
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(2,781 products)
- Apoptosis(6,260 products)
- Cell Cycle/Checkpoint(4,792 products)
- Chromatin/Epigenetics(2,440 products)
- Cytoskeletal Signaling(1,527 products)
- DNA Damage/DNA Repair(2,968 products)
- Endocrinology/Hormones(3,706 products)
- Enzyme(3,667 products)
- GPCR/G-Protein(9,005 products)
- Immunology and Inflammation(3,874 products)
- Influenza Virus(301 products)
- JAK/STAT signaling(414 products)
- MAPK Signaling(1,248 products)
- Membrane Transporter/Ion Channel(3,033 products)
- Metabolism(10,207 products)
- Microbiology/Virology(7,591 products)
- Neuroscience(10,382 products)
- Other Inhibitors(36,042 products)
- Oxidation-Reduction(42 products)
- PI3K/Akt/mTOR Signaling(1,444 products)
- Proteases/Proteasome(1,724 products)
- Stem Cell and Derivatives(825 products)
- Tyrosine Kinase/Adaptors(2,035 products)
- Ubiquitination(1,717 products)
Show 16 more subcategories
Found 66686 products of "Inhibitors"
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AF267
CAS:AF267 is a M1 muscarinic agonist that works by restoring cognitive impairments.Formula:C10H18N2OSPurity:98%Color and Shape:SolidMolecular weight:214.33EML741
CAS:<p>EML741 also inhibits DNMT1 (IC50, 3.1 μM), with no effect on DNMT3a or DNMT3b.</p>Formula:C31H49N5O2Purity:98%Color and Shape:SolidMolecular weight:523.75hDDAH-1-IN-1 TFA
CAS:hDDAH-1-IN-1 TFA is a selective non-amino acid catalytic site inhibitor of human dimethylarginine dimethylaminohydrolase-1 (hDDAH-1) (Ki: 18 μM).Formula:C12H22F6N4O5Purity:98%Color and Shape:SolidMolecular weight:416.32PI3Kγ inhibitor 6
CAS:PI3Kγ Inhibitor 6, a specific inhibitor of PI3Kγ, is utilized in the study of inflammatory and autoimmune diseases.Formula:C16H11NO5SColor and Shape:SolidMolecular weight:329.33TWIK-1/TREK-1-IN-2
CAS:TWIK-1/TREK-1-IN-2 (Compound 2g) serves as an inhibitor of both TWIK-1 and TREK-1, targeting the TREK-1 homodimer and TWIK-1/TREK-1 heterodimer with IC50 valuesFormula:C20H29F3N2O2Purity:98%Color and Shape:SolidMolecular weight:386.45PF-3774076
CAS:PF-3774076 is a CNS penetrant, potent, selective, partial agonist at the human α1A adrenoceptor. PF-3774076 is selective over α1B and α1D adrenoceptors.Formula:C14H15ClN2OColor and Shape:SolidMolecular weight:262.73Bicifadine hydrochloride
CAS:noradrenalin transporter antagonistFormula:C12H16ClNPurity:98%Color and Shape:SolidMolecular weight:209.715Thiosildenafil
CAS:Thiosildenafil is a derivative of the phosphodiesterase 5 (PDE5) inhibitor sildenafil.Formula:C22H30N6O3S2Color and Shape:SolidMolecular weight:490.64(5Z,2E)-CU-3
CAS:(5Z,2E)-CU-3 is a potent and selective inhibitor of DGKα isozyme with an IC50 value of 0.6 μM and inhibition of DGKα by competing ATP with a Km value of 0.48 mMFormula:C16H12N2O4S3Purity:99.02%Color and Shape:SolidMolecular weight:392.47Ref: TM-T10177
1mg48.00€5mg96.00€10mg169.00€25mg359.00€50mg615.00€100mg948.00€500mg1,890.00€1mL*10mM (DMSO)105.00€Otaplimastat
CAS:SP-8203 is a reactive oxygen species inhibitor and superoxide dismutase stimulant.Formula:C28H34N6O5Purity:98%Color and Shape:SolidMolecular weight:534.61Glemanserin
CAS:Glemanserin (MDL11939) is a specific 5-HT2A antagonist with Ki values of 0.54 nM, 2.5 nM and 2.89 nM for rabbit, human and rat 5-HT2A.Formula:C20H25NOPurity:99.93%Color and Shape:SolidMolecular weight:295.42Ref: TM-T22964
1mg40.00€5mg88.00€10mg126.00€25mg273.00€50mg432.00€100mg638.00€500mg1,359.00€1mL*10mM (DMSO)88.00€PP30
CAS:PP30 is an inhibitor of mTORC1 and mTORC2. It is selective within the PI3K family, inhibiting other PI3Ks only at high concentrations.Formula:C18H19N7OSPurity:98%Color and Shape:SolidMolecular weight:381.45Disulfamide
CAS:Disulfamide: Oral carbonic anhydrase inhibitor, IC50 0.07 μM, diuretic by blocking Na+/HCO3- reabsorption.Formula:C7H9ClN2O4S2Purity:98.65%Color and Shape:SolidMolecular weight:284.74Chlorpromazine Sulfone Hydrochloride
CAS:Chlorpromazine Sulfone Hydrochloride: metabolite of anti-psychotic, may inhibit N-methyltransferase.Formula:C17H20Cl2N2O2SColor and Shape:SolidMolecular weight:387.32Methotrexate-α-alanine
CAS:Methotrexate-alpha-alanine is a prodrug.Formula:C23H27N9O6Purity:98%Color and Shape:SolidMolecular weight:525.52Enocitabine
CAS:Enocitabine is a nucleoside analog.Formula:C31H55N3O6Purity:97.22%Color and Shape:SolidMolecular weight:565.78Flupentixol decanoate, (Z)-
CAS:Flupentixol decanoate, a dopamine antagonist, blocks dopamine receptors and actions of agonists.Formula:C33H43F3N2O2SColor and Shape:SolidMolecular weight:588.77Teglicar
CAS:Teglicar is a selective and reversible liver isoform of carnitine palmitoyl-transferase 1 (L-CPT1) inhibitor.Formula:C22H45N3O3Purity:98%Color and Shape:SolidMolecular weight:399.61Y-9738
CAS:Y-9738 is an agent of hypolipidemic.Formula:C15H16ClNO4Purity:98%Color and Shape:SolidMolecular weight:309.74Ulecaciclib
CAS:Ulecaciclib: oral, BBB-permeable CDK inhibitor; favorable pharmacokinetics; ki: 0.62 μM (CDK2/A), 3 nM (CDK6/D3), 0.2 nM (CDK4/D1), 0.63 μM (CDK7/H).Formula:C25H33FN8SColor and Shape:SolidMolecular weight:496.65
