Studies on organophosphorus compounds VII: Transformation of steroidal ketones with Lawesson's reagent into thioxo and heterofused steroids. Results of antimicrobial and antifungal activity

Phosphorus, Sulfur and Silicon and the Related Elements

Volumn 178, Issue 9, 2003, Pages 2003-2017

  Mohamed, Nadia R ^a   Elmegeed, Gamal A ^a   Younis, Magdi ^b  

^a NATIONAL RESEARCH CENTRE   (Egypt)

^b SOUTH VALLEY UNIVERSITY   (Egypt)

Author keywords

17 Thioxoandrosten 3 one; Antibacterial; Antifungal; Lawesson's reagent; Mercaptooxathiaphospholoandrosten 2 thione; Steroids; Thiazaphosphorinothieno steroids

Indexed keywords

17 BETA HYDROXY 2'' (4 METHOXYPHENYL) 1'',3'',2'' THIAZAPHOSPHORINO[5'',4'':4',5']THIENO[2',3':2,3] 5 ALPHA ANDROSARTAN 2'',6'' DITHIONE; 17 THIOXO 4 ANDROSTEN 3 ONE; 2'' (4 METHOXYPHENYL) 1'',3'',2'' THIAZAPHOSPHORINO[5'',4'':4',5']THIENO[2',3':2,3] 5 ALPHA CHOLESTAN 2'',6'' DITHIONE; 3 BETA MERCAPTO 2' (4 METHOXYPHENYL)SPIRO(5 ALPHA ANDROSTAN 17,4' DITHIAPHOSPHETAN) 2' THIONE; 3 BETA MERCAPTOSPIRO(ANDROSARTAN 17,4' DITHIAPHOSPHETAN)THIONE; 3,17 DITHIOXO 4 ANDROSTENE; 5' METHYL 2' (4 METHOXYPHENYL) 2' THIOXOTHIAPHOSPHOLO[3',4':16,17]ANDROST 4 EN 3 ONE; ANDROSTENEDIONE; ANTIFUNGAL AGENT; ANTIINFECTIVE AGENT; BIS [2' (4 METHOXYPHENYL)SPIRO(5 ALPHA ANDROSARTAN 17,4' DITHIAPHOSPHETAN) 2' THION 3 YL]SULFIDE; BIS(3 OXOPROSTA 4,17 DIEN 2 YL)SULFIDE; CARBOXYLIC ACID DERIVATIVE; EPIANDROSTERONE; ETHYL 2' AMINOTHIENO[2',3':2,3] 5 ALPHA CHOLESTAN CARBOXYLATE; KETONE; KETONE DERIVATIVE; METHYL GROUP; ORGANOPHOSPHORUS COMPOUND; PHENYL GROUP; PROGESTERONE DERIVATIVE; REAGENT; SPIRO COMPOUND; STEROID; STEROID HORMONE; SULFIDE; THIAPHOSPHOLO[3',4':16,17]ANDROSTEN 3 ONE; THIENO[2',3':2,3]ANDROSTAN; THIENO[2',3':2,3]CHOLESTAN; UNCLASSIFIED DRUG;

ANTIFUNGAL ACTIVITY; ANTIMICROBIAL ACTIVITY; ARTICLE; BACTERIUM; CHEMICAL REACTION; CONTROLLED STUDY; DRUG ACTIVITY; DRUG ISOLATION; DRUG SCREENING; DRUG SYNTHESIS; FUNGUS; IN VITRO STUDY; NONHUMAN; STUDY; YEAST;

EID: 0142200470     PISSN: 10426507     EISSN: None     Source Type: Journal    
DOI: 10.1080/10426500390228693     Document Type: Article

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