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(Z)-3-Benzo[1,3]dioxol-5-yl-2-(4-methoxy-phenyl)-acrylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96853-53-1

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96853-53-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96853-53-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,8,5 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 96853-53:
(7*9)+(6*6)+(5*8)+(4*5)+(3*3)+(2*5)+(1*3)=181
181 % 10 = 1
So 96853-53-1 is a valid CAS Registry Number.

96853-53-1Relevant academic research and scientific papers

STILBENES OF GNETUM ULA

Prakash, Satya,Khan, Mushtaq A.,Khan, Khaliquz Zaman,Zaman, Asif

, p. 622 - 624 (1985)

Key Word Index - Gnetum ula; Gnetaceae; stilbenes; structure; synthesis; structure revision. - Gnetin, a new stilbene isolated from Gnetum ula is assigned the structure 3,4-methylenedioxy-4'methoxy-trans-stilbene, 3 on the basis of spectroscopic data and synthesis.The structure 3,3',4-trihydroxy-2-methoxy-trans-stilbene, 1a earlier assigned to a trihydroxymonomethoxy stilbene is now revised to 3,4,5'-trihydroxy-3'-methoxy-trans-stilbene, 1b.

Design, synthesis and biological evaluation of 1-phenanthryl-tetrahydroisoquinoline derivatives as novel p21-activated kinase 4 (PAK4) inhibitors

Song, Shuai,Li, Xiaodong,Guo, Jing,Hao, Chenzhou,Feng, Yan,Guo, Bingyu,Liu, Tongchao,Zhang, Qiaoling,Zhang, Zhen,Li, Ruijuan,Wang, Jian,Lin, Bin,Li, Feng,Zhao, Dongmei,Cheng, Maosheng

, p. 3803 - 3818 (2015/03/30)

Functional versatility and elevated expression in cancers have promoted p21-activated kinase 4 (PAK4) as one of the first-in-class anti-cancer drug targets. In this study, a series of novel 1-phenanthryl-tetrahydroisoquinoline analogues have been designed and synthesized as a novel class of small-molecule PAK4 inhibitors to fit into the cavity of PAK4. All of the target compounds were evaluated for their in vitro PAK4 inhibitory activities and antiproliferative activities. Lead optimization identified all the derivatives with more potency than the lead compound, especially compound 21a. Moreover, compound 21a significantly induced the cell cycle in the G1/S phase, and inhibited migration and invasion of MCF-7 cells via the regulation of the PAK4-LIMK1-cofilin signaling pathway. A molecular modeling study showed possible novel binding modes between 21a and PAK4 and provided a structural basis for further structure-guided design of PAK4 inhibitors.

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