
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(2,942 products)
- Apoptosis(6,646 products)
- Cell Cycle/Checkpoint(4,921 products)
- Chromatin/Epigenetics(2,638 products)
- Cytoskeletal Signaling(1,594 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(3,959 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(7,955 products)
- Neuroscience(11,146 products)
- Other Inhibitors(35,856 products)
- Oxidation-Reduction(41 products)
- PI3K/Akt/mTOR Signaling(1,440 products)
- Proteases/Proteasome(1,693 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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Equisetin
CAS:Equisetin: a QSI from Fusarium equiseti, curbs P. aeruginosa virulence, fights Gram-positive bacteria & HIV-1 integrase; not antibacterial to Gram-negative.Formula:C22H31NO4Purity:98%Color and Shape:SolidMolecular weight:373.49EZH2-IN-12
EZH2-IN-12 (Compound 5) is a potent inhibitor of EZH2, which has potential for studies of CNS malignancies.Formula:C23H23Cl2N3O3Color and Shape:SolidMolecular weight:460.35Antifungal agent 43
Antifungal agent 43 inhibits biofilms with low toxicity to human cancer cells.Formula:C24H26N4Se2Color and Shape:SolidMolecular weight:528.41Beclabuvir
CAS:Beclabuvir blocks HCV NS5B polymerase at thumb site 1, effective on genotypes 1, 3, 4, 5 with IC50 <28 nM.Formula:C36H45N5O5SPurity:99.87% - 99.93%Color and Shape:SolidMolecular weight:659.84Enantiomer of Sofosbuvir
Inactive enantiomer of Sofosbuvir, used for chronic hepatitis C; lacks reported biological activity.Formula:C22H29FN3O9PPurity:98%Color and Shape:SolidMolecular weight:529.45EBI-907
CAS:EBI-907 is a potent, oral B-RafV600E inhibitor with an IC50 of 4.9 nM, over 10x stronger than Vemurafenib, and effective against key cancer kinases.Formula:C23H21ClF2N4O3SColor and Shape:SolidMolecular weight:506.95PF-06463922 acetate
CAS:PF-06463922 acetate: ALK/ROS1 inhibitor, brain- penetrable, active vs crizotinib-resistant mutants, in NSCLC trials.Formula:C23H23FN6O4Color and Shape:SolidMolecular weight:466.46LY 235959
CAS:LY 235959 is a NMDA receptor antagonist.Formula:C11H20NO5PPurity:98%Color and Shape:SolidMolecular weight:277.25Antitumor agent-37
Antitumor agent-37: strong anti-growth, anti-spread, induces DNA damage, apoptosis via Bcl-2/Bax/caspase3, boosts immune response.Formula:C16H18Cl2N2O4PtColor and Shape:SolidMolecular weight:568.32eIF4A3-IN-4
eIF4A3-IN-4 is a novel inhibitor of eIF4A (IC50: 8.6 μM).Formula:C24H20N2O5Color and Shape:SolidMolecular weight:416.43(Rel)-Factor B-IN-5
CAS:(Rel)-Factor B-IN-5 is a complement factor B inhibitor that can be used to study diseases associated with activation of the alternative complement pathway.Formula:C27H32N2O4Purity:>99.99%Color and Shape:SolidMolecular weight:448.55ART615
ART615 is a related isomer of ART558. ART615 inhibits Polθ by <10% at 12 μM and is able to act as a control for ART558 (IC50:7.9 nM).Formula:C21H21F3N4O2Color and Shape:SolidMolecular weight:418.41GP-1681
CAS:GP-1681, a G-protein coupled receptor (GPCR) agonist, is used potentially for the treatment of influenza infection.Formula:C24H30NaO5Purity:98%Color and Shape:SolidMolecular weight:421.48Samuraciclib
CAS:Samuraciclib (CT7001) is an oral CDK7 inhibitor with 41 nM IC50, notable for its high selectivity and potency against breast cancer cells.Formula:C22H30N6OColor and Shape:SolidMolecular weight:394.51GZN39838
CAS:GZN39838, a natural Kv1.2 blocker, induces C-type inactivation without blocking the outer pore.Formula:C22H30O6Color and Shape:SolidMolecular weight:390.474-Bromo A23187
CAS:4-Bromo A23187 is a halogenated analog of the calcium ionophore A-23187. 4-Bromo A23187 is a calcium modulator and induces apoptosis in different cells.Formula:C29H36BrN3O6Purity:98%Color and Shape:SolidMolecular weight:602.52CRV431
CAS:CRV431 is a novel Pan-Cyclophilin Inhibitor, potently inhibiting all cyclophilin isoforms tested - A, B, D, and G (IC50 values ranged from 1-7 nM).Formula:C67H122N12O13Color and Shape:SolidMolecular weight:1303.76Turoctocog alfa
CAS:Turoctocog alfa: recombinant FVIII from CHO cells for hemophilia A study.Color and Shape:SolidVEGFR2-IN-1
CAS:VEGFR2-IN-1 is a VEGFR2 inhibitor with antitumor activity used in the study of breast cancer.Formula:C22H18N6SPurity:98.15%Color and Shape:SolidMolecular weight:398.48

