Please use this identifier to cite or link to this item: http://localhost:80/xmlui/handle/123456789/14981
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dc.contributor.authorAnsari, Sumaira-
dc.contributor.authorMushtaq, Nousheen-
dc.contributor.authorAhmed, Ahsaan-
dc.contributor.authorAsghar, Saira-
dc.contributor.authorMunawar, Rabya-
dc.contributor.authorSaify, Zafar Saied-
dc.date.accessioned2022-12-13T09:34:56Z-
dc.date.available2022-12-13T09:34:56Z-
dc.date.issued2022-07-20-
dc.identifier.citationAnsari, S., Mushtaq, N., Ahmed, A., Asghar, S., Munawar, R., & Saify, Z. S. (2022). Synthesis, biological screening and docking studies of some indole derivatives as potential antioxidant. Pakistan Journal of Pharmaceutical Sciences, 35(4).en_US
dc.identifier.issn1011-601X-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/14981-
dc.description.abstractThe present study envisioned some antioxidant candidates having 1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole (TRY), 3-(2-bromoethyl)indole (BEI) and 7-azindole (AI) nucleus. Derivatives of these indole molecules were synthesized and their scavenging activity for reactive oxygen species (ROS) investigated by 2,2-diphenyl-1picrylhydrazyl (DPPH) radical scavenging assay. T3, T42 exhibited significant radical scavenging potential which is comparable to ascorbic acid (standard), while T36 appeared as most potent antioxidant by displaying better scavenging activity than standard molecule. Molecular docking study revealed good binding score and interactions of T36 with target human antioxidant enzyme (PDB code: 3MNG) validating the results of biological activity.en_US
dc.language.isoenen_US
dc.publisherKarachi:Pakistan Journal of Pharmaceutical Sciences, university of Karachi.en_US
dc.subject7-azaindoleen_US
dc.subject3-(2-bromoethyl)indoleen_US
dc.subjecttryptamine, 5-hydroxytryptamineen_US
dc.subjectreactive oxygen speciesen_US
dc.titleSynthesis, biological screening and docking studies of some indole derivatives as potential antioxidanten_US
dc.typeArticleen_US
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