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(98.572 produits)
- Par Biological Target(100.755 produits)
- Par usage/effets pharmacologiques(6.938 produits)
- Cryoconservation et composés associés aux cryoconservateurs(21 produits)
- Désinfectants, additifs pour les fluides pour bains chauffants et composés apparentés(28 produits)
- Hormones(467 produits)
- Biologie végétale(6.906 produits)
- Métabolites secondaires(14.368 produits)
130507 produits trouvés pour "Produits biochimiques et réactifs"
Trier par
Degré de pureté (%)
0
100
|
0
|
50
|
90
|
95
|
100
nNOS antibody
nNOS antibody was raised in rabbit using residues 19-31 [PRKGPPLPNGDTEC] of NOS as the immunogen.Degré de pureté :Min. 95%GMF beta protein
Region of GMF beta protein corresponding to amino acids SESLVVCDVA EDLVEKLRKF RFRKETNNAA IIMKIDKDKR LVVLDEELEG ISPDELKDEL PERQPRFIVY SYKYQHDDGR VSYPLCFIFS SPVGCKPEQQ MMYAGSKNKL VQTAELTKVF EIRNTEDLTE EWLREKLGFF H.Degré de pureté :Min. 95%RUFY1 antibody
The 6-Fluoro-3-indoxyl-beta-D-galactopyranoside is a powerful antituberculosis drug belonging to the class of rifamycins. It is known for its bactericidal activity against tuberculosis infection and has been extensively studied using advanced techniques like transcription-quantitative polymerase chain and patch-clamp technique. This active compound exhibits oxidative metabolites and undergoes hydrolysis by esterases, reduction by glutathione reductase, and oxidation by cytochrome p450 enzymes. It specifically targets Mycobacterium tuberculosis strains and inhibits cell growth in culture.Goat RBC antibody (Texas Red)
Goat RBC antibody (Texas Red) was raised in rabbit using goat erythrocytes as the immunogen.MAPK1 protein (His tag)
1-360 amino acids: MGSSHHHHHH SSGLVPRGSH MAAAAAAGAG PEMVRGQVFD VGPRYTNLSY IGEGAYGMVC SAYDNVNKVR VAIKKISPFE HQTYCQRTLR EIKILLRFRH ENIIGINDII RAPTIEQMKD VYIVQDLMET DLYKLLKTQH LSNDHICYFL YQILRGLKYI HSANVLHRDL KPSNLLLNTT CDLKICDFGL ARVADPDHDH TGFLTEYVAT RWYRAPEIML NSKGYTKSID IWSVGCILAE MLSNRPIFPG KHYLDQLNHI LGILGSPSQE DLNCIINLKA RNYLLSLPHK NKVPWNRLFP NADSKALDLL DKMLTFNPHK RIEVEQALAH PYLEQYYDPS DEPIAEAPFK FDMELDDLPK EKLKELIFEE TARFQPGYRSDegré de pureté :Min. 95%TXNDC5 Blocking Peptide
A synthetic peptide for use as a blocking control in assays to test for specificity of TXNDC5 antibody, catalog no. 70R-2551Degré de pureté :Min. 95%PEDX 4
CAS :PEDX-4 is a peptide that binds to the nicotinic acetylcholine receptor (nAChR). It blocks the nAChR by competing with acetylcholine for binding. PEDX-4 is a cell-permeable, high purity compound with a CAS number of 644990-68-1. This peptide can be used as a research tool in pharmacology and protein interactions. PEDX-4 has been shown to inhibit the activity of nAChRs in cells.Degré de pureté :Min. 95%Hsp90 α, His tagged human
CAS :Hsp90 α is a protein that belongs to the heat shock protein 90 family. It is involved in the regulation of energy metabolism, protein synthesis and cell physiology. Hsp90 α has been shown to be an important regulator of cellular function, such as cellular proliferation and differentiation. This protein binds to a number of natural compounds and drugs, including inhibitors that can regulate its activity. Hsp90 α has been shown to play a role in hyperproliferative diseases such as cancer because it regulates the expression of hsp90 target genes.Degré de pureté :Min. 95%Metazin
CAS :Metazin is a Chinese medicinal analog that has shown significant potential as an anticancer agent. It is a potent inhibitor of cyclin-dependent kinases, which are enzymes that regulate the cell cycle and play a critical role in tumor growth. Metazin has been shown to induce apoptosis in cancer cells, leading to their death and regression of tumors. This protein inhibitor is derived from human urine and has been extensively studied for its ability to inhibit cancer cell growth. In preclinical studies, Metazin has demonstrated promising results against a range of tumor types, making it a promising candidate for further development as an anticancer therapy.Formule :C11H19N7Degré de pureté :Min. 95%Masse moléculaire :249.32 g/mol1,2-Dipalmitoyl-3-decanoyl-rac-glycerol
CAS :Please enquire for more information about 1,2-Dipalmitoyl-3-decanoyl-rac-glycerol including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C45H86O6Degré de pureté :Min. 95%Masse moléculaire :723.2 g/molEletriptan hydrobromide
