(S)-Ro 32-0432 free base

Modify Date: 2024-01-12 08:55:07

(S)-Ro 32-0432 free base Structure
(S)-Ro 32-0432 free base structure
Common Name (S)-Ro 32-0432 free base
CAS Number 151342-35-7 Molecular Weight 452.55
Density N/A Boiling Point 711.9ºC at 760 mmHg
Molecular Formula C28H28N4O2 Melting Point N/A
MSDS N/A Flash Point 384.3ºC

 Use of (S)-Ro 32-0432 free base


(S)-Ro 32-0432 free base is a potent, selective, ATP-competitive and orally active PKC inhibitor. The IC50 values of (S)-Ro 32-0432 free base for PKCα, PKCβI, PKCβII, PKCγ and PKCε are 9.3 nM, 28 nM, 30 nM, 36.5 nM and 108.3 nM, respectively. (S)-Ro 32-0432 free base is also a selective G protein-coupled receptor kinase 5 (GRK5) inhibitor. (S)-Ro 32-0432 free base prevents T-cell activation and has the potential for chronic inflammatory and autoimmune diseases research[1][2].

 Names

Name bisindolylmaleimide X

 (S)-Ro 32-0432 free base Biological Activity

Description (S)-Ro 32-0432 free base is a potent, selective, ATP-competitive and orally active PKC inhibitor. The IC50 values of (S)-Ro 32-0432 free base for PKCα, PKCβI, PKCβII, PKCγ and PKCε are 9.3 nM, 28 nM, 30 nM, 36.5 nM and 108.3 nM, respectively. (S)-Ro 32-0432 free base is also a selective G protein-coupled receptor kinase 5 (GRK5) inhibitor. (S)-Ro 32-0432 free base prevents T-cell activation and has the potential for chronic inflammatory and autoimmune diseases research[1][2].
Related Catalog
References

[1]. A M Birchall, et al. Ro 32-0432, a Selective and Orally Active Inhibitor of Protein Kinase C Prevents T-cell Activation. J Pharmacol Exp Ther. 1994 Feb;268(2):922-9.  

[2]. Thakur Gurjeet Singh, et al. Ro 32-0432 Attenuates Mecamylamine-Precipitated Nicotine Withdrawal Syndrome in Mice. Naunyn Schmiedebergs Arch Pharmacol. 2013 Mar;386(3):197-204.  

 Chemical & Physical Properties

Boiling Point 711.9ºC at 760 mmHg
Molecular Formula C28H28N4O2
Molecular Weight 452.55
Flash Point 384.3ºC
Exact Mass 488.19800
PSA 59.27000
LogP 4.95500
Vapour Pressure 4.11E-20mmHg at 25°C