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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S107 hydrochloride
CAS:S107 hydrochloride stabilizes RyR2 by improving calstabin2 binding to mutant/PKA-phosphorylated channels.Formula:C11H16ClNOSPurity:98%Color and Shape:SolidMolecular weight:245.77ATR-IN-15
CAS:ATR-IN-15, an ATR kinase inhibitor, has an IC50 of 8 nM and also targets LoVo cells, DNA-PK, and PI3K with higher IC50 values.
Formula:C19H22N8OColor and Shape:SolidMolecular weight:378.43Galectin-3-IN-1
CAS:Galectin-3-IN-1 is a potent Gal-3 inhibitor, key in cancer-related metabolic processes.Formula:C18H26O10SColor and Shape:SolidMolecular weight:434.46G0507
CAS:G0507, a potent pyrrolopyrimidinedione, blocks E. coli growth by activating σE stress and targeting LolCDE ABC Transporter.Formula:C18H15N3O3SColor and Shape:SolidMolecular weight:353.39CLK1/2-IN-3
CAS:CLK1/2-IN-3 (Cpd-3) is a CLK1 and CLK2 inhibitor with antiproliferative activity that inhibits the activity of CLK and SRPK.Formula:C21H21N5O2Purity:99.04%Color and Shape:SolidMolecular weight:375.42CGP 36216 hydrochloride
CAS:CGP 36216 hydrochloride is a potent and selective antagonist of GABAB receptors (IC50: 43 μM).Formula:C5H14NO2PPurity:98%Color and Shape:SolidMolecular weight:151.14Multi-kinase-IN-2
CAS:Orally active Multi-kinase-IN-2 blocks angiokinases including VEGFR, PDGFR, FGFR, and more, reducing AKT/ERK phosphorylation and promoting apoptosis.Formula:C34H35N5O3Color and Shape:SolidMolecular weight:561.67KRAS G12D inhibitor 14
CAS:KRAS G12D inhibitor 14 is a potent inhibitor of KRAS G12D that binds KRAS G12D protein (Kd: 33 nM).
Formula:C20H19F3N4OSPurity:>99.99%Color and Shape:SolidMolecular weight:420.45KRP-297
CAS:KRP297 is a PPAR agonist potentially for the treatment of type 2 diabetes and dyslipidemia.Formula:C20H17F3N2O4SColor and Shape:SolidMolecular weight:438.42HJC0149
CAS:HJC0149 is a potent orally bioavailable signal transducer and activator of transcription 3 inhibitor.Formula:C15H10ClNO4SColor and Shape:SolidMolecular weight:335.76PF-04479745 tartrate
CAS:PF-04479745 (PF-4479745) is a selective 5-HT2C agonist with EC50 10 nM, effective in canine SUI models, not targeting 5-HT2A/B.Formula:C21H28N4O6Color and Shape:SolidMolecular weight:432.477(3S,5R)-Pitavastatin calcium
CAS:(3S,5R)-Pitavastatin calcium is the enantiomer of Pitavastatin which is a potent HMG-CoA reductase inhibitor.Formula:C25H26CaFNO4Purity:98%Color and Shape:SolidMolecular weight:463.562EBMI-13B
CAS:EBMI-13B is a potent and selective isozymes CA-VA and CA-VII activator.Formula:C10H14N4Purity:98%Color and Shape:SolidMolecular weight:190.24BChE-IN-14
CAS:BChE-IN-14 reverses cognitive decline, is safe for primary cells, crosses the blood-brain barrier, and selectively inhibits BChE (IC50: 0.011 μM for hBChE).Formula:C24H29NColor and Shape:SolidMolecular weight:331.49GSK 189254 HCl
CAS:GSK 189254A: histamine H3 antagonist, treats narcolepsy, may improve cognition and help with dementia, neuropathic pain.Formula:C21H26ClN3O2Purity:98%Color and Shape:SolidMolecular weight:387.9Mps-BAY2b
CAS:Mps-BAY2b is a novel MPS1 inhibitor.Formula:C20H23N5OColor and Shape:SolidMolecular weight:349.43FRAN-12
CAS:FRAN-12 is a histamine and 5-hydroxytryptamine antagonist with pressor properties.Formula:C19H21ClN4SColor and Shape:SolidMolecular weight:372.91Azalanstat mesylate
CAS:Azalanstat, an anti-obesity drug, inhibits cholesterol synthesis by targeting P450 enzyme lanosterol 14α-demethylase; reduces LDL more than HDL in hamsters.Formula:C23H28ClN3O5S2Color and Shape:SolidMolecular weight:526.063SGK1 inhibitor
CAS:SGK1 inhibitor targets SGK1/2 over SGK3, blocks GSK3β phosphorylation, lowers HCC1954 cell viability with BYL719, and reduces tumor growth in mice.Formula:C17H12Cl2N6O2SColor and Shape:SolidMolecular weight:435.29VEGFR-2-IN-6
CAS:VEGFR-2-IN-6 (WO 02/059110, example 64) is a potent inhibitor of VEGFR2, a crucial receptor involved in the regulation of angiogenesis [1].Formula:C20H21N7O2SPurity:99.01%Color and Shape:SolidMolecular weight:423.49
