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(2,763 products)
- Apoptosis(6,207 products)
- Cell Cycle/Checkpoint(4,810 products)
- Chromatin/Epigenetics(2,547 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(9,002 products)
- Immunology and Inflammation(3,751 products)
- Influenza Virus(298 products)
- JAK/STAT signaling(416 products)
- MAPK Signaling(1,245 products)
- Membrane Transporter/Ion Channel(3,103 products)
- Metabolism(10,129 products)
- Microbiology/Virology(7,570 products)
- Neuroscience(10,343 products)
- Other Inhibitors(35,810 products)
- Oxidation-Reduction(40 products)
- PI3K/Akt/mTOR Signaling(1,412 products)
- Proteases/Proteasome(1,682 products)
- Stem Cell and Derivatives(757 products)
- Tyrosine Kinase/Adaptors(1,954 products)
- Ubiquitination(1,715 products)
Show 16 more subcategories
Found 66606 products of "Inhibitors"
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EGFR-IN-59
CAS:EGFR-IN-59: EGFR inhibitor, IC50 = 190 nM, induces apoptosis, cytotoxic to A549 cells (IC50 = 8.62 μM) and WI38 cells (IC50 = 52.6 μM). Use: Various cancers.Formula:C27H23N5O4SColor and Shape:SolidMolecular weight:513.57UCSF648
CAS:UCSF648 (Compound 5A6-48) weakly activates MTNR1A and ADRA2A. UCSF648 is a chemical probe for the serotonin receptor 5-HT 5A [1].Formula:C15H19ClN2O2SColor and Shape:SolidMolecular weight:326.84Phosphoenol-3-bromopyruvate
CAS:Phosphoenol-3-bromopyruvate is a mechanism-based inhibitor of phosphoenolpyruvate carboxylase from maizeFormula:C3H4BrO6PColor and Shape:SolidMolecular weight:246.94Naxillin
CAS:Naxillin is a non-growth hormone like molecule that induces lateral root development.Formula:C13H10F3N3OSPurity:99.22%Color and Shape:SolidMolecular weight:313.3N-Methyl Duloxetine hydrochloride
CAS:N-Methyl Duloxetine hydrochloride elicits both tonic and use-dependent block of neuronal Na+ channels. N-Methyl Duloxetine hydrochloride is an analgesic.Formula:C19H22ClNOSPurity:98%Color and Shape:SolidMolecular weight:347.9Antileishmanial agent-7
CAS:Compound 23: Strong against Leishmania, IC50: 6.89 μM (L. donovani), 259 μM (L-6).Formula:C20H18O8Color and Shape:SolidMolecular weight:386.35Prodipine hydrochloride
CAS:Prodipine hydrochloride for purified and plasma Dipeptidyl peptidase IV (DPP IV) from the rabbit (IC50 of 4.5 μM and 30 μM, respectively).Formula:C20H26ClNPurity:98%Color and Shape:SolidMolecular weight:315.88SDZ 21009
CAS:β-adrenoceptor and 5-HT1A/1B receptor antagonistFormula:C19H28N2O4Purity:98%Color and Shape:SolidMolecular weight:348.44CI-898 HCl
CAS:CI-898 HCl: lipophilic antifolate, DHFR inhibitor, effective on methotrexate-resistant cancers, synergizes with other drugs in advanced P338 leukemia.Formula:C19H26Cl3N5O3Color and Shape:SolidMolecular weight:478.8LB-205
CAS:LB-205 is a Zn 2+ dependent pan-inhibitor of class I and class II HDACs. It also has a long half-life in vivo.Formula:C18H21N3O2SColor and Shape:SolidMolecular weight:343.44Avidinorubicin
CAS:Avidinorubicin is a novel anthracycline with platelet aggregation inhibitory activity.Formula:C60H86N4O22Color and Shape:SolidMolecular weight:1215.34T761-0184
CAS:T761-0184 is a potent antagonist of α7 nicotinic receptor (nAChR) [1].Formula:C16H20FN3OColor and Shape:SolidMolecular weight:289.35CCT373566
CAS:CCT373566: potent BCL6 degrader, oral, IC50 2.2 nM; hinders cell growth in vitro & shrinks tumors in vivo.Formula:C26H29ClF2N6O3Color and Shape:SolidMolecular weight:547FLT3/D835Y-IN-1
CAS:FLT3/D835Y-IN-1, an oral FLT3 inhibitor (IC50: FLT3 - 0.26 nM, D835Y - 0.18 nM), shows anticancer potential in AML research.Formula:C22H21N5O3Color and Shape:SolidMolecular weight:403.43A-1062
CAS:A-1062, a resolvase-binding inhibitor, inhibits resolvase binding to the res site.Formula:C18H10O6SPurity:98%Color and Shape:SolidMolecular weight:354.33Cyclic-di-GMP
CAS:Cyclic-di-GMP is a STING agonist and ubiquitous second messenger, which regulates the formation, motility and virulence of biofilms in various bacterial speciesFormula:C20H24N10O14P2Purity:98%Color and Shape:SolidMolecular weight:690.41IDO1-IN-15
CAS:IDO1-IN-15 is an effective IDO1 inhibitor with IC50 of 127 nM. The potency of IDO1-IN-15 against IDO1 enzyme is comparable with Epacadostat in vitro.Formula:C13H14BrFN6O3Color and Shape:SolidMolecular weight:401.19Thiamphenicol palmitate
CAS:Thiamphenicol palmitate is a Prodrug of Thiamphenicol, inhibiting the 50S subunit of the bacterial ribosome and protein translation.Formula:C28H45Cl2NO6SColor and Shape:SolidMolecular weight:594.63M 16287
CAS:M 16287 is a potent aldose reductase inhibitor.Formula:C11H7ClN2O5SColor and Shape:SolidMolecular weight:314.7Espatropate
CAS:Espatropate is a bronchodilator with antimuscarinic activity.Formula:C19H23N3O3Color and Shape:SolidMolecular weight:341.4
