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(2,833 products)
- Apoptosis(6,315 products)
- Cell Cycle/Checkpoint(4,875 products)
- Chromatin/Epigenetics(2,612 products)
- Cytoskeletal Signaling(1,566 products)
- DNA Damage/DNA Repair(2,872 products)
- Endocrinology/Hormones(3,754 products)
- Enzyme(3,672 products)
- GPCR/G-Protein(9,014 products)
- Immunology and Inflammation(3,901 products)
- Influenza Virus(300 products)
- JAK/STAT signaling(415 products)
- MAPK Signaling(1,256 products)
- Membrane Transporter/Ion Channel(3,154 products)
- Metabolism(10,139 products)
- Microbiology/Virology(7,620 products)
- Neuroscience(10,377 products)
- Other Inhibitors(35,852 products)
- Oxidation-Reduction(40 products)
- PI3K/Akt/mTOR Signaling(1,430 products)
- Proteases/Proteasome(1,691 products)
- Stem Cell and Derivatives(733 products)
- Tyrosine Kinase/Adaptors(1,983 products)
- Ubiquitination(1,726 products)
Show 16 more subcategories
Found 66522 products of "Inhibitors"
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STAT3-IN-3
CAS:STAT3-IN-3 is a potent and selective signal transducer inhibitor and transcription 3 (STAT3) activator.Formula:C27H26BrN3O6SPurity:98%Color and Shape:SolidMolecular weight:600.48SARS-CoV-2 Mpro-IN-9
CAS:SARS-CoV-2 Mpro-IN-9 (compound c7), a nonpeptidic, noncovalent inhibitor of SARS-CoV-2 main protease (Mpro), exhibits potent inhibitory action (IC50 = 0.085 μMFormula:C20H14N2O4Purity:99.74% - 99.89%Color and Shape:SolidMolecular weight:346.34Pentifylline
CAS:Pentifylline: vasodilator, blocks platelet clumping, curbs thromboxane A2, lowers free radicals, might protect nerves.Formula:C13H20N4O2Color and Shape:SolidMolecular weight:264.32SHP2 inhibitor LY6
CAS:SHP2 inhibitor LY6 (LY6) is a potent and selective SHP2 inhibitor (IC50: 9.8 μM) that blocks SHP2-mediated cell signaling and proliferation.Formula:C30H27Cl2N3O4Color and Shape:SolidMolecular weight:564.46KF 392
CAS:KF-392, an antiulcer drug, suppresses Shay ulcer and aspirin/stress/reserpine-induced gastric lesions in rats at 1-5 mg/kg doses orally.Formula:C8H12N2O4Color and Shape:SolidMolecular weight:200.192-TEDC
CAS:2-TEDC: Potent LOX inhibitor, blocks 5-LOX, 12-LOX, 15-LOX (IC50: 0.09, 0.013, 0.5 μM); aids atherosclerosis research.Formula:C16H13NO4SPurity:99.97%Color and Shape:SolidMolecular weight:315.34Bisdequalinium diacetate
CAS:Bisdequalinium diacetate is an antibacterial agentFormula:C44H64N4O4Purity:98%Color and Shape:SolidMolecular weight:713.01Purfalcamine
CAS:Purfalcamine, a selective PfCDPK1 inhibitor effective against malaria, has IC50 of 17 nM and EC50 of 230 nM; halts parasites at schizont stage.Formula:C29H33FN8OColor and Shape:SolidMolecular weight:528.62DSM267
CAS:DSM267 is a novel Plasmodium falciparum Dihydroorotate Dehydrogenase (PfDHODH) Inhibitor.Formula:C15H12F5N5Color and Shape:SolidMolecular weight:357.28A1AR antagonist 4
CAS:Compound 22: A1AR antagonist, pIC50 5.51, pKi 6.29, potent and selective.Formula:C23H25N3O2Color and Shape:SolidMolecular weight:375.46Penamecillin
CAS:Penamecillin (Wy 20788) is an orally active antibacterial agent.Formula:C19H22N2O6SColor and Shape:SolidMolecular weight:406.45YS-035 hydrochloride
CAS:inhibitor of outward K+ currentsFormula:C21H30ClNO4Purity:98%Color and Shape:SolidMolecular weight:395.92SK 946
CAS:SK 946 is a cognition activator.Formula:C15H21N3O2Color and Shape:SolidMolecular weight:275.352UR-3216
CAS:UR-3216 is a prodrug, selectively antagonizing GPIIb/IIIa receptors orally, with its active form, UR-2992, binding tightly to platelets.Formula:C27H29N7O7Purity:98%Color and Shape:SolidMolecular weight:563.56PNU-177864 hydrochloride
CAS:PNU-177864 hydrochloride is a potent, selective and orally active antagonist of dopamine D3 receptor.
