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(2,765 products)
- Apoptosis(6,237 products)
- Cell Cycle/Checkpoint(4,778 products)
- Chromatin/Epigenetics(2,426 products)
- Cytoskeletal Signaling(1,515 products)
- DNA Damage/DNA Repair(2,957 products)
- Endocrinology/Hormones(3,692 products)
- Enzyme(3,665 products)
- GPCR/G-Protein(8,968 products)
- Immunology and Inflammation(3,857 products)
- Influenza Virus(301 products)
- JAK/STAT signaling(413 products)
- MAPK Signaling(1,249 products)
- Membrane Transporter/Ion Channel(3,024 products)
- Metabolism(10,184 products)
- Microbiology/Virology(7,551 products)
- Neuroscience(10,359 products)
- Other Inhibitors(36,088 products)
- Oxidation-Reduction(43 products)
- PI3K/Akt/mTOR Signaling(1,444 products)
- Proteases/Proteasome(1,718 products)
- Stem Cell and Derivatives(825 products)
- Tyrosine Kinase/Adaptors(2,035 products)
- Ubiquitination(1,710 products)
Show 16 more subcategories
Found 66669 products of "Inhibitors"
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DGAT-1 inhibitor 2
CAS:DGAT-1 inhibitor 2: effective against obesity, targets enzyme in triglyceride synthesis for diabetes treatment.Formula:C24H28N4O3Purity:98.36%Color and Shape:SolidMolecular weight:420.5αvβ1 integrin-IN-1
CAS:<p>αvβ1 integrin-IN-1 is a potent and selective inhibitor of αvβ1 integrin (IC50 of 0.63 nM) with antifibrotic effects.</p>Formula:C26H34N6O6SPurity:99.74% - >99.99%Color and Shape:SolidMolecular weight:558.65GI 181771
CAS:GI 181771 is an agonist of the cholecystokinin 1 receptor. GI 181771 can be used in studies about obesity.Formula:C34H31N5O6Purity:95.02%Color and Shape:SolidMolecular weight:605.64VU0661013
CAS:VU0661013 is an effective and selective inhibitor of MCL-1.Formula:C39H39Cl2N5O4Purity:99.04%Color and Shape:SolidMolecular weight:712.66GW 833972A
CAS:<p>GW 833972A: selective CB2 agonist; reduces neural depolarization and citric acid cough in animals.</p>Formula:C18H14Cl2F3N5OPurity:99.93%Color and Shape:SoildMolecular weight:444.24ZED-1227
CAS:<p>ZED-1227 (TAK-227) is a TG2 inhibitor with anticancer activity that blocks inflammation-induced TG2 expression and activation for the treatment of Celiac Diseas</p>Formula:C26H36N6O6Purity:99.04%Color and Shape:SolidMolecular weight:528.6CFI-402257
CAS:<p>CFI-402257 is a selective inhibitor of Mps1/TTK kinase (Mps1 Ki = 0.09 nM; EC50 = 6.5 nM)and can be used in studies about hepatocellular carcinoma diseases.</p>Formula:C28H30N6O3Purity:96.66% - 99.51%Color and Shape:SolidMolecular weight:498.58Tenofovir amibufenamide
CAS:Tenofovir amibufenamide (HS-10234) 是一种 Tenofovir 前药，是一种具有口服活性的抗病毒化合物。Tenofovir amibufenamide 对乙型肝炎病毒 (HBV)具有抑制作用，可用于慢性乙型肝炎 (CHB) 研究。Formula:C22H31N6O5PPurity:99.19% - 99.87%Color and Shape:SolidMolecular weight:490.49Philanthotoxin 74 dihydrochloride
CAS:Philanthotoxin 74 dihydrochloride is an antagonist of AMPAR with IC50s of 263 and 296 nM for GluR3 and GluR1.Formula:C24H44Cl2N4O3Purity:99.75%Color and Shape:SolidMolecular weight:507.54GCN2-IN-7
CAS:GCN2-IN-7 is an inhibitor of the environmental sensing protein GCN2 with antitumor activity for the study of melanoma.Formula:C22H23BrN8OSPurity:99.12%Color and Shape:SolidMolecular weight:527.44Tyrphostin AG 538
CAS:Tyrphostin AG 538 is a chalcone compound, an IGF-1 receptor kinase inhibitor (IC₅0 : for 400 nM) that is potent, cell-permeable, reversible, and competitive.Formula:C16H11NO5Purity:98.75%Color and Shape:SoildMolecular weight:297.26CDDO-3P-Im
CAS:<p>CDDO-3P-Im is an orally active inhibitor of necroptosis with chemopreventive effects. CDDO-3P-Im can be used in studies about ischemia/reperfusion.</p>Formula:C39H46N4O3Purity:97.72%Color and Shape:SolidMolecular weight:618.81PHY34
CAS:PHY34 inhibits autophagy at nanomolar potency, with anti-tumor effects on HGSOC in vivo.Formula:C30H30O12Purity:98.71%Color and Shape:SolidMolecular weight:582.55PSB-603
CAS:<p>PSB-603 is a selective antagonist of Adenosine A2B receptor(Ki = 0.553 nM) with anti-inflammatory effects.</p>Formula:C24H25ClN6O4SPurity:97.13%Color and Shape:SolidMolecular weight:529.01GW-803430
CAS:GW-803430: potent MCH R1 antagonist, pIC50=9.3, orally effective against obesity in animals.Formula:C25H24ClN3O3SPurity:98.07%Color and Shape:SolidMolecular weight:481.997-BIA
CAS:7-BIA is a receptor-type protein tyrosine phosphatase D (PTPRD) inhibitor with anti-addictive properties and can be used in the study of neuropathic pain.Formula:C15H18O6Purity:≥98% - ≥98%Color and Shape:SolidMolecular weight:294.3JNJ-42253432
CAS:JNJ-42253432 is an oral active P2X7 antagonist capable of penetrating the central nervous system with a pKi value of 9.1 for rat and 7.9 for human P2X7 channelsFormula:C28H38N4OPurity:99.98%Color and Shape:SolidMolecular weight:446.63CCT365623
CAS:<p>CCT365623: oral Lysyl Oxidase inhibitor, potent, selective, good pharmacokinetics, anti-metastatic.</p>Formula:C18H17NO4S3Purity:97.299% - 99.49%Color and Shape:SolidMolecular weight:407.53α1 adrenoceptor-MO-1
CAS:α1 adrenoceptor-MO-1 (S enantiomer) has affinity at alpha 1 adrenergic receptor with alphalytic activity and analgesic action.Formula:C20H24ClN5OPurity:99.20% - 99.29%Color and Shape:SolidMolecular weight:385.89GSK-3 inhibitor 1
CAS:GSK-3 inhibitor 1 is a GSK-3 inhibitor.Formula:C22H17ClFN5O2Purity:98.42%Color and Shape:SolidMolecular weight:437.85
