
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(2,785 products)
- Apoptosis(6,253 products)
- Cell Cycle/Checkpoint(4,833 products)
- Chromatin/Epigenetics(2,588 products)
- Cytoskeletal Signaling(1,532 products)
- DNA Damage/DNA Repair(2,883 products)
- Endocrinology/Hormones(3,747 products)
- Enzyme(3,670 products)
- GPCR/G-Protein(8,977 products)
- Immunology and Inflammation(3,777 products)
- Influenza Virus(299 products)
- JAK/STAT signaling(415 products)
- MAPK Signaling(1,248 products)
- Membrane Transporter/Ion Channel(3,147 products)
- Metabolism(10,143 products)
- Microbiology/Virology(7,585 products)
- Neuroscience(10,341 products)
- Other Inhibitors(35,820 products)
- Oxidation-Reduction(40 products)
- PI3K/Akt/mTOR Signaling(1,413 products)
- Proteases/Proteasome(1,680 products)
- Stem Cell and Derivatives(747 products)
- Tyrosine Kinase/Adaptors(1,948 products)
- Ubiquitination(1,719 products)
Show 16 more subcategories
Found 66565 products of "Inhibitors"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Norbinaltorphimine dihydrochloride
CAS:Norbinaltorphimine dihydrochloride is a selective and potent κ opioid receptor antagonist that induces itch-associated responses in mice.Formula:C40H45Cl2N3O6Purity:98.17% - 99.88%Color and Shape:SolidMolecular weight:734.71Ref: TM-T12241
1mg35.00€5mg80.00€10mg114.00€25mg224.00€50mg388.00€100mg618.00€200mg859.00€1mL*10mM (DMSO)117.00€ETX0282
CAS:ETX0282, oral class A/C β-lactamase inhibitor, developed by Entasis with cefpodoxime for bacterial infections.Formula:C13H18FN3O5Color and Shape:SolidMolecular weight:315.30Ro 0437626
CAS:P2X1 purinergic receptor antagonistFormula:C27H35N5O4SPurity:98%Color and Shape:SolidMolecular weight:525.66TEI-9063
CAS:TEI-9063 is a stable and highly specific prostacyclin analogue of prostacyclin receptor in mast cell tumor p-815 cells.Formula:C23H38O4Color and Shape:SolidMolecular weight:378.55MDK6465
CAS:MDK6465 (PCSK9-IN-8b), CAS#1900686-46-5, is a liver-targeted PCSK9 synthesis inhibitor.Formula:C27H29ClFN9O4Color and Shape:SolidMolecular weight:598.03OUN58101
CAS:OUN58101, also MDK-8101/BI-D, is an RSV L-protein inhibitor with no formal name, first reported in patent WO 2005042530.Formula:C32H36N6O6Color and Shape:SolidMolecular weight:600.66Antitumor agent-51
Antitumor agent-51 targets osteosarcoma with 21.9 nM IC50, high selectivity, and low toxicity.Formula:C23H25N5O2SColor and Shape:SolidMolecular weight:435.54EGFR/HER2-IN-5
EGFR/HER2-IN-5: Irreversible, oral dual EGFR inhibitor, IC50 0.6 nM, targets L858R/T790M mutations, anti-tumor in vivo for lung cancer study.Color and Shape:Solid11-trans Leukotriene E4
CAS:Slow isomerization of the C-11 double bond of LTE4 leads to the formation of 11-trans LTE4. 11-trans LTE4 is equipotent to LTE4 in contracting guinea pig ileum.Formula:C23H37NO5SColor and Shape:SolidMolecular weight:439.61SP-471
SP-471 is a potent inhibitor of dengue virus (DENV) protease (IC50: 18 μM) and inhibits the inter- and intramolecular protease processes of DENV.Formula:C33H26BrN5Color and Shape:SolidMolecular weight:572.5Substituted piperidines-1
CAS:Substituted piperidines-1 can promote the release of growth hormone in humans and animals.Formula:C29H39N7O2Purity:98%Color and Shape:SolidMolecular weight:517.67Cilobamine mesylate
CAS:Cilobamine mesylate is a drug which acts as a norepinephrine-dopamine reuptake inhibitor (NDRI) and has stimulant and antidepressant effects.Formula:C18H27Cl2NO4SColor and Shape:SolidMolecular weight:424.38NI-Pano
NI-Pano (CH-03) is a novel hypoxia-activated KDAC inhibitor capable of O2-dependent release of the compound panobinostat.Formula:C26H28N6O4Color and Shape:SolidMolecular weight:488.54Polvitolimod
CAS:Polvitolimod is a TLR7 agonist used to treat infectious disease and cancer.Formula:C13H14FN5O4Color and Shape:SolidMolecular weight:323.28ZK 93426 hydrochloride
CAS:benzodiazepine receptor antagonist,competitiveFormula:C18H21ClN2O3Purity:98%Color and Shape:SolidMolecular weight:348.82ALK-IN-23
ALK-IN-23 inhibits ALK (IC50: 1.6-0.71 nM), hinders cancer cell spread, forms colonies in vitro, and reduces tumors in mice with low toxicity.Formula:C26H29ClN8O3SColor and Shape:SolidMolecular weight:569.08Antitubercular agent-15
Antitubercular agent-15 (5n): low toxicity, fights M. tuberculosis strains; MIC90 values range 0.73-18.8 μg/mL.Formula:C21H29FN2Color and Shape:SolidMolecular weight:328.47MRS2279
CAS:Selective, high affinity competitive antagonist of the P2Y1 receptorFormula:C13H18ClN5O8P2Purity:98%Color and Shape:SolidMolecular weight:469.71CLK1/4-IN-1
CLK1/4-IN-1 inhibits Clk1/4 (IC50: 9.7/6.6 nM), curbing T24 cell growth (GI50: 1.1 μM). Potential cancer research tool.Formula:C18H14ClNO4SColor and Shape:SolidMolecular weight:375.83FTO-IN-4
CAS:FTO-IN-4 is a potent and selective inhibitor of adiposity and obesity-associated protein (FTO).Formula:C22H16Cl2N6O6Color and Shape:SolidMolecular weight:531.31

