Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/3855
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dc.contributor.authorGodipurge S.S
dc.contributor.authorBiradar J.S
dc.contributor.authorBiradar N.J
dc.contributor.authorShivarudrappa H.P
dc.contributor.authorYallappa S
dc.contributor.authorHungund B.S
dc.contributor.authorSreedhara Ranganath Pai K.
dc.date.accessioned2020-06-12T15:01:54Z-
dc.date.available2020-06-12T15:01:54Z-
dc.date.issued2018
dc.identifier.citationChemistry of Natural Compounds , Vol. 54 , 1 , p. 142 - 146en_US
dc.identifier.uri10.1007/s10600-018-2277-3
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/3855-
dc.description.abstractTwo new alkaloids, designated as hypocretine 1 and 2, have been extracted from the aerial parts of Rivea hypocrateriformis, and their structures were established as 1-(4-(((1R,5S,6R)-(4-acetyl-2,6-dibutylphenoxy)-8-methyl-8-azabicyclo[3.2.1]octan-6-yl)oxy)-2,6-dibutylphenyl)ethan-1-one and 1-(4-((3-(4-acetyl-2-butyl-6-(4-hydroxybutyl)phenoxy)-8-methyl-8-azabicyclo[3.2.1]octan-6-yl)oxy)-2-butyl-6-(4-hydroxybutyl)phenyl)ethan-1-one. These alkaloids were further characterized by mass and NMR spectral data analysis. Further studies were conducted to evaluate their antihemolytic and cytotoxic activity. The extracted compounds exhibited potent antihemolytic activity against cow erythrocytes. The results of the MTT assay for cytotoxicity revealed the antiproliferative activity of compounds 1and 2 against MCF-7 breast cancer cell line. © 2018, Springer Science+Business Media, LLC, part of Springer Nature.en_US
dc.publisherSpringer New York LLC
dc.subjectalkaloids
dc.subjectantihemolytic activity
dc.subjectcytotoxicity
dc.subjecthypocretine compounds
dc.subjectRivea hypocrateriformis
dc.titleStructural Elucidation of Alkaloids from Aerial Parts of Rivea hypocrateriformis and Their Antihemolytic and Cytotoxic Activityen_US
dc.typeArticle
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