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(E)-1-(2,4-bis(allyloxy)-5-chlorophenyl)-3-(3,4-bis(allyloxy)phenyl)prop-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1522361-72-3

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1522361-72-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1522361-72-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,2,2,3,6 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1522361-72:
(9*1)+(8*5)+(7*2)+(6*2)+(5*3)+(4*6)+(3*1)+(2*7)+(1*2)=133
133 % 10 = 3
So 1522361-72-3 is a valid CAS Registry Number.

1522361-72-3Relevant academic research and scientific papers

New chalcone compound or pharmaceutically acceptable salt thereof having inhibitory activity on Hsp90 and medical use thereof

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Paragraph 0056; 0063-0065; 0081-0084, (2020/03/31)

The present invention relates to a novel chalcone compound or pharmaceutically acceptable salt thereof having inhibitory activity on Hsp90, and to medical use thereof. The charcone compound: has an excellent effect of inhibiting Hsp90; induces decomposition of Hsp90 client protein, which causes cancer or neurodegenerative diseases; and thus can be advantageously used for a pharmaceutical product or health-promotional food for treating or preventing Hsp90-mediated diseases such as cancer or neurodegenerative diseases. The chalcone compound or the pharmaceutically acceptable salt is represented by Chemical Formula 1 below.

Discovery of hybrid Hsp90 inhibitors and their anti-neoplastic effects against gefitinib-resistant non-small cell lung cancer (NSCLC)

Jeong, Chul-Ho,Park, Hee Baek,Jang, Won Jun,Jung, Su Hyun,Seo, Young Ho

supporting information, p. 224 - 227 (2014/01/17)

Heat shock protein 90 (Hsp90) represents an attractive cancer therapeutic target due to its role in the stabilization and maturation of many oncogenic proteins. We have designed a series of hybrid Hsp90 inhibitors by connecting the resorcinol ring of VER-

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