
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(2,847 products)
- Apoptosis(6,334 products)
- Cell Cycle/Checkpoint(4,889 products)
- Chromatin/Epigenetics(2,616 products)
- Cytoskeletal Signaling(1,579 products)
- DNA Damage/DNA Repair(2,868 products)
- Endocrinology/Hormones(3,753 products)
- Enzyme(3,673 products)
- GPCR/G-Protein(9,027 products)
- Immunology and Inflammation(3,938 products)
- Influenza Virus(300 products)
- JAK/STAT signaling(415 products)
- MAPK Signaling(1,259 products)
- Membrane Transporter/Ion Channel(3,160 products)
- Metabolism(10,131 products)
- Microbiology/Virology(7,628 products)
- Neuroscience(10,543 products)
- Other Inhibitors(35,859 products)
- Oxidation-Reduction(40 products)
- PI3K/Akt/mTOR Signaling(1,435 products)
- Proteases/Proteasome(1,692 products)
- Stem Cell and Derivatives(732 products)
- Tyrosine Kinase/Adaptors(1,991 products)
- Ubiquitination(1,727 products)
Show 16 more subcategories
Found 66512 products of "Inhibitors"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
CRV431
CAS:CRV431 is a novel Pan-Cyclophilin Inhibitor, potently inhibiting all cyclophilin isoforms tested - A, B, D, and G (IC50 values ranged from 1-7 nM).Formula:C67H122N12O13Color and Shape:SolidMolecular weight:1303.76Enpp-1-IN-12
ENPP1-IN-12 is a potent, oral ENPP1 inhibitor with a Ki of 41 nM and anti-tumor properties.Formula:C17H19N5O3SColor and Shape:SolidMolecular weight:373.43Daeatal
CAS:Dynorphin A ethylamide (1-9), the opioid activities were examined in the bioassays.Formula:C56H93N19O10Purity:98%Color and Shape:SolidMolecular weight:1192.46Turoctocog alfa
CAS:Turoctocog alfa: recombinant FVIII from CHO cells for hemophilia A study.Color and Shape:SolidTAI-95
CAS:TAI-95 is an inhibitor of highly expressed cancer protein 1 (Hec1).Formula:C24H23N5O3S2Color and Shape:SolidMolecular weight:493.60GLS-1-IN-1
GLS-1-IN-1 (compound 1d) is a GLS-1 inhibitor that inhibits Hep G2, MCF 7 and MCF 10A cells.Formula:C26H25FN4OSColor and Shape:SolidMolecular weight:460.57BRD7539
CAS:BRD7539B: PfDHODH inhibitor, IC50 0.033μM; selective vs HsDHODH, IC50 >50μM.Formula:C23H22FN3O2Purity:98%Color and Shape:SolidMolecular weight:391.443-IN-PP1
CAS:3-IN-PP1: PKD inhibitor (IC50: 94-108 nM for PKD1/2/3), broad anticancer agent for research.Formula:C17H18N6Color and Shape:SolidMolecular weight:306.36MEN-10354
CAS:MEN-10354 is a less potent and less selective NK-2 tachykinin receptor antagonist compared to the linear analog, R 396.Formula:C37H46N8O9Color and Shape:SolidMolecular weight:746.81COX-2-IN-12
COX-2-IN-12: Potent, selective COX-2 inhibitor, IC50=19.98μM, safe anti-inflammatory with low acute toxicity.Formula:C17H19NO3Color and Shape:SolidMolecular weight:285.34ATM Inhibitor-4
ATM Inhibitor -4: selective, potent (IC50: 0.32 nM), inhibits PI3K family, stable, stops mTOR at 1 μM.Formula:C26H29FN6O3Color and Shape:SolidMolecular weight:492.55TP-6076
CAS:TP-6076 is a fluorocycline antibiotic, inhibiting bacterial protein synthesis, exhibiting great antimicrobial activity against carbapenem-resistant A.Formula:C28H32F3N3O7Color and Shape:SolidMolecular weight:579.56TD-0212 TFA
CAS:TD-0212 TFA is an oral AT1 receptor antagonist & NEP inhibitor with pKi 8.9 & pIC50 9.2.Formula:C30H35F4N3O6SPurity:98%Color and Shape:SolidMolecular weight:641.67PF-06372222
CAS:PF-06372222: a small-molecule that modulates GCGR and antagonizes GLP-1R, affecting insulin and glucagon.Formula:C26H28F3N5O3Purity:98%Color and Shape:SolidMolecular weight:515.53nNOS-IN-25
CAS:nNOS-IN-25 is an effective, selective, and cell-permeable inhibitor of neuronal nitric oxide synthase.Formula:C21H22N4Purity:98%Color and Shape:SolidMolecular weight:330.43VEGFR-2-IN-13
VEGFR-2-IN-13 (Compound 19a) is a potent VEGFR-2 inhibitor (IC50: 3.4 nM). vEGFR-2-IN-13 arrests the HepG2 cell cycle in G2/M phase and induces apoptosis.Formula:C24H18N6O2SColor and Shape:SolidMolecular weight:454.5Suloctidil HCl
CAS:Suloctidil HCl is a peripheral vascular dilator.Formula:C20H36ClNOSColor and Shape:SolidMolecular weight:374.02Casuarinin
CAS:Casuarinin, an ellagitannin found in pomegranates and certain Casuarina/Stachyurus plants, is a carbonic anhydrase inhibitor and astringent.Formula:C41H28O26Color and Shape:SolidMolecular weight:936.65PI3K-IN-35
CAS:PI3K-IN-35 (6l) selectively inhibits PI3K-α, β, δ (IC50: 13.98, 7.22, 10.94 μM), blocks G2/M phase, induces apoptosis, and is useful in leukemia research.Formula:C25H23N7O2Color and Shape:SolidMolecular weight:453.5CCR7 Ligand 1
CAS:CCR7-Cmp2105 is a thiadiazole-dioxide allosteric antagonist for CCR7 with a Kd of 3 nM and IC50 of 7.3 μM against arrestin binding.Formula:C22H29N5O5SColor and Shape:SolidMolecular weight:475.56

