New enantiomeric fluorine-containing derivatives of sulforaphane: Synthesis, absolute configurations and biological activity

European Journal of Medicinal Chemistry

Volumn 76, Issue , 2014, Pages 332-342

  Kiełbasiński, Piotr ^a   Łuczak, Jerzy ^a   Cierpiał, Tomasz ^a   Błaszczyk, Jarosław ^a   Sieroń, Lesław ^b   Wiktorska, Katarzyna ^c   Lubelska, Katarzyna ^c   Milczarek, Małgorzata ^c   Chilmończyk, Zdzisław ^c  

^a CENTRE OF MOLECULAR AND MACROMOLECULAR STUDIES   (Poland)

^b LODZ UNIVERSITY OF TECHNOLOGY   (Poland)

^c NATIONAL MEDICINES INSTITUTE   (Poland)

Author keywords

Isothiocyanates; Melanoma; Organofluorine compounds; Sulforaphane; Sulfoxides

Indexed keywords

4 ISOTHIOCYANATO 1 BUTYL 2' ,2' ,2' TRIFLUOROETHYL SULFOXIDE; 4 ISOTHIOCYANATO 1 BUTYL TRIFLUOROMETHYL SULFOXIDE; 4 N PHTHALIMIDO 1 BUTYL TRIFLUOROMETHYL SULFOXIDE; 5 ISOTHIOCYANATO 1 PENTYL 2',2',2' TRIFLUOROETHYL SULFOXIDE; CARBENE; CARBON; FLUORINE; SULFORAPHANE; SULFUR; UNCLASSIFIED DRUG; ISOTHIOCYANIC ACID DERIVATIVE; SULFORAFAN;

ARTICLE; BIOLOGICAL ACTIVITY; CANCER GROWTH; CONTROLLED STUDY; CYTOTOXICITY; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOMER; IN VITRO STUDY; MELANOMA CELL; STEREOCHEMISTRY; CHEMICAL STRUCTURE; CHEMISTRY; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; STEREOISOMERISM; SYNTHESIS;

FLUORINE; ISOTHIOCYANATES; MAGNETIC RESONANCE SPECTROSCOPY; MASS SPECTROMETRY; MODELS, MOLECULAR; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 84896821056     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2014.02.036     Document Type: Article

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