Synthesis and cytotoxic activity of nitric oxide-releasing isosteviol derivatives

Bioorganic and Medicinal Chemistry Letters

Volumn 24, Issue 9, 2014, Pages 2202-2205

  Wang, Ting Ting ^a,b   Liu, Yan ^a   Chen, Li ^a  

^a CHINA PHARMACEUTICAL UNIVERSITY   (China)

^b Zhenjiang Center for Disease Control and Prevention   (China)

Author keywords

Cytotoxicity; Furoxan; Isosteviol; NO donor; Structural modification

Indexed keywords

ANTINEOPLASTIC AGENT; BARDOXOLONE METHYL; COMPTOTHECIN; ENT 16 OXOBEYERAN 19 OIC ACID; NITRIC OXIDE; UNCLASSIFIED DRUG; ISOSTEVIOL; KAURANE DERIVATIVE; NITRIC OXIDE DONOR; CAMPTOTHECIN; CYTOTOXIC AGENT; DITERPENE; ISOSTEVIOL DERIVATIVE; OXIME DERIVATIVE;

ACIDIFICATION; ARTICLE; BAEYER VILLIGER REACTION; CANCER CELL CULTURE; CANCER INHIBITION; CELL STRAIN HEPG2; CONTROLLED STUDY; DRUG CYTOTOXICITY; DRUG SYNTHESIS; HUMAN; HUMAN CELL; IC 50; IN VITRO STUDY; MTT ASSAY; ROOM TEMPERATURE; CELL PROLIFERATION; CHEMISTRY; DRUG EFFECTS; NEOPLASMS; SYNTHESIS; TUMOR CELL LINE; ANTIPROLIFERATIVE ACTIVITY; CYTOTOXICITY; DRUG POTENCY; HEPG2 CELL LINE; IC50; STRUCTURE ACTIVITY RELATION; ANTINEOPLASTIC ACTIVITY; METASTATIC MELANOMA;

ANTINEOPLASTIC AGENTS; CELL LINE, TUMOR; CELL PROLIFERATION; DITERPENES, KAURANE; HUMANS; NEOPLASMS; NITRIC OXIDE DONORS;

EID: 84899096731     PISSN: 0960894X     EISSN: 14643405     Source Type: Journal    
DOI: 10.1016/j.bmcl.2014.03.004     Document Type: Article

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