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Benzoic acid, 4-(cyclopropylamino)-3-nitro-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

579514-76-4

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579514-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 579514-76-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,9,5,1 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 579514-76:
(8*5)+(7*7)+(6*9)+(5*5)+(4*1)+(3*4)+(2*7)+(1*6)=204
204 % 10 = 4
So 579514-76-4 is a valid CAS Registry Number.

579514-76-4Downstream Products

579514-76-4Relevant academic research and scientific papers

Discovery and optimization of 1-(1H-indol-1-yl)ethanone derivatives as CBP/EP300 bromodomain inhibitors for the treatment of castration-resistant prostate cancer

Xiang, Qiuping,Wang, Chao,Zhang, Yan,Xue, Xiaoqian,Song, Ming,Zhang, Cheng,Li, Chenchang,Wu, Chun,Li, Kuai,Hui, Xiaoyan,Zhou, Yulai,Smaill, Jeff B.,Patterson, Adam V.,Wu, Donghai,Ding, Ke,Xu, Yong

, p. 238 - 252 (2018/02/15)

The CREB (cAMP responsive element binding protein) binding protein (CBP) and its homolog EP300 have emerged as new therapeutic targets for the treatment of cancer and inflammatory diseases. Here we report the identification, optimization and evaluation of 1-(1H-indol-1-yl)ethanone derivatives as CBP/EP300 inhibitors starting from fragment-based virtual screening (FBVS). A cocrystal structure of the inhibitor (22e) in complex with CBP provides a solid structural basis for further optimization. The most potent compound 32h binds to the CBP bromodomain and has an IC50 value of 0.037 μM in the AlphaScreen assay which was 2 times more potent than the reported CBP bromodomain inhibitor SGC-CBP30 in our hands. 32h also exhibit high selectivity for CBP/EP300 over other bromodomain-containing proteins. Notably, the ester derivative (29h) of compound 32h markedly inhibits cell growth in several prostate cancer cell lines including LNCaP, 22Rv1 and LNCaP derived C4-2B. Compound 29h suppresses the mRNA expression of full length AR (AR-FL), AR target genes and other oncogene in LNCaP cells. 29h also reduces the expression of PSA, the biomarker of prostate cancer. CBP/EP300 inhibitor 29h represents a promising lead compound for the development of new therapeutics for the treatment of castration-resistant prostate cancer.

TETRAHYDROQUINOXALINES AND THEIR USE AS M2 ACETYLCHOLINE RECEPTOR AGONISTS

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Page/Page column 28-29, (2008/06/13)

The invention relates to tetrahydroquinoxalines of formula (I), in which A, X, R1, R2, R3, R4, and R are defined as cited in claim 1, to a method for their production and to the use thereof for producing medicaments for the treatment and/or prophylaxis of diseases, in particular cardiovascular diseases.

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