Article
Chemistry, Applied
Xue-Wei Yan, Si-Yu Du, Xiao-Tong Wang, Kong-Kai Zhu, Lei Fang
Summary: Two new monoterpenoid indole alkaloids, named taberibogines E and F (1 and 2), together with three known ones (3-5), were isolated from the stems of Tabernaemontana bovina Lour (Apocynaceae). Their structures and absolute configurations were elucidated through NMR and HRESIMS data, NMR calculations, and DP4+ probability analyses. Compounds 1 and 2 exhibited inhibitory effects on LPS-induced nitric oxide (NO) production in RAW 264.7 macrophages.
NATURAL PRODUCT RESEARCH
(2023)
Article
Chemistry, Medicinal
Andre Nehemie Bitombo, Auguste Abouem A. Zintchem, Alex De Theodore Atchade, Norbert Mbabi Nyemeck Ii, Dominique Serge Ngono Bikobo, Christian G. Bochet, Dieudonn Emmanuel Pegnyemb
Summary: In this study, thirteen compounds, including five new carboxy-indole alkaloids and one known alkaloid, were isolated from the trunk bark of a plant in the Apocynaceae family. These compounds exhibited good in vitro antiplasmodial activities against two strains of Plasmodium falciparum. Of particular interest were penduflorines A and B, as well as tabernaemontine, which showed significant inhibitory activities against the parasites.
Article
Biochemistry & Molecular Biology
Shun-Qing Chen, Jia Jia, Jing-Yao Hu, Jun Wu, Wen-Ting Sun, Mingxin Zheng, Xi Wang, Kong-Kai Zhu, Cheng-Shi Jiang, Sheng-Ping Yang, Juan Zhang, Shou-Bao Wang, You-Sheng Cai
Summary: Phytochemical investigation on the aerial parts of Tabernaemontana bufalina Lour. led to the identification of several new alkaloids and known indole alkaloids. The structures and absolute configurations of the new alkaloids were determined by spectroscopic and computational methods. Some of these alkaloids exhibited significant bioactivity, demonstrating potential for drug development.
Article
Biochemistry & Molecular Biology
Sheng Li, Ling-Ling Han, Ke-Pu Huang, Ye-Han Ma, Ling-Li Guo, Yarong Guo, Xiaoqian Ran, Yong-Gang Yao, Xiao-Jiang Hao, Rongcan Luo, Yu Zhang
Summary: Eleven monoterpenoid indole alkaloids, including three new ones, tabercrassines A-C (1-3), were isolated from the seeds of Tabernaemontana crassa. Tabercrassine A (1) is an ibogan-ibogan-type bisindole alkaloid formed by the polymerization of two classic ibogan-type monomers through a C3 unit aliphatic chain. Their structures were determined by HRESIMS, NMR, and ECD spectra. Cellular assays showed that alkaloids 1-3 reduce A beta 42 production and inhibit phospho-tau (Thr217) associated with Alzheimer's disease [AD] mediated pathways, indicating their potential against AD.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
(2023)
Article
Chemistry, Applied
Frederico Luiz Reis, Luciana Adolpho, Ana Lucia Tasca Gois Ruiz, Euclesio Simionatto, Ionara Irion Dalcol, Marco Aurelio Mostardeiro, Ademir Farias Morel
Summary: Four alkaloids were isolated from the stem bark of T. catharinensis and tested for antiproliferative activity in tumor cell lines. The alkaloid affinisine showed the most promising results with cytotoxic effects against various tumor cell strains and high selectivity rates compared to non-tumor cells.
NATURAL PRODUCT RESEARCH
(2022)
Article
Biochemistry & Molecular Biology
Jing Chen, Yang Yu, Jing Wu, Mei-Fen Bao, Sumet Kongkiatpaiboon, Johann Schinnerl, Xiang-Hai Cai
Summary: The study explored the influence of artificial cultivation on the chemical composition of the same plant species, leading to the discovery of several undescribed bioactive alkaloids in the leaves of Tabernaemontana divaricata 'Dwaft'. Among the isolated alkaloids, taberdivarines A and B were particularly noteworthy for their unique structure. Compound 6 showed significant cytotoxic activity against three human cancer cell lines, indicating its potential as a lead compound for further research.
BIOORGANIC CHEMISTRY
(2021)
Article
Plant Sciences
Miao Zhang, Si-Yu Du, Jie Liu, Xue Zhao, Jia-Ning Liu, Cheng-Shi Jiang, Kong-Kai Zhu, Lei Fang
Summary: Two new monoterpenoid indole alkaloids, taberibogines A and B, along with four known compounds, were isolated from the stems of Tabernaemontana bovina. The structures of these compounds were elucidated using comprehensive spectroscopic analysis and computational methods. Compounds 1-2 were found to have inhibitory effects on LPS-induced NO production in RAW 264.7 macrophages.
