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Bioactive benzofuran derivatives: Moracins A-Z in medicinal chemistry

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dc.contributor.authorNaik, Ravi-
dc.contributor.authorHarmalkar, Dipesh S.-
dc.contributor.authorXu, Xuezhen-
dc.contributor.authorJang, Kyusic-
dc.contributor.authorLee, Kyeong-
dc.date.accessioned2024-09-26T14:00:34Z-
dc.date.available2024-09-26T14:00:34Z-
dc.date.issued2015-01-
dc.identifier.issn0223-5234-
dc.identifier.issn1768-3254-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/25290-
dc.description.abstractBenzofuran heterocycles are fundamental structural units in a variety of biologically active natural products as well as synthetic materials. Over the time, benzofuran derivatives have attracted many researchers due to the broad scope of their biological activity, which include anticancer, antimicrobial, immunomodulatory, antioxidant and anti-inflammatory properties. Egonol, homoegonol and moracin families are biologically active natural products containing benzofuran heterocycle as basic structural units. This paper focuses on the moracin family (moracin A to Z). Morus, a genus of flowering plants in the family Moraceae, comprises 10-16 species of deciduous trees commonly known as mulberries. The root bark, stem bark and leaves of Morus alba, M. lhou, Mows macroura are the main sources for aryl-benzofuran derivatives including the moracins. A large volume of research has been carried out on moracins and their derivatives, which has shown the pharmacological importance of this benzofuran heterocyclic nucleus. In this mini-review, we attempt to highlight the importance of moracins, as they have been a major source for drug development. Herein, we also summarize the current state of the art concerning the synthesis and medicinal use of moracins A Z. (C) 2014 Elsevier Masson SAS. All rights reserved.-
dc.format.extent15-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER-
dc.titleBioactive benzofuran derivatives: Moracins A-Z in medicinal chemistry-
dc.typeArticle-
dc.publisher.location프랑스-
dc.identifier.doi10.1016/j.ejmech.2014.11.047-
dc.identifier.scopusid2-s2.0-84913582348-
dc.identifier.wosid000348951900031-
dc.identifier.bibliographicCitationEUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, v.90, pp 379 - 393-
dc.citation.titleEUROPEAN JOURNAL OF MEDICINAL CHEMISTRY-
dc.citation.volume90-
dc.citation.startPage379-
dc.citation.endPage393-
dc.type.docTypeReview-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.subject.keywordPlusCULTIVATED MULBERRY TREE-
dc.subject.keywordPlusDIELS-ALDER ADDUCTS-
dc.subject.keywordPlusMORUS-ALBA L.-
dc.subject.keywordPlusROOT BARK-
dc.subject.keywordPlusDISEASED MULBERRY-
dc.subject.keywordPlus2-ARYLBENZOFURAN DERIVATIVES-
dc.subject.keywordPlusANTIMICROBIAL ACTIVITY-
dc.subject.keywordPlusSTAPHYLOCOCCUS-AUREUS-
dc.subject.keywordPlusAROMATASE INHIBITORS-
dc.subject.keywordPlusANTIOXIDANT ACTIVITY-
dc.subject.keywordAuthorBenzofuran-
dc.subject.keywordAuthorMoracins-
dc.subject.keywordAuthorMulberries-
dc.subject.keywordAuthorBiological activity-
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