1415609-37-8

Basic information

• Product Name: 5-chloro-3-(4-(2-(dimethylamino)ethoxy)-3-methoxybenzyliden)indolin-2-one
• Synonyms: 5-chloro-3-(4-(2-(dimethylamino)ethoxy)-3-methoxybenzyliden)indolin-2-one
• CAS NO: 1415609-37-8
• Molecular Weight: 372.851
• Mol File: 1415609-37-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 5-chloro-3-(4-(2-(dimethylamino)ethoxy)-3-methoxybenzyliden)indolin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5-chloro-3-(4-(2-(dimethylamino)ethoxy)-3-methoxybenzyliden)indolin-2-one(1415609-37-8)
• EPA Substance Registry System: 5-chloro-3-(4-(2-(dimethylamino)ethoxy)-3-methoxybenzyliden)indolin-2-one(1415609-37-8)

Safety Data

• Hazardous Substances Data: 1415609-37-8(Hazardous Substances Data)

Upstream product

• 17630-75-0 5-chloro-indolin-2-one 
• 55589-46-3 4-(2-(dimethylamino)ethoxy)-3-methoxybenzaldehyde 
• 121-33-5 vanillin 

Relevant articles and documents

Indolinone based LRRK2 kinase inhibitors with a key hydrogen bond

The most prevalent leucine-rich repeat kinase 2 (LRRK2) mutation G2019S is associated with Parkinson's disease (PD). It enhances kinase activity and has been identified in both familial and sporadic cases. Kinase activity was reported to be required for LRRK2 mutants to exert their toxic effects. Hence LRRK2 kinase inhibition may be a promising therapeutic target for PD. Here we report on the discovery and characterization of indolinone based LRRK2 inhibitors. Indolinone 15b, the most potent and selective inhibitor of the present series, is characterized by an IC50of 15 nM against wild-type LRRK2 and 10 nM against the LRRK2 G2019S mutant, respectively. Compound 15b was further evaluated in a kinase panel including 46 human protein kinases and in a zebrafish embryo phenotype assay, which enabled toxicity determination in whole organisms.