4.6 Article

Novel C,N-chelate platinum(II) antitumor complexes bearing a lipophilic ethisterone pendant

期刊

JOURNAL OF INORGANIC BIOCHEMISTRY
卷 105, 期 4, 页码 525-531

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jinorgbio.2010.12.005

关键词

Platinum complexes; Cytotoxicity; Lipophilicity; Steroidal derivative; DNA

资金

  1. Ministerio de Educacion y Ciencia of Spain
  2. FEDER [CTQ2008-02178/BQU, CTQ2008-01402]
  3. Fundacion Seneca-CARM [08666/PI/08, 04509/GERM/06]

向作者/读者索取更多资源

The novel steroidal carrier ligand 17-alpha[4'-ethynyl-dimethylbenzylamine]-17-beta-testosterone (ET-dmba 1) and the steroid - C,N-chelate platinum(II) derivatives [Pt(ET-dmba)Cl(L)] (L = DMSO (2) and PTA (3; PTA = 1,3,5-triaza-7-phosphaadamantane)) have been prepared. Values of IC50 were calculated for the new platinum complexes 2 and 3 against a panel of human tumor cell lines representative of ovarian (A2780 and A2780cisR) and breast cancers (T47D). At 48 h incubation time complexes 2 and 3 show very low resistance factors (RF of <2) against an A2780 cell line which has acquired resistant to cisplatin and were more active than cisplatin (about 4-fold for 3) in T47D (AR+, AR = androgen receptor). Compound 1 retains a moderate degree of relative binding affinity (RBA = 0.94%) for androgen receptors. The cytotoxicity of the non steroidal platinum analogues [Pt(dmba)Cl(L)] (dmba = dimethylbenzylamine; L = DMSO (4) and PTA (5)) has also been studied for comparison purposes. Theoretical calculations at the BP86/def2-TZVP level of theory on complex 3 have been undertaken. (C) 2010 Elsevier Inc. All rights reserved.

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