6E-hydroximinosteroid homodimerization by cross-metathesis processes.

Abstract:

:A rapid and efficient synthesis of 6E-hydroximinosteroid homodimers is described. The two new compounds were linked at position 3 of the steroid nucleus via a ruthenium catalyzed cross-metathesis reaction. The cytotoxic activity of these compounds was evaluated in vitro on human lung carcinoma A549 (ATCC CCL-185), colon adenocarcinoma HCT-116 (ATCC CCL-247), human caucasian glioblastoma multiforme T98G (ECACC 92090213) and human pancreatic adenocarcinoma PSN1 (ECACC 94060601) tumour cells. Homodimer 10b presented selective activity against HCT-116, although they are not highly toxic when compared with the monomer counterparts.

journal_name

Steroids

journal_title

Steroids

authors

Rega M,Jiménez C,Rodríguez J

doi

10.1016/j.steroids.2007.03.014

subject

Has Abstract

pub_date

2007-10-01 00:00:00

pages

729-35

issue

11-12

eissn

0039-128X

issn

1878-5867

pii

S0039-128X(07)00058-X

journal_volume

72

pub_type

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