
Inhibitors
Subcategories of "Inhibitors"
- Angiogenesis(2,810 products)
- Apoptosis(6,297 products)
- Cell Cycle/Checkpoint(4,846 products)
- Chromatin/Epigenetics(2,540 products)
- Cytoskeletal Signaling(1,552 products)
- DNA Damage/DNA Repair(2,911 products)
- Endocrinology/Hormones(3,707 products)
- Enzyme(3,671 products)
- GPCR/G-Protein(9,023 products)
- Immunology and Inflammation(3,897 products)
- Influenza Virus(302 products)
- JAK/STAT signaling(417 products)
- MAPK Signaling(1,248 products)
- Membrane Transporter/Ion Channel(3,097 products)
- Metabolism(10,148 products)
- Microbiology/Virology(7,623 products)
- Neuroscience(10,358 products)
- Other Inhibitors(35,910 products)
- Oxidation-Reduction(40 products)
- PI3K/Akt/mTOR Signaling(1,437 products)
- Proteases/Proteasome(1,706 products)
- Stem Cell and Derivatives(783 products)
- Tyrosine Kinase/Adaptors(2,008 products)
- Ubiquitination(1,721 products)
Found 66616 products of "Inhibitors"
HBV-IN-38
CAS:HBV-IN-38 (Example 193), an HBV DNA inhibitor with an EC50 value of ≤100 nM, serves as a research tool for investigating viral infections [1].
Formula:C18H16F3N5O4S2Purity:98%Color and Shape:SolidMolecular weight:487.48AEF0117
CAS:AEF0117 is a signaling inhibitor of CB1-SSi that inhibits cannabinoid self-administration and can be used to study cannabis withdrawal.
Formula:C29H40O3Purity:99.58%Color and Shape:SolidMolecular weight:436.63Antitumor photosensitizer-1
CAS:Antitumor Photosensitizer-1 (Compound 8) is a potent photosensitizer with remarkable photodynamic anti-tumor properties and minimal skin photo-toxicity,
Formula:C42H51N5O6Color and Shape:SolidMolecular weight:721.88BTK-IN-27
CAS:BTK-IN-27 (example 8), a potent BTK inhibitor with an IC50 of 0.2 nM, demonstrates anti-proliferative effects in TMD8 cells with an IC50 of less than 5 nM.
Formula:C31H35N7O2Purity:98%Color and Shape:SolidMolecular weight:537.66JAK1-IN-11
CAS:JAK1-IN-11 (compound 11) serves as a potent inhibitor of Janus kinases, exhibiting nanomolar inhibitory concentrations with IC50 values of 0.02 nM (JAK1) and 0.
Formula:C26H36N6O4SPurity:98%Color and Shape:SolidMolecular weight:528.67PHI-101
CAS:PHI-101 is a checkpoint kinase 2 (Chk2) inhibitor that can be used for the study of refractory acute myeloid leukemia (AML) and ovarian cancer.
Formula:C19H19FN4O2SPurity:99.4%Color and Shape:SolidMolecular weight:386.44Ifetroban
CAS:Ifetroban is a potent and selective TxA2/PGH2 receptor antagonist.
Formula:C25H32N2O5Color and Shape:SolidMolecular weight:440.53Cortivazol
CAS:Cortivazol is an Anti-Inflammatory Drug.Formula:C32H38N2O5Purity:98%Color and Shape:SolidMolecular weight:530.65BPH-628
CAS:BPH-628 is a bioactive chemical.
Formula:C20H20O7P2Color and Shape:SolidMolecular weight:434.32ALS-I-41
CAS:ALS-I-41 is a novel, potent and selective antagonist of oxytocin receptor.Formula:C30H38FN3O6SPurity:98%Color and Shape:SolidMolecular weight:587.7hDHODH-IN-8
hDHODH-IN-8 is a potent human dihydroorotic dehydrogenase (hDHODH) inhibitor (IC50: 16 nM) that exhibits potent antiproliferative effects and has good water solubility, with potential for oncology studies, especially in lymphoma.
Formula:C21H15F6N3O4Purity:98%Molecular weight:487.35Ifetroban sodium
CAS:Ifetroban sodium (BMS-180291), oral TXA2/PGH2 antagonist for researching heart, stroke, BP, thrombosis.
Formula:C25H31N2NaO5Color and Shape:SolidMolecular weight:462.522ROCK-IN-6
CAS:ROCK-IN-6, a selective ROCK2 inhibitor, exhibits potent inhibition with an IC50 of 2.19 nM and holds promise for research into glaucoma and retinal diseases [1
Formula:C19H19N5O8SPurity:98%Color and Shape:SolidMolecular weight:477.45Dimethandrolone Undecanoate
CAS:Dimethandrolone Undecanoate (DMAU) is a novel orally available androgen with progestational activity and is a potential male contraceptive compound.Formula:C31H50O3Purity:99.65% - >99.99%Color and Shape:SolidMolecular weight:470.73Ref: TM-T27176
Discontinued productDG026
CAS:DG026 selectively inhibits IRAP, reducing its cross-presentation in dendritic cells without affecting ERAP1.Formula:C35H40N3O4PPurity:98%Color and Shape:SolidMolecular weight:597.68ZK824859 hydrochloride
ZK824859 hydrochloride: oral uPA inhibitor with IC50 of 79 nM (uPA), 1580 nM (tPA), 1330 nM (fibrin).Formula:C23H23ClF2N2O4Color and Shape:SolidMolecular weight:464.89

