
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(2,776 products)
- Apoptosis(6,256 products)
- Cell Cycle/Checkpoint(4,788 products)
- Chromatin/Epigenetics(2,435 products)
- Cytoskeletal Signaling(1,522 products)
- DNA Damage/DNA Repair(2,964 products)
- Endocrinology/Hormones(3,706 products)
- Enzyme(3,668 products)
- GPCR/G-Protein(8,997 products)
- Immunology and Inflammation(3,862 products)
- Influenza Virus(301 products)
- JAK/STAT signaling(414 products)
- MAPK Signaling(1,249 products)
- Membrane Transporter/Ion Channel(3,027 products)
- Metabolism(10,206 products)
- Microbiology/Virology(7,577 products)
- Neuroscience(10,378 products)
- Other Inhibitors(36,080 products)
- Oxidation-Reduction(43 products)
- PI3K/Akt/mTOR Signaling(1,446 products)
- Proteases/Proteasome(1,726 products)
- Stem Cell and Derivatives(825 products)
- Tyrosine Kinase/Adaptors(2,039 products)
- Ubiquitination(1,714 products)
Show 16 more subcategories
Found 66691 products of "Inhibitors"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Novocebrin
CAS:Novocebrin is a central nervous system activator.Formula:C20H22ClNOS2Purity:98%Color and Shape:SolidMolecular weight:391.98(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:434.463TYK2-IN-11
CAS:TYK2-IN-11 (5B) selectively inhibits TYK2 (IC50: 0.016 nM) and JAK1 (IC50: 0.31 nM), aiding autoimmune and inflammatory disease research.Formula:C18H17N5O3SColor and Shape:SolidMolecular weight:383.42CAY10669
CAS:CAY10669 inhibits PCAF (IC50 = 662 μM), is twice as potent as anacardic acid, and reduces H4 acetylation in HepG2 cells at 30-60 μM.Formula:C20H22O4Color and Shape:SolidMolecular weight:326.39(R)-Gyramide A hydrochloride
CAS:(R)-Gyramide A HCl inhibits DNA gyrase in bacteria (IC50: 875 μM), with MIC 10-80 μM against P. aeruginosa & E. coli, sparing topoisomerase IV.Formula:C21H28ClFN2O3SColor and Shape:SolidMolecular weight:442.97AZD-3783
CAS:AZD-3783 is a selective 5-hydroxytryptamine 1B receptor antagonist with probable antidepressant and anxiolytic activity.Formula:C26H34N4O4Color and Shape:SolidMolecular weight:466.57Isoxepac
CAS:Isoxepac (Olopatadine USP Related Compound C) is a non-steroidal anti-antiphlogistic agent and analgesic.Formula:C16H12O4Purity:99.86%Color and Shape:Light-Yellow To Pale-White Crystalline PowderMolecular weight:268.26P18IN003
CAS:P18IN003 is a selective and effective p18(INK4C) inhibitor that inhibits the activity of p18 protein and can be used to study in vitro expansion ofFormula:C17H16N2O3Purity:99%Color and Shape:SolidMolecular weight:296.32Pifoxime
CAS:Pifoxime: a NSAID with COX-1/2 inhibition, used in anti-inflammatory treatment and neuropsychiatric studies.Formula:C15H20N2O3Color and Shape:SolidMolecular weight:276.33Fadaltran
CAS:Fadaltran is an α2-adrenoreceptor antagonist.Formula:C24H29N5O2Color and Shape:SolidMolecular weight:419.52FAAH inhibitor 1
CAS:FAAH inhibitor 1 (Benzothiazole analog 3) is an effective FAAH inhibitor with an IC50 of 18 nM.Formula:C24H23N3O3S3Purity:99.6%Color and Shape:SolidMolecular weight:497.65Chlordantoin
CAS:Chlordantoin is an antifungal agent with the potential for vaginal candidiasis treatment.Formula:C11H17Cl3N2O2SPurity:98%Color and Shape:SolidMolecular weight:347.69DHODH-IN-15
CAS:DHODH-IN-15, a hydroxyfuran analogue of A771726, inhibits rat liver DHODH with an IC50 of 11 μM, and is used for rheumatoid arthritis.Formula:C15H11N3O3Purity:99.8%Color and Shape:SolidMolecular weight:281.27UCL-1972
