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(2,763 products)
- Apoptosis(6,205 products)
- Cell Cycle/Checkpoint(4,812 products)
- Chromatin/Epigenetics(2,553 products)
- Cytoskeletal Signaling(1,520 products)
- DNA Damage/DNA Repair(2,906 products)
- Endocrinology/Hormones(3,703 products)
- Enzyme(3,671 products)
- GPCR/G-Protein(8,965 products)
- Immunology and Inflammation(3,749 products)
- Influenza Virus(297 products)
- JAK/STAT signaling(414 products)
- MAPK Signaling(1,244 products)
- Membrane Transporter/Ion Channel(3,118 products)
- Metabolism(10,123 products)
- Microbiology/Virology(7,569 products)
- Neuroscience(10,314 products)
- Other Inhibitors(35,804 products)
- Oxidation-Reduction(40 products)
- PI3K/Akt/mTOR Signaling(1,411 products)
- Proteases/Proteasome(1,681 products)
- Stem Cell and Derivatives(752 products)
- Tyrosine Kinase/Adaptors(1,947 products)
- Ubiquitination(1,716 products)
Show 16 more subcategories
Found 66604 products of "Inhibitors"
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Nrf2 activator-2
Compound O15, an Osthole derivative, is a potent Nrf2 agonist with an EC50 of 2.9 μM; it inhibits Keap1-Nrf2 binding and Nrf2 ubiquitination.Formula:C20H17BrO3Color and Shape:SolidMolecular weight:385.25JAK-IN-23
"JAK-IN-23: oral dual JAK/STAT & NF-κB inhibitor; JAK1 (IC50: 8.9 nM), JAK2 (15 nM), JAK3 (46.2 nM); for IBD research."Formula:C23H22Cl2N4OColor and Shape:SolidMolecular weight:441.35Antitubercular 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:533.51K252d
CAS:K252d: indolocarbazole alkaloid in Nocardiopsis; inhibits PKC in rat brain and bovine heart phosphodiesterase.
Formula:C26H23N3O5Color and Shape:SolidMolecular weight:457.48LSD1/ER-IN-1
LSD1/ER-IN-1 inhibits ER & LSD1 (IC50: 1.55 μM), and fights MCF-7 breast cancer (IC50: 8.79 μM).Formula:C23H18FNO6SColor and Shape:SolidMolecular weight:455.46HbF inducer-1
HbF inducer-1 is a fetal hemoglobin inducer which is orally bioavailable.Formula:C18H19N3O3Color and Shape:SolidMolecular weight:325.36Moxaverine hydrochloride
CAS:Moxaverine HCL, a papaverine derivative, is in Phase III trials for treating ocular blood flow in macular degeneration and glaucoma.Formula:C20H22ClNO2Color and Shape:SolidMolecular weight:343.85CU-2010
CAS:CU-2010 is a synthetic compound that reduces blood loss and aids recovery post-cardiac surgery.Formula:C37H42N6O6SColor and Shape:SolidMolecular weight:698.83THR-β agonist 4
CAS:THR-β agonist 4 is a potent agonist of THR-β.Formula:C16H11Cl2F2N5O6SColor and Shape:SolidMolecular weight:510.26Gly-7-MAD-MDCPT
CAS:Gly-7-MAD-MDCPT: anticancer Camptothecin with IC50 of 10-1000 nM against diverse cancers.
Formula:C24H22N4O7Color and Shape:SolidMolecular weight:478.45FPI-1465
CAS:FPI-1465: Dual serine-β-lactamase & PBP inhibitor; IC50 PBP2=1.0 μg/mL; Kd CTX-M-15=0.011μM, OXA-48=5.3μM.Formula:C11H18N4O7SColor and Shape:SolidMolecular weight:350.35Calphostin I
CAS:Calphostins, from Cladosporium fungus, inhibit PKC. Notably, calphostin C is a potent biochemical tool.Formula:C44H38O15Color and Shape:SolidMolecular weight:806.76Thiomuscimol hydrobromide
CAS:Thiomuscimol hydrobromide is an agonist of GABAA receptor.Formula:C4H6N2OSPurity:98%Color and Shape:SolidMolecular weight:130.17MtTMPK-IN-5
MtTMPK-IN-5 inhibits Mtb TMPK with IC50 of 34 μM and fights tuberculosis with MIC of 12.5 μM, aiding TB research.Formula:C21H23N5O2Color and Shape:SolidMolecular weight:377.44ONO-8809
CAS:ONO-8809: Thromboxane A2 antagonist, reduces airway hyperresponse, macrophage accumulation, and MMP-9 in SHRSP brains.Formula:C30H46BrNO4SPurity:98%Color and Shape:SolidMolecular weight:596.66SSTR5 antagonist 2 hydrochloride
SSTR5 antagonist 2 hydrochloride: potent, oral SSTR5 blocker with potential in type 2 diabetes research.Formula:C32H36ClFN2O5Color and Shape:SolidMolecular weight:583.09AY-22,252
CAS:AY-22,252 is an inhibitor of beef heart & rat brain nucleoside-3',5'- monophosphate phosphodiesterase.Formula:C27H37NaO7Color and Shape:SolidMolecular weight:496.57D-473
CAS:D-473 is a novel orally active triple reuptake inhibitor targeting dopamine, serotonin and norepinephrine transporters.
Formula:C26H27F2NO3Color and Shape:SolidMolecular weight:439.49Latrunculin M
CAS:Latrunculin M, a novel marine toxin, disrupts microfilament organization in cultured cells.Formula:C21H33NO5SColor and Shape:SolidMolecular weight:411.55Topo I/COX-2-IN-2
Compound W10 is a dual inhibitor of Topo I (IC50: 0.90μM) and COX-2 (IC50: 2.31μM), inducing cancer cell apoptosis via mitochondria.Formula:C24H25ClN4OColor and Shape:SolidMolecular weight:420.93
