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(2,805 products)
- Apoptosis(6,292 products)
- Cell Cycle/Checkpoint(4,820 products)
- Chromatin/Epigenetics(2,490 products)
- Cytoskeletal Signaling(1,544 products)
- DNA Damage/DNA Repair(2,940 products)
- Endocrinology/Hormones(3,706 products)
- Enzyme(3,670 products)
- GPCR/G-Protein(9,024 products)
- Immunology and Inflammation(3,902 products)
- Influenza Virus(302 products)
- JAK/STAT signaling(417 products)
- MAPK Signaling(1,247 products)
- Membrane Transporter/Ion Channel(3,078 products)
- Metabolism(10,178 products)
- Microbiology/Virology(7,618 products)
- Neuroscience(10,367 products)
- Other Inhibitors(35,951 products)
- Oxidation-Reduction(41 products)
- PI3K/Akt/mTOR Signaling(1,442 products)
- Proteases/Proteasome(1,716 products)
- Stem Cell and Derivatives(801 products)
- Tyrosine Kinase/Adaptors(2,030 products)
- Ubiquitination(1,722 products)
Show 16 more subcategories
Found 66630 products of "Inhibitors"
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ChE/Aβ1-42-IN-1
ChE/Aβ1-42-IN-1 (compound 28) is a potent aggregation inhibitor of ChE and Aβ 1-42 with excellent BBB permeability.Formula:C19H24N2O3Color and Shape:SolidMolecular weight:328.41SHR902275
CAS:SHR902275: potent RAF inhibitor, hits RAS mutations, oral use. cRAF IC50=1.6 nM, bRAFwt IC50=10 nM, bRAFV600E IC50=5.7 nM, hinders cell growth.Formula:C26H23F3N4O4Color and Shape:SolidMolecular weight:512.48Ganciclovir monophosphonate
CAS:Ganciclovir monophosphate treats CMV, inhibiting replication in human/animal strains (IC50: 0.01μM).Formula:C10H16N5O6PColor and Shape:SolidMolecular weight:333.24STING agonist-20
CAS:STING agonist-20: potent, aids in XMT-2056 synthesis, used as a cancer vaccine adjuvant.Formula:C36H39N11O8Color and Shape:SolidMolecular weight:753.76L 156903
CAS:L 156903 is a bioactive chemical. It also inhibits the binding of neurotensin to brain tissue.Formula:C35H41N7O5SColor and Shape:SolidMolecular weight:671.81AL-GDa62
AL-GDa62, a gastric cancer treatment lead, has EC50 of 3.2 μM (MCF10A-WT) and 2 μM (MCF10A-CDH1 -/-).Formula:C24H28FN3OColor and Shape:SolidMolecular weight:393.5AK-295
CAS:AK 295, also known as CX 295, is a dipeptide inhibitor of alpha-ketoamide calpain.Formula:C26H40N4O6Color and Shape:SolidMolecular weight:504.62TP-030-1
CAS:TP-030-1, RIPK1 inhibitor: K(i) hRIPK1 at 3.9nM, IC50 mRIPK1 at 4.2μM; targets inflammation, neurodegeneration research.Formula:C23H22N4O3Color and Shape:SolidMolecular weight:402.45AS2575959
CAS:AS2575959 is a novel GPR40 agonist, exhibiting glucose metabolism improvement and synergistic effect with sitagliptin on insulin and incretin secretion.Formula:C32H35NaO7Color and Shape:SolidMolecular weight:554.6148BMS-741672
CAS:BMS-741672 is a potent, selective CCR2 antagonist for the treatment of neuropathic pain.Formula:C25H33F3N6O2Color and Shape:SolidMolecular weight:506.56Sinulatumolin E
CAS:Sinulatumolin E, a terpenoid, inhibits TNF-α (IC 50: 3.6 μM); has anti-inflammatory properties.Formula:C15H22O2Color and Shape:SolidMolecular weight:234.33PIM1-IN-3
PIM1-IN-3 (HL8) selectively blocks PIM1, induces Colo320 cell apoptosis, and may be researched for cancer.Formula:C27H25BrN6OColor and Shape:SolidMolecular weight:529.43Vindeburnol
CAS:Vindeburnol is a cerebral vasodilator vincamine analog that bears neuroprotective properties.Formula:C17H20N2OColor and Shape:SolidMolecular weight:268.35NRX-2663
CAS:NRX-2663 boosts β-catenin binding to E3 ligase SCFβ-TrCP (Kd: 54.8 nM, EC50: 22.9 nM).Formula:C20H13F3N2O5Color and Shape:SolidMolecular weight:418.32A4B17
A4B17 is an inhibitor of androgen receptor N-terminal with potential for androgen-responsive prostate cancer treatment.Formula:C14H7F4NSColor and Shape:SolidMolecular weight:297.27Nrf2 activator-6
CAS:Nrf2 activator-6, a tetrahydroisoquinoline, inhibits Kelch-Nrf2 at 5 nM IC50 (WO2021214470A1).Formula:C31H37ClFN5O5Color and Shape:SolidMolecular weight:614.11NTPDase-IN-2
CAS:NTPDase-IN-2 inhibits h-NTPDase-2/-8 (IC50: 0.04, 2.27 µM), non-competitive for h-NTPDase-1/-2 (Km: 74 µM); useful in cancer, immune, bacterial research.Formula:C24H20FN3OS2Color and Shape:SolidMolecular weight:449.56PI3K-IN-29
CAS:PI3K-IN-29: Strong PI3K block, inhibits Akt phosphorylation. IC50: U87MG 0.264µM, HeLa 2.04µM, HL60 1.14µM.Formula:C27H22ClN7O3SColor and Shape:SolidMolecular weight:560.03BSc5367
CAS:BSc5367 inhibits Nek1 kinase (IC50: 11.5 nM), key in cell cycle, DNA repair, impacting ALS, PKD, cancer.
Formula:C20H15N3O2Color and Shape:SoildMolecular weight:329.35Ataprost
CAS:Ataprost (ONO 41483), an oral Carboprostacyclin analogue, is 2.6x more potent in inhibiting ADP-induced platelet aggregation and can relieve coronary spasm.Formula:C21H32O4Color and Shape:SolidMolecular weight:348.48
