Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/21490
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dc.contributor.authorMinu, Maninder-
dc.contributor.authorJindal, Dharam Paul-
dc.contributor.authorLeclercq, G-
dc.contributor.authorBorras, M-
dc.date.accessioned2013-10-04T10:26:18Z-
dc.date.available2013-10-04T10:26:18Z-
dc.date.issued2003-01-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/21490-
dc.description166-172en_US
dc.description.abstractThe synthesis of 16-arylidene derivatives 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14 and 15 is described. These compounds have been tested at NCI, Bethesda, for their antineoplastic acti vity against the cell panel consisting of 60-cell lines and the compounds 3, 4, 5, 6 and 7 have also been tested for their in vitro estrogenic / antiestrogenic activity ; induction of ERE dependent luciferase induction was measured (MVLN cells).en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.42B(01) [January 2003]en_US
dc.titleSynthesis and biological activity of 16-arylidene derivatives of estrone and estrone methyl etheren_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.42B(01) [January 2003]

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