An efficient synthesis of SK-658 and its analogs as potent histone deacetylase inhibitors

Bioorganic Chemistry

Volumn 59, Issue , 2015, Pages 145-150

  Shahidul Islam, Md ^a,b   Nurul Islam, Md ^a,b   Ashraful Hoque, Md ^a,b   Nishino, Norikazu ^a   Kato, Tamaki ^a   Kim, Hyun Jung ^c   Ito, Akihiro ^d   Yoshida, Minoru ^d  

^a KYUSHU INSTITUTE OF TECHNOLOGY   (Japan)

^b UNIVERSITY OF RAJSHAHI   (Bangladesh)

^c Department of Biochemistry and Molecular Biology Faculty of Science University of Rajshahi ^*  (South Korea)

^d RIKEN   (Japan)

Author keywords

Histone deacetylase inhibitor; SK 658 analogs; SS hybrid; Zinc binding group

Indexed keywords

DISULFIDE; HISTONE DEACETYLASE 1; HISTONE DEACETYLASE 4; HISTONE DEACETYLASE 6; HISTONE DEACETYLASE INHIBITOR; SK 658; THIOESTER; UNCLASSIFIED DRUG; VORINOSTAT; HISTONE DEACETYLASE; HYDROXAMIC ACID; ZINC;

ARTICLE; CONCENTRATION RESPONSE; CONTROLLED STUDY; DRUG DESIGN; DRUG POTENCY; DRUG SYNTHESIS; ENZYME INHIBITION; HUMAN; HUMAN CELL; HYDROPHOBICITY; PRIORITY JOURNAL; STRUCTURE ACTIVITY RELATION; BINDING SITE; CHEMICAL STRUCTURE; CHEMISTRY; METABOLISM; SYNTHESIS;

BINDING SITES; HISTONE DEACETYLASE INHIBITORS; HISTONE DEACETYLASES; HUMANS; HYDROXAMIC ACIDS; MODELS, MOLECULAR; STRUCTURE-ACTIVITY RELATIONSHIP; ZINC;

EID: 84925233415     PISSN: 00452068     EISSN: 10902120     Source Type: Journal    
DOI: 10.1016/j.bioorg.2015.02.009     Document Type: Article

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