
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(2,764 products)
- Apoptosis(6,204 products)
- Cell Cycle/Checkpoint(4,811 products)
- Chromatin/Epigenetics(2,553 products)
- Cytoskeletal Signaling(1,519 products)
- DNA Damage/DNA Repair(2,906 products)
- Endocrinology/Hormones(3,703 products)
- Enzyme(3,671 products)
- GPCR/G-Protein(8,966 products)
- Immunology and Inflammation(3,748 products)
- Influenza Virus(297 products)
- JAK/STAT signaling(414 products)
- MAPK Signaling(1,244 products)
- Membrane Transporter/Ion Channel(3,119 products)
- Metabolism(10,122 products)
- Microbiology/Virology(7,569 products)
- Neuroscience(10,314 products)
- Other Inhibitors(35,802 products)
- Oxidation-Reduction(40 products)
- PI3K/Akt/mTOR Signaling(1,411 products)
- Proteases/Proteasome(1,681 products)
- Stem Cell and Derivatives(752 products)
- Tyrosine Kinase/Adaptors(1,947 products)
- Ubiquitination(1,716 products)
Show 16 more subcategories
Found 66604 products of "Inhibitors"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
RORγt Inverse agonist 2
CAS:RORγt Inverse agonist 2 is a selective, orally active inverse agonist of RORγt(EC50 of 119 nM).Formula:C27H25F8NO5SPurity:98%Color and Shape:SolidMolecular weight:627.54Ketomethylenebestatin
CAS:Ketomethylenebestatin, a weaker carba-analog of aminopeptidase inhibitor bestatin, is 10x less potent.Formula:C17H25NO4Purity:98%Color and Shape:SolidMolecular weight:307.38RSK4-IN-1
CAS:RSK4-IN-1 is a compound exhibiting potent inhibition of RSK4, demonstrated by an IC50 value of 9.5 nM.Formula:C19H20F2N4O3Color and Shape:SolidMolecular weight:390.38Heme Oxygenase-1-IN-2
Heme Oxygenase-1-IN-2 is a novel inhibitor of heme oxygenase-1 (HO-1), displaying potent antiproliferative activity in vitro, with an IC50 value of 0.95 μM.Formula:C19H18ClN3OColor and Shape:SolidMolecular weight:339.82PD-1/PD-L1-IN-23
CAS:PD-1/PD-L1-IN-23: potent, oral PD-1/PD-L1 inhibitor; L7's ester prodrug; exhibits strong antitumor effects.Formula:C32H30BrCl2N3O6Color and Shape:SolidMolecular weight:703.41Calphostin B
CAS:Calphostins, PKC inhibitors from Cladosporium fungus, include A, B, C, D, I; C is most potent.Formula:C37H34O11Color and Shape:SolidMolecular weight:654.66DNA-PK-IN-6
CAS:DNA-PK-IN-6 inhibits DNA-PKcs, disrupting tumor DNA repair and triggering apoptosis; enhances radiotherapy and targets various tumors (WO2021197159A1).Formula:C19H21N7OColor and Shape:SolidMolecular weight:363.422,3-dinor-11β-Prostaglandin F2α
CAS:2,3-dinor-11β-Prostaglandin F2α (2,3-dinor-11β-PGF2α) was recovered from the urine of both normal monkeys and humans when infused with radiolabeled PGD2, whereFormula:C18H30O5Color and Shape:SolidMolecular weight:326.43VVD-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:429.36EGFR-IN-35
CAS:EGFR-IN-35, an acrylamide-based EGFR inhibitor, shows promise for EGFR mutation-related cancers like NSCLC.Formula:C25H24ClN7O2Color and Shape:SolidMolecular weight:489.96S-HP210
S-HP210: selective GR modulator, blocks NF-κB (IC50: 1.92 μM), non-toxic to mouse fibroblasts.Formula:C22H19N3O2S2Color and Shape:SolidMolecular weight:421.54PX-316
CAS:PX-316: AKT inhibitor, reduces Akt activity by 78% in HT-29 xenografts, effective against MCF-7 and HT-29 cancers, well-tolerated intravenously.Formula:C28H57O10PColor and Shape:SolidMolecular weight:584.72Isoleucyl tRNA synthetase-IN-1
CAS:Isoleucyl tRNA synthetase-IN-1 is a selective and potent inhibitor (Ki: 88 nM) that targets isoleucyl tRNA synthetase (IleRS).Formula:C23H35N5O7SColor and Shape:SolidMolecular weight:525.62Cas9-IN-1
Cas9-IN-1 is a potent inhibitor of Cas9 with an IC50 value of 7.02 μM. Cas9-IN-1 acts by binding apo-Cas9 and blocking the formation of the Cas9:gRNA complex.Formula:C17H11Cl2F3N2O3SColor and Shape:SolidMolecular weight:451.25PRN694
CAS:PRN694 is a potent, irreversible ITK/RLK inhibitor with IC50s: 0.3/1.4 nM; offers lasting effector cell suppression.Formula:C28H35F2N5O2SPurity:98%Color and Shape:SolidMolecular weight:543.67MRS2279
CAS:Selective, high affinity competitive antagonist of the P2Y1 receptorFormula:C13H18ClN5O8P2Purity:98%Color and Shape:SolidMolecular weight:469.71ODN 21158
CAS:ODN 21158 is a potent, non-cytotoxic inhibitor of G-modified TLR3 and TLR9. ODN 21158 dose-dependently inhibits IFN-α secretion.Color and Shape:SolidBleomycin Free Base
CAS:Bleomycin Free Base, a glycopeptide antibiotic, halts DNA function and treats solid tumors.Formula:C55H84N17O21S3Color and Shape:SolidMolecular weight:1415.55PSB 36
CAS:A1 adenosine receptor antagonistFormula:C21H30N4O3Purity:98%Color and Shape:SolidMolecular weight:386.49GSK-1264
CAS:GSK-1264: allosteric HIV integrase inhibitor, halts viral replication & abnormal protein multimerization.Formula:C26H28FNO5Color and Shape:SolidMolecular weight:453.5

