نمایش مختصر رکورد

dc.contributor.authorJarrahpour, Aliasgharen_US
dc.contributor.authorHeiran, Roghayehen_US
dc.contributor.authorSinou, Véroniqueen_US
dc.contributor.authorLatour, Christineen_US
dc.contributor.authorBouktab, Lamia Djouhrien_US
dc.contributor.authorLatour, Christineen_US
dc.contributor.authorSheikh, Javeden_US
dc.contributor.authorBEN HADDA, Taibien_US
dc.date.accessioned1399-07-09T06:55:42Zfa_IR
dc.date.accessioned2020-09-30T06:55:43Z
dc.date.available1399-07-09T06:55:42Zfa_IR
dc.date.available2020-09-30T06:55:43Z
dc.date.issued2019-01-01en_US
dc.date.issued1397-10-11fa_IR
dc.date.submitted2016-07-30en_US
dc.date.submitted1395-05-09fa_IR
dc.identifier.citationJarrahpour, Aliasghar, Heiran, Roghayeh, Sinou, Véronique, Latour, Christine, Bouktab, Lamia Djouhri, Latour, Christine, Sheikh, Javed, BEN HADDA, Taibi. (2019). Synthesis of New β-Lactams Bearing the Biologically Important Morpholine Ring and POM Analyses of Their Antimicrobial and Antimalarial Activities. Iranian Journal of Pharmaceutical Research, 18(1), 34-48. doi: 10.22037/ijpr.2019.2348en_US
dc.identifier.issn1735-0328
dc.identifier.issn1726-6890
dc.identifier.urihttps://dx.doi.org/10.22037/ijpr.2019.2348
dc.identifier.urihttp://ijpr.sbmu.ac.ir/article_2348.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/312181
dc.description.abstractSome new b-lactams bearing biologically important morpholine ring have been synthesized by acylation of amino b-lactams in the presence of morpholine-4-carbonyl chloride. These novel β-lactams were prepared under mild reaction conditions without any solvent in short reaction times. Their biological activities have been examined against microbial agents such as Staphylococcus aureus (S. aureus), Escherichia coli (E. coli), Pseudomonas aeruginosa (P. aeruginosa) and fungi such as Candida albicans (C. albicans) and Candida glabrata (C. glabrata). They have been also tested against Plasmodium falciparum K14 resistant strain and showed moderate to good IC50 values.en_US
dc.format.extent702
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherSchool of Pharmacy, Shahid Beheshti University of Medical Sciencesen_US
dc.relation.ispartofIranian Journal of Pharmaceutical Researchen_US
dc.relation.isversionofhttps://dx.doi.org/10.22037/ijpr.2019.2348
dc.subjectb-Lactamen_US
dc.subject2-Azetidinonesen_US
dc.subjectAcylationen_US
dc.subjectAntimalarial activitiesen_US
dc.subjectPOM analysesen_US
dc.subjectMedicinal chemistryen_US
dc.titleSynthesis of New β-Lactams Bearing the Biologically Important Morpholine Ring and POM Analyses of Their Antimicrobial and Antimalarial Activitiesen_US
dc.typeTexten_US
dc.typeResearch articleen_US
dc.contributor.departmentDepartment of Chemistry, College of Sciences, Shiraz University, Shiraz, Iranen_US
dc.contributor.departmentDepartment of Chemistry, College of Sciences, Shiraz University, Shiraz, Iranen_US
dc.contributor.departmentUMR-MD3 Relation hoˆte-parasites, Physiopathologie and Pharmacologie, Faculte´ de Pharmacie, Aix-Marseille Universite´, Bd Jean Moulin, Marseille, 13385, France.en_US
dc.contributor.departmentUMR-MD3 Relation hoˆte-parasites, Physiopathologie and Pharmacologie, Faculte´ de Pharmacie, Aix-Marseille Universite´, Bd Jean Moulin, Marseille, 13385, France.en_US
dc.contributor.departmentCentre de Recherche en Cance´rologie de Marseille (CRCM), UM 105, CNRS, UMR7258, Institut Paoli Calmettes, Inserm, U1068, Faculte´ de Pharmacie, Aix-Marseille Universite´, Bd Jean Moulin, Marseille, 13385, France.en_US
dc.contributor.departmentCentre de Recherche en Cance´rologie de Marseille (CRCM), UM 105, CNRS, UMR7258, Institut Paoli Calmettes, Inserm, U1068, Faculte´ de Pharmacie, Aix-Marseille Universite´, Bd Jean Moulin, Marseille, 13385, France.en_US
dc.contributor.departmentDepartment of Chemistry, Dhote Bandhu Science College, Gondia, 441614 India.en_US
dc.contributor.departmentLaboratoire de Chimie des Matériaux (LCM), Département de Chimie, Facultés des Sciences, Université Mohammed Premier, Oujda, 60000, Morocco.en_US
dc.citation.volume18
dc.citation.issue1
dc.citation.spage34
dc.citation.epage48


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