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"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Carbonic anhydrase inhibitor 3
Carbonic anhydrase inhibitor 3 (compound 11g) is an inhibitor of carbonic anhydrase II that reduces the intraocular pressure in glaucomatous rabbits [1].Formula:C15H17N3O3SColor and Shape:SolidMolecular weight:319.38Teslexivir
CAS:Teslexivir is a topical antiviral agent that is an effective and selective inhibitor of the interaction between two essential viral proteins, E1 and E2.Formula:C35H36BrN3O4Purity:98%Color and Shape:SolidMolecular weight:642.58AFP-07 free acid
CAS:AFP 07 free acid is a 7,7-difluoroprostacyclin derivative. It also acts as a selective and highly potent agonist for the IP receptor.Formula:C22H30F2O5Purity:98%Color and Shape:SolidMolecular weight:412.47Ganciclovir monophosphonate
CAS:Ganciclovir monophosphate treats CMV, inhibiting replication in human/animal strains (IC50: 0.01μM).Formula:C10H16N5O6PColor and Shape:SolidMolecular weight:333.24AK-295
CAS:AK 295, also known as CX 295, is a dipeptide inhibitor of alpha-ketoamide calpain.Formula:C26H40N4O6Color and Shape:SolidMolecular weight:504.62APN/AKT-IN-1
APN/AKT-IN-1, a dual APN (IC50=0.21μM) & AKT (IC50=0.27μM) inhibitor, hinders GSK3β phosphorylation.Formula:C18H27N7O3Color and Shape:SolidMolecular weight:389.45Tuvatidine
CAS:Tuvatidine is a histamine 2 receptor antagonist.Formula:C10H17N9O2S3Color and Shape:SolidMolecular weight:391.5AZ13824374
AZ13824374: potent, selective ATAD2 inhibitor; anti-proliferative in breast cancer; pIC50: FRET 8.2, NanoBRET 6.2.Formula:C30H39FN8O2Color and Shape:SolidMolecular weight:562.68Antitrypanosomal agent 6
Compound 18a: potent vs. T. brucei (IC50: 0.47 μM), >2x efficacy compared to Nifurtimox, good ADME, binds AT-rich DNA.Formula:C22H29Cl2N5OColor and Shape:SolidMolecular weight:450.49-O-Demethyltrigonostemone
CAS:9-O-Demethyltrigonostemone is a natural IDO1 inhibitor, cytotoxic and antiplasmodial agent from the Roots of Strophioblachia fimbricalyx.Formula:C19H20O4Color and Shape:SolidMolecular weight:312.36Ladirubicin
CAS:Ladirubicin, as an anthracyclines analog is the leading compound of alkylcyclines.Formula:C29H31NO11SColor and Shape:SolidMolecular weight:601.62GL0388
GL0388, a Bax activator, induces apoptosis, hinders breast cancer growth, and has IC50 of 0.299-1.57 μM.Formula:C21H17FN2OColor and Shape:SolidMolecular weight:332.37Antibiotic MA 144M1
CAS:Antibiotic MA 144M1, an anthracycline, targets gram-positive bacteria and animal tumors; derived from Streptomyces fermentation or aclacinomycin A conversion.Formula:C42H55NO15Color and Shape:SolidMolecular weight:813.88MK-2748
CAS:MK-2748 is an inhibitor of NS3 protease, hepatitis C virus.Formula:C42H56N6O10SColor and Shape:SolidMolecular weight:836.99COX-2/NO-IN-1
COX-2/NO-IN-1: oral iNOS & NO blocker (IC50=3.52μM), COX-2 supressor, anti-inflammatory, protects kidneys.Formula:C15H15NO3Color and Shape:SolidMolecular weight:257.28L5-DA
L5-DA, a G-quadruplex ligand, stabilizes G4s in HeLa cells, induces apoptosis, and is cytotoxic with an IC50 of 4.3 μM.Formula:C32H34N6O2Color and Shape:SolidMolecular weight:534.65Anticancer agent 78
Anticancer agent 78: anti-aromatase (IC50=0.9 μM), cytotoxic, potential in breast cancer research.Formula:C19H14BrNO4Color and Shape:SolidMolecular weight:400.22hTrkA-IN-2
hTrkA-IN-2 is a selective hTrkA metamorphosis inhibitor (IC50: 3.9 nM).Formula:C24H22F3N5O3Color and Shape:SolidMolecular weight:485.46Aplaviroc hydrochloride
CAS:Aplaviroc, a potent CCR5 inhibitor, binds selectively, blocking HIV entry and specific monoclonal antibody attachment in vitro.Formula:C33H44ClN3O6Color and Shape:SolidMolecular weight:614.17Cdc7-IN-11
CAS:Cdc7-IN-11 is a potent inhibitor of Cdc7 (IC50 ≤ 1 nM) and can be used in the study of proliferative diseases.Formula:C20H22F2N4O2SColor and Shape:SolidMolecular weight:420.48