CAS :Eletriptan hydrobromide is a medicinal compound that has been found to have anticancer properties. It works by inhibiting the activity of certain proteins, such as kinases, which are involved in the growth and survival of cancer cells. Studies have shown that Eletriptan hydrobromide can induce apoptosis (cell death) in human and Chinese hamster ovary tumor cells, and can also inhibit cell cycle progression. This compound is an analog of other protein kinase inhibitors that have been used in cancer treatment. Eletriptan hydrobromide has potential therapeutic applications for various types of cancer and is currently being studied for its efficacy in treating different malignancies.Formule :C22H29BrN2O3SDegré de pureté :Min. 95%Masse moléculaire :481.4 g/molSpirohexenolide A
CAS :Spirohexenolide A is a potent inhibitor of cancer cell replication. It has been shown to inhibit the growth of various types of cancer cells, including those found in human tumors and urine. This compound works by inhibiting the activity of kinases, which are enzymes that play a key role in cell division and proliferation. Spirohexenolide A is an analog of methotrexate, a chemotherapy drug commonly used to treat cancer. However, unlike methotrexate, spirohexenolide A does not cause significant toxicity or side effects. Studies have also shown that spirohexenolide A can induce apoptosis (programmed cell death) in cancer cells, making it a promising candidate for cancer therapy. Additionally, this compound has been found to be a potent inhibitor of astaxanthin kinase in Chinese hamster ovary cells.Formule :C25H28O5Degré de pureté :Min. 95%Masse moléculaire :408.5 g/mol2-Eicosenoic acid
CAS :2-Eicosenoic acid is a medicinal compound that has shown potential as an anticancer agent. It works by inhibiting the activity of kinases, which are enzymes that regulate cell growth and division. Studies have shown that this compound can induce apoptosis (programmed cell death) in cancer cells, making it a promising candidate for cancer treatment. Additionally, 2-Eicosenoic acid has been found to inhibit the growth of tumors in Chinese hamsters and reduce protein levels in urine samples from cancer patients. This compound is an analog of xylan, a complex carbohydrate found in plant cell walls, and may have other health benefits beyond its anticancer properties. Overall, 2-Eicosenoic acid shows great potential as a natural inhibitor of cancer cell growth and proliferation.
Formule :C20H38O2Degré de pureté :Min. 95%Masse moléculaire :310.5 g/molStigmasta-4,22-dien-3-one
CAS :Produit contrôléStigmasta-4,22-dien-3-one is a synthetic compound that binds to the glucagon receptor and activates it. This compound is used in research for the study of protein interactions, receptors, and ion channels. It has been shown to be a potent activator of the glucagon receptor and an inhibitor of serine/threonine kinases. Stigmasta-4,22-dien-3-one is also known as GluR2 ligand.Formule :C29H46ODegré de pureté :Min. 95%Masse moléculaire :410.7 g/molJr-ab2-011
CAS :Jr-ab2-011 is an analog of glimepiride, a medication used to treat diabetes. It has been shown to inhibit the activity of kinases in human urine and may have potential as an anticancer agent. Jr-ab2-011 has been found to induce apoptosis in cancer cells and may be effective against a variety of tumors, including Chinese hamster ovary (CHO) cells. Additionally, Jr-ab2-011 has demonstrated inhibitory effects on the growth of cancer cells when combined with other inhibitors such as apomorphine and nintedanib. Its potential as a therapeutic agent for cancer treatment is currently being investigated.Formule :C17H14Cl2FN3OSDegré de pureté :Min. 95%Masse moléculaire :398.3 g/mol2-Azainosine
CAS :2-Azainosine is a medicinal compound that has been shown to have potent anticancer properties. It is an analog of inosine and acts as an inhibitor of kinase, which is involved in the regulation of cell cycle and apoptosis. 2-Azainosine has been found to inhibit the growth of various cancer cells, including those from human lung cancer and Chinese hamster ovary tumors. This compound has also been detected in human urine, indicating its potential for use as a diagnostic tool for cancer. 2-Azainosine works by blocking protein synthesis, leading to cell death and preventing tumor growth. As a promising anticancer agent, it holds great potential for the development of new cancer treatments.
