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2,3,5-tri-O-benzyl-L-xylose-dibenzyl dithioacetal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

169514-86-7

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169514-86-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 169514-86-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,5,1 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 169514-86:
(8*1)+(7*6)+(6*9)+(5*5)+(4*1)+(3*4)+(2*8)+(1*6)=167
167 % 10 = 7
So 169514-86-7 is a valid CAS Registry Number.

169514-86-7Relevant academic research and scientific papers

Synthesis and biological activity of certain 4'-thio-D- arabinofuranosylpurine nucleosides

Secrist III, John A.,Tiwari, Kamal N.,Shortnacy-Fowler, Anita T.,Messini, Lea,Riordan, James M.,Montgomery, John A.,Meyers, Scott C.,Ealick, Steven E.

, p. 3865 - 3871 (1998)

A series of 4'-thio-D-arabinofuranosylpurine nucleosides was prepared and evaluated as potential anticancer agents. The details of a convenient and high-yielding synthesis of the carbohydrate precursor 1-O-acetyl-2,3,5-tri- O-benzyl-4-thio-D-arabinofurano

Preparation of thioarabinofuranosyl compounds and use thereof

-

, (2008/06/13)

Patients suffering from cancer are treated by being administered a compound represented by the following formula: wherein each R individually is H or an aliphatic or aromatic acyl group; A is selected from the group consisting of wherein X is selected from the group consisting of hydrogen, fluorine, alkoxy, alkyl, haloalkyl, alkenyl, haloalkenyl, alkynyl, amino, monoalkylamino, dialkylamino, cyano and nitro. The above compounds also inhibit DNA replication in mammalian cells,

The synthesis and biological activity of certain 4'-thionucleosides

Secrist III,Parker,Tiwari,Messini,Shaddix,Rose,Bennett Jr.,Montgomery

, p. 675 - 686 (2007/10/02)

Results are presented on the synthesis and biological activity of several types of 4'-thionucleosides as potential anticancer agents. Detailed studies on the mechanism of action of 4'-thiothymidine are also presented.

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