Journal of Asian Natural Products Research
ISSN: 1028-6020 (Print) 1477-2213 (Online) Journal homepage: http://www.tandfonline.com/loi/ganp20
Cytototoxic constituents from the bark of Chisocheton cumingianus (Meliaceae)
Dewa Gede Katja, Kindi Farabi, Nurlelasari, Desi Harneti, Tri Mayanti, Unang Supratman, Khalijah Awang & Hideo Hayashi
To cite this article: Dewa Gede Katja, Kindi Farabi, Nurlelasari, Desi Harneti, Tri Mayanti, Unang Supratman, Khalijah Awang & Hideo Hayashi (2016): Cytototoxic constituents from the bark of Chisocheton cumingianus (Meliaceae), Journal of Asian Natural Products Research, DOI: 10.1080/10286020.2016.1196671
To link to this article: http://dx.doi.org/10.1080/10286020.2016.1196671
Published online: 22 Jun 2016.
Submit your article to this journal
View related articles
View Crossmark data
Full Terms & Conditions of access and use can be found at http://www.tandfonline.com/action/journalInformation?journalCode=ganp20
Download by: [Universitas Padjadjaran] Date: 22 June 2016, At: 18:38 Contens
Review Autophagy-inducing natural compounds: a treasure resource for developing therapeutics against tissue fibrosis Xiao-xi Lv, Shan-shan Liu & Zhuo-Wei Hu Pages: 101-108 Published online: 02 Mar 2017 Abstract | Full Text | References | PDF (1076 KB) |
86Views 2CrossRef citations 1Altmetric review Recent progression in the utilization of autophagy-regulating nature compound as anti-liver fibrosis agents Mao-Xu Ge, Hong-Wei He, Rong-Guang Shao & Hong Liu Pages: 109-113 Published online: 29 Jan 2017 Abstract | Full Text | References | PDF (611 KB) |
100Views 1CrossRef citations 0Altmetric
Original Articles Article Four new compounds from the rhizome of Aristolochia championii Xin Wang, Guo-Ru Shi, Yan-Fei Liu, Ruo-Yun Chen & De-Quan Yu Pages: 114-120 Published online: 25 Dec 2016 Abstract | Full Text | References | PDF (644 KB) |
78Views 0CrossRef citations 1Altmetric
Article Four new C10-polyacetylene glycosides from the rhizomes of Atractylodes lancea Kuo Xu, Zi-Ming Feng, Ya-Nan Yang, Jian-Shuang Jiang & Pei-Cheng Zhang Pages: 121-127 Published online: 28 Oct 2016 Abstract | Full Text | References | PDF (614 KB) |
111Views 1CrossRef citations 1Altmetric
Article Apocynin derivatives from Iris tectorum Chun-Lei Zhang, Guo-Ru Shi, Yan-Fei Liu, Yan Wang, Ruo-Yun Chen & De-Quan Yu Pages: 128-133 Published online: 12 Jan 2017 Abstract | Full Text | References | PDF (474 KB) |
73Views 0CrossRef citations 1Altmetric
Article Three new isobenzofuranone derivatives from the fruiting bodies of Hericium erinaceus Xu-Li Wang, Jie Gao, Jing Li, Hong-Ping Long, Ping-Sheng Xu, Kang-Ping Xu & Gui-Shan Tan Pages: 134-139 Published online: 31 May 2016 Abstract | Full Text | References | PDF (605 KB) |
101Views 3CrossRef citations 0Altmetric
Article Three new 1-(p-hydroxybenzyl)phenanthrenes from Bletilla striata S Xiao, Fu-Ming Yuan, Mao-Sheng Zhang, Shou-Yang Yu, Ji-Da Li, Xiao-Dong Yi & De-Lin Xu Pages: 140-144 Published online: 31 May 2016 Abstract | Full Text | References | PDF (454 KB) |
85Views 1CrossRef citations 1Altmetric
Article Monoterpenes and sesquiterpenes from the marine sediment-derived fungus Eutypella scoparia FS46 Hong-Xin Liu, Ling Zhang, Yu-Chan Chen, Zhang-Hua Sun, Qing-Ling Pan, Hao-Hua Li & Wei-Min Zhang Pages: 145-151 Published online: 03 Jun 2016 Abstract | Full Text | References | PDF (727 KB) |
102Views 1CrossRef citations 0Altmetric
Article Two new sesquiterpenes from the aerial parts of Schizonepeta tenuifolia Li-Zi Zhao, Yue Jin, Xiao-Min Han, Qing-Long Chu & Jun-Shan Yang Pages: 152-156 Published online: 07 Jun 2016 Abstract | Full Text | References | PDF (431 KB) |
66Views 1CrossRef citations 0Altmetric
Article Renchangianins F and G: two new sesquiterpenoids from Kadsura renchangiana Li-Qing Deng, Guo-Wei Wang, Si-Yu Zhou, Jing-Qiu Ge, Zhi-Hua Liao, Dao-Feng Chen & Min Chen Pages: 157-163 Published online: 10 Jun 2016 Abstract | Full Text | References | PDF (635 KB) | Supplemental |
88Views 1CrossRef citations 0Altmetric
Article Two new phenolic compounds and antitumor activities of asparinin A from Asparagus officinalis Xue-Mei Li, Jin-Long Cai, Le Wang, Wen-Xiang Wang, Hong-Lian Ai & Zi-Chao Mao Pages: 164-171 Published online: 13 Sep 2016 Abstract | Full Text | References | PDF (678 KB) |
