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955879-83-1

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955879-83-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 955879-83-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,5,8,7 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 955879-83:
(8*9)+(7*5)+(6*5)+(5*8)+(4*7)+(3*9)+(2*8)+(1*3)=251
251 % 10 = 1
So 955879-83-1 is a valid CAS Registry Number.

955879-83-1Upstream product

955879-83-1Downstream Products

955879-83-1Relevant academic research and scientific papers

The discovery of substituted 4-(3-hydroxyanilino)-quinolines as potent RET kinase inhibitors

Graham Robinett,Freemerman, Alex J.,Skinner, Michael A.,Shewchuk, Lisa,Lackey, Karen

, p. 5886 - 5893 (2007)

Substituted 4-(3-hydroxyanilino)-quinoline compounds, initially identified as small-molecule inhibitors of src family kinases, have been evaluated as potential inhibitors of RET kinase. Three compounds, 38, 31, and 40, had Ki's of 3, 25, and 50

AMINO-QUINOLINES AS KINASE INHIBITORS

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Page/Page column 70, (2018/06/22)

Disclosed are compounds having the formula:wherein R 1 , R 2 , R 3 and Z are as defined herein, and methods of making and using the same.

AMINO-QUINOLINES AS KINASE INHIBITORS

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Page/Page column 81, (2018/05/15)

Disclosed are compounds having the formula: wherein R1, R2, R3 and Z are as defined herein, and methods of making and using the same.

SUBSTITUTED QUINOXALINE DERIVATIVES

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Page/Page column 147, (2016/11/28)

The present invention relates to substituted quinoxaline derivatives. These compounds are useful for the prevention and/or treatment of several medical conditions including hyperproliferative disorders and diseases.

AMINO-QUINOLINES AS KINASE INHIBITORS

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Paragraph 0137; 0138, (2016/10/31)

Disclosed are compounds having the formula: wherein R1, R2, R3 and Z are as defined herein, and methods of making and using the same.

Compounds and Methods of Treatment

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Page/Page column 21, (2008/12/08)

A derivative, which is useful as a ret kinase inhibitor is described herein. The described invention also includes methods of using the same in the treatment of diseases mediated by inappropriate ret kinase activity.

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