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(2,782 products)
- Apoptosis(6,263 products)
- Cell Cycle/Checkpoint(4,792 products)
- Chromatin/Epigenetics(2,441 products)
- Cytoskeletal Signaling(1,528 products)
- DNA Damage/DNA Repair(2,965 products)
- Endocrinology/Hormones(3,707 products)
- Enzyme(3,667 products)
- GPCR/G-Protein(9,009 products)
- Immunology and Inflammation(3,875 products)
- Influenza Virus(301 products)
- JAK/STAT signaling(414 products)
- MAPK Signaling(1,248 products)
- Membrane Transporter/Ion Channel(3,033 products)
- Metabolism(10,209 products)
- Microbiology/Virology(7,592 products)
- Neuroscience(10,381 products)
- Other Inhibitors(36,040 products)
- Oxidation-Reduction(42 products)
- PI3K/Akt/mTOR Signaling(1,442 products)
- Proteases/Proteasome(1,724 products)
- Stem Cell and Derivatives(826 products)
- Tyrosine Kinase/Adaptors(2,035 products)
- Ubiquitination(1,717 products)
Show 16 more subcategories
Found 66683 products of "Inhibitors"
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CP 81282
CAS:CP 81282 inhibits human renin and endothiapepsin.Formula:C32H47F2N5O6Color and Shape:SolidMolecular weight:635.74c-Fms-IN-10
CAS:c-Fms-IN-10 is a thieno[3,2-d]pyrimidine derivative, an FMS kinase inhibitor with IC50 of 2 nM, exhibiting anti-tumor properties.Formula:C22H19N7OSPurity:98%Color and Shape:SolidMolecular weight:429.5ARN19874
CAS:ARN19874 is a selective, reversible uncompetitive N-acylphosphatidylethanolamine phospholipase D (NAPE-PLD) activity inhibitor. With an IC50 of ~34 μM[1].Formula:C19H14N4O4SPurity:98%Color and Shape:SolidMolecular weight:394.4PCSK9 modulator-4
CAS:Compound 21, a potent PCSK9 modulator (EC50=0.15 nM), targets LDL-C for hyperlipidemia research.Formula:C17H11F2N3OColor and Shape:SolidMolecular weight:311.29Amiglumide
CAS:Amiglumide is a non-peptide cholecystokinin antagonist.Formula:C26H36N2O4Color and Shape:SolidMolecular weight:440.58Iobenguane I 131
CAS:<p>Iobenguane I 131 targets sympathetic tissue and tumors; used in cancer treatment and imaging. MIBG blocks neurons, collects in adrenal medulla.</p>Formula:C8H10IN3Color and Shape:SolidMolecular weight:279.09FQ
CAS:FQ is a novel reversible inhibitor of mixed-type tyrosinase.Formula:C14H9FN2OColor and Shape:SolidMolecular weight:240.23RGH-5526
CAS:RGH-5526: novel antihypertensive, boosts hypothalamic NA turnover, reduces blood pressure via decreased sympathetic nerve activity.Formula:C16H25N5O3Purity:98%Color and Shape:SolidMolecular weight:335.4(Rac)-AZD 6482
CAS:(Rac)-AZD 6482 is the racemate of AZD 6482. AZD 6482 is a potent and selective inhibitor of p110β (IC50 of 0.69 nM).Formula:C22H24N4O4Color and Shape:SolidMolecular weight:408.45BI1002494
CAS:BI1002494 is an effective and selective Syk inhibitor.Formula:C23H25N3O5Purity:98%Color and Shape:SolidMolecular weight:423.46Tarafenacin
CAS:Tarafenacin is a highly selective M3 muscarinic receptor antagonist (Ki= 0.19 nM), ~200 fold selectivity over the M2 receptor.Formula:C21H20F4N2O2Purity:98%Color and Shape:SolidMolecular weight:408.39(S)-HexylHIBO
CAS:Group I mGlu receptor antagonistFormula:C12H20N2O4Purity:98%Color and Shape:SolidMolecular weight:256.3BRD4 Inhibitor-25
BRD4 Inhibitor-25 blocks BRD4 (BD1: IC50 0.82 μM, BD2: 1.94 μM), induces cell death in ovarian cancer, used in cancer research.Formula:C29H27N5O6SColor and Shape:SolidMolecular weight:573.62AF267
CAS:AF267 is a M1 muscarinic agonist that works by restoring cognitive impairments.Formula:C10H18N2OSPurity:98%Color and Shape:SolidMolecular weight:214.33Disulfamide
CAS:Disulfamide: Oral carbonic anhydrase inhibitor, IC50 0.07 μM, diuretic by blocking Na+/HCO3- reabsorption.Formula:C7H9ClN2O4S2Purity:98.65%Color and Shape:SolidMolecular weight:284.74SN 003
CAS:SN 003 is a CRF1 antagonist.Formula:C19H25N5O2Purity:98%Color and Shape:SolidMolecular weight:355.43BMS-566394
CAS:BMS-566394 is a potent, exceptionally selective inhibitor of TNF-α converting enzyme (TACE).Formula:C22H21F3N4O4Color and Shape:SolidMolecular weight:462.42Amadinone
CAS:Amadinone is an androgen antagonist.Formula:C20H25ClO3Color and Shape:SolidMolecular weight:348.86IRFI-165
CAS:IRFI-165 is an adenosine A1 receptor inhibitorFormula:C16H18N4Color and Shape:SolidMolecular weight:266.34JNJ-61803534
CAS:JNJ-61803534: RORγt inverse agonist, IC50=9.6 nM, oral, anti-inflammatory, reduces IL-17A in T cells.Formula:C23H23Cl2F6N3O4SColor and Shape:SolidMolecular weight:622.41