128Views 0CrossRef citations 0Altmetric
Article Synthesis of pogostone by one-step Han-Bin Chen, Jiang-Tao Zhou, Yu-Hong Liu, Zhen-Biao Zhang, Ya-Xian Zhan, Zi-Ren Su & Hui-Fang Zeng Pages: 172-175 Published online: 31 May 2016 Abstract | Full Text | References | PDF (346 KB) |
85Views 0CrossRef citations 0Altmetric
Article Ferulic acid induces proliferation and differentiation of rat osteoblasts in vitro through cGMP/PKGII/ENaC signaling Jian-Lin Gao, Jun Chen, Guo-Zhu Yang, Li Lu, Xing-Yan Lu, Huan-Huan Jia, Xiao-Dong Jin, Hao Zhang & Qing-Nan Li Pages: 176-187 Published online: 27 Dec 2016 Abstract | Full Text | References | PDF (2129 KB) |
67Views 0CrossRef citations 0Altmetric
Note note Cytotoxic diterpenoids from Pteris ensiformis Yu-Sheng Shi, Yan Zhang, Wen-Zhong Hu, Li-Hong Zhang, Xi Chen, Ning Zhang, Guang Li & Li-Yan Tan Pages: 188-193 Published online: 02 Mar 2017 Abstract | Full Text | References | PDF (504 KB) |
51Views 1CrossRef citations 0Altmetric
Notes note Cytototoxic constituents from the bark of Chisocheton cumingianus (Meliaceae) Dewa Gede Katja, Kindi Farabi, Nurlelasari, Desi Harneti, Tri Mayanti, Unang Supratman, Khalijah Awang & Hideo Hayashi Pages: 194-200 Published online: 22 Jun 2016 Abstract | Full Text | References | PDF (704 KB) | Journal of Asian Natural Products Research, 2016 http://dx.doi.org/10.1080/10286020.2016.1196671
Cytototoxic constituents from the bark of Chisocheton cumingianus (Meliaceae)
Dewa Gede Katjaa,b, Kindi Farabia, Nurlelasaria, Desi Harnetia, Tri Mayantia, Unang Supratmana, Khalijah Awangc and Hideo Hayashid
aFaculty of Mathematics and Natural Sciences, Department of Chemistry, Universitas Padjadjaran, Jatinangor 45363, Indonesia; bFaculty of Mathematics and Natural Sciences, Department of Chemistry, Universitas Sam Ratulangi, Manado 95115, Indonesia; cFaculty of Science, Department of Chemistry, University of Malaya, Kuala Lumpur 59100, Malaysia; dDivision of Applied Life Sciences, Graduate School of Life and Environmental Sciences, Osaka Prefecture University, Osaka 599-8531, Japan
ABSTRACT ARTICLE HISTORY A new lanostane-type triterpenoid, 3β-hydroxy-25-ethyl-lanost- Received 11 January 2016 9(11),24(24′)-diene (1), along with 3β-hydroxy-lanost-7-ene (2) Accepted 30 May 2016 and β-sitosterol-3-O-acetate (3) was isolated from the stem bark of KEYWORDS C. cumingianus. The chemical structure of the new compound was Lanostane-type triterpenoid; elucidated on the basis of spectroscopic data. All of the compounds Chisocheton cumingianus; were evaluated for their cytotoxic effects against P-388 murine cytotoxic activity; Meliaceae leukemia cells. Compounds 1-3 showed cytotoxicity against P-388
murine leukemia cells with IC50 values of 28.8 ± 0.10, 4.29 ± 0.03, and 100.18 ± 0.16 μg/ml, respectively.
1. Introduction The genus Chisocheton, the second largest genus of the family Meliaceae, consists of more than 50 species and is distributed across Nepal, India, Bhutan, Myanmar, South China, Thailand, Indonesia, Malaysia, and Papua New Guinea 1[ ]. Previous phytochemical studies on Chisocheton plants reported the presence of compounds with interesting biological activ- ities including sesquiterpenoids [2], dammarane-type triterpenoids [2,3], tirucallane-type Downloaded by [Universitas Padjadjaran] at 18:38 22 June 2016 triterpenoids [4], apo-tirucallane-type triterpenoids [4,5], limonoids [6–11], steroids [10], and phenolics [3]. As part of our studies on anticancer candidate compounds from Indonesian Chicocheton plants, the methanolic extract from the bark of Chisocheton cuminganus showed significant cytotoxic activity against P-388 murine leukimia cells. C. cuminganus is a higher plant and widely distributed in the northern part of Sulawesi island in Indonesia [12]. Its bark has been used as an Indonesian folk medicine for reducing fever, treating contused wounds, and skin diseases [12,13]. The isolation, structure elucidation, and cytotoxic evaluation of these isolated compounds are described herein.
CONTACT Unang Supratman [email protected] © 2016 Informa UK Limited, trading as Taylor & Francis Group