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(2,941 products)
- Apoptosis(6,644 products)
- Cell Cycle/Checkpoint(4,921 products)
- Chromatin/Epigenetics(2,638 products)
- Cytoskeletal Signaling(1,593 products)
- DNA Damage/DNA Repair(2,864 products)
- Endocrinology/Hormones(3,765 products)
- Enzyme(3,675 products)
- GPCR/G-Protein(9,485 products)
- Immunology and Inflammation(3,958 products)
- Influenza Virus(301 products)
- JAK/STAT signaling(418 products)
- MAPK Signaling(1,271 products)
- Membrane Transporter/Ion Channel(3,406 products)
- Metabolism(10,175 products)
- Microbiology/Virology(7,951 products)
- Neuroscience(11,146 products)
- Other Inhibitors(35,855 products)
- Oxidation-Reduction(41 products)
- PI3K/Akt/mTOR Signaling(1,440 products)
- Proteases/Proteasome(1,692 products)
- Stem Cell and Derivatives(732 products)
- Tyrosine Kinase/Adaptors(1,989 products)
- Ubiquitination(1,745 products)
Show 16 more subcategories
Found 66507 products of "Inhibitors"
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Teoprolol
CAS:Teoprolol is a blocker of β-adrenergic receptor.Formula:C23H30N6O4Purity:98%Color and Shape:SolidMolecular weight:454.52TIY-7
TIY-7 is a selective, orally active inhibitor of the promyosin receptor kinase (TRK) enzyme. TIY-7 exhibited anti-tumour effects in a mouse xenograft model.Color and Shape:SolidSJG-136
CAS:SJG-136 is a DNA cross-linking agent (XL50: 45 nM for pBR322 DNA).Formula:C31H32N4O6Purity:98%Color and Shape:SolidMolecular weight:556.61KIRA9
KIRA9 inhibits IRE1 with a 4.8 μM IC50, blocking ER-stress-induced mRNA decay and apoptosis by fully binding IRE1's ATP site.Formula:C27H27F3N6O3SColor and Shape:SolidMolecular weight:572.6Leukotriene F-4 sulfone
CAS:Leukotriene F-4 sulfone induces vascular permeability changes.Formula:C28H44N2O10SColor and Shape:SolidMolecular weight:600.72PI3K-IN-35
CAS:PI3K-IN-35 (6l) selectively inhibits PI3K-α, β, δ (IC50: 13.98, 7.22, 10.94 μM), blocks G2/M phase, induces apoptosis, and is useful in leukemia research.Formula:C25H23N7O2Color and Shape:SolidMolecular weight:453.5Antibacterial agent 87
Antibacterial agent 87 is an effective antibacterial agent that acts on MRSA (MIC: 0.125 μg/ml), MRSE (MIC: 0.0625 μg/ml) and S. aureus (MIC: 0.0625 μg/ml).Formula:C31H46N2O6SColor and Shape:SolidMolecular weight:574.77GNTI dihydrochloride
CAS:κ opioid receptor antagonistFormula:C27H30ClN5O3Purity:98%Color and Shape:SolidMolecular weight:508.01Diacylglycerol acyltransferase inhibitor-1
CAS:Diacylglycerol Acyltransferase Inhibitor-1, a diacylglycerol acyltransferase (DGAT1) inhibitor, effectively suppresses the activity of DGAT1.Formula:C21H23N5O2Purity:98%Color and Shape:SolidMolecular weight:377.44TLR7/8 antagonist 2
TLR7/8 antagonist 2: potent, orally active, IC50: 4.9 nM (TLR7), 0.6 nM (TLR8); potential for lupus therapy research.Formula:C22H26FN5Color and Shape:SolidMolecular weight:379.47MAO-B-IN-7
MAO-B-IN-7 inhibits MAO-B/AChE, crossing the blood-brain barrier; IC50: 41/87 nM (h/eel AChE), 0.3 μM (MAO-B). Reduces oxidative stress and neuroinflammation.Formula:C25H31NO4Color and Shape:SolidMolecular weight:409.52FLT3-IN-13
FLT3-IN-13 inhibits topoisomerase II/FLT3 in leukemia with IC50 of 2.26 μM, causes G2/M arrest, and promotes apoptosis.Formula:C20H14N4O2Color and Shape:SolidMolecular weight:342.35Lu 26-046
CAS:Lu 26-046 is a muscarinic receptor agonist.Formula:C10H12N2OSColor and Shape:SolidMolecular weight:208.28FTI 276 TFA
CAS:FTI 276 TFA targets plasmodium falciparum & humans, inhibits PFT with IC50s: 0.9 nM (parasite) & 0.5 nM (human).Formula:C23H28F3N3O5S2Color and Shape:SolidMolecular weight:547.61cis-RdRP-IN-5
Cis-RdRP-IN-5 is an effective inhibitor of the influenza virus RNA-dependent RNA polymerase (RdRP), employed in influenza virus research.Formula:C23H21N3O5Color and Shape:SolidMolecular weight:419.43trans-Doxercalciferol
CAS:trans-Doxercalciferol is an isomer of Doxercalciferol. Doxercalciferol is an activator of the Vitamin D receptor and prevents renal disease.Formula:C28H44O2Purity:98%Color and Shape:SolidMolecular weight:412.65Carbonic anhydrase inhibitor 10
CA inhibitor 10 targets MCF-7 cells, IC50: 11.9 μM; potent h CA IX inhibitor, Ki: 6.2 nM. Anti-cancer research.Formula:C14H17N5O3SColor and Shape:SolidMolecular weight:335.38Aristoforin
CAS:Aristoforin is a SIRT1 and SIRT2 inhibitor that induces cell cycle arrest, shows potent antitumor effects, and inhibits lymphangiogenesis in vivo.Formula:C37H54O6Color and Shape:SolidMolecular weight:594.82(R)-CSN5i-3
CAS:(R)-CSN5i-3 is CSN5i-3 of the R configuration.Formula:C28H29F2N5O2Purity:99.76% - 99.97%Color and Shape:SolidMolecular weight:505.56CDK2-IN-9
CDK2-IN-9: potent CDK2 inhibitor (IC50: 0.63 μM), anti-proliferative, arrests S/G2M cell cycle, induces apoptosis, promising for melanoma study.Formula:C21H16ClN3O4SColor and Shape:SolidMolecular weight:441.89
