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3303-37-5

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3303-37-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3303-37-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,0 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3303-37:
(6*3)+(5*3)+(4*0)+(3*3)+(2*3)+(1*7)=55
55 % 10 = 5
So 3303-37-5 is a valid CAS Registry Number.

3303-37-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name H-ALA-NLE-OH

1.2 Other means of identification

Product number -
Other names L-ALANYL-L-NORLEUCINE

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:3303-37-5 SDS

3303-37-5Downstream Products

3303-37-5Relevant articles and documents

Selection of DNA-Encoded Dynamic Chemical Libraries for Direct Inhibitor Discovery

Deng, Yuqing,Huang, Yiran,Lam, Fong Sang,Li, Xiaoyu,Meng, Ling,Peng, Jianzhao,Shen, Wenyin,Song, Yinan,Xie, Chao,Xiong, Feng,Zhang, Jianfu,Zhou, Yu

, p. 14965 - 14972 (2020)

Dynamic combinatorial libraries (DCLs) is a powerful tool for ligand discovery in biomedical research; however, the application of DCLs has been hampered by their low diversity. Recently, the concept of DNA encoding has been employed in DCLs to create DNA-encoded dynamic libraries (DEDLs); however, all current DEDLs are limited to fragment identification, and a challenging process of fragment linking is required after selection. We report an anchor-directed DEDL approach that can identify full ligand structures from large-scale DEDLs. This method is also able to convert unbiased libraries into focused ones targeting specific protein classes. We demonstrated this method by selecting DEDLs against five proteins, and novel inhibitors were identified for all targets. Notably, several selective BD1/BD2 inhibitors were identified from the selections against bromodomain 4 (BRD4), an important anti-cancer drug target. This work may provide a broadly applicable method for inhibitor discovery.

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