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 About 8 results found for searched term "92-13-7" (0.129 seconds)

Cat.No.  Name Target
M2911 Riviciclib hydrochloride (P276-00) CDK
Riviciclib hydrochloride
Riviciclib hydrochloride (P276-00) is an effective CDK inhibitor, inhibiting CDK9-CyclinT1, CDK4-cyclin D1, CDK1-Cyclinb with IC50 values of 20 nM, 63 nM, respectively. 79 nM. Riviciclib hydrochloride (P276-00) has anti-tumor activity against Cisplatin resistant cells.
M9882 Roflumilast N-oxide PDE
Roflumilast N-oxide is a phosphodiesterase 4 inhibitor.
M30915 Pilocarpine  AChR/AChE
Pilocarpine is a selective M3-type muscarinic acetylcholine receptor (M3 muscarinic receptor) agonist.
M53191 Carperitide Endothelin Receptor
Carperitide (Atrial Natriuretic Peptide (ANP) (1-28), human, porcine) is a 28-amino acid hormone, that is normally produced and secreted by the human heart in response to cardiac injury and mechanical stretch.
M2003 PF-04929113 HSP
SNX-5422
PF-04929113 (SNX-5422) is a potent and selective Hsp90 inhibitor with Kd of 41 nM. SNX-5422 (PF-04929113) also induces Her-2 degradation, with an IC50 of 37 nM.
M30879 AR-9281 Epoxide Hydrolase
APAU
AR9281 (APAU) is a potent, selective and orally active soluble epoxide hydrolase (s-EH) inhibitor. AR-9281 can inhibits human sEH (HsEH) and murine sEH (MsEH) with IC50 values of 13.8 nM and 1.7 nM, respectively. AR9281 can be used for the research of inflammation, hypertension and type 2 diabetes.
M41263 ZINC475239213 Anti-infection
ZINC475239213 is an inhibitor of the SARS-CoV-2 Nsp14 N7-Methyltransferase (IC50: 20 μM).
M41379 BMS-561392 formate TNF Receptor
DPC 333 formate
BMS-561392 formate is a TNF alpha-converting enzyme (TACE) inhibitor. BMS-561392 is also an ADAM17 blocker. BMS-561392 can be used for research of inflammatory bowel disease.



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