
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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Carbonic anhydrase inhibitor 13
CAS:Carbonic anhydrase inhibitor 13 (compound 7) is a potent inhibitor of carbonic anhydrase (CA).Formula:C17H15N5O3S2Color and Shape:SolidMolecular weight:401.46RPR-200765A Mesylayte
CAS:RPR-200765A selectively inhibits p38 MAP kinase, blocks TNFalpha in vitro (EC50 = 110 nM) and in mice (ED50 = 6 mg/kg), and shows promise in RA treatment.Formula:C24H25FN4O4Color and Shape:SolidMolecular weight:452.48LY-2599506
CAS:LY-2599506 is a novel glucokinase activator.Formula:C21H25N3O4SColor and Shape:SolidMolecular weight:415.51Tubulin polymerization-IN-18
CAS:Tubulin aggregation-IN-18 (compound 3) is a potent tubulin aggregation inhibitor with potential for breast cancer and drug-resistant colon cancer studies.Formula:C25H25NO6Color and Shape:SolidMolecular weight:435.47HDAC-IN-49
HDAC-IN-49: potent, broad HDAC inhibitor; IC50s: 10-1880 nM for HDAC1-6; strong anti-leukemic, low toxicity to healthy cells.Formula:C26H27FN4O4Color and Shape:SolidMolecular weight:478.52B-Raf IN 6
CAS:B-Raf IN 6: potent B-Raf kinase inhibitor, IC50 of 1.7 nM, doesn't target PXR, metabolically stable, potential in cancer research.Formula:C24H21F3N6O2S2Color and Shape:SolidMolecular weight:546.59LG190155
CAS:LG190155 is a VDR agonist that regulates calcium, bone metabolism, and cell growth.Formula:C31H44O4Color and Shape:SolidMolecular weight:480.68Risotilide
CAS:Risotilide is a voltage-dependent potassium channel inhibitor. It can prolong cardiac action potentials and refractory periods.Formula:C15H27N3O4S2Purity:98%Color and Shape:SolidMolecular weight:377.52Tramazoline hydrochloride
CAS:Tramazoline hydrochloride: a nasal decongestant in sprays, it's an α-adrenergic agonist reducing mucus secretion.Formula:C13H18ClN3Color and Shape:SolidMolecular weight:251.76SC 46944
CAS:SC 46944 is a highly potent human renin inhibitor.Formula:C34H55N3O7Color and Shape:SolidMolecular weight:617.82ZLY032
CAS:ZLY032 is a FFAR1 and PPARδ agonist (EC50: 68 nM & 102 nM), selective over PPARα/γ, lowers glucose, cholesterol, and improves NASH in mice.Formula:C22H18F3NO4SColor and Shape:SolidMolecular weight:449.44EGFR-IN-542
CAS:EGFR-IN-542 is a novel EGFR inhibitor reducing cardiac inflammation, fibrosis, and dysfunction, promising for obesity complications.Formula:C23H18FN5Color and Shape:SolidMolecular weight:383.42AFN941
CAS:AFN941 is a staurosporine analog, acting as a Jak3-specific inhibitor.Formula:C28H30N4O3Color and Shape:SolidMolecular weight:470.56COX-2-IN-11
CAS:COX-2-IN-11 (compound 7b2) is a potent and selective COX-2 inhibitor. COX-2-IN-11 has the potential in inflammation disease research[1].Formula:C12H12OS3Color and Shape:SolidMolecular weight:268.42BMS-187745
CAS:BMS-187745 is a squalene synthase inhibitor.Formula:C16H19O7PSColor and Shape:SolidMolecular weight:386.36SM 21
CAS:SM 21 is a sigma(2) antagonist.Formula:C18H24ClNO3Purity:98%Color and Shape:SolidMolecular weight:337.84IHVR-11029
CAS:IHVR-11029 inhibits ER α-glucosidase, combats hemorrhagic fever viruses, and hinders enveloped virus morphogenesis.Formula:C18H27F2NO5Color and Shape:SolidMolecular weight:375.41Adenosine receptor inhibitor 1
CAS:Potent, selective adenosine receptor blocker with strong affinity, especially A2A (Ki 68.5 nM). Promising for cancer, neurodegeneration study.Formula:C17H19ClFN5O3Color and Shape:SolidMolecular weight:395.82AChE/MAO-IN-1
AChE/MAO-IN-1 is a potent inhibitor of human acetylcholinesterase (AChE), monoamine oxidase A (MAO-A), and monoamine oxidase B (MAO-B), demonstrating inhibitoryFormula:C23H26N2O3Color and Shape:SolidMolecular weight:378.46PWT33597 mesylate
CAS:PWT33597 (VDC-597) is an oral PI3K alpha/mTOR dual inhibitor, potentially causing cancer cell death and growth inhibition.Formula:C27H34F2N8O7S2Color and Shape:SolidMolecular weight:684.7348
