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1234479-76-5

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  • 6H- Pyrimido[4, 5- b] [1, 4] benzodiazepin- 6- one, 5, 11- dihydro- 2- [[2- methoxy- 4- (4- methyl- 1- piperazinyl) phenyl] amino] - 5, 11- dimethyl-

    Cas No: 1234479-76-5

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1234479-76-5 Usage

Uses

ERK5-IN-1 is a potent selective ERK5 inhibitor, inhibiting EGFR-induced ERK5 autophosphorylation and ERK5 enzymatic activity. Orally bioavailable.

Check Digit Verification of cas no

The CAS Registry Mumber 1234479-76-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,4,4,7 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1234479-76:
(9*1)+(8*2)+(7*3)+(6*4)+(5*4)+(4*7)+(3*9)+(2*7)+(1*6)=165
165 % 10 = 5
So 1234479-76-5 is a valid CAS Registry Number.

1234479-76-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-{[2-Methoxy-4-(4-methyl-1-piperazinyl)phenyl]amino}-5,11-dimeth yl-5,11-dihydro-6H-pyrimido[4,5-b][1,4]benzodiazepin-6-one

1.2 Other means of identification

Product number -
Other names LRRK2-IN-1

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1234479-76-5 SDS

1234479-76-5Downstream Products

1234479-76-5Relevant articles and documents

Discovery of a benzo[e]pyrimido-[5,4-b][1,4]diazepin-6(11H)-one as a potent and selective inhibitor of big MAP kinase 1

Deng, Xianming,Yang, Qingkai,Kwiatkowski, Nicholas,Sim, Taebo,McDermott, Ultan,Settleman, Jeffrey E.,Lee, Jiing-Dwan,Gray, Nathanael S.

, p. 195 - 200 (2011/05/03)

Kinome-wide selectivity profiling of a collection of 2-amino-pyrido[2,3-d] pyrimidines followed by cellular structure-activity relationship-guided optimization resulted in the identification of moderately potent and selective inhibitors of BMK1/ERK5 exemp

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