
Inhibitors
Inhibitors are molecules that bind to enzymes, receptors, or other proteins to reduce or block their biological activity. These compounds are widely used in research to study biological pathways, understand disease mechanisms, and develop therapeutic drugs. Inhibitors play a crucial role in the treatment of various diseases, including cancer, cardiovascular diseases, and infections. At CymitQuimica, we provide a diverse range of high-quality inhibitors to support your research in biochemistry, cell biology, and pharmaceutical development.
Subcategories of "Inhibitors"
- Angiogenesis(2,797 products)
- Apoptosis(6,259 products)
- Cell Cycle/Checkpoint(4,836 products)
- Chromatin/Epigenetics(2,592 products)
- Cytoskeletal Signaling(1,534 products)
- DNA Damage/DNA Repair(2,880 products)
- Endocrinology/Hormones(3,748 products)
- Enzyme(3,670 products)
- GPCR/G-Protein(8,985 products)
- Immunology and Inflammation(3,797 products)
- Influenza Virus(299 products)
- JAK/STAT signaling(415 products)
- MAPK Signaling(1,250 products)
- Membrane Transporter/Ion Channel(3,148 products)
- Metabolism(10,144 products)
- Microbiology/Virology(7,591 products)
- Neuroscience(10,345 products)
- Other Inhibitors(35,830 products)
- Oxidation-Reduction(40 products)
- PI3K/Akt/mTOR Signaling(1,421 products)
- Proteases/Proteasome(1,681 products)
- Stem Cell and Derivatives(748 products)
- Tyrosine Kinase/Adaptors(1,961 products)
- Ubiquitination(1,721 products)
Show 16 more subcategories
Found 66564 products of "Inhibitors"
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LY 186126
CAS:LY 186126 is a potent cGI-PDE inhibitor with reversible, high affinity (Ka = 6 nM) binding to a single class of SaR binding sites.Formula:C16H19N3O2Purity:98%Color and Shape:SolidMolecular weight:285.34PD 120697
CAS:PD 120697 is a dopamine antagonist with central dopamine agonist properties.Formula:C11H15N3SPurity:98%Color and Shape:SolidMolecular weight:221.32Y2 Antagonist 36
CAS:Y2 Antagonist 36 is a highly potent, soluble and selective antagonist of NPY Y2.Formula:C27H29ClN4O3Color and Shape:SolidMolecular weight:493sEH inhibitor-14
CAS:sEH inhibitor-14, a benzoxazolone-5-urea analogue, acts as an efficient soluble Epoxide Hydrolase (sEH) inhibitor, demonstrating significant activity with anFormula:C16H12F3N3O4Color and Shape:SoildMolecular weight:367.28LP 20 hydrochloride
CAS:ligand of the 5-HT7 receptorFormula:C17H21ClN2OPurity:98%Color and Shape:SolidMolecular weight:304.81SH-053-S-CH3-2'F
CAS:SH-053-S-CH3-2'F is a potent and selective agonist of GABAA receptors.Formula:C23H18FN3O2Color and Shape:SolidMolecular weight:387.41CAY10760
CAS:CAY10760 inhibits RAD51-BRCA2 interaction (EC50=19 μM), reduces homologous recombination by 54%, and hinders BxPC-3/Capan-1 cancer cell proliferation.Formula:C28H24ClN3O3Color and Shape:SolidMolecular weight:485.96AC-155
CAS:AC-155 is a bamifylline metabolite in human plasma that may induce apoptosis selectively in cancer cells.Formula:C16H19N5O2Color and Shape:SolidMolecular weight:313.35NCI172112
CAS:NCI172112 is is used to develop antitumor agents effective against CNS tumors.Formula:C14H23Cl2N3O2Purity:98%Color and Shape:SolidMolecular weight:336.26Tyrphostin AG 568
CAS:Tyrphostin AG 568 promotes Tyrphostin-induced inhibition of p210bcr-abl tyrosine kinase activity. It also induces K562 to differentiate.Formula:C13H9N5O2Purity:98%Color and Shape:SolidMolecular weight:267.24CAM 4750
CAS:CAM 4750 is a nonpeptide tachykinin NK1 receptor antagonist.Formula:C30H31ClN4O4Color and Shape:SolidMolecular weight:547.05HI5
CAS:HI5: potent tubulin/IDO inhibitor, IC50 70 nM (HeLa), blocks kynurenine, G2/M arrest, spurs T cell activity, & triggers apoptosis.Formula:C42H43N5O8Color and Shape:SolidMolecular weight:745.82Z-VAE(OMe)-fmk
CAS:Z-VAE(OMe)-fmk: an irreversible, cell-permeable UCHL1 inhibitor, binds ubiquitin's C-terminal site.Formula:C23H32FN3O7Color and Shape:SolidMolecular weight:481.51EZH2-IN-11
CAS:EZH2-IN-11, a potent E2HZ inhibitor with potential for cancer treatment, is highlighted in patent WO2019204490A1.Formula:C28H36ClN3O5SColor and Shape:SolidMolecular weight:562.12DRL-17822
CAS:DRL-17822 is a Cholesteryl Ester Transfer Protein (CETP) inhibitor.Formula:C30H31F6N7Color and Shape:SolidMolecular weight:603.6KAI-407
CAS:KAI407, a non-8-aminoquinoline, kills early Plasmodium cynomolgi liver parasites with IC50 of 0.69μM for hypnozoites; similar to primaquine efficacy.Formula:C22H14F3N5OColor and Shape:SolidMolecular weight:421.37TJ08
CAS:TJ08 has anticancer properties and can effectively induce G1/S phase blockade while promoting apoptosis in a variety of cancer cells.Formula:C22H16FN3O4Purity:99.89%Color and Shape:SolidMolecular weight:405.38Halofuginone hydrobromide
CAS:Halofuginone specifically inhibits collagen type I and MMP-2 gene expression, which may result in the suppression of angiogenesis and tumor cell growth.Formula:C16H17BrClN3O3·HBrPurity:97.01% - 99.73%Color and Shape:SolidMolecular weight:495.59Ref: TM-T3524
1mg34.00€2mg49.00€5mg74.00€10mg106.00€25mg207.00€50mg310.00€100mg469.00€500mg897.00€1mL*10mM (DMSO)84.00€LT175
CAS:LT175 is a dual PPARα/γ partial agonist, insulin sensitizer, orally active, with lower adipogeny (EC50: hPPARα 0.22μm, mPPARα 0.26μm, hPPARγ 0.48μm).Formula:C21H18O3Color and Shape:SolidMolecular weight:318.37
