Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16433
Title: Synthesis and biological activity of some D-ring modified estrone derivatives
Authors: Gupta, Ranju
Jindal, Dharam Paul
Borras, M
Legros, N
Leclercq, G
Issue Date: May-1999
Publisher: NISCAIR-CSIR, India
Abstract: 3-Methoxy-17-aza-D-homo-1,3,5(10)-estratrienc-16, 17a-dione 3, 16, 17a-dioxo-17-aza-D-homo-1,3,5(10)-estratrien-3-yl acctate 12 and a series of related compounds have been synthesised from 3-methoxy-16-oximino- 1,3,5 (10)-estrairian-17- one 1 and 3-hydroxy-16-oximino- 1,3,5 (10)-estnttrien-17-one 2, respectively. The compounds 3 (DPJ-280), 14 (DPJ-369), 17 (DPJ-370), 18 (DPJ-354), 19 (DPJ-320), 21 (DPJ- 321 ), 22 (DPJ-374) and (DPJ-284) have been evaluated for their estrogenic/antiestrogenic effects and the compounds 3-7,8,9,10,12,15,16,18,20,21,23 and 24 have been screened for antineoplastic activity at NCI, Bethesda.
Page(s): 563-571
Appears in Collections:IJC-B Vol.38B(05) [May 1999]

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