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3-Pyrrolidinecarboxylic acid, 4-hydroxy-1-(phenylmethyl)-, ethyl ester, (3S,4R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

849935-77-9

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849935-77-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 849935-77-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,9,3 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 849935-77:
(8*8)+(7*4)+(6*9)+(5*9)+(4*3)+(3*5)+(2*7)+(1*7)=239
239 % 10 = 9
So 849935-77-9 is a valid CAS Registry Number.

849935-77-9SDS

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 ethyl (3S,4R)-1-benzyl-4-hydroxypyrrolidine-3-carboxylate

1.2 Other means of identification

Product number -
Other names (3S,4R)-1-N-benzyl-4-hydroxypyrrolidine-3-carboxylic acid ethyl ester

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:849935-77-9 SDS

849935-77-9Relevant academic research and scientific papers

An aza-nucleoside, fragment-like inhibitor of the DNA repair enzyme alkyladenine glycosylase (AAG)

Al Yahyaei, Balqees,Chu, Shuyu,Elliott, Ruan M.,Howlin, Brendan J.,Imperato, Manuel,Lopez, Arnaud,Mas Claret, Eduard,Meira, Lisiane B.,Whelligan, Daniel K.

, (2020/04/23)

The DNA repair enzyme AAG has been shown in mice to promote tissue necrosis in response to ischaemic reperfusion or treatment with alkylating agents. A chemical probe inhibitor is required for investigations of the biological mechanism causing this phenomenon and as a lead for drugs that are potentially protective against tissue damage from organ failure and transplantation, and alkylative chemotherapy. Herein, we describe the rationale behind the choice of arylmethylpyrrolidines as appropriate aza-nucleoside mimics for an inhibitor followed by their synthesis and the first use of a microplate-based assay for quantification of their inhibition of AAG. We finally report the discovery of an imidazol-4-ylmethylpyrrolidine as a fragment-sized, weak inhibitor of AAG.

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