Synthesis and antiproliferative activity of A-ring aromatised and conduritol-like steroidal compounds

Steroids

Volumn 70, Issue 14, 2005, Pages 922-932

  Milić, Dragana ^a   Kop, Tatjana ^a   Juranić, Zorica ^b   Gašić, Miroslav J ^a   Tinant, Bernard ^c   Pocsfalvi, Gabriella ^d   Šolaja, Bogdan A ^a  

^a UNIVERSITY OF BELGRADE   (Serbia)

^b INSTITUTE FOR ONCOLOGY AND RADIOLOGY OF SERBIA   (Serbia)

^c Unité CSTR   (Serbia)

^d CNR   (Italy)

Author keywords

Anticancer activity; Aromatization; Conduritol; Rearrangement

Indexed keywords

1,3 DIACETOXY 4 BROMOESTRA 1,3,5(10) TRIEN 17 ONE; 1,4 DIACETOXYESTRA 1,3,5(10) TRIEN 17 ONE; 10BETA ACETOXY 4BETA,5BETA EPOXYESTR 1 EN 3,17 DIONE; 10BETA ACETOXYESTRA 1,4 DIEN 3,17 DIONE; 2,3 DIHYDROXYESTR 5(10) EN 1,4,17 TRIONE; 3,4 DIACETOXY 2 BROMOESTRA 1,3,5(10),9(11) TETRAEN 17 ONE; 3BETA,4BETA,17BETA TRIACETOXYESTR 1 EN 5BETA,10BETA DIOL; 4BETA,5BETA,10BETA TRIHYDROXYESTR 1 EN 3,17 DIONE; ACID; ALKADIENE; HYDROXYL GROUP; PHENOL; STEROID; TRIFLUOROMETHANESULFONIC ACID; TRIFLUOROMETHANESULFONIC ACID TRIMETHYLSILYL ESTER; UNCLASSIFIED DRUG;

ACETYLATION; ANTINEOPLASTIC ACTIVITY; AROMATIZATION; ARTICLE; CATALYSIS; CATALYST; CONTROLLED STUDY; DRUG ACTIVITY; DRUG SCREENING; DRUG STRUCTURE; DRUG SYNTHESIS; FEMALE; HUMAN; HUMAN CELL; MALE; PRECURSOR; REACTION ANALYSIS; RING OPENING; X RAY CRYSTALLOGRAPHY;

EID: 27844533964     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.steroids.2005.07.001     Document Type: Article

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