
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(2,811 products)
- Apoptosis(6,295 products)
- Cell Cycle/Checkpoint(4,842 products)
- Chromatin/Epigenetics(2,526 products)
- Cytoskeletal Signaling(1,550 products)
- DNA Damage/DNA Repair(2,917 products)
- Endocrinology/Hormones(3,708 products)
- Enzyme(3,671 products)
- GPCR/G-Protein(9,024 products)
- Immunology and Inflammation(3,896 products)
- Influenza Virus(302 products)
- JAK/STAT signaling(418 products)
- MAPK Signaling(1,248 products)
- Membrane Transporter/Ion Channel(3,094 products)
- Metabolism(10,157 products)
- Microbiology/Virology(7,623 products)
- Neuroscience(10,360 products)
- Other Inhibitors(35,913 products)
- Oxidation-Reduction(40 products)
- PI3K/Akt/mTOR Signaling(1,440 products)
- Proteases/Proteasome(1,711 products)
- Stem Cell and Derivatives(792 products)
- Tyrosine Kinase/Adaptors(2,013 products)
- Ubiquitination(1,722 products)
Show 16 more subcategories
Found 66619 products of "Inhibitors"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
GP-1681
CAS:GP-1681, a G-protein coupled receptor (GPCR) agonist, is used potentially for the treatment of influenza infection.Formula:C24H30NaO5Purity:98%Color and Shape:SolidMolecular weight:421.48NTPDase-IN-2
CAS:NTPDase-IN-2 inhibits h-NTPDase-2/-8 (IC50: 0.04, 2.27 µM), non-competitive for h-NTPDase-1/-2 (Km: 74 µM); useful in cancer, immune, bacterial research.Formula:C24H20FN3OS2Color and Shape:SolidMolecular weight:449.56PI3K-IN-29
CAS:PI3K-IN-29: Strong PI3K block, inhibits Akt phosphorylation. IC50: U87MG 0.264µM, HeLa 2.04µM, HL60 1.14µM.Formula:C27H22ClN7O3SColor and Shape:SolidMolecular weight:560.03BSc5367
CAS:BSc5367 inhibits Nek1 kinase (IC50: 11.5 nM), key in cell cycle, DNA repair, impacting ALS, PKD, cancer.
Formula:C20H15N3O2Color and Shape:SoildMolecular weight:329.35RORγt/DHODH-IN-3
RORγt/DHODH-IN-3 (compound (S)-14d) is a potent, orally active dual inhibitor of RORγt (IC50: 0.098 μM) and DHODH (IC50: 0.432 μM).RORγt/DHODH-IN-1 hasFormula:C24H26ClF6N3O3SColor and Shape:SolidMolecular weight:585.99FPDT
FPDT combats glioblastoma by inhibiting the AKT pathway; IC50: >100 μM (astrocytes), 45-68 μM (GBM cells).Formula:C16H12FNO2SColor and Shape:SolidMolecular weight:301.34Ribocil-C R enantiomer
Ribocil-C R enantiomer is the R enantiomer of Ribocil-C. Ribocil-C is a highly selective bacterial riboflavin riboswitches inhibitor.Formula:C21H21N7OSPurity:98%Color and Shape:SolidMolecular weight:419.5Silvestrol
CAS:Silvestrol is a eukaryotic translation initiation factor 4A inhibitor. Silvestrol causes autophagy and caspase-mediated apoptosis.Formula:C34H38O13Purity:98%Color and Shape:SolidMolecular weight:654.66STA-1474
CAS:STA-1474, a soluble prodrug of ganetespib (STA-9090), becomes a strong HSP90 inhibitor effective against canine tumors.Formula:C20H21N4O6PColor and Shape:SolidMolecular weight:444.38Y1 receptor antagonist 1
CAS:Y1 receptor antagonist 1 is an antagonist of neuropeptide Y1 receptor.Formula:C28H33N5O3Purity:98.17%Color and Shape:SolidMolecular weight:487.59K203
K203 is a potent tabun-inhibited AChE reactivator and is an important antidote to organophosphorus poisoning.Formula:C16H18Br2N4O2Color and Shape:SolidMolecular weight:458.15Sequoiaflavone
CAS:Sequoiaflavone is a biflavone isolated from Ginkgo biloba.Formula:C31H20O10Color and Shape:SolidMolecular weight:552.48GSK1820795A
CAS:GSK1820795A: Telmisartan analog, selective hGPR132a antagonist, blocks yeast activation by N-acylamides, angiotensin II antagonist, partial PPARγ agonist.Formula:C35H34N8Color and Shape:SolidMolecular weight:566.7Pralatrexate, (R)-
CAS:Pralatrexate is a high-affinity DHFR inhibitor targeting RFC-1, used in cancer treatment and immunosuppression.Formula:C23H23N7O5Purity:98%Color and Shape:SolidMolecular weight:477.47AChE-IN-24
AChE-IN-24: Strong AChE blocker, crosses blood-brain barrier, IC50=0.053 μM, useful for AD research.Formula:C22H30N2O4S2Color and Shape:SolidMolecular weight:450.61L-744832
CAS:L-744832, also known as L-744,832, is a potent Farnesyltransferase inhibitor with potential anticancer activity.Formula:C26H45N3O6S2Color and Shape:SolidMolecular weight:559.78Soyacerebroside II
CAS:Soyacerebroside II is a Ca2+ ionophore; both I and II inhibit IL-18 in PBMCs and modulate immune responses.Formula:C40H75NO9Purity:98%Color and Shape:SolidMolecular weight:714.02XP-524
CAS:XP-524: BET & EP300 inhibitor, suppresses KRAS tumors in vivo, targets PDAC, boosts immune response.Formula:C30H28N6O3SColor and Shape:SolidMolecular weight:552.65GSK864
CAS:GSK864 is an inhibitor of isocitrate dehydrogenase 1 (IDH1) mutant. GSK864 inhibits IDH1 mutants R132C, R132H, and R132G (IC50: 8.8, 15.2, and 16.6 nM).Formula:C30H31FN6O4Purity:97.07%Color and Shape:SolidMolecular weight:558.6SSR-182289A (Free)
CAS:SSR-182289A (Free) is a thrombin inhibitor.Formula:C30H33F2N5O4SPurity:98%Color and Shape:SolidMolecular weight:597.68

