Thiazolidinediones as a privileged structural scaffold in PPAR agonists: A review

Authors

  • Fajeelath Fathima Department of Pharmaceutical Chemistry, Grace College of Pharmacy, Kodunthirapully, Palakkad-678501, Kerala
  • Baskar Lakshmanan Department of Pharmaceutical Chemistry, Grace College of Pharmacy, Kodunthirapully, Palakkad-678501, Kerala

DOI:

https://doi.org/10.7439/ijpc.v6i5.3287

Abstract

Thiazolidinediones are a versatile scaffold of connecting various classes of organic compounds with a unique structural feature of hydrogen bonding donor and the hydrogen bonding acceptor region. An extensive number of research has been carried out on thiazolidinedione derivatives as a potent class of PPAR-? agonists. The present review focuses on the chemistry and PPAR- agonistic activity of diverse classes of phenyl and heterocyclic based thiazolidinediones

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Author Biographies

  • Fajeelath Fathima, Department of Pharmaceutical Chemistry, Grace College of Pharmacy, Kodunthirapully, Palakkad-678501, Kerala
    DEPARTMENT OF PHARMACEUTICAL CHEMISTRY
  • Baskar Lakshmanan, Department of Pharmaceutical Chemistry, Grace College of Pharmacy, Kodunthirapully, Palakkad-678501, Kerala
    PHD at birla institute; Ranchi

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2016-05-30

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Thiazolidinediones as a privileged structural scaffold in PPAR agonists: A review. Int J of Pharm Chem [Internet]. 2016 May 30 [cited 2026 Jan. 3];6(5):124-41. Available from: https://ssjournals.co.in/index.php/ijpc/article/view/3287