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"
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DYRKs-IN-1
CAS:DYRKs-IN-1 has antitumor activity.
Formula:C30H30ClN7O4Purity:98%Color and Shape:SolidMolecular weight:588.06IRAK4-IN-15
CAS:IRAK4-IN-15: selective IRAK4 inhibitor, IC50 0.002 μM, good PK, low clearance, synergizes with Acalabrutinib in MyD88/CD79 mutant ABC-DLBCL.Formula:C25H29FN10Color and Shape:SolidMolecular weight:488.56JAK1-IN-9
CAS:JAK1-IN-9 (compound 23a) is a potent, selective inhibitor of JAK1, demonstrating an IC50 of 72 nM.Formula:C16H13IN6Color and Shape:SolidMolecular weight:416.22HS-731
CAS:HS-731 is a μ-Opioid Receptor Agonist.Formula:C20H26N2O5Color and Shape:SolidMolecular weight:374.43Topoisomerase II inhibitor 6
Topoisomerase II inhibitor 6, a potent tryptanthrin derivative, blocks G2 phase in CCRF-CEM cells, induces DNA breaks, and may be used for cancer research.Formula:C19H18N4O2Color and Shape:SolidMolecular weight:334.37EGFR-IN-17
EGFR-IN-17: potent, selective EGFR inhibitor, IC50 of 0.2 nM, overcomes C797S drug resistance.Formula:C27H31ClN7O3PColor and Shape:SolidMolecular weight:568.01AL-6556
CAS:AL-6556 is a prostaglandin DP receptor agonist.Formula:C20H33ClO5Color and Shape:SolidMolecular weight:388.93SSTR4 agonist 4
CAS:SSTR4 agonist 4, potent in pain research, shows promise in rodent pain models, with potential for Alzheimer's due to hippocampus activity.Formula:C19H26N4OColor and Shape:SolidMolecular weight:326.44PD-1/PD-L1-IN-30
CAS:PD-1/PD-L1-IN-30: Cancer research inhibitor with 0.018 μM IC50.Formula:C29H28F3NO5Color and Shape:SolidMolecular weight:527.53PIM1-IN-3
PIM1-IN-3 (HL8) selectively blocks PIM1, induces Colo320 cell apoptosis, and may be researched for cancer.Formula:C27H25BrN6OColor and Shape:SolidMolecular weight:529.43Antitumor agent-54
Compound C11 inhibits 14-3-3η protein (KD: 35 μM), targets liver cancer cells, blocks G1-S phase, and induces apoptosis.Formula:C29H32N2O3Color and Shape:SolidMolecular weight:456.58Tubulin inhibitor 16
Tubulin inhibitor 16 is a potent tubulin inhibitor with antiproliferative activity. Tubulin inhibitor 16 exhibits cytotoxicity in HepG2 cells [1].Formula:C16H12FNO2Color and Shape:SolidMolecular weight:269.27KPH2f
CAS:KPH2f: dual URAT1/GLUT9 inhibitor, orally active, IC50: 0.24μM (URAT1), 9.37μM (GLUT9), minimal OAT1/ABCG2 impact.Formula:C24H16N3NaO2SColor and Shape:SolidMolecular weight:433.46Isobetanin
CAS:Isobetanin is a betacyanin that has been shown to enhance vitexin-2-O-xyloside mediated inhibition of proliferation of T24 bladder cancer cells.
Formula:C24H26N2O13Color and Shape:SolidMolecular weight:550.47Carbonic anhydrase inhibitor 3
Carbonic anhydrase inhibitor 3 (compound 11g) is an inhibitor of carbonic anhydrase II that reduces the intraocular pressure in glaucomatous rabbits [1].Formula:C15H17N3O3SColor and Shape:SolidMolecular weight:319.38Sinulatumolin E
CAS:Sinulatumolin E, a terpenoid, inhibits TNF-α (IC 50: 3.6 μM); has anti-inflammatory properties.Formula:C15H22O2Color and Shape:SolidMolecular weight:234.33G12Si-1
G12Si-1 selectively binds and inhibits K-Ras(G12S) to block oncogenic signaling and nucleotide exchange.Formula:C29H32ClN5O3Color and Shape:SolidMolecular weight:534.05PROTAC CDK12/13 Degrader-1
PROTAC CDK12/13 Degrader-1 (7f) selectively degrades CDK12/13 at nanomolar potency, targeting breast cancer.Color and Shape:SolidNovokinin
CAS:Angiotensin AT2 receptor agonistFormula:C39H61N11O7Purity:98%Color and Shape:SolidMolecular weight:795.97Spliceostatin A
CAS:Spliceostatin A is an anticancer agent and splicing inhibitor that induces apoptosis by inducing cell cycle arrest in the G1 and G2/M phases.Formula:C28H43NO8Purity:94.66%Color and Shape:SolidMolecular weight:521.643
