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137965-01-6

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137965-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137965-01-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,9,6 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 137965-01:
(8*1)+(7*3)+(6*7)+(5*9)+(4*6)+(3*5)+(2*0)+(1*1)=156
156 % 10 = 6
So 137965-01-6 is a valid CAS Registry Number.

137965-01-6Downstream Products

137965-01-6Relevant articles and documents

In search of flavivirus inhibitors: Evaluation of different tritylated nucleoside analogues

Chatelain, Grégory,Debing, Yannick,De Burghgraeve, Tine,Zmurko, Joanna,Saudi, Milind,Rozenski, Jef,Neyts, Johan,Van Aerschot, Arthur

supporting information, p. 249 - 255 (2013/10/01)

Following up on a hit that was identified in a large scale cell-based antiviral screening effort, a series of triphenylmethyl alkylated nucleoside analogues were synthesized and evaluated for their in vitro antiviral activities against the dengue virus (DENV) and the yellow fever virus (YFV). Hereto, trityl moieties were attached at various positions of the sugar ring combined with subtle variations of the heterocyclic base. Several triphenylmethyl modified nucleosides were uncovered being endowed with submicromolar in vitro antiviral activity against the YFV. The most selective inhibitor in this series was 3′,5′-bis-O-tritylated-5-chlorouridine (1b) affording a selectivity index of over 90, whereas the 3′,5′-bis-O-tritylated inosine congener (5b) displayed the highest activity, but proved more toxic. The finding of these lipophilic structures being endowed with high antiviral activity for flaviviruses, should stimulate the interest for further structureeactivity research.

A synthesis of 9-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)adenine and hypoxanthine. An effect of C3'-endo to C2'-endo conformational shift on the reaction course of 2'-hydroxyl group with DAST

Pankiewicz,Krzeminski,Ciszewski,Ren,Watanabe

, p. 553 - 559 (2007/10/02)

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