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4H-Pyrazolo[3,4-d]pyrimidin-4-one, 1-(3-bromophenyl)-1,5-dihydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

650628-15-2

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650628-15-2 Usage

Potential biological activities

anti-inflammatory, anti-cancer, anti-microbial effects
Valuable tool for medicinal chemistry and drug design
Potential applications in the development of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 650628-15-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,0,6,2 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 650628-15:
(8*6)+(7*5)+(6*0)+(5*6)+(4*2)+(3*8)+(2*1)+(1*5)=152
152 % 10 = 2
So 650628-15-2 is a valid CAS Registry Number.

650628-15-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-bromophenyl)-2H-pyrazolo[3,4-d]pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 4H-Pyrazolo[3,4-d]pyrimidin-4-one,1-(3-bromophenyl)-1,5-dihydro

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:650628-15-2 SDS

650628-15-2Relevant academic research and scientific papers

Novel pyrazolopyrimidine derivatives as GSK-3 inhibitors

Peat, Andrew J.,Boucheron, Joyce A.,Dickerson, Scott H.,Garrido, Dulce,Mills, Wendy,Peckham, Jennifer,Preugschat, Frank,Smalley, Terrence,Schweiker, Stephanie L.,Wilson, Jayme R.,Wang, Tony Y.,Zhou, Huiqiang Q.,Thomson, Stephen A.

, p. 2121 - 2125 (2007/10/03)

A series of [1-aryl-1H-pyrazolo[3,4-d]pyrimidin-4-yl]arylhydrazones were discovered as novel inhibitors glycogen synthase kinase-3 (GSK-3). Based on initial modeling a detailed SAR was constructed. Modification of the interior binding aryl ring (Ar1) determined this to be a tight binding region with little room for modification. As predicted from the model, a large variety of modifications could be incorporated into the hydrazone aryl ring. This work led to GSK-3 inhibitors in the low nano-molar range.

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