Фитотерапия

Iridoid and bis-iridoid glucosides from the fruit of Gardenia jasminoides

Hai-Bo Li a,1, Yang Yu b,1, Zhen-Zhong Wang c, Yi Dai b, Hao Gao b, Wei Xiao a,c,⁎, Xin-Sheng Yao b,d,⁎ a Nanjing University of Chinese Medicine, Nanjing 210000, PR China b Institute of Traditional Chinese Medicine & Natural Products, College of Pharmacy, Jinan University, Guangzhou 510632, PR China c Jiangsu Kanion Pharmaceutical, Lianyungang 222000, PR China d Shenyang Pharmqaceutical University, Shenyang 110016, PR China a r t i c l e i n f o a b s t r a c t Article history: Received 23 January 2013 Accepted in revised form 29 March 2013 Available online 6 April 2013

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‘Bacoside B’ — the need remains for establishing identity

Mundkinajeddu Deepak ⁎, Agarwal Amit Research and Development Centre, Natural Remedies Private Limited, Bangalore, India a r t i c l e i n f o a b s t r a c t Article history: Received 17 December 2012 Accepted in revised form 5 March 2013 Available online 16 March 2013 Bacopa monnieri is fast gaining popularity for its beneficial effects on cognition and memory. The active constituents of the plant were putatively identified as ‘bacosides A and B’ in older publications. Subsequently ‘bacoside A’ was identified as a mixture of four saponins [bacoside

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Simultaneous determination of arctiin and its metabolites in rat urine and feces by HPLC

Wei Wang a, Qiang Pan b, Xue-Ying Han a, Jing Wang a, Ri-Qiu Tan a, Fan He a, De-Qiang Dou a,⁎, Ting-Guo Kang a,⁎⁎ a School of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, China b Liaoning Provincial Institute for Food and Drug Control, Shenyang, China a r t i c l e i n f o a b s t r a c t Article history: Received 9 December 2012 Accepted in revised form 18 January 2013 Available online 1 February 2013 Arctiin, an important lignan compound in Fructus Arctii, has been reported to possess

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Microbial transformation of 20(S)-protopanaxadiol by Absidia corymbifera. Cytotoxic activity of the metabolites against human prostate cancer cells

Guangtong Chen a, Min Yang b, Shaojun Nong a, Xue Yang a, Yong Ling a, Donggeng Wang a, Xinyang Wang a, Wei Zhang a,⁎ a School of Medicine, Nantong University, 19 Qi Xiu Road, Nantong 226001, PR China b National Engineering Laboratory for TCM Standardization Technology, Shanghai Research Center for TCM Modernization, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 501 Hai Ke Road, Shanghai 201203, PR China a r t i c l e i n f o a b s t r a c t Article history: Received 24 July 2012 Accepted in revised form 16 September 2012 Available online 28 September 2012

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Goniolandrene A and B from Goniothalamus macrophyllus

Norkamilah Abdullah a, Hamidah Sahibul-Anwar a, Sharinah Ideris a, Tomoyo Hasuda b, Yukio Hitotsuyanagi b, Koichi Takeya b, Marc Diederich c, CheeYan Choo a,⁎ a MedChem Herbal Research Group, Faculty of Pharmacy, Universiti Teknologi MARA, 42300 Puncak Alam, Selangor, Malaysia b Tokyo University of Pharmacy and Life Science, 1432-1 Horinouchi, Hajiochi, Tokyo 192-03, Japan c Laboratoire de Biologie Moléculaire et Cellulaire du Cancer, Fondation de Recherche Cancer et Sang, Hôpital Kirchberg, 9 Rue Edward Steichen, 2540 Luxembourg, Luxembourg a r t i c l e i n f o a b s t r a c t

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Four new hemiterpenoid derivatives from Taxillus chinensis

Bo Ding a,b,1, Yi Dai a,b,1, Yun-Long Hou c, Xiao-Meng Wu a,b, Xue Chen c, Xin-Sheng Yao a,b,d,⁎ a Institute of Traditional Chinese Medicine & Natural Products, College of Pharmacy, Jinan University, Guangzhou 510632, PR China b Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drugs Research, Guangzhou 510632, PR China c State-Province Key Laboratory of Biomedicine-Pharmaceutics of China, Department of Pharmacology, Harbin Medical University, Harbin 150086, PR China

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New sesquiterpenes and phenolic compound from Ficus foveolata

Pathom Somwong a, Rutt Suttisri a,⁎, Anumart Buakeaw b a Department of Pharmacognosy and Pharmaceutical Botany, Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok 10330, Thailand b Institute of Biotechnology and Genetic Engineering, Chulalongkorn University, Bangkok 10330, Thailand a r t i c l e i n f o a b s t r a c t Article history: Received 21 November 2012 Accepted in revised form 17 December 2012 Available online 27 December 2012 Two new eudesmane-type sesquiterpenes, named foveolide A (1) and foveoeudesmenone (2),

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Bioactive carbazole alkaloids from Murraya koenigii (L.) Spreng

Qinge Ma, Jin Tian, Jianbo Yang, Aiguo Wang, Tengfei Ji, Yangai Wang, Yalun Su ⁎ State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China a r t i c l e i n f o a b s t r a c t Article history: Received 17 December 2012 Accepted in revised form 27 February 2013 Available online 14 March 2013 Four new carbazole alkaloids (1–4) and fourteen known carbazole alkaloids (5–18) were

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A new hepatotoxic triterpenoid ketone from Curculigo orchioides

Wei Jiao a,⁎, Xiaozhen Chen a, Haibo Wang a, Runhua Lu b, Huawu Shao a,⁎ a Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610041, China b Department of Applied Chemistry, College of Sciences, China Agricultural University, Beijing 100094, China a r t i c l e i n f o a b s t r a c t Article history: Received 27 July 2012 Accepted in revised form 24 October 2012 Available online 2 November 2012 To investigate hepatotoxic constituents, a new cycloartane-type triterpenoid ketone together

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Structural characterization and radioprotection of bone marrow hematopoiesis of two novel polysaccharides from the root of Angelica sinensis (Oliv.) Diels

Lu Zhao a,b,c,1, Yin Wang c,1, Han-lin Shen b, Xu-dong Shen c, Yan Nie a, Ying Wang a, Ting Han a, Ming Yin b, Qiao-yan Zhang a,⁎ a School of Pharmacy, Second Military Medical University, Shanghai, 200433, China b School of Pharmacy, Shanghai Jiaotong University, Shanghai, 200240, China c People's Liberation Army (PLA) 455 Hospital, Shanghai, 200050, China a r t i c l e i n f o a b s t r a c t Article history: Received 1 May 2012 Accepted in revised form 18 September 2012 Available online 12 October 2012 Two novel homogeneous polysaccharides, APS-1a and APS-3a were successfully isolated from

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