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575473-97-1

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575473-97-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 575473-97-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,5,4,7 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 575473-97:
(8*5)+(7*7)+(6*5)+(5*4)+(4*7)+(3*3)+(2*9)+(1*7)=201
201 % 10 = 1
So 575473-97-1 is a valid CAS Registry Number.

575473-97-1SDS

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 7-amino-2,2-dimethyl-4H-pyrido[3,2-b][1,4]oxazin-3-one

1.2 Other means of identification

Product number -
Other names -

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:575473-97-1 SDS

575473-97-1Downstream Products

575473-97-1Relevant articles and documents

Y08060: A Selective BET Inhibitor for Treatment of Prostate Cancer

Xiang, Qiuping,Zhang, Yan,Li, Jiaguo,Xue, Xiaoqian,Wang, Chao,Song, Ming,Zhang, Cheng,Wang, Rui,Li, Chenchang,Wu, Chun,Zhou, Yulai,Yang, Xiaohong,Li, Guohui,Ding, Ke,Xu, Yong

, p. 262 - 267 (2018)

Prostate cancer is a commonly diagnosed cancer and a leading cause of cancer-related deaths. The bromodomain and extra terminal domain (BET) family proteins have emerged as potential therapeutic targets for the treatment of castration-resistant prostate cancer. A series of 2,2-dimethyl-2H-benzo[b][1,4]oxazin-3(4H)-one derivatives were designed and synthesized as selective bromodomain containing protein 4 (BRD4) inhibitors. The compounds potently inhibit BRD4(1) with nanomolar IC50 values and exhibit high selectivity over most non-BET subfamily members. One of the representative compounds 36 (Y08060) effectively suppresses cell growth, colony formation, and expression of androgen receptor (AR), AR regulated genes, and MYC in prostate cancer cell lines. In in vivo studies, 36 demonstrates a good PK profile with high oral bioavailability (61.54%) and is a promising lead compound for further prostate cancer drug development.

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