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Design, synthesis and cytotoxic studies on the simplified oxy analog of eleutherobin

  • S. Chandrasekhar
  • , V. Jagadeshwar
  • , Ch Narsihmulu
  • , M. Sarangapani
  • , D. R. Krishna
  • , J. Vidyasagar
  • , Dolly Vijay
  • , G. Narahari Sastry

Research output: Contribution to journalArticlepeer-review

Abstract

A straight forward entry into nine membered B ring of eleutherobin as oxy analog and its cyctotoxic properties on HBL cell lines is described. Molecular modeling studies were carried out to ascertain the binding of the model compound to the active site of β-tubulin.

Original languageEnglish (US)
Pages (from-to)3687-3689
Number of pages3
JournalBioorganic and Medicinal Chemistry Letters
Volume14
Issue number14
DOIs
StatePublished - Jul 16 2004
Externally publishedYes

Bibliographical note

Funding Information:
V.J. and C.N.G. thank CSIR, New Delhi for the financial assistance. Research grants for the project from DST, New Delhi is acknowledged.

Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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