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Design and synthesis of 3,5-disubstituted 1,2,4-oxadiazole containing retinoids from a retinoic acid receptor agonist

  • Bhaskar C. Das
  • , Xiang Ying Tang
  • , Swarnava Sanyal
  • , Seetaram Mohapatra
  • , Patrick Rogler
  • , Sabita Nayak
  • , Todd Evans
  • Albert Einstein College of Medicine
  • Ravenshaw University
  • Cornell University

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

We previously synthesized novel retinoid libraries, and after screening for bioactivity found one compound BT10 that functions as a specific agonist for retinoic acid receptors. This lead compound was further derivatized using SAR and LRD to obtain 3,5-disubstituted-1,2,4-oxadiazole-containing retinoids. The new oxadiazole (amide bioisosters)-containing retinoids (compounds 1, 2, 3, 4, 5, and 6) were synthesized in 42-65% yield by reacting with (E)-4-((3-ethyl,2-4, 4,4-trimethylcyclohex-2-enylidene)methyl)benzoic acid and phenyl substituted amidoxime in DMF using CDI as the coupling reagent. The biological activities of the synthesized compounds are currently being evaluated.

Original languageEnglish
Pages (from-to)2433-2435
Number of pages3
JournalTetrahedron Letters
Volume52
Issue number19
DOIs
StatePublished - May 11 2011

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