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(2,765 products)
- Apoptosis(6,237 products)
- Cell Cycle/Checkpoint(4,778 products)
- Chromatin/Epigenetics(2,426 products)
- Cytoskeletal Signaling(1,515 products)
- DNA Damage/DNA Repair(2,957 products)
- Endocrinology/Hormones(3,692 products)
- Enzyme(3,665 products)
- GPCR/G-Protein(8,968 products)
- Immunology and Inflammation(3,857 products)
- Influenza Virus(301 products)
- JAK/STAT signaling(413 products)
- MAPK Signaling(1,249 products)
- Membrane Transporter/Ion Channel(3,024 products)
- Metabolism(10,184 products)
- Microbiology/Virology(7,551 products)
- Neuroscience(10,359 products)
- Other Inhibitors(36,088 products)
- Oxidation-Reduction(43 products)
- PI3K/Akt/mTOR Signaling(1,444 products)
- Proteases/Proteasome(1,718 products)
- Stem Cell and Derivatives(825 products)
- Tyrosine Kinase/Adaptors(2,035 products)
- Ubiquitination(1,710 products)
Show 16 more subcategories
Found 66669 products of "Inhibitors"
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THR-β agonist 4
CAS:THR-β agonist 4 is a potent agonist of THR-β.Formula:C16H11Cl2F2N5O6SColor and Shape:SolidMolecular weight:510.26CDK7-IN-17
CAS:CDK7-IN-17, a pyrimidine-based CDK7 inhibitor, shows promise for various cancers, especially with abnormal transcription.Formula:C24H26F3N6OPPurity:99.60%Color and Shape:SolidMolecular weight:502.47AZ14145845
AZ14145845 is an in vivo potent and highly selective type I1/2 Mer/Axl bispecific kinase inhibitor.Formula:C32H35N9OColor and Shape:SolidMolecular weight:561.68Aplaviroc
CAS:Aplaviroc (AK 602), a SDP derivative, is a CCR5 antagonist. With IC50s of 0.1-0.4 nM for HIV-1Ba-L, HIV-1JRFL and HIV-1MOKW.Formula:C33H43N3O6Purity:97.98% - 98.26%Color and Shape:SolidMolecular weight:577.71Nurr1 agonist 1
Nurr1 agonist 1 is an inverse agonist tool for the neuroprotective transcription factor Nurr1 which is an appealing target to treat neurodegenerative diseases.Formula:C16H14N2O2Color and Shape:SolidMolecular weight:266.29BMS-681
CAS:BMS-681 is a CCR2 antagonist blocking chemokine binding, aiding control of inflammatory and neurodegenerative diseases.Formula:C26H36F3N5OColor and Shape:SolidMolecular weight:491.59E6201
CAS:E6201, a dual kinase inhibitor, blocks MEK1/FLT3 and has anti-tumor/psoriasis effects with low IC50s: ERK2 (5.2 nM), JNK (91 nM), p38 MAPK (19 nM).Formula:C21H27NO6Color and Shape:SolidMolecular weight:389.44Dazucorilant
CAS:Dazucorilant (CORT113176), a selective non-steroidal GR modulator, has high affinity with a K i <1 nM, useful for neurological research.Formula:C29H22F4N4O3SColor and Shape:SolidMolecular weight:582.57MEIS-IN-3
MEIS-IN-3 is a potent inhibitor of MEIS.Formula:C25H26N2O4Color and Shape:SolidMolecular weight:418.48LSD1-IN-16
LSD1-IN-16 (4b) inhibits LSD1, MAO-A/B; IC50: 0.015-0.366 μM. Halts prostate cancer cell growth; IC50: 15.2 μM.Formula:C20H18N2OSColor and Shape:SolidMolecular weight:334.43Antitumor agent-48
Antitumor agent-48, a 2,3-dehydrosilybin derivative, exhibits cytotoxicity on MCF-7, NCI-H1299, HepG2, HT29 cells; IC50 ranging 8.06-16.51 µM.Formula:C35H34N2O14Color and Shape:SolidMolecular weight:706.65Vimirogant hydrochloride
Vimirogant (VTP-43742) HCl: Oral, selective RORγt inhibitor (IC50: 17 nM, Ki: 3.5 nM), >1000x selectivity over RORα/β, targets Th17, not Th1/2/Treg.Formula:C27H36ClF3N4O3SColor and Shape:SolidMolecular weight:588.21487VEGFR-2/DHFR-IN-2
VEGFR-2/DHFR-IN-2 inhibits VEGFR-2 & DHFR (IC50: 0.623 & 9.085 μM), toxic to C26, HepG2, MCF7 cells (IC50: 3.59-8.38 μM), promising for cancer study.Formula:C21H21NO4Color and Shape:SolidMolecular weight:351.4HMG499
CAS:HMG499 inhibits HMG-CoA reductase (IC50: 0.41μM), reduces statin-induced HMGCR, lowers cholesterol, and lessens atherosclerosis.Formula:C33H54O3Purity:98%Color and Shape:SolidMolecular weight:498.78D6808
D6808: selective c-Met inhibitor, IC50=2.9 nM, induces apoptosis and cell cycle arrest, for NSCLC/gastric cancer research.Formula:C30H25F3N6O2Color and Shape:SolidMolecular weight:558.55Aniline-MPB-amino-C3-PBD
CAS:Aniline-MPB-amino-C3-PBD is a cytotoxic agent comprised of the non-alkylating group. It is a sequence-selective DNA minor-groove binding agent.Formula:C42H46N8O6Purity:98%Color and Shape:SolidMolecular weight:758.86hCAII-IN-4
CAS:hCAII-IN-4 (Compound 12j) is a potent inhibitor of human carbonic anhydrase II (hCA II), exhibiting an inhibitory concentration (IC50) of 7.78 μM.Formula:C31H23NO9Color and Shape:SolidMolecular weight:553.52DH376
CAS:DH376 inhibits DAGLα in a time and dose dependent manner in mouse brain. DH376 shows picomolar activity.Formula:C31H28F2N4O3Color and Shape:SolidMolecular weight:542.58Rubropunctatin
CAS:Rubropunctatin is a monascus pigment with very potent cancer cell proliferation inhibitory effects.Formula:C21H23NO4Color and Shape:SolidMolecular weight:353.41Pamiparib maleate
CAS:Pamiparib (BGB-290) is a selective PARP inhibitor that blocks DNA repair and promotes apoptosis.Formula:C44H42F2N8O14Purity:98%Color and Shape:SolidMolecular weight:944.859
