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Diterpenoids of the Cassane Type from Caesalpinia decapetala.
Qiao, Yuben; Xu, Qianqian; Hu, Zhengxi; Li, Xiao-Nian; Xiang, Ming; Liu, Junjun; Huang, Jinfeng; Zhu, Hucheng; Wang, Jianping; Luo, Zengwei; Xue, Yongbo; Zhang, Yonghui.
Affiliation
  • Qiao Y; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation and Department of Pharmacology, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology , Wuhan 430030, Hubei Province, People's Republic of China.
  • Xu Q; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation and Department of Pharmacology, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology , Wuhan 430030, Hubei Province, People's Republic of China.
  • Hu Z; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation and Department of Pharmacology, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology , Wuhan 430030, Hubei Province, People's Republic of China.
  • Li XN; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences , Kunming 650204, Yunnan Province, People's Republic of China.
  • Xiang M; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation and Department of Pharmacology, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology , Wuhan 430030, Hubei Province, People's Republic of China.
  • Liu J; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation and Department of Pharmacology, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology , Wuhan 430030, Hubei Province, People's Republic of China.
  • Huang J; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation and Department of Pharmacology, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology , Wuhan 430030, Hubei Province, People's Republic of China.
  • Zhu H; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation and Department of Pharmacology, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology , Wuhan 430030, Hubei Province, People's Republic of China.
  • Wang J; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation and Department of Pharmacology, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology , Wuhan 430030, Hubei Province, People's Republic of China.
  • Luo Z; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation and Department of Pharmacology, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology , Wuhan 430030, Hubei Province, People's Republic of China.
  • Xue Y; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation and Department of Pharmacology, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology , Wuhan 430030, Hubei Province, People's Republic of China.
  • Zhang Y; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation and Department of Pharmacology, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology , Wuhan 430030, Hubei Province, People's Republic of China.
J Nat Prod ; 79(12): 3134-3142, 2016 Dec 23.
Article in En | MEDLINE | ID: mdl-27966950
ABSTRACT
Eighteen compounds, including eight new cassane-type furanoditerpenoids, 3ß-hydroxyphanginin H (1), 3ß-acetoxyphanginin H (2), 7ß-acetoxyphanginin H (3), 7ß-hydroxyphanginin H (4), 4-epi-3ß-hydroxycaesalpinilinn (5), 4-epi-3ß-acetoxycaesalpinilinn (6), 20-acetoxytaepeenin D (7), and tomocin E (8), along with 10 known compounds (9-18) were isolated from the roots of Caesalpinia decapetala. Compounds 1-13 were isolated from C. decapetala for the first time. The new compounds with their absolute configurations were determined by extensive spectroscopic analysis, single-crystal X-ray diffraction, and electronic circular dichroism calculations. Compounds 1, 4, 5, 7, and 11 exhibited inhibitory activities against the SW1990 human pancreatic cancer cell line with IC50 values ranging from 2.9 to 8.9 µM.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Drugs, Chinese Herbal / Caesalpinia / Diterpenes / Antineoplastic Agents, Phytogenic Limits: Animals / Humans / Male Language: En Journal: J Nat Prod Year: 2016 Type: Article

Full text: 1 Database: MEDLINE Main subject: Drugs, Chinese Herbal / Caesalpinia / Diterpenes / Antineoplastic Agents, Phytogenic Limits: Animals / Humans / Male Language: En Journal: J Nat Prod Year: 2016 Type: Article