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  • Keri, Rangappa S. (author)

An overview of benzo[b]thiophene-based medicinal chemistry

  • Article/chapterEnglish2017

Publisher, publication year, extent ...

  • Elsevier Masson SAS,2017
  • printrdacarrier

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  • LIBRIS-ID:oai:DiVA.org:umu-140647
  • https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-140647URI
  • https://doi.org/10.1016/j.ejmech.2017.07.038DOI

Supplementary language notes

  • Language:English
  • Summary in:English

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  • Subject category:ref swepub-contenttype
  • Subject category:for swepub-publicationtype

Notes

  • Among sulfur containing heterocycles, benzothiophene and its derivatives are at the focus as these candidates have structural similarities with active compounds to develop new potent lead molecules in drug design. Benzo[b]thiophene scaffold is one of the privileged structures in drug discovery as this core exhibits various biological activities allowing them to act as anti-microbial, anti-cancer, anti-inflammatory, anti-oxidant, anti-tubercular, anti-diabetic, anti-convulsant agents and many more. Further, numerous benzothiophene-based compounds as clinical drugs have been extensively used to treat various types of diseases with high therapeutic potency, which has led to their extensive developments. Due to the wide range of biological activities of benzothiophene, their structure activity relationships (SAR) have generated interest among medicinal chemists, and this has culminated in the discovery of several lead molecules against numerous diseases. The present review is endeavoring to highlight the progress in the various pharmacological activities of benzo[b]thiophene derivatives. It is hoped that this review will be helpful for new thoughts in the quest for rational designs of more active and less toxic benzothiophene-based medicinal drugs, as well as more effective diagnostic agents and pathologic probes. Also, SAR studies that highlight the chemical groups responsible for evoking the potential activities of benzothiophene derivatives are studied and compared.

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  • Chand, KaramUmeå universitet,Kemiska institutionen(Swepub:umu)kach0026 (author)
  • Budagumpi, Srinivasa (author)
  • Somappa, Sasidhar Balappa (author)
  • Patil, Siddappa A. (author)
  • Nagaraja, Bhari Mallanna (author)
  • Umeå universitetKemiska institutionen (creator_code:org_t)

Related titles

  • In:European Journal of Medicinal Chemistry: Elsevier Masson SAS138, s. 1002-10330223-52341768-3254

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