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(2,762 products)
- Apoptosis(6,206 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(9,002 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(3,106 products)
- Metabolism(10,125 products)
- Microbiology/Virology(7,567 products)
- Neuroscience(10,343 products)
- Other Inhibitors(35,806 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(1,949 products)
- Ubiquitination(1,716 products)
Show 16 more subcategories
Found 66605 products of "Inhibitors"
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GPX4-IN-2
CAS:GPX4-IN-2 is a potent inhibitor of GPX4, exhibiting antiproliferative activity. It holds potential for cancer research applications.Formula:C30H40N2OColor and Shape:SolidMolecular weight:444.65LY2922083
CAS:LY2922083: Potent, selective GPR40 agonist; lowers glucose, boosts insulin and GLP-1.Formula:C31H33NO3SColor and Shape:SolidMolecular weight:499.66RU28362
CAS:RU28362 is an agonist of glucocorticoid receptor.Formula:C23H28O3Color and Shape:SolidMolecular weight:352.47A-357300
CAS:A-357300: potent reversible MetAP2 inhibitor, IC50=0.12 uM; promising for neuroblastoma treatment.Formula:C15H22ClN3O3SColor and Shape:SolidMolecular weight:359.87DuP-532
CAS:DuP-532, an angiotensin type 1 receptor antagonist, is used potentially for the treatment of hypertension and heart failure.Formula:C23H19F5N6O2Color and Shape:SolidMolecular weight:506.43β-Catenin modulator-5
CAS:β-Catenin Modulator-5 (Compound IIa-84), an oxazole and thiazole-based compound, serves as a potent and selective modulator of β-Catenin [1].Formula:C21H22N2O2SColor and Shape:SolidMolecular weight:366.48Naxagolide free base
CAS:Naxagolide is a sustained release formulation. It is a dopamine agonist.Formula:C15H21NO2Purity:98%Color and Shape:SolidMolecular weight:247.33HBV-IN-30
CAS:HBV-IN-30, a flavone derivative, inhibits cccDNA in HBV research.Formula:C22H18BrClO6Color and Shape:SolidMolecular weight:493.73erythro-Austrobailignan-6
CAS:Erythro-Austrobailignan-6: orally active, anti-cancer, inhibits DNA topoisomerases, induces apoptosis, boosts p38/JNK phosphorylation.Formula:C20H24O4Color and Shape:SolidMolecular weight:328.4ICMT-IN-14
CAS:ICMT-IN-14 (compound 50) serves as an inhibitor of isoprenylcysteine carboxyl methyltransferase (ICMT), exhibiting potent activity with an IC50 of 0.025 μM [1].Formula:C21H25ClFNOColor and Shape:SolidMolecular weight:361.88Inflachromene
CAS:Inflachromene (ICM) is an inhibitor of HMGB1 and HMGB expression with anti-inflammatory activity.Inflachromene is used in the study of epilepsy.Formula:C21H19N3O4Purity:97.36% - 99.88%Color and Shape:SolidMolecular weight:377.39Ref: TM-T24167
1mg109.00€5mg260.00€10mg416.00€25mg710.00€50mg973.00€100mg1,314.00€1mL*10mM (DMSO)286.00€QR-0217
CAS:QR-0217 is a potent inhibitor of both Aβ1-40 and α-synuclein aggregation, exhibiting an IC50 of 7.5 µM for Aβ1-40.Formula:C19H13NO3Color and Shape:SolidMolecular weight:303.31Benzoadenosine
CAS:Benzoadenosine suppresses kinase activity slightly less than does adenosine.Formula:C14H15N5O4Purity:98%Color and Shape:SolidMolecular weight:317.3P-1075
CAS:P-1075 activates SUR2-KIR6 channels at 45 nM; may open mitoKATP channels and protect the heart.Formula:C12H17N5Purity:99.85%Color and Shape:SolidMolecular weight:231.3Ref: TM-T16420
1mg57.00€5mg119.00€10mg192.00€25mg349.00€50mg530.00€100mg708.00€200mg964.00€1mL*10mM (DMSO)90.00€SID 26681509
CAS:SID 26681509 is a selective, reversible and competitive human cathepsin L inhibitor (IC50 of 56 nM).Formula:C27H33N5O5SPurity:99.18%Color and Shape:SolidMolecular weight:539.65Ref: TM-T12909
1mg63.00€5mg137.00€10mg205.00€25mg414.00€50mg618.00€100mg882.00€1mL*10mM (DMSO)163.00€Z-YVAD-CMK
CAS:Z-YVAD-CMK is an inhibitor of both caspase-1 and caspase-3, as referenced in [1].Formula:C30H37ClN4O9Purity:98%Color and Shape:SolidMolecular weight:633.09ENT-C225
CAS:ENT-C225 is a potent TrkB neurotrophin receptor (TrkBR) activator with neuroprotective activity for the study of Alzheimer's disease and Parkinson's disease.Formula:C26H40N4O5Purity:99.36% - 99.36%Color and Shape:SolidMolecular weight:488.62Pomaglumetad methionil hydrochloride
CAS:LY2140023 hydrochloride: oral methionine prodrug of LY404039, a selective mGlu2/3 agonist, studied for schizophrenia.Formula:C12H19ClN2O7S2Purity:98.57%Color and Shape:SolidMolecular weight:402.87Lifirafenib
CAS:Lifirafenib (Beigene-283) is a potent inhibitor of RAF family kinases and EGFR in biochemical assays with IC50 of 23, 29 and 495 nM for the recombinantFormula:C25H17F3N4O3Purity:97.99% - 98%Color and Shape:SolidMolecular weight:478.42Ref: TM-T22272
1mg34.00€5mg65.00€10mg92.00€25mg180.00€50mgTo inquire100mgTo inquire1mL*10mM (DMSO)94.00€VU0463271
CAS:VU0463271: KCC2 antagonist, IC50 61 nM, >100x selective over NKCC1, inactive on other GPCRs, channels, transporters.
Formula:C19H18N4OS2Purity:97.84% - 99.55%Color and Shape:SolidMolecular weight:382.5
