>C.I. Mordant green 4 may be absorbed through skin contact and may cause irritation, dermatitis, allergic reactions, or photosensitivity in some people.br&gt;br&gt;<br>Coding: <br>1) Section <br>2) Plant diseases <br>3) Magnetic <br>4) Human immunodeficiency</p>

<p>Peptide Decanoyl-RWKFGGFKWR-OH is a Research Peptide with significant interest within the field academic and medical research. This peptide is available for purchase at Cymit Quimica in multiple sizes and with a specification of your choice.</p>

<p>Prasugrel is a thienopyridine prodrug that inhibits the enzyme ADP-dependent P2Y purinergic receptor. Prasugrel inhibits platelet aggregation and the formation of blood clots by blocking the conversion of ADP to ATP on the surface of platelets, thus preventing the release of serotonin from platelets. The reaction products formed by prasugrel are similar to those formed by clopidogrel and include hydrogen sulfate ions and a thiol-containing metabolite. It has also been shown to have potent cytotoxic activity against melanoma cells and anti-inflammatory properties.</p>

<p>Peptide H-KKKKKKWLGSALIGALLPSVVGLFQ-NH2 is a Research Peptide with significant interest within the field academic and medical research. This peptide is available for purchase at Cymit Quimica in multiple sizes and with a specification of your choice.</p>

<p>GSK-lsd1 dihydrochloride is a potent chemical inhibitor, which is derived synthetically to target LSD1, a histone demethylase involved in epigenetic regulation. It functions by inhibiting the enzymatic activity of LSD1, thereby affecting the methylation status of histones, a critical process in regulating gene expression. This inhibition leads to alterations in the transcriptional programs of cells, particularly those in oncogenic pathways.</p>

<p>Myelin PLP (180-199) is a peptide that has been shown to be immunogenic and biochemically active. It belongs to the group of peptides and biochemicals, which are organic compounds of high molecular weight. Myelin PLP (180-199) is an immunogenic compound that can be used as a vaccine adjuvant. It also has been shown to have anti-inflammatory activities, which may be due to its ability to inhibit prostaglandin synthesis.</p>

<p>N-MCT is an analog of a naturally occurring protein found in human urine that has been shown to have potent anticancer properties. It works by inhibiting specific kinases involved in cancer cell growth and promoting apoptosis, or programmed cell death, in cancer cells. N-MCT has been studied extensively for its potential as a medicinal inhibitor of tumor growth and has shown promising results in preclinical trials. This compound has the ability to disrupt the cell cycle of cancer cells, preventing them from dividing and spreading throughout the body. Its unique mechanism of action makes it a promising candidate for future cancer therapies.</p>