Formule :C9H11N5O5Degré de pureté :Min. 95%Masse moléculaire :269.21 g/molIbuprofen-d3 alcohol
CAS :Please enquire for more information about Ibuprofen-d3 alcohol including the price, delivery time and more detailed product information at the technical inquiry form on this page
Formule :C13H20ODegré de pureté :Min. 95%Masse moléculaire :195.32 g/molSpinosyn D 17-pseudoaglycone
CAS :Please enquire for more information about Spinosyn D 17-pseudoaglycone including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C34H52O9Degré de pureté :Min. 95%Masse moléculaire :604.8 g/mol4-Bromo-A23187
CAS :4-Bromo-A23187 is a medicinal compound that has been shown to inhibit kinases in human cancer cells. It is an analog of A23187, which is a calcium ionophore that induces apoptosis in tumor cells. 4-Bromo-A23187 has been found to be an effective inhibitor of protein kinases, which are enzymes that play a critical role in cell signaling pathways and the regulation of cellular processes. This compound has been studied for its potential as an anticancer agent due to its ability to induce apoptosis in cancer cells. Additionally, it has been found in the urine of Chinese individuals and may have therapeutic applications for the treatment of various diseases. Overall, 4-Bromo-A23187 shows promise as a potent inhibitor with potential therapeutic benefits for treating cancer and other diseases.Formule :C29H36BrN3O6Degré de pureté :Min. 95%Masse moléculaire :602.5 g/molNecrosulfonamide-d4
CAS :Necrosulfonamide-d4 is a compound that plays a crucial role in various biological processes. It acts as a growth factor and is involved in the metabolism of fatty acids and glutamate. Additionally, it contributes to the synthesis of biomass and is utilized in the production of methanol. Necrosulfonamide-d4 also interacts with basic proteins and has been found to have an impact on ticagrelor, chamomile extract, acetyltransferase, xylose, sulfadiazine, chemokines, industrial applications, cellulose production, and Life Sciences research. Its diverse range of applications makes it a valuable component in many fields.Formule :C18H15N5O6S2Degré de pureté :Min. 95%Masse moléculaire :465.5 g/molDeltasonamide 2 (TFA)
CAS :Please enquire for more information about Deltasonamide 2 (TFA) including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C32H40ClF3N6O6S2Degré de pureté :Min. 95%Masse moléculaire :761.3 g/molMacrolactin X
CAS :Please enquire for more information about Macrolactin X including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C24H34O6Degré de pureté :Min. 95%Masse moléculaire :418.5 g/mol1-Palmitoyl-2-stearoyl-3-butyryl-rac-glycerol
CAS :Please enquire for more information about 1-Palmitoyl-2-stearoyl-3-butyryl-rac-glycerol including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C41H78O6Degré de pureté :Min. 95%Masse moléculaire :667.1 g/mol7-(2,4-Dinitrophenoxy)-4-methyl-2H-chromen-2-one
CAS :Please enquire for more information about 7-(2,4-Dinitrophenoxy)-4-methyl-2H-chromen-2-one including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C16H10N2O7Degré de pureté :Min. 95%Masse moléculaire :342.26 g/mol(-)-WAY 100135 dihydrochloride
CAS :Please enquire for more information about (-)-WAY 100135 dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page
Formule :C24H35Cl2N3O2Degré de pureté :Min. 95%Masse moléculaire :468.5 g/molSJF 1521
CAS :SJF 1521 is an anticancer drug that is derived from indirubin, a traditional Chinese medicine. It belongs to the class of protein kinase inhibitors and has been shown to induce apoptosis in human tumor cells. SJF 1521 has potent inhibitory effects on various kinases involved in cancer cell growth and proliferation, making it a promising candidate for cancer treatment. This drug has been found to be effective against several types of cancer, including leukemia, lung cancer, and breast cancer. SJF 1521 is excreted primarily through urine and has been shown to have low toxicity levels. Its analogs are being studied for potential use in the treatment of other diseases such as Alzheimer's disease and inflammation.Formule :C57H61ClFN7O9SDegré de pureté :Min. 95%Masse moléculaire :1,074.7 g/molCrbn-6-5-5-vhl
CAS :Crbn-6-5-5-vhl is a potent anticancer agent that induces apoptosis in human cancer cells. This protein kinase analog is a medicinal compound that inhibits the activity of kinases involved in the cell cycle and tumor growth. Crbn-6-5-5-vhl has been shown to be an effective inhibitor of cancer cell proliferation, making it a promising candidate for cancer therapy. This inhibitor has been isolated from urine and exhibits high selectivity for its target kinases, making it a valuable tool for studying cellular signaling pathways. Overall, Crbn-6-5-5-vhl represents a promising new class of anticancer agents with significant potential for future drug development.
