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(2,939 products)
- Apoptosis(6,643 products)
- Cell Cycle/Checkpoint(4,918 products)
- Chromatin/Epigenetics(2,633 products)
- Cytoskeletal Signaling(1,595 products)
- DNA Damage/DNA Repair(2,868 products)
- Endocrinology/Hormones(3,765 products)
- Enzyme(3,675 products)
- GPCR/G-Protein(9,484 products)
- Immunology and Inflammation(3,958 products)
- Influenza Virus(301 products)
- JAK/STAT signaling(417 products)
- MAPK Signaling(1,272 products)
- Membrane Transporter/Ion Channel(3,404 products)
- Metabolism(10,179 products)
- Microbiology/Virology(7,953 products)
- Neuroscience(11,146 products)
- Other Inhibitors(35,856 products)
- Oxidation-Reduction(41 products)
- PI3K/Akt/mTOR Signaling(1,439 products)
- Proteases/Proteasome(1,692 products)
- Stem Cell and Derivatives(733 products)
- Tyrosine Kinase/Adaptors(1,992 products)
- Ubiquitination(1,745 products)
Show 16 more subcategories
Found 66508 products of "Inhibitors"
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Demethoxyviridin
CAS:Demethoxyviridin inhibits mammalian Ptdlns 3-kinase (p110) and is antifungal.Formula:C19H14O5Purity:98%Color and Shape:SolidMolecular weight:322.31IAB15
CAS:IAB15 is a potent inhibitor of T-type calcium channel that can be used in the research of epilepsy [1].Formula:C15H14F3NO2Color and Shape:SolidMolecular weight:297.27Mu opioid receptor antagonist 4
Compound 31: Potent, selective MOR antagonist; crosses blood-brain barrier; Ki & EC50: 0.38 nM; useful for OUD research.Formula:C25H28N2O4SColor and Shape:SolidMolecular weight:452.57Glutamate-5-kinase-IN-1
Glutamate-5-kinase-IN-1 is a potent G5K inhibitor with a 4.1 μM MIC, showing promise in anti-TB research.Formula:C20H18N2OColor and Shape:SolidMolecular weight:302.37Detoxin D1
CAS:Detoxin D1 is a selective blasticidin S antagonist.Formula:C28H41N3O8Purity:98%Color and Shape:SolidMolecular weight:547.64Antifungal agent 13
CAS:Antifungal agent 13 demonstrates significant antifungal activity against Sclerotinia sclerotiorum, achieving an EC50 of 1.25 mg/L.Formula:C21H16ClF3N4OColor and Shape:SolidMolecular weight:432.83SJF 8240
CAS:c-MET degrader with foretinib linked to VHL ligand; reduces c-MET in 6h, hampers AKT, halts GTL16 cells (IC50=66.7nM), acts on exon-14-less c-MET.
Formula:C58H65F2N7O11SColor and Shape:SolidMolecular weight:1106.25CYP1B1-IN-2
CYP1B1-IN-2 (compound 9j) is a highly potent and selective inhibitor of CYP1B1, a cytochrome P450 enzyme. It exhibits an IC50 value of 0.52 nM [1].Formula:C20H11F3O2Color and Shape:SolidMolecular weight:340.3PD-1/PD-L1-IN-16
PD-1/PD-L1-IN-16 is a potent inhibitor of PD-1/PD-L1 (IC50: 53.2 nM) and has shown research potential for tumour immunotherapy.Formula:C34H30N4O4Color and Shape:SolidMolecular weight:558.63(S)-MALT1-IN-5
CAS:(S)-MALT1-IN-5: Potent MALT1 protease inhibitor, may help in abnormal T/B-cell signalling and MALT1-linked diseases.Formula:C17H17ClF2N6O3Color and Shape:SolidMolecular weight:426.80Vindeburnol
CAS:Vindeburnol is a cerebral vasodilator vincamine analog that bears neuroprotective properties.Formula:C17H20N2OColor and Shape:SolidMolecular weight:268.35Metocurine chloride
CAS:Metocurine: a muscle relaxant, not for kidney failure patients as it's kidney-excreted.Formula:C40H48Cl2N2O6Color and Shape:SolidMolecular weight:723.72COX-2/PI3K-IN-1
COX-2/PI3K-IN-1 (compound 5d) is a potent inhibitor of PI3K (IC50: 1.14 nM). COX-2/PI3K-IN-1 is a selective inhibitor of COX-2 (Ki: 3.24 nM).Formula:C19H14ClN5S2Color and Shape:SolidMolecular weight:411.93Anticancer agent 35
Compound 10, a sulfonylurea, inhibits A549, A431, PACA2 cells with IC50s: 18.1, 4.0, 18.9 μg/mL.Formula:C15H13N3O3S3Color and Shape:SolidMolecular weight:379.48Antibacterial agent 62
Novel anti-TB agent 62 is a redox compound with bactericidal activity against active and dormant bacteria.Formula:C24H33BrN2O2Color and Shape:SolidMolecular weight:461.44FTI-2148
CAS:FTI-2148 blocks RAS-related FT-1 & GGT-1; IC50: 1.4 nM & 1.7 μM.Formula:C24H28N4O3SPurity:98%Color and Shape:SolidMolecular weight:452.57Mesulergine hydrochloride
CAS:5-HT2A and 2C receptor antagonistFormula:C18H27ClN4O2SPurity:98%Color and Shape:SolidMolecular weight:398.95JNJ-1250132
CAS:JNJ-1250132 is a steroidal progesterone receptor modulator that inhibits binding of the receptor to DNA in vitro.Formula:C33H41NO4Color and Shape:SolidMolecular weight:515.68DNA-PK-IN-2
CAS:DNA-PK-IN-2 is an inhibitor of the DNA-PK enzyme complex, useful in cancer research.Formula:C20H23N5O3Color and Shape:SolidMolecular weight:381.43PfPKG-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:492
