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(2,939 products)
- Apoptosis(6,643 products)
- Cell Cycle/Checkpoint(4,918 products)
- Chromatin/Epigenetics(2,633 products)
- Cytoskeletal Signaling(1,595 products)
- DNA Damage/DNA Repair(2,868 products)
- Endocrinology/Hormones(3,765 products)
- Enzyme(3,675 products)
- GPCR/G-Protein(9,484 products)
- Immunology and Inflammation(3,958 products)
- Influenza Virus(301 products)
- JAK/STAT signaling(417 products)
- MAPK Signaling(1,272 products)
- Membrane Transporter/Ion Channel(3,404 products)
- Metabolism(10,179 products)
- Microbiology/Virology(7,953 products)
- Neuroscience(11,146 products)
- Other Inhibitors(35,856 products)
- Oxidation-Reduction(41 products)
- PI3K/Akt/mTOR Signaling(1,439 products)
- Proteases/Proteasome(1,692 products)
- Stem Cell and Derivatives(733 products)
- Tyrosine Kinase/Adaptors(1,992 products)
- Ubiquitination(1,745 products)
Show 16 more subcategories
Found 66508 products of "Inhibitors"
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LT-850-166
LT-850-166 is a potent inhibitor of FLT3 and has shown efficacy in overcoming a wide range of FLT3 mutations.Formula:C30H29Cl2N7OColor and Shape:SolidMolecular weight:574.5CREB-IN-1 TFA
CREB-IN-1 TFA: Potent oral CREB inhibitor, IC50 of 0.18 μM, suppresses breast cancer cell growth.Color and Shape:SolidSqualamine lactate
CAS:Squalamine lactate is an aminosterol compound discovered in the tissues of the dogfish shark, with antimicrobial activity.Formula:C37H71N3O8SPurity:98%Color and Shape:SolidMolecular weight:718.04AChE-IN-25
AChE-IN-25: selective, potent AChE inhibitor, non-competitive, IC50 = 2.95 μM, for Alzheimer's research.Formula:C20H15ClN4O4SColor and Shape:SolidMolecular weight:442.88STA 2
CAS:STA 2 is an analogue of TXA2, a thromboxane receptor in the colonic epithelium.Formula:C21H34O3SColor and Shape:SolidMolecular weight:366.56L162389
CAS:L162389 is an angiotensin II receptor antagonist with a balanced affinity for AT1 and AT2 receptor and stimulates the conversion of phosphatidylinositol.Formula:C31H38N4O4SPurity:99.11% - 99.57%Color and Shape:SolidMolecular weight:562.72Udifitimod
CAS:Udifitimod (BMS-986166) is a potent, selective, and orally active modulator of the S1P1R receptor, showing potential for research in autoimmune diseases.Formula:C25H33NO2Color and Shape:SolidMolecular weight:379.54Tyk2-IN-3
CAS:Tyk2-IN-3 is an inhibitor of Tyk2 pseudokinase (IC50: 485 nM).Formula:C25H24N6O3S2Purity:98%Color and Shape:SolidMolecular weight:520.63TX2-121-1
CAS:TX2-121-1 targets HER3 for proteasome-mediated degradation to inhibit HER3-dependent signalling and growth.Formula:C42H52N8O3Purity:98%Color and Shape:SolidMolecular weight:716.91Nrf2 activator-2
Compound O15, an Osthole derivative, is a potent Nrf2 agonist with an EC50 of 2.9 μM; it inhibits Keap1-Nrf2 binding and Nrf2 ubiquitination.Formula:C20H17BrO3Color and Shape:SolidMolecular weight:385.25WAY-855
CAS:WAY-855 is an EAAT2-preferring, nonsubstrate inhibitor of high-affinity glutamate uptake.Formula:C9H11NO4Color and Shape:SolidMolecular weight:197.19Rostratin A
CAS:Rostratin A, a disulfide from Exserohilum rostratum, is cytotoxic to HCT-116 cells with an IC50 of 8.5 μg/mL.Formula:C18H24N2O6S2Color and Shape:SolidMolecular weight:428.52IACS-8779 disodium
CAS:IACS-8779 disodium: potent STING agonist, strong systemic anti-tumor effects, effective in melanoma model.Formula:C21H23N9Na2O10P2S2Color and Shape:SolidMolecular weight:733.52Chitin synthase inhibitor 12
Chitin synthase inhibitor 12: potent CHS blocker (IC50: 0.16 mM), broad-spectrum antifungal, effective against resistant strains. Useful in IFI research.Formula:C23H21ClFN3O5Color and Shape:SolidMolecular weight:473.88Bizelesin
CAS:Bizelesin, a synthetic antineoplastic agent, binds DNA, disrupts replication, triggers cell-cycle arrest, and induces senescence.Formula:C43H36Cl2N8O5Color and Shape:SolidMolecular weight:815.7TrxR-IN-2
TrxR-IN-2 is a potential thioredoxin reductase (TrxR) inhibitor. TrxR-IN-2 has research value in the chemotherapy of drug-resistant hepatocellular carcinoma.Formula:C22H22N4O4Color and Shape:SolidMolecular weight:406.43PI3K-IN-27
CAS:PI3K-IN-27 is a potent PI3K inhibitor, relevant for cancer and immune disease research. See patent WO2021233227A1.Formula:C30H26F2N6O2SColor and Shape:SolidMolecular weight:572.63HPK1-IN-3
HPK1-IN-3: Selective HPK1 inhibitor, ATP-competitive, IC50=0.25nM; boosts IL-2 in PBMCs, EC50=108nM.Formula:C23H22F4N6O2Color and Shape:SolidMolecular weight:490.45GLS1 Inhibitor-6
GLS1 Inhibitor-6: IC50=68nM, 220x more selective for GLS2, has anti-tumor and pro-apoptosis effects.Formula:C37H52N6O3SColor and Shape:SolidMolecular weight:660.91GNE-431
CAS:GNE-431: potent, selective noncovalent Btk inhibitor, IC50=3.2 nM; effective against C481R, T474I, T474M mutants, may counter ibrutinib resistance.Formula:C30H32N10O2Color and Shape:SolidMolecular weight:564.64
