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1-[2,3-di-O-benzoyl-5-O-(p-monomethoxytrityl)-β-D-ribofuranosyl]-1H-1,2,4-triazole-3-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

190141-29-8

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190141-29-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 190141-29-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,1,4 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 190141-29:
(8*1)+(7*9)+(6*0)+(5*1)+(4*4)+(3*1)+(2*2)+(1*9)=108
108 % 10 = 8
So 190141-29-8 is a valid CAS Registry Number.

190141-29-8Relevant academic research and scientific papers

Nucleotides: Part LII. Synthesis and biological activity of new base- modified (2'- 5')oligoadenylate trimers

Kvasyuk,Kulak,Tkachenko,Sentyureva,Mikhailopulo,Suhadolnik,Henderson,Horvath,Guan,Pfleiderer

, p. 1053 - 1060 (2007/10/03)

Some new (2'- 5')oligoadenylate trimers, i.e., 22-28 containing the antiviral nucleoside ribavirin (= 1-(β-D-ribofuranosyl)-1H-1,2,4-triazole- 3-carboxamide; 7) and the synthetic cytokine 6-(benzylamino)purine riboside (= N6-benzyladenosine; 1) in different positions of the trimer, have been synthesized by the posphotriester method. The selectively blocked nucleosides 2-6 and 8-11 and the 2'-phosphodiesters 13 and 14, used for the oligonucleotide syntheses, were synthesized from the corresponding unprotected ribonucleosides 1 and 7, and isolated by silica-gel column chromatography. The fully deblocked trimers 22-28 were purified by ion- exchange chromatography on DEAE-Servavell 23-SS. The newly synthesized compounds were characterized by physical means. The ability of synthesized trimers to inhibit HIV-1 replication and to improve RNase L activation were investigated Some of the synthesized trimers showed also biological inhibition of HIV-1 reverse transcriptase and HIV-1-induced syncytia formation. It was shown that Ado(Bn)-containing trimers inhibited HIV-1- induced syncytia formation > 1500-fold, independently of the position of the Ado(Bn) residue in the oligomer chain.

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