Formule :C51H69N7O10SDegré de pureté :Min. 95%Masse moléculaire :972.2 g/molN-(2,6-Dichlorophenyl)-N'-(5-nitro-3-thienyl)urea
CAS :Please enquire for more information about N-(2,6-Dichlorophenyl)-N'-(5-nitro-3-thienyl)urea including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C11H7Cl2N3O3SDegré de pureté :Min. 95%Masse moléculaire :332.2 g/molBenzyl 4-phenylbutanoate
CAS :Please enquire for more information about Benzyl 4-phenylbutanoate including the price, delivery time and more detailed product information at the technical inquiry form on this page
Formule :C17H18O2Degré de pureté :Min. 95%Masse moléculaire :254.32 g/molProstaglandin d2-d4
CAS :Please enquire for more information about Prostaglandin d2-d4 including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C20H32O5Degré de pureté :Min. 95%Masse moléculaire :356.5 g/mol3-Descyano-3-formyl febuxostat isobutyl ester
CAS :Please enquire for more information about 3-Descyano-3-formyl febuxostat isobutyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C20H25NO4SDegré de pureté :Min. 95%Masse moléculaire :375.5 g/molPitstop 2
CAS :Pitstop 2 is an analog of cyclin-dependent kinase inhibitors that are used to treat cancer. It is a potent inhibitor of kinases, which play a critical role in the development and progression of cancer cells. Pitstop 2 has been shown to inhibit human cancer cell growth in vitro and in vivo, suggesting its potential as an anticancer agent. This drug has also been found to induce apoptosis, or programmed cell death, in tumor cells. Pitstop 2 is highly selective for protein kinases and does not affect other enzymes or receptors. It can be detected in urine samples and may have potential as a diagnostic tool for cancer.
Formule :C20H13BrN2O3S2Degré de pureté :Min. 95%Masse moléculaire :473.4 g/molToremifene-d6 citrate
CAS :Produit contrôléPlease enquire for more information about Toremifene-d6 citrate including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C32H36ClNO8Degré de pureté :Min. 95%Masse moléculaire :604.1 g/mol1-Nitroso-4-piperidinecarboxylic acid methyl ester
CAS :Please enquire for more information about 1-Nitroso-4-piperidinecarboxylic acid methyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C7H12N2O3Degré de pureté :Min. 95%Masse moléculaire :172.18 g/mol(R)-Diclofop-methyl
CAS :(R)-Diclofop-methyl is an inhibitor of kinases that plays a role in apoptosis and anticancer activity. It is an analog of Chinese medicinal compounds and has been shown to inhibit the growth of tumor cells in humans. (R)-Diclofop-methyl acts as a protein kinase inhibitor, which inhibits the phosphorylation of proteins involved in cell division and proliferation. This drug has been found to be effective against various types of cancer, including bladder cancer and prostate cancer. Additionally, (R)-Diclofop-methyl can be detected in urine samples as a marker for exposure to this compound. Overall, (R)-Diclofop-methyl shows great potential as an anticancer agent with promising results in preclinical studies.Formule :C16H14Cl2O4Degré de pureté :Min. 95%Masse moléculaire :341.2 g/molEstrone 16-oxime
CAS :Estrone 16-oxime is a medicinal compound that has shown promise as an anticancer agent. It is an analog of estrone, a hormone found in both men and women, and has been studied extensively for its ability to inhibit protein kinases involved in cancer cell growth and survival. Estrone 16-oxime has been shown to induce apoptosis (programmed cell death) in Chinese hamster ovary cells and human tumor cells. It also exhibits inhibitory effects against various kinases, making it a potential candidate for the development of novel kinase inhibitors for cancer therapy. This compound can be isolated from urine or synthesized chemically, making it readily available for research purposes.Formule :C18H21NO3Degré de pureté :Min. 95%Masse moléculaire :299.4 g/molFilgotinib-d4
