
Inhibitors
Subcategories of "Inhibitors"
- Angiogenesis(2,756 products)
- Apoptosis(6,188 products)
- Cell Cycle/Checkpoint(4,808 products)
- Chromatin/Epigenetics(2,575 products)
- Cytoskeletal Signaling(1,503 products)
- DNA Damage/DNA Repair(2,891 products)
- Endocrinology/Hormones(3,702 products)
- Enzyme(3,671 products)
- GPCR/G-Protein(8,965 products)
- Immunology and Inflammation(3,700 products)
- Influenza Virus(296 products)
- JAK/STAT signaling(414 products)
- MAPK Signaling(1,248 products)
- Membrane Transporter/Ion Channel(3,136 products)
- Metabolism(10,099 products)
- Microbiology/Virology(7,554 products)
- Neuroscience(10,303 products)
- Other Inhibitors(35,767 products)
- Oxidation-Reduction(39 products)
- PI3K/Akt/mTOR Signaling(1,402 products)
- Proteases/Proteasome(1,672 products)
- Stem Cell and Derivatives(742 products)
- Tyrosine Kinase/Adaptors(1,922 products)
- Ubiquitination(1,716 products)
Found 66572 products of "Inhibitors"
Mal-cyclohexane-Gly-Gly-Phe-Gly-Exatecan
CAS:Mal-cyclohexane-Gly-Gly-Phe-Gly-Exatecan is a linker molecule employed in the synthesis of antibody-drug conjugates (ADCs), demonstrating potent antitumor
Formula:C55H60FN9O13Color and Shape:SolidMolecular weight:1074.12STAT3-IN-18
CAS:STAT3-IN-18 (compound SPP), a platinum (IV) complex featuring an axial ligand from sandalwood, suppresses the JAK2-STAT3 pathway in breast cancer (BC) cells and
Formula:C18H24Cl2N2O6PtPurity:98%Color and Shape:SolidMolecular weight:630.38Civorebrutinib
CAS:Civorebrutinib (WS-413) is an inhibitor of Bruton's tyrosine kinase that exhibits antineoplastic activity [1].
Formula:C23H22ClN7O2Color and Shape:SolidMolecular weight:463.92Mal-VC-PAB-PNP-CDN-A
CAS:Mal-VC-PAB-PNP-CDN-A is a conjugate comprised of an agent and a linker, utilized in antibody-drug conjugates (ADC) [1] [2].
Formula:C51H67N17O20P2Color and Shape:SolidMolecular weight:1300.13SHP2-IN-14
CAS:SHP2-IN-14 (compound 27) is a potent, orally active allosteric inhibitor of SHP2, displaying strong anti-tumor activity with an IC50 of 7 nM.
Formula:C22H20Cl2N8OColor and Shape:SolidMolecular weight:483.35Azilsartan mepixetil potassium
CAS:Azilsartan medoxomil potassium (QR-01019K), an angiotensin II receptor antagonist, exhibits a potent and sustained antihypertensive effect, along with a more
Formula:C36H33KN6O8Color and Shape:SolidMolecular weight:716.78Davelizomib
CAS:Davelizomib is a proteasome inhibitor that exhibits antineoplastic activity [1].
Formula:C21H26BF2N3O7Purity:98%Color and Shape:SolidMolecular weight:481.25CYY292
CAS:CYY292 is a chemical compound acting as an inhibitor of PDGFRα, PDGFRβ, FGFR1, -2, and -3, with respective IC50 values of 5.35, 4.6, 28, 28, and 78 nM.
Formula:C24H28N8OColor and Shape:SolidMolecular weight:444.53Bumetanide sodium
CAS:Bumetanide sodium, a potent diuretic, blocks NKCC1 (IC50: 0.68 μM) and NKCC2 (IC50: 4.0 μM).Formula:C17H19N2NaO5SColor and Shape:SolidMolecular weight:386.4URAT1&XO inhibitor 1
CAS:URAT1&XO Inhibitor 1 (compound 29) serves as a dual inhibitor with IC50 values of approximately 10 μM for URAT1 and 1.01 μM for Xanthine Oxidase.
Formula:C20H13N5O3SPurity:98%Color and Shape:SolidMolecular weight:403.41TrkB-IN-1
CAS:TrkB-IN-1 is a potent, orally active agonist of the TrkB receptor, with favorable pharmacokinetic (PK) properties.
Formula:C19H16N2O6Purity:98%Color and Shape:SolidMolecular weight:368.34PHI-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:440.53DG026
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:464.89hDHODH-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:487.35ROCK-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:477.45Cortivazol
CAS:Cortivazol is an Anti-Inflammatory Drug.Formula:C32H38N2O5Purity:98%Color and Shape:SolidMolecular weight:530.65Dimethandrolone 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 productALS-I-41
CAS:ALS-I-41 is a novel, potent and selective antagonist of oxytocin receptor.Formula:C30H38FN3O6SPurity:98%Color and Shape:SolidMolecular weight:587.7Ifetroban sodium
CAS:Ifetroban sodium (BMS-180291), oral TXA2/PGH2 antagonist for researching heart, stroke, BP, thrombosis.
Formula:C25H31N2NaO5Color and Shape:SolidMolecular weight:462.522BPH-628
CAS:BPH-628 is a bioactive chemical.
Formula:C20H20O7P2Color and Shape:SolidMolecular weight:434.32

