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dc.contributor.authorAli, Eslam M. H.-
dc.contributor.authorAbdel-Maksoud, Mohammed S.-
dc.contributor.authorOh, Chang-Hyun-
dc.date.accessioned2024-01-19T20:30:14Z-
dc.date.available2024-01-19T20:30:14Z-
dc.date.created2022-01-10-
dc.date.issued2019-04-01-
dc.identifier.issn0968-0896-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/120116-
dc.description.abstractThienopyrimidine scaffold is a fused heterocyclic ring system that structurally can be considered as adenine, the purine base that is found in both DNA and RNA-bioisosteres. Thienopyrimidines exist in three distinct isomeric forms. The current review discusses thieno[2,3-d] pyrimidine as a one of the opulent heterocycles in drug discovery. Its broad range of medical applications such as anticancer, anti-inflammatory, anti-microbial, and CNS protective agents has inspired us to study its structure-activity relationship (SAR), along with its relevant synthetic strategies. The present review briefly summarizes synthetic approaches for the preparation of thieno[2,3-d] pyrimidine derivatives. In addition, the promising biological activities of this scaffold are also illustrated with explanatory diagrams for their SAR studies.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectRECEPTOR TYROSINE KINASE-
dc.subjectINITIATION-FACTOR 4E-
dc.subjectBIOLOGICAL EVALUATION-
dc.subjectDERIVATIVES BEARING-
dc.subjectANTICANCER ACTIVITY-
dc.subject3-D PYRIMIDINE-
dc.subjectTHIENO 2-
dc.subjectSUBSTITUTED THIENOPYRIMIDINES-
dc.subjectSTRUCTURAL MODIFICATIONS-
dc.subjectANTIBACTERIAL AGENTS-
dc.titleThieno[2,3-d] pyrimidine as a promising scaffold in medicinal chemistry: Recent advances-
dc.typeArticle-
dc.identifier.doi10.1016/j.bmc.2019.02.044-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBIOORGANIC & MEDICINAL CHEMISTRY, v.27, no.7, pp.1159 - 1194-
dc.citation.titleBIOORGANIC & MEDICINAL CHEMISTRY-
dc.citation.volume27-
dc.citation.number7-
dc.citation.startPage1159-
dc.citation.endPage1194-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000461168400002-
dc.identifier.scopusid2-s2.0-85062071370-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeReview-
dc.subject.keywordPlusRECEPTOR TYROSINE KINASE-
dc.subject.keywordPlusINITIATION-FACTOR 4E-
dc.subject.keywordPlusBIOLOGICAL EVALUATION-
dc.subject.keywordPlusDERIVATIVES BEARING-
dc.subject.keywordPlusANTICANCER ACTIVITY-
dc.subject.keywordPlus3-D PYRIMIDINE-
dc.subject.keywordPlusTHIENO 2-
dc.subject.keywordPlusSUBSTITUTED THIENOPYRIMIDINES-
dc.subject.keywordPlusSTRUCTURAL MODIFICATIONS-
dc.subject.keywordPlusANTIBACTERIAL AGENTS-
dc.subject.keywordAuthorThienopyrimidine-
dc.subject.keywordAuthorAnti-inflammatory-
dc.subject.keywordAuthorAnticancer-
dc.subject.keywordAuthorAntimicrobial-
dc.subject.keywordAuthorAntiviral-
dc.subject.keywordAuthorCNS protective agents-
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