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Org Lett ; 22(3): 929-933, 2020 02 07.
Article in English | MEDLINE | ID: mdl-31916776

ABSTRACT

Crokonoid A (1), a highly rearranged diterpenoid featuring a dual-bridged tricyclo[4.4.1.11,4]dodecane-2,11-dione ring system and its two possible ent-kaurene diterpenoid precursors (2 and 3), was isolated and structurally characterized by solid data from Croton kongensis. Compound 1 exhibited significant cytotoxicity against HL-60 and A-549 cell lines with IC50 values of 1.24 ± 0.56 and 1.92 ± 0.60 µM, respectively.


Subject(s)
Antineoplastic Agents, Phytogenic/pharmacology , Croton/chemistry , Diterpenes/pharmacology , A549 Cells , Antineoplastic Agents, Phytogenic/chemistry , Antineoplastic Agents, Phytogenic/isolation & purification , Cell Line, Tumor , Cell Proliferation/drug effects , Diterpenes/chemistry , Diterpenes/isolation & purification , Drug Screening Assays, Antitumor , HL-60 Cells , Humans , Molecular Structure , Stereoisomerism
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