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1079097-24-7

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1079097-24-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1079097-24-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,9,0,9 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1079097-24:
(9*1)+(8*0)+(7*7)+(6*9)+(5*0)+(4*9)+(3*7)+(2*2)+(1*4)=177
177 % 10 = 7
So 1079097-24-7 is a valid CAS Registry Number.

1079097-24-7Downstream Products

1079097-24-7Relevant articles and documents

Discovery of novel potent and selective dipeptide hepatitis C virus NS3/4A serine protease inhibitors

Raboisson, Pierre,Lin, Tse-I,Kock, Herman de,Vendeville, Sandrine,Vreken, Wim Van de,McGowan, David,Tahri, Abdellah,Hu, Lili,Lenz, Oliver,Delouvroy, Frederic,Surleraux, Dominique,Wigerinck, Piet,Nilsson, Magnus,Rosenquist, Asa,Samuelsson, Bertil,Simmen, Kenneth

scheme or table, p. 5095 - 5100 (2009/06/18)

Starting from the previously reported HCV NS3/4A protease inhibitor BILN 2061 (1), we have used a fast-follower approach to identify a novel series of HCV NS3/4A protease inhibitors in which (i) the P3 amino moiety and its capping group have been truncated, (ii) a sulfonamide is introduced in the P1 cyclopropyl amino acid, (iii) the position 8 of the quinoline is substituted with a methyl or halo group, and (iv) the ring size of the macrocycle has been reduced to 14 atoms. SAR analysis performed with a limited set of compounds led to the identification of N-{17-[8-chloro-2-(4-isopropylthiazol-2-yl)-7-methoxyquinolin-4-yloxy]-2,14-dioxo-3,15-diazatricyclo [13.3.0.0 [Bartenschlager, R.; Lohmann, V. J. Gen. Virol. 2000, 81, 1631; Vincent Soriano, Antonio Madejon, Eugenia Vispo, Pablo Labarga, Javier Garcia-Samaniego, Luz Martin-Carbonero, Julie Sheldon, Marcelle Bottecchia, Paula Tuma, Pablo Barreiro Expert Opin. Emerg. Drugs, 2008, 13, 1-19]]octadec-7-ene-4-carbonyl}(1-methylcyclopropyl)(1-methylcyclopropyl)sulfonamide 19l an extremely potent (Ki = 0.20 nM, EC50 = 3.7 nM), selective, and orally bioavailable dipeptide NS3/4A protease inhibitor, which has features attractive for further preclinical development.

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