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(2,795 products)
- Apoptosis(6,256 products)
- Cell Cycle/Checkpoint(4,836 products)
- Chromatin/Epigenetics(2,591 products)
- Cytoskeletal Signaling(1,534 products)
- DNA Damage/DNA Repair(2,880 products)
- Endocrinology/Hormones(3,748 products)
- Enzyme(3,670 products)
- GPCR/G-Protein(8,981 products)
- Immunology and Inflammation(3,789 products)
- Influenza Virus(299 products)
- JAK/STAT signaling(415 products)
- MAPK Signaling(1,250 products)
- Membrane Transporter/Ion Channel(3,148 products)
- Metabolism(10,143 products)
- Microbiology/Virology(7,591 products)
- Neuroscience(10,343 products)
- Other Inhibitors(35,823 products)
- Oxidation-Reduction(40 products)
- PI3K/Akt/mTOR Signaling(1,420 products)
- Proteases/Proteasome(1,680 products)
- Stem Cell and Derivatives(748 products)
- Tyrosine Kinase/Adaptors(1,958 products)
- Ubiquitination(1,720 products)
Show 16 more subcategories
Found 66564 products of "Inhibitors"
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BI 703704
CAS:BI 703704, a soluble guanylate cyclase (sGC) activator, inhibits the progression of diabetic nephropathy in the ZSF1 rat [1].Formula:C32H37N3O4SPurity:98%Color and Shape:SolidMolecular weight:559.72ST362
CAS:ST362, an anticancer agent, acts by disrupting DNA repair and halting growth in prostate, colon, lung and breast cancer cells.Formula:C25H21NO6SPurity:98%Color and Shape:SolidMolecular weight:463.5FTI-2628
CAS:FTI-2628 is a novel inhibitor of protein farnesyltransferase (FT), inhibiting the growth of P. falciparum in red blood cells and suppressing parasitemia.Formula:C31H34N4O3SColor and Shape:SolidMolecular weight:542.69FGI-106
CAS:FGI-106 combats Ebola, Rift Valley, Dengue Fever, HCV, and HIV-1; EC50s range from 100-900 nM.Formula:C28H38N6Purity:98%Color and Shape:SolidMolecular weight:458.64Axl-IN-3
Axl-IN-3 is a selective, potent and orally active inhibitor of AXL kinase (IC50: 41.5 nM) and has a low inhibitory effect on other kinases.Formula:C24H25ClN6O2Color and Shape:SolidMolecular weight:464.95ZL-Pin13
CAS:ZL-Pin13: potent Pin1 inhibitor (IC50: 67 nM), halts MDA-MB-231 cell growth, reduces Pin1 substrates.Formula:C24H23ClN2O3SColor and Shape:SoildMolecular weight:454.97SP-471
SP-471 is a potent inhibitor of dengue virus (DENV) protease (IC50: 18 μM) and inhibits the inter- and intramolecular protease processes of DENV.Formula:C33H26BrN5Color and Shape:SolidMolecular weight:572.5RXR antagonist 2
RXR antagonist 2 is a potent antagonist of RXR (Ki: 0.391 μM, Kd: 0.281 μM). RXR antagonist 2 has shown research potential for RXR-related diseases.Formula:C29H35F3N2O3Color and Shape:SolidMolecular weight:516.6Tubulin inhibitor 19
Tubulin inhibitor 19 (9b), a potent indole chalcone, strongly blocks tubulin, valuable in cancer studies.Formula:C21H23NO5Color and Shape:SolidMolecular weight:369.41Freselestat quarterhydrate
ONO-6818 quarterhydrate: oral neutrophil elastase inhibitor, Ki 12.2 nM; >100x less effective on other proteases; strong anti-inflammatory.Formula:C23H30N6O5Color and Shape:SolidMolecular weight:457.03SMCypI C31
SMCypIC31, a non-peptide cyclophilin inhibitor, blocks PPIase at 0.1 μM IC50 and fights various HCV genotypes (EC50: 1.20-7.76 μM).Formula:C27H30N4O2SColor and Shape:SolidMolecular weight:474.62PD-1/PD-L1-IN-13
PD-1/PD-L1-IN-13 is a potent immune checkpoint PD-1/PD-L1 inhibitor with an IC50 value of 10.2 nM for PD-1/PD- L1 interaction.PD-1/PD-L1-IN-13 promotes CD8+ T-Formula:C36H34ClF2N3O9Color and Shape:SolidMolecular weight:726.12VVD-118313
CAS:VVD-118313 (5a) is a potent JAK1 inhibitor targeting allosteric cysteine, blocking cytokine signaling for cancer research.Formula:C19H22Cl2N2O3SColor and Shape:SolidMolecular weight:429.36Antiangiogenic agent 2
Antiangiogenic agent 2 (compound 3b) is a potent inhibitor of thymidine phosphorylase (IC50: 39.71 μM) and exhibits anti-angiogenic effects.
Formula:C26H26FN3O4Color and Shape:SolidMolecular weight:463.5GT-055
GT-055 (LCB18-055) is a novel inhibitor of broad-spectrum β-lactamase.Formula:C13H20F3N5O8SColor and Shape:SolidMolecular weight:463.39GR 83895
CAS:GR 83895 is an antagonist of prototype fibrinogen receptor.Formula:C29H39N9O8SPurity:98%Color and Shape:SolidMolecular weight:673.74FTO-IN-4
CAS:FTO-IN-4 is a potent and selective inhibitor of adiposity and obesity-associated protein (FTO).Formula:C22H16Cl2N6O6Color and Shape:SolidMolecular weight:531.31CLK1/4-IN-1
CLK1/4-IN-1 inhibits Clk1/4 (IC50: 9.7/6.6 nM), curbing T24 cell growth (GI50: 1.1 μM). Potential cancer research tool.Formula:C18H14ClNO4SColor and Shape:SolidMolecular weight:375.83Antibacterial agent 76
Antibacterial agent 76 (compound 9) is a potent antibacterial agent.Formula:C23H27N3O2SColor and Shape:SolidMolecular weight:409.54LY210073
CAS:LY210073 is an antagonist of the Leukotriene B4 (LTB4) receptor (IC50: 6.2 nM).Formula:C30H28O8Purity:98%Color and Shape:SolidMolecular weight:516.54