CAS:UCL-1972, a Histamine H3 Receptor Antagonist, used to treat cognitive disorders.Formula:C15H22N2O3Color and Shape:SolidMolecular weight:278.35Cdc7-IN-17
CAS:Cdc7-IN-17 is a potent inhibitor of CDC7 with an IC 50 of <10 μM that can be used in cancer research [1].Formula:C13H15N5OSColor and Shape:SolidMolecular weight:289.36MRS-1191
CAS:MRS-1191 is an effective and selective A3 adenosine receptor antagonist (KB: 92 nM, a Ki: 31.4 nM for human A3 receptor and an IC50: 120 nM for CHO cells).Formula:C31H27NO4Color and Shape:SolidMolecular weight:477.55(RS)-4-Carboxyphenylglycine
CAS:(RS)-4-Carboxyphenylglycine is a racemic mixture. (S)-4-Carboxyphenylglycine is a selective mGlu1α receptor antagonist.Formula:C9H9NO4Purity:97.22% - >99.99%Color and Shape:SolidMolecular weight:195.17Bay 41-4109
CAS:BAY 41-4109 is a potent inhibitor of human hepatitis B virus (HBV)(IC50 : 53 nM).Formula:C18H13ClF3N3O2Color and Shape:SolidMolecular weight:395.76Sortin2
CAS:Sortin2 is a sorting inhibitor that acts upstream from the morphological marker of lateral root primordium formation, the mitotic activity.Formula:C16H12ClNO5S3Purity:98%Color and Shape:SolidMolecular weight:429.92Dexamethasone oxetanone
CAS:Dex-Ox, a selective glucocorticoid derivative of Dex, exhibits antiglucocorticoid and antiprogestin activities, targeting PR A/B isoforms.Formula:C22H27FO4Color and Shape:SolidMolecular weight:374.45R-SKF-38393A HCl
CAS:R(+)-SKF-38393A is a D1 dopamine receptor agonist and also is a more active enantiomer of (±)-SKF-38393A.Formula:C16H18ClNO2Purity:98%Color and Shape:SolidMolecular weight:291.77Bisindolylmaleimide II
CAS:protein kinase C (PKC) inhibitorFormula:C27H26N4O2Purity:98%Color and Shape:SolidMolecular weight:438.52LSD1-IN-14
CAS:LSD1-IN-14: potent LSD1 inhibitor, IC50 0.89 μM; hinders A549/THP-1 cell growth, induces tumor cell apoptosis.Formula:C21H24FN5Color and Shape:SolidMolecular weight:365.45NKP-1339
CAS:NKP-1339 (IT-139) induces G2/M cell cycle arrest, blockage of DNA synthesis, and induction of apoptosis via the mitochondrial pathway.Formula:C14H12Cl4N4NaRuPurity:98%Color and Shape:SolidMolecular weight:502.14NCGC00247743
CAS:NCGC00247743 is an inhibitor of histone lysine demethylase KDM4.Formula:C24H29N3O2Purity:98%Color and Shape:SolidMolecular weight:391.516BrW
CAS:6BrW is an analog of tryptophan effector.Formula:C11H11BrN2O2Purity:98%Color and Shape:SolidMolecular weight:283.12hDHODH-IN-9
CAS:hDHODH-IN-9 is a potent hDHODH inhibitor, IC50=0.34 μM, toxic to MCF-7/A375 cells, promising for cancer research.Formula:C21H21NO4Color and Shape:SolidMolecular weight:351.4AZD1446 HCl
CAS:AZD1446 (TC-6683) is a selective α4β2 receptor agonist, showing promise in treating cognitive deficits and Alzheimer's.Formula:C11H14Cl2N2O2Color and Shape:SolidMolecular weight:277.15PF-739
CAS:PF-739 is an AMPK agonist that has been shown to activate AMPK in hepatocytes and skeletal muscle.Formula:C23H23ClN2O5Purity:98%Color and Shape:SolidMolecular weight:442.89BC12-4
CAS:BC12-4 is a novel potent inhibitor of IL-2 secretion, it has potent immunomodulatory activity.Formula:C19H14N2O3Color and Shape:SolidMolecular weight:318.33BLT-3
CAS:BLT-3 is a novel scavenger receptor BI (SR-BI) inhibitor.Formula:C19H13NOPurity:98%Color and Shape:SolidMolecular weight:271.31ISC-4
