Synthesis and biological evaluation of C-12 triazole and oxadiazole analogs of salvinorin A

Bioorganic and Medicinal Chemistry Letters

Volumn 19, Issue 5, 2009, Pages 1301-1304

  Yang, Lu ^a   Xu, Wei ^b   Chen, Feng ^a   Liu Chen, Lee Yuan ^b   Ma, Zhongze ^a   Lee, David Y W ^a  

^a MCLEAN HOSPITAL   (United States)

^b University School of Medicine   (United States)

Author keywords

Antagonist; Salvinorin A; Triazole

Indexed keywords

OXADIAZOLE DERIVATIVE; SALVINORIN A; TRIAZOLE DERIVATIVE;

ARTICLE; CHROMATOGRAPHY; DRUG ACTIVITY; DRUG RECEPTOR BINDING; DRUG SCREENING; DRUG STRUCTURE; DRUG SYNTHESIS; HYDROGEN BOND; NONHUMAN; SALVIA;

ANIMALS; CARBON; CHO CELLS; CRICETINAE; CRICETULUS; DITERPENES, CLERODANE; DOSE-RESPONSE RELATIONSHIP, DRUG; DRUG EVALUATION, PRECLINICAL; HUMANS; MICE; OXADIAZOLES; PROTEIN BINDING; RATS; STRUCTURE-ACTIVITY RELATIONSHIP; TRIAZOLES;

SALVIA DIVINORUM;

EID: 60449110147     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2009.01.078     Document Type: Article

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