Formula:C18H22ClF3N2O3SPurity:99.95%Color and Shape:SolidMolecular weight:438.89NPA101.3
CAS:NPA101.3 is a a Second-Generation RET/VEGFR2 Inhibitor. It is a potential clinical candidate for RET-driven cancers.Formula:C29H28N4O4SColor and Shape:SolidMolecular weight:528.62AY 29315
CAS:AY 29315 is a histamine H2-receptor antagonist with antisecretory and antiulcer activities.Formula:C25H41N7O3SColor and Shape:SolidMolecular weight:519.7GR 100679
CAS:GR 100679 is an antagonist of NK2 receptor.Formula:C34H44N6O5Purity:98%Color and Shape:SolidMolecular weight:616.75Antiviral agent 9
Antiviral agent 9: EC50 0.006 nM vs HIV-1, 300x more selective than TAF.Formula:C38H50N7O8PColor and Shape:SolidMolecular weight:763.82LY 393558
CAS:Dual 5-HT1B/1D receptor antagonistFormula:C26H31FN4O4S2Purity:98%Color and Shape:SolidMolecular weight:546.68KRAS G12C inhibitor 39
CAS:KRAS G12C inhibitor 39 effectively targets KRAS G12C, a key protein in cancer research.Formula:C37H43N9O2Color and Shape:SolidMolecular weight:645.8FGFR-IN-3
CAS:FGFR-IN-3: potent, oral FGFR modulator, BBB-penetrating, neuroprotective, potential in neurodegeneration study.Formula:C18H27F2N5O2Color and Shape:SolidMolecular weight:383.44GNF179 (Metabolite)
CAS:GNF179 metabolite is a potent (4.8 nM vs. W2 strain) derivative of 8,8-dimethyl IP with strong in vitro stability and oral bioavailability.Formula:C14H16FN3Purity:98%Color and Shape:SolidMolecular weight:245.3TIPP
CAS:TIPP is an agent of delta opioid antagonist.Formula:C37H38N4O6Purity:98%Color and Shape:SolidMolecular weight:634.72K114
CAS:K114 binds tightly to amyloid fibrils (EC50: 20-30 nM). K114 is an efficient detector of semen-derived enhancer of virus infection (SEVI).Formula:C22H17BrO2Purity:98%Color and Shape:SolidMolecular weight:393.27ALK-IN-22
CAS:ALK-IN-22 suppresses ALK and mutants (IC50: 2.3-3.7 nM), hinders phosphorylation, and induces apoptosis in tumor studies.Formula:C24H24ClN7O2Color and Shape:SolidMolecular weight:477.95Influenza virus-IN-2
CAS:Influenza virus-IN-2 (compound 19) has anti-influenza A virus activities that is a potent inhibitor of influenza virus with an CC 50 of 150.85 μM and EC 50 of 2Formula:C17H17NO5Color and Shape:SolidMolecular weight:315.32JNJ 10191584 maleate
CAS:JNJ 10191584 maleate (VUF6002 maleate) is an orally active and selective antagonist of H4 receptor (Ki = 26 nM).Formula:C17H19ClN4O5Purity:99.37%Color and Shape:SolidMolecular weight:394.81AMG-221
CAS:AMG-221: potent 11β-HSD1 inhibitor, lowers glucose & insulin, reduces obesity in mice.Formula:C14H22N2OSPurity:98%Color and Shape:SolidMolecular weight:266.4VUF14738
CAS:VUF14738 is a robust and fatigue-resistant photoswitchable GPCR antagonist.Formula:C25H32N4O2Color and Shape:SolidMolecular weight:420.55LV-320
CAS:LV-320, potent ATG4B inhibitor; IC50: 24.5 μM, Kd: 16 μM. Blocks autophagy, stable, non-toxic, active in vivo. Useful for ATG4B research in cancer.Formula:C29H26ClNO2S2Purity:98%Color and Shape:SolidMolecular weight:520.11L-(-)-threo-3-Hydroxyaspartic acid
CAS:L-(-)-threo-3-Hydroxyaspartic acid is an EAAT1-4 inhibitor/non-transportable EAAT5 inhibitor.Formula:C4H7NO5Purity:98%Color and Shape:SolidMolecular weight:149.1JMI-346
CAS:JMI-346: Anti-malarial, inhibits P. falciparum (CQS, CQR), IC50: 13 μM (3D7), 33 μM (RKL-9), targets PfFP-2 protease.Formula:C19H20N4O2Color and Shape:SolidMolecular weight:336.39N-(5-((2-Methylene-3-(((octadecylamino)carbonyl)oxy)propoxy)carbonyl)pentyl)pyridinium
