Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Evagelia S. Arsenou"'
Autor:
Evagelia S. Arsenou, George Pairas, Manolis A. Fousteris, Anna I. Koutsourea, Sotiris S. Nikolaropoulos, Athanasios A. Papageorgiou
Publikováno v:
Bioorganic & Medicinal Chemistry. 16:5207-5215
The synthesis and the in vivo evaluation against leukemias P388 and L1210 of six new alkylating steroidal esters are described. The esteric derivatives incorporating the 17β-acetamido-B-lactamic steroidal skeleton exhibited increased antileukemic ac
Autor:
Anna I, Koutsourea, Manolis A, Fousteris, Evagelia S, Arsenou, Athanasios, Papageorgiou, George N, Pairas, Sotiris S, Nikolaropoulos
Publikováno v:
In vivo (Athens, Greece). 22(3)
Recent structure-antileukemic activity studies showed that the steroidal part of complex molecules containing DNA alkylators does not play only the role of the "biological carrier". New such compounds designed to possess an allylic 7-ketone showed en
Autor:
Dionysios Mourelatos, Sotiris S. Nikolaropoulos, Athanasios A. Papageorgiou, Manolis A. Fousteris, Anna I. Koutsourea, Evagelia S. Arsenou
Publikováno v:
Anti-cancer drugs. 18(9)
This study was designed as a rational continuation of our research regarding the functional requirements essential for the antileukemic activity of compounds comprising an alkylating moiety and a modified steroid. The steroidal esteric derivatives of
Autor:
Sotiris S. Nikolaropoulos, Manolis A. Fousteris, Dionysios Mourelatos, Athanasios A. Papageorgiou, Anna I. Koutsourea, Evagelia S. Arsenou
Publikováno v:
Anti-cancer drugs. 16(10)
We have studied the effect of modification of the B-steroidal ring to lactamic on the anti-leukemic potency of D-modified and D-non-modified steroidal esters of chlorambucil's active metabolite. The compounds synthesized were studied against leukemia
Autor:
Manolis A, Fousteris, Anna I, Koutsourea, Evagelia S, Arsenou, Athanasios, Papageorgiou, Dionisis, Mourelato, Sotiris S, Nikolaropoulos
Publikováno v:
Anticancer research. 22(4)
The increase of the damaging effects on specific DNA sequences and the reduction of the subsequent toxicity of nitrogen mustards has been achieved by their chemical conjugation with modified steroids through an esteric bond. In an attempt to study th