CAS:ISC-4 is an Akt inhibitor, which activates prostate apoptosis response protein-4 and reduces colon tumor growth in a nude mouse model.Formula:C11H13NSeColor and Shape:SolidMolecular weight:238.19MS438
CAS:MS438 is an effective agonist of the TSH receptor.Formula:C20H17F3N2O3Purity:98%Color and Shape:SolidMolecular weight:390.36SC57666
CAS:SC57666 is a highly selective COX2 inhibitor (IC50 at 26 nM) that shows no activity against COX1.Formula:C18H17FO2SPurity:98.83%Color and Shape:SolidMolecular weight:316.39UR 8225
CAS:UR 8225 is a potassium channel activator with cardiovascular activity.Formula:C18H14N2O2Color and Shape:SolidMolecular weight:290.32M&B 39279
CAS:M&B 39279 is a potent inhibitor of plant, yeast and mouse protoporphyrinogen oxidase.Formula:C11H5Cl2F3N4Color and Shape:SolidMolecular weight:321.09Liguzinediol
CAS:Liguzinediol, a potent positive inotropic agent, inhibits myocardial cell apoptosis.Formula:C8H12N2O2Purity:98%Color and Shape:SolidMolecular weight:168.192614W94
CAS:2614W94 is a selective inhibitor of MAO-A with IC50 of 5 nM and Ki of 1.6 nM.Formula:C15H11F3O4SPurity:99.6%Color and Shape:SolidMolecular weight:344.318-Nitro-cGMP
CAS:8-Nitro-cGMP is a unique cytoprotective mediator which inhibits oxidative stress. 8-Nitro-cGMP is also a probe of the protein S-guanylation.Formula:C10H11N6O9PColor and Shape:SolidMolecular weight:390.20Tubulin polymerization-IN-16
CAS:Compound 5g is a potent tubulin aggregation inhibitor, disrupting microtubules and causing G2/M arrest in SGC-7901 cells.Formula:C24H27N5O5Color and Shape:SolidMolecular weight:465.5cis-Ned 19
CAS:nicotinic acid adenine dinucleotide phosphate (NAADP) antagonistFormula:C30H31FN4O3Purity:98%Color and Shape:SolidMolecular weight:514.59Influenza virus-IN-4
CAS:Influenza virus-IN-4 (compound 11e) is a potent inhibitor of influenza virus neuraminidase, acting on H5N1 (IC50: 3.4 μM), H5N2 (IC50: 0.094 μM), H5N6 (IC50: 0.Formula:C23H31FN2O4Color and Shape:SolidMolecular weight:418.5R78206
CAS:R 78206 is a pyridazinamine derivative that suppresses the formation of poliovirus eclipse particles.Formula:C22H29N3O3Purity:98%Color and Shape:SolidMolecular weight:383.48Sirtuin modulator 4
CAS:Sirtuin modulator 4 inhibits SIRT1 (EC50: 51-100 μM), may extend cell life and prevent diseases like diabetes and cancer.Formula:C18H10N2O2SColor and Shape:SolidMolecular weight:318.35SR 3576
CAS:JNK3 inhibitor, potent and selectiveFormula:C27H27N5O5Purity:98%Color and Shape:SolidMolecular weight:501.53CJ 036878
CAS:CJ 036878 was developed as an antagonist of the N-methyl-D-aspartate receptor NR2B subunit.Formula:C22H21NO3Color and Shape:SolidMolecular weight:347.41PUN-96956
CAS:PUN-96956, a BAM inhibitor lacking a formal name, impacts OMP folding/insertion. Named via MedKoo Nomenclature.Formula:C21H33ClN2Color and Shape:SolidMolecular weight:348.95Hexbutinol methiodide
CAS:<p>Hexbutinol methiodide is an inhibitor of muscarinic receptors.</p>Formula:C22H34INO2Color and Shape:SolidMolecular weight:471.42HDAC ligand-1
CAS:HDAC ligand-1 is a synthetic precursor utilized in the production of PROTAC-based HDAC degraders [1].Formula:C7H8N2OPurity:98%Color and Shape:SolidMolecular weight:136.15Burimamide
CAS:Burimamide is an antagonist of histamine. It appears to block both H2 and H3 histamine receptors.Formula:C9H16N4SPurity:98%Color and Shape:SolidMolecular weight:212.32
