Chemical Structure : MCUF-42
货号: PC-22560Not For Human Use, Lab Use Only.
MCUF-42 is a selective, positive allosteric modulator (PAM) of guanylyl cyclase B (GC-B) receptor, dose-dependently potentiates CNP-induced cGMP with EC50 of 0.8 uM (Emax = 86%), enhances the binding affinity between GC-B and its natural ligand C-type natriuretic peptide (CNP).
大包装,大折扣!
E-mail: sales@probechem.com
Tech Support: tech@probechem.com
MCUF-42 is a selective, positive allosteric modulator (PAM) of guanylyl cyclase B (GC-B) receptor, dose-dependently potentiates CNP-induced cGMP with EC50 of 0.8 uM (Emax = 86%), enhances the binding affinity between GC-B and its natural ligand C-type natriuretic peptide (CNP).
In the absence of CNP, MCUF-42 possesses no cGMP-generating activity in HEK293 GC-B cells.
MCUF-42 is a PAM without agonistic activity.
MCUF-42 binds to human GC-B with KD of 710 nM in SPR assays.
MCUF-42 (1, 5, and 10 µM) enhances the cGMP generation of CNP in human cardiac fibroblasts (HCFs).
MCUF-42 enhances CNP mediated inhibition of HCF proliferation triggered by profibrotic TGFβ1.
分子量 | 393.33 | |
分子式 | C19H18Cl2N2OS | |
外观性状 | Solid | |
储存条件 |
|
|
Solubility |
10 mM in DMSO |
1. Ma X, et al. PNAS Nexus. 2024 Jun 6;3(6):pgae225.
备案号:沪ICP备16042516号-1 Copyright © 2022 probechem.com. All Rights Reserved. probechem Copyright