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(1E,4E)-1-(2,4-dimethoxy-6-((E)-4-methoxystyryl)phenyl)-5-(2-fluorophenyl)penta-1,4-dien-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1357567-07-7

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1357567-07-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1357567-07-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,7,5,6 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1357567-07:
(9*1)+(8*3)+(7*5)+(6*7)+(5*5)+(4*6)+(3*7)+(2*0)+(1*7)=187
187 % 10 = 7
So 1357567-07-7 is a valid CAS Registry Number.

1357567-07-7Downstream Products

1357567-07-7Relevant academic research and scientific papers

pentadienone-resveratrol derivative, a method for producing the same, and an anticancer drug containing the same

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Paragraph 0163; 0166; 0167; 0173, (2019/03/28)

The present invention relates to a pentadienone-resveratrol derivative useful as an anti-cancer drug, a preparing method thereof, and an anti-cancer drug including the same. The pentadienone-resveratrol derivative comprises a compound represented by chemi

Synthesis, biological evaluation and molecular docking studies of resveratrol derivatives possessing curcumin moiety as potent antitubulin agents

Ruan, Ban-Feng,Lu, Xiang,Li, Ting-Ting,Tang, Jian-Feng,Wei, Yao,Wang, Xiao-Liang,Zheng, Shi-Li,Yao, Ri-Sheng,Zhu, Hai-Liang

experimental part, p. 1113 - 1121 (2012/02/17)

A series of resveratrol derivatives possessing curcumin moiety were synthesized and evaluated for their antiproliferative activity against three cancer cell lines including murine melanoma B16-F10, human hepatoma HepG2 and human lung carcinoma A549. Among them, compound C5 displayed the most potent in vitro antiproliferative activity against B16-F10 with IC50 value of 0.71 μg/mL. Compound C5 also exhibited good tubulin polymerization inhibitory activity with IC50 value of 1.45 μg/mL. Furthermore, docking simulation was carried out to position C5 into the tubulin-colchicine binding site to determine the probable binding mode.

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