Journal of Natural Products · 2002 · 27 citations · 7 references
Life SciencesBotanyPharmacologyCancer PharmacologyPlant BiochemistryStructure-activity RelationshipsMedicinal Plant KnowledgeMedicinal PlantsOrganic AcidsStructure-activity Relationship AnalysisAnticancer ActivityAnticancer Natural ProductsEpstein-barr Virus LatencyEpstein-barr Virus OncogenesisPlant-derived Natural ProductsTumor Promoter Mechanisms
A new nor-labdane-type diterpene, 15-nor-labda-8(17),12E-dien-13,19-dienoic acid (1), along with five known diterpenes, 15-nor-14-oxolabda-8(17),12E-dien-19-oic acid (2), trans-communic acid (3), sandaracopimaric acid (4), dehydroabietic acid (5), and abieta-8,11,13-triene-15,18-diol (6), was isolated from the cones of Pinus luchuensis. The structure of 1 was established by chemical and spectroscopic methods. Among these isolates, compounds 2, 4, and 6 showed potent inhibitory effects on Epstein-Barr virus early antigen (EBV-EA) activation induced by the tumor promoter 12-O-tetradecanoylphorbol 13-acetate.
7
Anti-tumor-Promoting Activity of Diterpenes from Excoecaria agallocha.
Tenji Konishi, Midori Takasaki, Harukuni Tokuda et al. · Biological and Pharmaceutical Bulletin · 1998 · 57 citations · Full text
Life Sciences, Botany, Oncology +14
Cancer chemopreventive agents, serratane-type triterpenoids from Picea jezoensis
Reiko Tanaka, Toshifumi Minami, Kazuhiro Tsujimoto et al. · Cancer Letters · 2001 · 36 citations
Medicine, Oncology, Pharmacology +14
Dehydroabietane diterpenes from Nepeta teydea
Braulio M. Fraga, Teresa Mestres, Carmen E. Díaz et al. · Phytochemistry · 1994 · 32 citations