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1798792-42-3

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1798792-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1798792-42-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,7,9,8,7,9 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1798792-42:
(9*1)+(8*7)+(7*9)+(6*8)+(5*7)+(4*9)+(3*2)+(2*4)+(1*2)=263
263 % 10 = 3
So 1798792-42-3 is a valid CAS Registry Number.

1798792-42-3Downstream Products

1798792-42-3Relevant articles and documents

Discovery and Preclinical Characterization of BIIB091, a Reversible, Selective BTK Inhibitor for the Treatment of Multiple Sclerosis

Hopkins, Brian T.,Bame, Eris,Bajrami, Bekim,Black, Cheryl,Bohnert, Tonika,Boiselle, Carrie,Burdette, Doug,Burns, Jeremy C.,Delva, Luisette,Donaldson, Douglas,Grater, Richard,Gu, Chungang,Hoemberger, Marc,Johnson, Josh,Kapadnis, Sudarshan,King, Kris,Lulla, Mukesh,Ma, Bin,Marx, Isaac,Magee, Tom,Meissner, Robert,Metrick, Claire M.,Mingueneau, Michael,Murugan, Paramasivam,Otipoby, Kevin L.,Polack, Evelyne,Poreci, Urjana,Prince, Robin,Roach, Allie M.,Rowbottom, Chris,Santoro, Joseph C.,Schroeder, Patricia,Tang, Hao,Tien, Eric,Zhang, Fengmei,Lyssikatos, Joseph

supporting information, p. 1206 - 1224 (2021/11/18)

Multiple Sclerosis is a chronic autoimmune neurodegenerative disorder of the central nervous system (CNS) that is characterized by inflammation, demyelination, and axonal injury leading to permeant disability. In the early stage of MS, inflammation is the

BENZOAZEPINE ANALOGS AS INHIBITING AGENTS FOR BRUTON'S TYROSINE KINASE

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Page/Page column 126; 128, (2018/11/10)

Provided are compounds of Formula (I), or pharmaceutically acceptable salts thereof, and methods for their production and compounds of formula (I) for use in treating a disease responsive to the inhibition of Bruton's tyrosine.

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

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Paragraph 0499, (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.

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