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(2,856 products)
- Apoptosis(6,375 products)
- Cell Cycle/Checkpoint(4,913 products)
- Chromatin/Epigenetics(2,633 products)
- Cytoskeletal Signaling(1,590 products)
- DNA Damage/DNA Repair(2,868 products)
- Endocrinology/Hormones(3,765 products)
- Enzyme(3,673 products)
- GPCR/G-Protein(9,055 products)
- Immunology and Inflammation(3,953 products)
- Influenza Virus(300 products)
- JAK/STAT signaling(417 products)
- MAPK Signaling(1,259 products)
- Membrane Transporter/Ion Channel(3,162 products)
- Metabolism(10,157 products)
- Microbiology/Virology(7,674 products)
- Neuroscience(10,550 products)
- Other Inhibitors(35,861 products)
- Oxidation-Reduction(41 products)
- PI3K/Akt/mTOR Signaling(1,438 products)
- Proteases/Proteasome(1,692 products)
- Stem Cell and Derivatives(733 products)
- Tyrosine Kinase/Adaptors(1,992 products)
- Ubiquitination(1,744 products)
Show 16 more subcategories
Found 66511 products of "Inhibitors"
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Figopitant
CAS:Figopitant is a tachykinin neurokinin-1 antagonist.Formula:C27H31F6N3OColor and Shape:SolidMolecular weight:527.54AZ8838
CAS:AZ8838 is an effective, competitive, allosteric, orally active non-peptide small molecule antagonist of PAR2 with a pK i of 6.4 for hPAR2 [1].Formula:C13H15FN2OColor and Shape:SolidMolecular weight:234.27JJO-1
CAS:JJO-1 is a bi-quinoline activating all AMPK αβγ isoforms except γ3; it requires low ATP and is unaffected by γ mutations or β deletions.Formula:C19H13N3Color and Shape:SolidMolecular weight:283.33MC4343
MC4343, a potent dual inhibitor targeting both EZH2 and histone deacetylase, presents promising potential for cancer research applications.Formula:C36H41N5O4Color and Shape:SolidMolecular weight:607.74SX-576
CAS:SX-576: potential pulmonary inflammation treatment, non-competitive boronic acid CXCR1/2 antagonist.Formula:C20H15BF4N2O4SColor and Shape:SolidMolecular weight:466.21F2276-0099
CAS:F2276-0099 is a PCAF/GCN5 BRD inhibitorFormula:C19H20N2O4Color and Shape:SolidMolecular weight:340.37Looplure
CAS:Looplure is a chemosterilant, insect attractant and repellent.Formula:C14H26O2Color and Shape:SolidMolecular weight:226.35Antitumor agent-46
Antitumor agent-46 shows strong activity against MCF-7 cells; IC50: 2.08 µM.Formula:C36H40N2O11Color and Shape:SolidMolecular weight:676.71FTase-IN-1
CAS:FTase-IN-1, a potent FTase inhibitor, has an IC50 of 0.35 μM with strong antitumor activity and cytotoxicity.Formula:C23H16N2O2SColor and Shape:SolidMolecular weight:384.45CB 3703
CAS:CB 3703 is an inhibitor of dihydrofolate reductase and thymidylate synthase.Formula:C22H24N6O5Color and Shape:SolidMolecular weight:452.46Flavipin
CAS:Flavipin: Ahr agonist, alters Ahr genes in T cells/macrophages, disrupts Arid5a, scavenges DPPH (IC50=7.2μM), inhibits α-glucosidase (IC50=33.8μM).Formula:C9H8O5Color and Shape:SolidMolecular weight:196.16Thionalide
CAS:Thionalide can transport these cpds from liver to bile.Formula:C12H11NOSColor and Shape:SolidMolecular weight:217.29IKKß-IN-124
CAS:IKKβ-IN-124 blocks NF-κB by inhibiting IκBα phosphorylation and securing IKKβ in inactive form.Formula:C17H26Cl2N2O3SColor and Shape:SolidMolecular weight:409.37Butixirate
CAS:Butixirate is a biochemical.Formula:C28H33NO2Color and Shape:SolidMolecular weight:415.577INU-101
CAS:INU-101: oral 11β-HSD1 inhibitor improves insulin sensitivity and reduces blood glucose, potential type 2 diabetes treatment.Formula:C21H28FN3O4SColor and Shape:SolidMolecular weight:437.53AZD2906
CAS:AZD2906: selective GR agonist with human/rat IC50s - 2.2/0.3 nM (PBMC), 41.6/7.5 nM (blood); induces rat bone marrow micronuclei.Formula:C26H25FN4O3Color and Shape:SolidMolecular weight:460.5VUF10132
CAS:VUF10132 is a full inverse CXCR3 N3.35A agonist.Formula:C19H13BrCl4N2O2Purity:98%Color and Shape:SolidMolecular weight:523.03TASP0433864
CAS:TASP0433864 enhances mGlu2 activity; EC50: 199 nM (human), 206 nM (rat); not an agonist.Formula:C18H23N3O3Purity:98%Color and Shape:SolidMolecular weight:329.39KAA-276 free base
CAS:KAA-276: potent, long-lasting histamine H1 antagonist with minimal irritation; for asthma via inhalation.Formula:C31H35FN4O2Color and Shape:SolidMolecular weight:514.63
