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(E)-methyl 3-methoxy-2-(2-(((2-(phenylamino)-5,6,7,8-tetrahydroquinazolin-4-yl)oxy)methyl)phenyl)acrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1257598-91-6

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  • (E)-methyl 3-methoxy-2-(2-(((2-(phenylamino)-5,6,7,8-tetrahydroquinazolin-4-yl)oxy)methyl)phenyl)acrylate

    Cas No: 1257598-91-6

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  • (E)-methyl 3-methoxy-2-(2-(((2-(phenylamino)-5,6,7,8-tetrahydroquinazolin-4-yl)oxy)methyl)phenyl)acrylate

    Cas No: 1257598-91-6

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1257598-91-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1257598-91-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,7,5,9 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1257598-91:
(9*1)+(8*2)+(7*5)+(6*7)+(5*5)+(4*9)+(3*8)+(2*9)+(1*1)=206
206 % 10 = 6
So 1257598-91-6 is a valid CAS Registry Number.

1257598-91-6Downstream Products

1257598-91-6Relevant articles and documents

Synthesis of novel strobilurin-pyrimidine derivatives and their antiproliferative activity against human cancer cell lines

Chai, Baoshan,Wang, Shuyang,Yu, Wenquan,Li, Huichao,Song, Chuanjun,Xu, Ying,Liu, Changling,Chang, Junbiao

, p. 3505 - 3510 (2013/07/28)

A series of new strobilurin-pyrimidine analogs were designed and synthesized based on the structures of our previously discovered antiproliferative compounds I and II. Biological evaluation with two human cancer cell lines (A549 and HL60) showed that most of these compounds possessed moderate to potent antiproliferative activity. Two potent candidates (8f, IC50 = 2.2 nM and 11d, IC50 = 3.4 nM) were identified with nanomolar activity against leukemia cancer cell line HL60 for further development. This activity represents a 1000- to 2500-fold improvement compared to the parent compounds I and II and is 20- to 30-fold better than the chemotherapy drug, doxorubicin. The present work provides strong incentive for further development of these strobilurin-pyrimidine analogs as potential antitumor agents for the treatment of leukemia.

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