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(2,762 products)
- Apoptosis(6,207 products)
- Cell Cycle/Checkpoint(4,810 products)
- Chromatin/Epigenetics(2,548 products)
- Cytoskeletal Signaling(1,520 products)
- DNA Damage/DNA Repair(2,908 products)
- Endocrinology/Hormones(3,703 products)
- Enzyme(3,671 products)
- GPCR/G-Protein(9,001 products)
- Immunology and Inflammation(3,751 products)
- Influenza Virus(298 products)
- JAK/STAT signaling(416 products)
- MAPK Signaling(1,246 products)
- Membrane Transporter/Ion Channel(3,103 products)
- Metabolism(10,130 products)
- Microbiology/Virology(7,570 products)
- Neuroscience(10,341 products)
- Other Inhibitors(35,810 products)
- Oxidation-Reduction(40 products)
- PI3K/Akt/mTOR Signaling(1,413 products)
- Proteases/Proteasome(1,682 products)
- Stem Cell and Derivatives(758 products)
- Tyrosine Kinase/Adaptors(1,954 products)
- Ubiquitination(1,715 products)
Show 16 more subcategories
Found 66606 products of "Inhibitors"
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K203
K203 is a potent tabun-inhibited AChE reactivator and is an important antidote to organophosphorus poisoning.Formula:C16H18Br2N4O2Color and Shape:SolidMolecular weight:458.15STA-1474
CAS:STA-1474, a soluble prodrug of ganetespib (STA-9090), becomes a strong HSP90 inhibitor effective against canine tumors.Formula:C20H21N4O6PColor and Shape:SolidMolecular weight:444.38AL-6556
CAS:AL-6556 is a prostaglandin DP receptor agonist.Formula:C20H33ClO5Color and Shape:SolidMolecular weight:388.93ATX inhibitor 12
Oral ATX inhibitor 12 (IC50: 1.72 nM) at 60 mg/kg prevents lung damage in C57Bl/6J mice.
Formula:C30H34FN5O2Color and Shape:SolidMolecular weight:515.62Antimalarial agent 9
Antimalarial 9, a quinoline-imidazole derivative, effectively targets CQ-susceptible (IC50-0.14 μM) and MDR strains (IC50-0.41 μM) with low toxicity.Formula:C28H32BrN3O2Color and Shape:SolidMolecular weight:522.48Antibacterial agent 80
Antibacterial agent 80 (compound 20) has antibacterial activity [1].Formula:C14H21N3S2Color and Shape:SolidMolecular weight:295.47Cbl-b-IN-2
CAS:Cbl-b-IN-2 is an oral E3 enzyme inhibitor for immune-modulated diseases and cancer research.Formula:C29H30F5N5O2Color and Shape:SolidMolecular weight:575.57CD73-IN-7
CAS:CD73-IN-7: potent inhibitor of CD73, blocks adenosine production to treat tumors.
Formula:C13H11ClN4O2Color and Shape:SolidMolecular weight:290.7Mu opioid receptor antagonist 3
Potent, selective MOR antagonist (compound 26); crosses blood-brain barrier. Ki: 0.24 nM, EC50: 0.54 nM; for studying OUD.Formula:C25H28N2O4SColor and Shape:SolidMolecular weight:452.57FGFR4-IN-9
FGFR4-IN-9 is a selective inhibitor of FGFR4 (IC50: 75.3 nM) that effectively inhibits the growth and angiogenesis of hepatocellular carcinoma cells.Formula:C24H22ClF3N4O4Color and Shape:SolidMolecular weight:522.9BSc5367
CAS:BSc5367 inhibits Nek1 kinase (IC50: 11.5 nM), key in cell cycle, DNA repair, impacting ALS, PKD, cancer.
Formula:C20H15N3O2Color and Shape:SoildMolecular weight:329.35Enpp-1-IN-7
Enpp-1-IN-7: potent enpp-1 inhibitor, broad specificity, potential in cancer/infectious disease research. (WO2021203772A1)Formula:C18H19N7O4SColor and Shape:SolidMolecular weight:429.45Tubulin polymerization-IN-34
"Tubulin-IN-34 inhibits oxazolylisoindole microtubule assembly, selective for VL51 lymphoma."Formula:C31H35N3O6Color and Shape:SolidMolecular weight:545.63MRS-2339
CAS:MRS-2339 is a P2X receptor activator.Formula:C12H15ClN5O6PColor and Shape:SolidMolecular weight:391.70S-HP210
S-HP210: selective GR modulator, blocks NF-κB (IC50: 1.92 μM), non-toxic to mouse fibroblasts.Formula:C22H19N3O2S2Color and Shape:SolidMolecular weight:421.54NSC381467
CAS:NSC381467: Potent, oral EGFR-TK inhibitor with strong antiproliferative effects, promising for cancer research.Formula:C20H16O7Color and Shape:SolidMolecular weight:368.34PI3K-IN-29
CAS:PI3K-IN-29: Strong PI3K block, inhibits Akt phosphorylation. IC50: U87MG 0.264µM, HeLa 2.04µM, HL60 1.14µM.Formula:C27H22ClN7O3SColor and Shape:SolidMolecular weight:560.03ZLM-66
ZLM-66: Doravirine analog, HIV-1 NNRTI inhibitor, IC50: 41nM, EC50: HIV-1 13nM, cIAP1 0.32nM; useful in AIDS research.
Color and Shape:SolidZurletrectinib
CAS:Zurletrectinib is a tyrosine kinase inhibitor with potential as an antineoplastic agent.Formula:C19H19F2N7O2Color and Shape:SolidMolecular weight:415.4MK-1220
CAS:MK-1220 is a novel Macrocyclic Inhibitor of Hepatitis C Virus NS3/4A Protease with Improved Preclinical Plasma Exposure.Formula:C40H53N5O9SColor and Shape:SolidMolecular weight:779.94
