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Please use this identifier to cite or link to this item: http://repository.iitr.ac.in/handle/123456789/1439
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dc.contributor.authorKumar N.-
dc.contributor.authorKumar S.-
dc.contributor.authorAbbat S.-
dc.contributor.authorNikhil K.-
dc.contributor.authorSondhi S.M.-
dc.contributor.authorBharatam P.V.-
dc.contributor.authorRoy, Partha-
dc.contributor.authorPruthi V.-
dc.date.accessioned2020-09-30T11:39:05Z-
dc.date.available2020-09-30T11:39:05Z-
dc.date.issued2016-
dc.identifier.citationMedicinal Chemistry Research (2016), 25(6): 1175-1192-
dc.identifier.issn10542523-
dc.identifier.urihttps://doi.org/10.1007/s00044-016-1562-6-
dc.identifier.urihttp://repository.iitr.ac.in/handle/123456789/1439-
dc.description.abstractAbstract: The design and microwave-assisted synthesis of four series (IIIa–IIIo, Va–Vg, VIIa–VIIg and IXa–IXe) of mono and bis-amide derivatives of ferulic acid have been achieved under solvent-free conditions and, subsequently characterized by spectroscopic techniques. During thermal analysis, all the compounds were found stable up to 100 °C and decomposed through single step at higher temperature. The derivatives were screened for their in vitro cytotoxicity and antioxidant activity, respectively and observed that compound Vb was most active against breast (MCF-7; IC50 = 07.49 µM and MDA-MB-231; IC50 = 07.28 µM), Vd against lung (A549; IC50 = 07.11 µM) and liver (HepG2; IC50 = 08.32 µM), and Ve against cervical (HeLa; IC50 = 07.14 µM) cancer cell lines, while compounds IIIf, IIIl, IIIo, VIIe and IXa–IXe were found to exhibit the strong antioxidant activity with respect to their parent molecule. Previous reports for the biological applications of ferulic acid amides also confirmed the importance of work presented here. The 3D-QSAR studies for anticancer and antioxidant activities were also performed by using CoMFA, and the corresponding contour maps of electrostatic and steric fields have been computed. Statistical analysis between experimental and CoMFA-predicted data for pIC50 have been accomplished by curve fitting analysis which showed the significant correlation. Graphical Abstract: [Figure not available: see fulltext.] © 2016, Springer Science+Business Media New York.-
dc.language.isoen_US-
dc.publisherBirkhauser Boston-
dc.relation.ispartofMedicinal Chemistry Research-
dc.subject3D-QSAR-
dc.subjectAmide derivatives-
dc.subjectAnticancer and antioxidant activity-
dc.subjectCoMFA-
dc.subjectFerulic acid-
dc.titleFerulic acid amide derivatives as anticancer and antioxidant agents: synthesis, thermal, biological and computational studies-
dc.typeArticle-
dc.scopusid57210345407-
dc.scopusid57216459762-
dc.scopusid56380640600-
dc.scopusid57192281884-
dc.scopusid7006090710-
dc.scopusid7003812504-
dc.scopusid35509207200-
dc.scopusid18837702800-
dc.affiliationKumar, N., Department of Biotechnology, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand 247667, India-
dc.affiliationKumar, S., Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee, 247667, India-
dc.affiliationAbbat, S., Department of Pharmacoinformatics, NIPER, S.A.S. Nagar, Mohali, 160062, India-
dc.affiliationNikhil, K., Department of Biotechnology, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand 247667, India-
dc.affiliationSondhi, S.M., Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee, 247667, India-
dc.affiliationBharatam, P.V., Department of Medicinal Chemistry, NIPER, S.A.S. Nagar, Mohali, 160062, India-
dc.affiliationRoy, P., Department of Biotechnology, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand 247667, India-
dc.affiliationPruthi, V., Department of Biotechnology, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand 247667, India-
dc.description.correspondingauthorKumar, N.; Department of Biotechnology, Indian Institute of Technology RoorkeeIndia; email: nareshkumariitr@gmail.com-
Appears in Collections:Journal Publications [BT]

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