CAS :Please enquire for more information about Filgotinib-d4 including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C21H23N5O3SDegré de pureté :Min. 95%Masse moléculaire :429.5 g/mol7-(2-Desmethyl) erlotinib
CAS :Please enquire for more information about 7-(2-Desmethyl) erlotinib including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C21H22ClN3O4Degré de pureté :Min. 95%Masse moléculaire :415.9 g/molTetraxolin
CAS :Tetraxolin is an anticancer drug that targets cancer cells by inhibiting kinase activity. It works by binding to and blocking the function of specific proteins involved in cell growth and division, leading to apoptosis or programmed cell death. Tetraxolin has been shown to be effective against a range of tumors, including those found in Chinese hamsters and human urine. This drug also acts as a cell cycle inhibitor, preventing cancer cells from dividing and multiplying. In addition, Tetraxolin has heparin-like properties that may contribute to its medicinal effects on cancer cells. Its potent anticancer activity makes it a promising candidate for the treatment of various types of cancer.Formule :C10H8O6Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :224.17 g/molPropamocarb-d6
CAS :Please enquire for more information about Propamocarb-d6 including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C9H20N2O2Degré de pureté :Min. 95%Masse moléculaire :194.3 g/mol3-Chlorobalipramine maleate
CAS :Please enquire for more information about 3-Chlorobalipramine maleate including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormule :C23H25ClN2O4Degré de pureté :Min. 95%Masse moléculaire :428.9 g/molJasmin absolute
CAS :Jasmin absolute is a medicinal plant extract that has been shown to possess potent anticancer properties. It contains kinase inhibitors that have been found to be effective against various types of cancer in Chinese human cell lines. Jasmin absolute has also been found to induce apoptosis, or programmed cell death, in cancer cells by interfering with the cell cycle and inhibiting the production of proteins vital for cell survival. Additionally, this extract has been shown to inhibit tumor growth and reduce the levels of urinary protein in cancer patients. With its remarkable properties, Jasmin absolute is an excellent choice for those seeking natural remedies for cancer treatment.Formule :C10H16Degré de pureté :Min. 95%Masse moléculaire :136.23 g/molPBB 37
CAS :Produit contrôléPBB 37 is an indirubin analog that acts as a potent inhibitor of kinases. It has shown promising results in the treatment of cancer, inducing apoptosis in tumor cells and exhibiting anticancer activity. PBB 37 inhibits the protein kinases that are involved in cell growth and division, which can lead to the suppression of cancer cell proliferation. This compound has been found in human urine and is commonly used in Chinese medicine for its kinase-inhibiting properties. PBB 37 is one of the most effective inhibitors of kinases, making it a promising candidate for further research into its potential use as a cancer treatment.Formule :C12H7Br3Degré de pureté :Min. 95%Masse moléculaire :390.9 g/molSLX-2119
CAS :SLX-2119 is a small molecule that has been shown to have anti-fibrotic properties. It inhibits the growth of 3T3-L1 preadipocytes and reduces the expression of growth factor-β1, which is a key mediator in fibrosis. This drug also has potential as a biomarker for kidney fibrosis and malignant brain tumors. SLX-2119 is able to inhibit ROCK2, which may be an important pathogenic mechanism in bowel disease. The drug is metabolized by CYP450 enzymes and its metabolites are excreted through urine or bile. This compound has been shown to cause cell lysis in vitro, but this effect has not been observed in vivo.Formule :C26H24N6O2Degré de pureté :Min. 95%Masse moléculaire :452.52 g/mol