PHYTOCHEMISTRY LETTERS
(2021)
Article
Chemistry, Applied
Lingling Han, Kepu Huang, Chen Chen, Wentao Zhu, Yehan Ma, Xiaojiang Hao, Hongping He, Yu Zhang
Summary: Two new alkaloids, Taberdines L (1) and M (2), were isolated from the twigs and leaves of Tabernaemontana divaricata, together with six known alkaloids. Taberdine L (1) is the first optically active natural member of the allo iboga class of alkaloids with an ethyl side chain in a bridgehead position. The structures, including absolute configurations, were elucidated using a combination of MS, NMR, and ECD calculation, and the cytotoxic activities of 1 and 2 against five human cancer cell lines were also evaluated.
NATURAL PRODUCT RESEARCH
(2022)
Article
Chemistry, Organic
Wen-Tao Zhu, Chen Chen, Qian Zhao, Ling-Ling Han, Min Yang, Xiao-Jiang Hao, Yu Zhang
Summary: Tabercetimines A-D, four new quaternary monoterpenoid indole alkaloids with rare skeleton characterized by a quinuclidine moiety, were isolated from the stems of Tabernaemontana divaricata. Their structures and absolute configurations were elucidated through extensive analysis of MS, NMR, ECD, and X-ray diffraction, and a possible biogenetic pathway of 1 was also proposed.
TETRAHEDRON LETTERS
(2021)
Article
Plant Sciences
Ninh Thi Ngoc, Tran Hong Quang, Nguyen Huu Quan, Tran Thi Hong Hanh, Nguyen Xuan Cuong, Nguyen Van Thanh, Chu Hoang Ha, Nguyen Hoai Nam, Chau Van Minh
Summary: Phytochemical investigation of Tabernaemontana bovina leaves and twigs led to the isolation of 10 monoterpenoid indole alkaloids, including two new compounds. One of the new compounds, taberbovinine B, demonstrated an unusual ring C/D cleavage. Compounds 2 and 8 exhibited weak cytotoxicity against various cancer cell lines, while other compounds showed different levels of toxicity against specific cancer cells.
PHYTOCHEMISTRY LETTERS
(2022)
Review
Plant Sciences
Clarissa Marcelle Naidoo, Yougasphree Naidoo, Yaser Hassan Dewir, Hosakatte Niranjana Murthy, Salah El-Hendawy, Nasser Al-Suhaibani
Summary: The study focuses on the medicinal potential and biological activities of several species within the genus Tabernaemontana, specifically analyzing the major alkaloidal components and their pharmacological value. Research indicates that plants within the Tabernaemontana genus have significant medicinal potential, warranting further in-depth investigation.
Article
Chemistry, Organic
Guanqun Zhan, Fuxin Zhang, Kailing Yang, Tao Yang, Ruixi Zhou, Xueqing Ma, Nan Wang, Zengjun Guo
Summary: A new compound and four known compounds were isolated from Alstonia scholaris. The new compound has a unique carbon skeleton and shows potential anti-inflammatory activity.
ORGANIC & BIOMOLECULAR CHEMISTRY
(2023)
Article
Chemistry, Physical
Yu-qi Li, Jing Cai, Jia-xin Cheng, Sheng-zhi Su, Toshihiro Akihisa, Wen-yuan Liu, Feng Feng, Jie Zhang
Summary: This study investigated the chemical constituents of Alstonia mairei and isolated twenty-four monoterpenoid indole alkaloids. Four new compounds were discovered. The structures of these compounds were characterized using various techniques. The cytotoxic activities of the isolated compounds were evaluated, and several compounds demonstrated potent inhibitory activities against A549 lung cancer cells.
JOURNAL OF MOLECULAR STRUCTURE
(2022)
Article
Chemistry, Organic
Sin-Yee Tang, Min-Phin Ng, Chun-Hoe Tan, Kae-Shin Sim, Kuan-Hon Lim, Kien-Thai Yong, Yun-Yee Low, Siew-Huah Lim
Summary: Eight undescribed indole alkaloids were isolated and their structures were determined. Some of these compounds showed cytotoxicity against cancer cells.
Article
Biochemistry & Molecular Biology
Zhi-Wen Liu, Min Song, Jun-Ya Wang, De-Zhi Wang, Biao Sun, Lei Shi, Ren-Wang Jiang, Min Ma, Xiao-Qi Zhang
Summary: Eight unprecedented monoterpenoid indole alkaloid (MIA) adducts and dimers, melofusinines A-H (1-8), and three undescribed melodinus-type MIA monomers, melofusinines I-K (9-11), were isolated from Melodinus fusiformis. Compounds 1 and 2 are hybrid indole alkaloids incorporating an aspidospermatan-type MIA with a monoterpenoid alkaloid unit. Compounds 3-8 are the first MIA dimers constructed through an aspidospermatan-type monomer and a rearranged melodinus-type monomer.
