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dc.contributor.authorHiremath S.P
dc.contributor.authorAshok C
dc.contributor.authorRao S.H.
dc.date.accessioned2020-06-12T15:08:14Z-
dc.date.available2020-06-12T15:08:14Z-
dc.date.issued1993
dc.identifier.citationBiological and Pharmaceutical Bulletin , Vol. 16 , 1 , p. 36 - 38en_US
dc.identifier.uri10.1248/bpb.16.36
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5555-
dc.description.abstractOf the 21 compounds evaluated for antiimplantation and abortifacient activities, compounds (A1, A2, A4 and B1) and compounds (C1, C2, D1 and D3) were found to exhibit 40% and 30% antimplantation activity, respectively, in female rats when given orally on days 1-5 postcoitum. The remaining 13 compounds were found to be inactive. All of the 21 compounds were also tested for the abortifacient activity, but all were found to be inactive. © 1993, The Pharmaceutical Society of Japan. All rights reserved.en_US
dc.subjectabortifacient activity
dc.subjectantiimplantation
dc.subjectindole derivative
dc.titlePossible antifertility agents belonging to substituted indolesen_US
dc.typeArticle
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