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4-chloro-6-(1-methyl-1H-pyrazol-4-yl)-7-(phenylsulfonyl)-7H-pyrrolo[2,3-d]pyrimidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1607005-69-5

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1607005-69-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1607005-69-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,7,0,0 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1607005-69:
(9*1)+(8*6)+(7*0)+(6*7)+(5*0)+(4*0)+(3*5)+(2*6)+(1*9)=135
135 % 10 = 5
So 1607005-69-5 is a valid CAS Registry Number.

1607005-69-5Relevant academic research and scientific papers

C-Kit inhibitor and application thereof

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Paragraph 0024-0026, (2018/07/30)

The invention discloses a C-Kit inhibitor compound shown by formula I and a stereoisomer or pharmaceutically acceptable salt thereof, wherein R1 is hydroxyl, cyano, C1-4 alkyl, halogen or halogen substituted C1-4 alkyl; R2 is hydrogen, hydroxyl, cyano, alkyl, halogen or halogen substituted C1-4 alkyl; R3 is hydrogen, hydroxyl, cyano, C1-4 alkyl, halogen or halogen substituted C1-4 alkyl. The invention also provides application of the compound and the stereoisomer or pharmaceutically acceptable salt thereof in preparing drugs for preventing or treating the diseases mediated by C-Kit, especiallymutant C-Kit. The formula I is shown in the description.

BIARYL COMPOUNDS USEFUL FOR THE TREATMENT OF HUMAN DISEASES IN ONCOLOGY, NEUROLOGY AND IMMUNOLOGY

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Paragraph 0246; 0265, (2015/06/25)

The present invention provides compounds and compositions thereof which are useful as inhibitors of Bruton's tyrosine kinase and which exhibit desirable characteristics for the same.

INHIBITORS OF BRUTON'S TYROSINE KINASE

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Page/Page column 110; 111, (2014/05/24)

This application discloses compounds according to generic Formula I: wherein all variables are defined as described herein, which inhibit Btk. The compounds disclosed herein are useful to modulate the activity of Btk and treat diseases associated with exc

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