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(2,758 products)
- Apoptosis(6,191 products)
- Cell Cycle/Checkpoint(4,808 products)
- Chromatin/Epigenetics(2,580 products)
- Cytoskeletal Signaling(1,503 products)
- DNA Damage/DNA Repair(2,887 products)
- Endocrinology/Hormones(3,702 products)
- Enzyme(3,671 products)
- GPCR/G-Protein(8,965 products)
- Immunology and Inflammation(3,700 products)
- Influenza Virus(296 products)
- JAK/STAT signaling(414 products)
- MAPK Signaling(1,248 products)
- Membrane Transporter/Ion Channel(3,136 products)
- Metabolism(10,096 products)
- Microbiology/Virology(7,554 products)
- Neuroscience(10,304 products)
- Other Inhibitors(35,764 products)
- Oxidation-Reduction(39 products)
- PI3K/Akt/mTOR Signaling(1,402 products)
- Proteases/Proteasome(1,672 products)
- Stem Cell and Derivatives(741 products)
- Tyrosine Kinase/Adaptors(1,922 products)
- Ubiquitination(1,716 products)
Show 16 more subcategories
Found 66571 products of "Inhibitors"
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GSK699
CAS:GSK699 is a potent, cell penetrant PCAF/GCN5 PROTAC.
Formula:C45H51BrN8O7Color and Shape:SolidMolecular weight:895.84AM-6494
CAS:AM-6494 is a potent and orally active BACE1 inhibitor (IC50: 0.4 nM) with in vivo selectivity over BACE2 (IC50: 18.6 nM).Formula:C22H21F2N5O3SPurity:98%Color and Shape:SolidMolecular weight:473.5GR-71251
CAS:GR-71251 is a Tachykinin receptor antagonist.
Formula:C74H105N19O13Color and Shape:SolidMolecular weight:1468.74Anticancer agent 45
Anticancer agent 46, potent and selective, induces apoptosis, is cytotoxic to cancer cells, with low toxicity to human lymphocytes.Formula:C22H14ClN3O6S2Color and Shape:SolidMolecular weight:515.95Aplaviroc hydrochloride
CAS:Aplaviroc, a potent CCR5 inhibitor, binds selectively, blocking HIV entry and specific monoclonal antibody attachment in vitro.Formula:C33H44ClN3O6Color and Shape:SolidMolecular weight:614.17Cgs 25155
CAS:Cgs 25155 is an orally active inhibitor of NEP 24.11.Formula:C25H34N2O6SPurity:98%Color and Shape:SolidMolecular weight:490.61BI-4916
CAS:BI-4916 is a phosphoglycerate dehydrogenase (PHGDH) inhibitor that inhibits SSP and reduces cancer cell migration.Formula:C23H24Cl2N2O6SPurity:98.55%Color and Shape:SolidMolecular weight:527.42D6808
D6808: selective c-Met inhibitor, IC50=2.9 nM, induces apoptosis and cell cycle arrest, for NSCLC/gastric cancer research.Formula:C30H25F3N6O2Color and Shape:SolidMolecular weight:558.55PIKfyve-IN-1
PIKfyve-IN-1: potent, cell-active inhibitor for PIKfyve research, IC50=6.9 nM.Formula:C20H21N5Color and Shape:SolidMolecular weight:331.41JAK2 JH2 binder-1
CAS:JAK2 JH2 binder-1: potent, selective, Ki=37.1 nM, potential for studying myeloproliferative neoplasms.Formula:C29H25N7O6SColor and Shape:SolidMolecular weight:599.62Chitinase-IN-4
Chitinase-IN-4 (compound 8f) is a potent and selective inhibitor of OfChi-h with an IC50 value of 0.1 μM and good insecticidal activity.Formula:C21H24ClN7Color and Shape:SolidMolecular weight:409.92PfPKG-IN-1
PfPKG-IN-1, an imidazole-based inhibitor, targets the Plasmodium falciparum cyclic guanosine monophosphate-dependent protein kinase (PfPKG).Formula:C24H22ClN7OSColor and Shape:SolidMolecular weight:492SphK1-IN-2
SphK1-IN-2: SphK1 inhibitor, IC50: 19.81 nM; less effective on SphK2. Induces apoptosis, hinders cancer cell growth.Formula:C27H30BrNO4SColor and Shape:SolidMolecular weight:544.5Aurora A inhibitor 1
CAS:Aurora A inhibitor 1: potent, selective, targets cancer-linked Aurora A overexpression, potential for cancer research. (WO2021147974A1, 49)Formula:C25H28ClF2N5O2Color and Shape:SolidMolecular weight:503.97SPR-00305
CAS:SPR-00305 is a novel potent inhibitor of the mvfr pathwayFormula:C24H19ClN2O3Color and Shape:SolidMolecular weight:418.87PSMA-1007
CAS:PSMA-1007 is a novel Glu-Ureido-type prostate-specific membrane antigen (PSMA) inhibitor.Formula:C49H55FN8O16Color and Shape:SolidMolecular weight:1030.01Antitubercular agent-22
Antitubercular agent-22 combats Candida albicans (MIC: 2.34 μg/ml) and M. tuberculosis (MIC: 2 μg/ml).Formula:C24H28FN5O8Color and Shape:SolidMolecular weight:533.51Ibafloxacine
CAS:Ibafloxacine (R835) is a fluoroquinolone antibiotic that is used exclusively in veterinary applications and shows zero good bacteriostatic effect againstFormula:C15H14FNO3Purity:97.67%Color and Shape:SolidMolecular weight:275.27LSD1-IN-16
LSD1-IN-16 (4b) inhibits LSD1, MAO-A/B; IC50: 0.015-0.366 μM. Halts prostate cancer cell growth; IC50: 15.2 μM.Formula:C20H18N2OSColor and Shape:SolidMolecular weight:334.43CAII-IN-1
CAII-IN-1 (3n) is a selective bovine CA-II inhibitor with 10.3 μM IC50, used in carbonic anhydrase disorder studies.Formula:C19H21FN4SColor and Shape:SolidMolecular weight:356.46
