
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(2,763 products)
- Apoptosis(6,208 products)
- Cell Cycle/Checkpoint(4,813 products)
- Chromatin/Epigenetics(2,555 products)
- Cytoskeletal Signaling(1,516 products)
- DNA Damage/DNA Repair(2,904 products)
- Endocrinology/Hormones(3,703 products)
- Enzyme(3,671 products)
- GPCR/G-Protein(8,965 products)
- Immunology and Inflammation(3,747 products)
- Influenza Virus(298 products)
- JAK/STAT signaling(414 products)
- MAPK Signaling(1,244 products)
- Membrane Transporter/Ion Channel(3,119 products)
- Metabolism(10,115 products)
- Microbiology/Virology(7,570 products)
- Neuroscience(10,315 products)
- Other Inhibitors(35,799 products)
- Oxidation-Reduction(40 products)
- PI3K/Akt/mTOR Signaling(1,410 products)
- Proteases/Proteasome(1,678 products)
- Stem Cell and Derivatives(750 products)
- Tyrosine Kinase/Adaptors(1,945 products)
- Ubiquitination(1,716 products)
Show 16 more subcategories
Found 66603 products of "Inhibitors"
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VMY-2-95
CAS:VMY-2-95 is an α4β2 nicotinic acetylcholine receptors (nAChRs) selective desensitizer.Formula:C17H16N2OColor and Shape:SolidMolecular weight:264.32Tripolin A
CAS:Tripolin A is a specific non-ATP competitive inhibitor of Aurora A kinase(Aurora A and Aurora B with IC50 values of 1.5 μM and 7 μM, respectively)Formula:C15H11NO3Purity:98%Color and Shape:SolidMolecular weight:253.25SMAPP1
CAS:SMAPP1 is an activator of protein phosphatase 1 (PP1). SMAPP1 induces PP1 activity in vitro and activates latent HIV-1 provirus in cultured and primary T cells.Formula:C27H25N5O5S2Purity:98%Color and Shape:SolidMolecular weight:563.65ZM223
CAS:ZM223 is an inhibitor of NEDD8 activating enzyme (NAE).Formula:C23H17F3N4O2S2Purity:99.73%Color and Shape:SolidMolecular weight:502.53Ref: TM-T13412
1mg109.00€2mg163.00€5mg241.00€10mg354.00€25mg532.00€50mg745.00€100mg1,018.00€500mg2,035.00€MAO-B-IN-23
CAS:MAO-B-IN-23, also known as Compound 11f, is a reversible and competitive monoamine oxidase B (MAO-B) inhibitor with an IC50 value of 1.44 μM and a Ki of 0.51 μMFormula:C19H18BrNOPurity:98%Color and Shape:SolidMolecular weight:356.26Febuprol
CAS:Febuprol: choleretic, bile-stimulating, lipid-lowering, and anticonvulsant drug.Formula:C13H20O3Purity:98%Color and Shape:SolidMolecular weight:224.3Angiogenesis agent 1
CAS:Compound C-31, a salidroside-based glycoside, activates HIF-1α and may aid in diabetic limb ischemia studies.Formula:C20H24O7Purity:98%Color and Shape:SolidMolecular weight:376.4TWS-119
CAS:TWS-119 blocks GSK-3β, prompting neuronal formation in mouse stem cells.Formula:C22H16F6N4O6Color and Shape:SolidMolecular weight:546.38QF0301B
CAS:QF0301B is a potent α1-adrenergic receptor antagonist with inhibitory effects on α2-adrenergic receptors, 5-HT2A and histamine H1 receptors.Formula:C23H28N2O2Purity:>99.99%Color and Shape:SolidMolecular weight:364.485-HT3 antagonist 3
CAS:5-HT3 antagonist 3 (Compound 15b) is a high-affinity 5-HT3 receptor antagonist. It binds to 5-HT3 receptors in rat brain cortical membranes (Ki: 0.25 nM).Formula:C20H21N3OPurity:99.9%Color and Shape:SolidMolecular weight:319.4Ref: TM-T10162
1mg109.00€2mg163.00€5mg243.00€10mg355.00€25mg532.00€50mg750.00€100mg1,009.00€500mgTo inquireEtibendazole
CAS:Etibendazole is a microtubule inhibitor.Formula:C18H16FN3O4Color and Shape:SolidMolecular weight:357.34NLX-219
CAS:NLX-219 is a selective 5-HT1A receptor-biased agonists.Formula:C21H23ClF2N2O2Color and Shape:SolidMolecular weight:408.87Cefcanel daloxate
CAS:Cefcanel daloxate is a pro-drug of KY-087.Formula:C27H27N5O9S3Purity:98%Color and Shape:SolidMolecular weight:661.73(±)-AC 7954 hydrochloride
CAS:(±)-AC 7954 hydrochloride is a urotensin-II (UT) receptor activator.Formula:C19H21Cl2NO2Purity:99.97%Color and Shape:White SolidMolecular weight:366.28Ref: TM-T22476
1mg50.00€5mg111.00€10mg164.00€25mg268.00€50mg389.00€100mg532.00€200mg705.00€1mL*10mM (DMSO)119.00€FK409
CAS:FK409 is a cell permeable NO donor which produces vasorelaxation.Formula:C8H13N3O4Color and Shape:SolidMolecular weight:215.21S.pombe lumazine synthase-IN-1
CAS:S.pombe lumazine synthase-IN-1 inhibits lumazine synthases: Ki of 243μM for S.pombe, 9.6μM for M.tuberculosis.Formula:C14H13N3O6Color and Shape:SolidMolecular weight:319.27β-glycosidase-IN-1
CAS:β-glycosidase-IN-1 is a piperidine derivative, and is an inhibitor of β-glycosidase. It has hypoglycemic activity.Formula:C13H23NO5Purity:98%Color and Shape:SolidMolecular weight:273.33(R)-OR-S1
CAS:(R)-OR-S1 is a SAM-competitive, highly selective, orally bioavailable dual inhibitor of EZH1/2.Formula:C26H34BrN3O4Purity:98%Color and Shape:SolidMolecular weight:532.47CHD-5
CAS:CHD-5 is a selective antagonist of the aryl hydrocarbon receptor (AhR).Formula:C19H17N3O2Color and Shape:SolidMolecular weight:319.36NT2 Purpurin
CAS:NT2 Purpurin is used in photodynamic therapy of induced tumors.Formula:C41H52N4O2Color and Shape:SolidMolecular weight:632.88