CAS:N-(5-((2-Methylene-3-(((octadecylamino)carbonyl)oxy)propoxy)carbonyl)pentyl)pyridinium is a platelet activating factor antagonist.Formula:C34H59BrN2O4Color and Shape:SolidMolecular weight:639.75Antibacterial agent 67
CAS:Antibacterial agent 67 blocks succinate dehydrogenase more effectively than haloperidol, with IC50 of 0.03 μM vs 4.40 μM.Formula:C24H15F6N5OColor and Shape:SolidMolecular weight:503.4(R)-PS210
CAS:(R)-PS210, the R enantiomer of PS210 is a substrate-selective allosteric PDK1 activator with an (AC50 of 1.8 μM).Formula:C19H15F3O5Color and Shape:SolidMolecular weight:380.31PF 4800567 hydrochloride
CAS:casein kinase 1ε inhibitorFormula:C17H19Cl2N5O2Purity:98%Color and Shape:SolidMolecular weight:396.27BMMP
CAS:BMMP is a novel postentry inhibitor of human immunodeficiency virus type 1 (HIV-1) replication.Formula:C13H11N3S2Color and Shape:SolidMolecular weight:273.38Butopiprine
CAS:Butopiprine is a cough suppressant with antispasmodic, local anesthetic and antitussive activity.Formula:C19H29NO3Purity:98%Color and Shape:SolidMolecular weight:319.44CIA-1 hcl(452087-38-6 Free base)
CAS:CIA-1 inhibits the nuclear receptor COUP-TFII, with IC50s ranging from 1.2 μM to 7.6 μM in prostate cancer cell lines.CIA-1 inhibits the growth of a variety ofFormula:C17H20ClN3O2SPurity:99.02%Color and Shape:SolidMolecular weight:365.88IKK2-IN-4
CAS:IKK2-IN-4(IKK2 Inhibitor VI) is a highly potent IKK-2 inhibitor with an IC50 value of 25 nM. IKK2-IN-4 inhibited the production of TNF-α in PBMC induced by LPS.Formula:C12H11N3O2SPurity:99.83%Color and Shape:SolidMolecular weight:261.3Ref: TM-T36524
1mg108.00€5mg261.00€10mg401.00€25mg622.00€50mg837.00€100mg1,125.00€200mg1,504.00€500µg82.00€(3S,5R)-Fluvastatin sodium
CAS:(3S,5R)-Fluvastatin sodium: synthetic HMG-CoA reductase inhibitor, IC50 8 nM, boosts vascular cell antioxidant defense.Formula:C24H26FNNaO4Purity:98%Color and Shape:SolidMolecular weight:434.463Stampidine
CAS:Stampidine prevents HIV-1, effective against resistant strains at subnanomolar levels.Formula:C20H23BrN3O8PPurity:98%Color and Shape:SolidMolecular weight:544.29SWE101
CAS:SWE101 is a potent human and rat soluble epoxide hydrolase (sEH)-P inhibitor(IC50s of 4 μM and 2.8 μM, respectively).Formula:C19H15Cl2NO3Purity:98%Color and Shape:SolidMolecular weight:376.23Clanobutin
CAS:Clanobutin inhibits gluconeogenesis and acts as a choleretic and digestion-stimulating agent.Formula:C18H18ClNO4Color and Shape:SolidMolecular weight:347.79Antitrypanosomal agent 4
CAS:Compound 19: potent, blood-brain penetrant antitrypanosomal; IC50: T. cruzi 1.2 μM, T.b. brucei 70 nM.Formula:C18H14ClN3O5SColor and Shape:SolidMolecular weight:419.84Asocainol hydrochloride
CAS:Asocainol hydrochloride, an antiarrhythmic, blocks Ca2+ influx and alters Na+ action potentials.Formula:C27H32ClNO3Color and Shape:SolidMolecular weight:454.01PI3K/mTOR Inhibitor-13
CAS:PI3K/mTOR Inhibitor-13, an oral dual blocker of PI3K and mTOR, may treat sexual diseases, solid tumors, and IPF.Formula:C20H13F2N5O3SColor and Shape:SolidMolecular weight:441.41Jineol
CAS:Jineol (NSC-694081) is a quinoline alkaloid from Scolopendra subspinipes. Jineol shows cytotoxic activity against the growth of human tumor cell lines in vitro.Formula:C9H7NO2Purity:99.55%Color and Shape:SolidMolecular weight:161.16Ref: TM-T32291
1mg56.00€5mg133.00€10mg205.00€25mg350.00€50mg515.00€100mg732.00€200mg973.00€1mL*10mM (DMSO)105.00€Fadaltran
CAS:Fadaltran is an α2-adrenoreceptor antagonist.Formula:C24H29N5O2Color and Shape:SolidMolecular weight:419.52
