Efficient synthesis of benzamide riboside, a potential anticancer agent

Laurent F. Bonnac, Guang Yao Gao, Liqiang Chen, Steven E. Patterson, Hiremagalur N. Jayaram, Krzysztof W. Pankiewicz

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

An efficient five step synthesis of benzamide riboside (BR) amenable for a large scale synthesis has been developed. It allows for extensive pre-clinical studies of BR as a potential anticancer agent.

Original languageEnglish
Pages (from-to)1249-1253
Number of pages5
JournalNucleosides, Nucleotides and Nucleic Acids
Volume26
Issue number10-12
DOIs
StatePublished - Oct 2007

Fingerprint

Antineoplastic Agents
3-(1-deoxyribofuranosyl)benzamide
Clinical Studies

Keywords

  • Anticancer agent
  • Benzamide riboside

ASJC Scopus subject areas

  • Genetics
  • Biochemistry

Cite this

Bonnac, L. F., Gao, G. Y., Chen, L., Patterson, S. E., Jayaram, H. N., & Pankiewicz, K. W. (2007). Efficient synthesis of benzamide riboside, a potential anticancer agent. Nucleosides, Nucleotides and Nucleic Acids, 26(10-12), 1249-1253. https://doi.org/10.1080/15257770701528222

Efficient synthesis of benzamide riboside, a potential anticancer agent. / Bonnac, Laurent F.; Gao, Guang Yao; Chen, Liqiang; Patterson, Steven E.; Jayaram, Hiremagalur N.; Pankiewicz, Krzysztof W.

In: Nucleosides, Nucleotides and Nucleic Acids, Vol. 26, No. 10-12, 10.2007, p. 1249-1253.

Research output: Contribution to journalArticle

Bonnac, LF, Gao, GY, Chen, L, Patterson, SE, Jayaram, HN & Pankiewicz, KW 2007, 'Efficient synthesis of benzamide riboside, a potential anticancer agent', Nucleosides, Nucleotides and Nucleic Acids, vol. 26, no. 10-12, pp. 1249-1253. https://doi.org/10.1080/15257770701528222
Bonnac, Laurent F. ; Gao, Guang Yao ; Chen, Liqiang ; Patterson, Steven E. ; Jayaram, Hiremagalur N. ; Pankiewicz, Krzysztof W. / Efficient synthesis of benzamide riboside, a potential anticancer agent. In: Nucleosides, Nucleotides and Nucleic Acids. 2007 ; Vol. 26, No. 10-12. pp. 1249-1253.
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