Article
Plant Sciences
Mei-Ling Han, Jin-Xin Zhao, Hong-Chun Liu, Gang Ni, Jian Ding, Sheng-Ping Yang, Jian-Min Yue
JOURNAL OF NATURAL PRODUCTS
(2015)
Article
Plant Sciences
Yang Yu, Li-She Gan, Sheng-Ping Yang, Li Sheng, Qun-Fang Liu, Shao-Nong Chen, Jia Li, Jian-Min Yue
JOURNAL OF NATURAL PRODUCTS
(2016)
Article
Plant Sciences
Si-Yuan Zhou, Fengkai Fan, Ji-Zheng Sun, Ziyan Guo, Wen-Ting Sun, Ling Chen, Qing-Qing Tang, Guofu Qiu, Sheng-Ping Yang, Jianqing Yu, You-Sheng Cai
PHYTOCHEMISTRY LETTERS
(2018)
Article
Orthopedics
Shengping Yang, Rui Zhang, Qingling Zhu, Guan Wang, Xuanxi Ding, Jianmin Wang
ACTA ORTHOPAEDICA ET TRAUMATOLOGICA TURCICA
(2014)
Article
Chemistry, Multidisciplinary
Jinbiao Xu, Gang Ni, Shengping Yang, Jianmin Yue
CHINESE JOURNAL OF CHEMISTRY
(2013)
Article
Chemistry, Medicinal
Sheng-Ping Yang, Xiao-Wei Zhang, Jing Ai, Li-She Gan, Jin-Biao Xu, Ying Wang, Zu-Shang Su, Lu Wang, Jian Ding, Mei-Yu Geng, Jian-Min Yue
JOURNAL OF MEDICINAL CHEMISTRY
(2012)
Article
Plant Sciences
You-Sheng Cai, Ariel M. Sarotti, Ting-Lan Zhou, Rong Huang, Guofu Qiu, Congkui Tian, Ze-Hong Miao, Attila Mandi, Tibor Kurtan, Shugeng Cao, Sheng-Ping Yang
JOURNAL OF NATURAL PRODUCTS
(2018)
Article
Chemistry, Organic
Jia Liu, Xiu-Feng He, Gai-Hong Wang, Emilio F. Merino, Sheng-Ping Yang, Rong-Xiu Zhu, Li-She Gan, Hua Zhang, Maria B. Cassera, He-Yao Wang, David G. I. Kingston, Jian-Min Yue
JOURNAL OF ORGANIC CHEMISTRY
(2014)
Article
Chemistry, Organic
Yao Wang, Qun-Fang Liu, Ji-Jun Xue, Yu Zhou, Huang-Chao Yu, Sheng-Ping Yang, Bo Zhang, Jian-Ping Zuo, Ying Li, Jian-Min Yue
Article
Chemistry, Organic
Gang Ni, Hua Zhang, Hong-Chun Liu, Sheng-Ping Yang, Mei-Yu Geng, Jian-Min Yue
Article
Biotechnology & Applied Microbiology
Li Miao, Xueling Wang, Wei Jiang, Shengping Yang, Huiru Zhou, Youpeng Zhai, Xiaojian Zhou, Kunming Dong
WORLD JOURNAL OF MICROBIOLOGY & BIOTECHNOLOGY
(2013)
Article
Plant Sciences
You-Sheng Cai, Cong Wang, Congkui Tian, Wen-Tin Sun, Ling Chen, Di Xiao, Si-Yuan Zhou, Guofu Qiu, Jianqing Yu, Kongkai Zhu, Sheng-Ping Yang
JOURNAL OF NATURAL PRODUCTS
(2019)
Article
Chemistry, Medicinal
Xi Wang, Fuqian Wang, Jun Wu, Shun-Qing Chen, Cheng-Shi Jiang, Sheng-Ping Yang, Cong Wang, You-Sheng Cai
Summary: Novel and known Lycopodium alkaloids were isolated and identified from Lycopodium japonicum Thunb., but unfortunately, all compounds showed no significant inhibitory effects on acetylcholinesterase and alpha-glucosidase.
Article
Biochemistry & Molecular Biology
Shun-Qing Chen, Jia Jia, Jing-Yao Hu, Jun Wu, Wen-Ting Sun, Mingxin Zheng, Xi Wang, Kong-Kai Zhu, Cheng-Shi Jiang, Sheng-Ping Yang, Juan Zhang, Shou-Bao Wang, You-Sheng Cai
Summary: Phytochemical investigation on the aerial parts of Tabernaemontana bufalina Lour. led to the identification of several new alkaloids and known indole alkaloids. The structures and absolute configurations of the new alkaloids were determined by spectroscopic and computational methods. Some of these alkaloids exhibited significant bioactivity, demonstrating potential for drug development.