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(2,797 products)
- Apoptosis(6,259 products)
- Cell Cycle/Checkpoint(4,836 products)
- Chromatin/Epigenetics(2,592 products)
- Cytoskeletal Signaling(1,534 products)
- DNA Damage/DNA Repair(2,880 products)
- Endocrinology/Hormones(3,748 products)
- Enzyme(3,670 products)
- GPCR/G-Protein(8,985 products)
- Immunology and Inflammation(3,797 products)
- Influenza Virus(299 products)
- JAK/STAT signaling(415 products)
- MAPK Signaling(1,250 products)
- Membrane Transporter/Ion Channel(3,148 products)
- Metabolism(10,144 products)
- Microbiology/Virology(7,591 products)
- Neuroscience(10,345 products)
- Other Inhibitors(35,830 products)
- Oxidation-Reduction(40 products)
- PI3K/Akt/mTOR Signaling(1,421 products)
- Proteases/Proteasome(1,681 products)
- Stem Cell and Derivatives(748 products)
- Tyrosine Kinase/Adaptors(1,961 products)
- Ubiquitination(1,721 products)
Show 16 more subcategories
Found 66564 products of "Inhibitors"
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Cav 2.2/3.2 blocker 1
Compound 9e is a Cav 2.2/3.2 blocker; IC50: 1.22 μM & 80 μM, respectively; penetrates CNS.Formula:C28H30N2O3Color and Shape:SolidMolecular weight:442.55DDCPPB-Glu
CAS:DDCPPB-Glu is a 6-5 fused ring heterocycle antifolate that shows antitumor activity.Formula:C22H27N5O5Purity:98%Color and Shape:SolidMolecular weight:441.48(R)-Atuveciclib
CAS:Atuveciclib (BAY-1143572) is a potent and highly selective, oral PTEFb / CDK9 inhibitor that inhibits CDK9 / CycT1 with an IC 50 of 13 nM [1].Formula:C18H18FN5O2SPurity:98%Color and Shape:SolidMolecular weight:387.43Dyrk1A/α-synuclein-IN-2
Dyrk1A/α-synuclein-IN-2 (Compound b20) is a dual inhibitor of Dyrk1A and α-synuclein aggregation that acts on α-synuclein (IC50: 7.8 μM).Formula:C21H16N4O4SColor and Shape:SolidMolecular weight:420.44HER2-IN-7
CAS:HER2-IN-7 is a potent HER2 inhibitor with potential for researching ErbB-related diseases, especially cancer.Formula:C28H26F3N7O3Color and Shape:SolidMolecular weight:565.55EGFR-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:489.96RET-IN-7
CAS:RET-IN-7 exhibits strong inhibitory effects against RET kinase in vitro and shows significant efficacy in treating RET-driven tumor xenografts in mice throughFormula:C22H24ClFN6O2Color and Shape:SolidMolecular weight:458.92CCR4 antagonist 2
CAS:CCR4 antagonist 2 (Compound 31) is a novel potent, orally bioavailable small molecule antagonists of CC chemokine receptor 4 (CCR4) that inhibits TregFormula:C26H28Cl2N6OPurity:98%Color and Shape:SolidMolecular weight:511.45RBM10-8
CAS:RBM10-8 irreversibly inhibits human sphingosine-1- phosphate lyase (hS1PL) while behaving also as an enzyme substrate.Formula:C17H36NO5PColor and Shape:SolidMolecular weight:365.45Calphostin D
CAS:Calphostins, PKC inhibitors from Cladosporium cladosporioides, include A, B, C, D, I; C is most potent.Formula:C30H30O10Color and Shape:SolidMolecular weight:550.55AChE/BACE1/GSK3β-IN-1
AChE/BACE1/GSK3β-IN-1 is an orally active, blood-brain barrier-transparent, moderately bioavailable triple inhibitor of AChE/BACE1/GSK3β.Formula:C26H27FN2O4Color and Shape:SolidMolecular weight:450.5Cimpuciclib tosylate
CAS:Cimpuciclib tosylate, a selective CDK4 inhibitor (IC50: 0.49 nM), exhibits anti-tumor activity.Formula:C37H43FN8O4SColor and Shape:SolidMolecular weight:714.85P-gp modulator 2
P-gp modulator 2 (Compound 27) is a potent competitive and metabotropic P-glycoprotein (P-gp) modulator.Formula:C22H20BrN3O4Color and Shape:SolidMolecular weight:470.32G-744
CAS:G-744 is a selective and orally active inhibitor of Btk (IC50: 2 nM).Formula:C29H29N5O3SPurity:98%Color and Shape:SolidMolecular weight:527.64AChE/GSK-3β-IN-1
CAS:AChE/GSK-3β-IN-1 is a potent dual AChE/GSK-3β inhibitor that crosses the blood-brain barrier and acts on hAChE (IC50: 1.2 nM), hBChE (IC50: 149.8 nM) and hGSK-Formula:C31H35N7O3SColor and Shape:SolidMolecular weight:585.72PTP1B-IN-18
PTP1B-IN-18 is an orally active, fully mixed protein tyrosine phosphatase 1B (PTP1B) inhibitor (Ki: 35.2 μM).PTP1B-IN-18 can be used to study type 2 diabetes.Formula:C26H19N3O4SColor and Shape:SolidMolecular weight:469.51BET-IN-1
BET-IN-1 is a potent inhibitor of BET, exhibiting good brain permeability and a reasonable metabolic stability.Formula:C23H24ClFN4O3SColor and Shape:SolidMolecular weight:490.98Mesulergine
CAS:Mesulergine is metabolized into dopaminergic agonists.Formula:C18H26N4O2SColor and Shape:SolidMolecular weight:362.49CHK1-IN-4
CAS:CHK1-IN-4 is a potent inhibitor of checkpoint kinase 1 (chk1) and potently inhibits chk1 phosphorylation in the tumor cells with anti-tumor activity.Formula:C18H18BrN7O2Purity:98%Color and Shape:SolidMolecular weight:444.29Transthyretin-IN-1
Transthyretin-IN-1 inhibits TTR fibril formation, aiding Alzheimer’s research.Formula:C10H9Br2NO4Color and Shape:SolidMolecular weight:366.99
