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1 . periforoside¢ñ
ÏàËÆ¶È:59.4%
Chinese Pharmaceutical Journal 2011 46 823-826
Study on Chemical Constituents of Periploca forrestii Schlecht.
XU Ran,ZHANG Yuan-hu,ZHAO Yan-tao
Structure 13C NMR ̼Æ×Ä£Äâͼ
2 . (16¦Á,20R,24S)-2,16,20,25-tetrahydroxy-24-methoxycucurbita-1,5-diene-3,11,22-trione 2-O-¦Â-D-glucopyranoside
37H56O13 ÏàËÆ¶È:59.4%
Journal of Natural Products 2011 74 2431-2437
Cucurbitane Glucosides from the Root of Machilus yaoshansis
Maoluo Gan, Mingtao Liu, Bo Liu, Sheng Lin, Yanling Zhang, Jiachen Zi, Weixia Song, Fei Ye, Xiaoguang Chen, and Jiangong Shi
Structure 13C NMR ̼Æ×Ä£Äâͼ
3 . 2¦Á,19¦Á-dihydroxy-3-oxo-olean-12-en-oic acid 28-¦Â-D-glucopyranoside
C36H56O10 ÏàËÆ¶È:59.4%
Indian Journal of Chemistry Section B 2001 40B 354-356
New constituent from the roots of Terminalia arjuna: antifungal agent
B K Chouksey, S K Srivastava
Structure 13C NMR ̼Æ×Ä£Äâͼ
4 . Isoarvenin III
C36H54O12 ÏàËÆ¶È:59.4%
Journal of Asian Natural Products Research 2012 14 528-532
Chemical constituents from the fruits of Trichosanthes kirilowii
Xue-Mei Fan, Gang Chen, Yi Sha, Xuan Lu, Ming-Xi Shen, Hong-Mei Ma & Yue-Hu Pei
Structure 13C NMR ̼Æ×Ä£Äâͼ
5 . sigmoiside F
C36H60O8 ÏàËÆ¶È:56.7%
Zeitschrift f¨¹r Naturforschung B 2008 63b 101-104
Sigmoiside F and Propyloxyamyrin, Two New Triterpenoid Derivatives from Erythrina sigmoidea (Fabaceae)
Jacques Kouam, Alain L. Meli, Muhammad I. Choudhary, and Zacharias T. Fomum
Structure 13C NMR ̼Æ×Ä£Äâͼ
6 . 9¦Â,25-cyclo 3¦Â-O-(¦Â-D-glucopyranosyl)echynocystic acid
C36H56O9 ÏàËÆ¶È:56.7%
Journal of Ethnopharmacology 2011 135 78-87
Chemical constituents from the stem bark of Symplocos paniculata Thunb. with antimicrobial, analgesic and anti-inflammatory activities
Ruchi Badoni Semwal, Deepak Kumar Semwal, Ravindra Semwal, Randhir Singh, Mohan Singh Maniyari Rawat
Structure 13C NMR ̼Æ×Ä£Äâͼ
7 . cucurbitacin B
C30H42O6 ÏàËÆ¶È:56.7%
Shoyakugaku Zasshi 1993 47 334-337
Isolation and Identification of Cytotoxic Principles from Chrysosplenium japonicum MAXIM. (Saxifragaceae)
ARISAWA MUNEHISA, TAKESHIMA YUMIKO, BAI HUA, HAYASHI TOSHIMITSU
Structure 13C NMR ̼Æ×Ä£Äâͼ
8 . (20R,22R)-6¦Â,14¦Á-dihydroxy-2,3:20,22-bis(isopropylidenedioxy)-5¦Á-cholesta-7,25-diene
ÏàËÆ¶È:55%
Russian Journal of Organic Chemistry 2005 41 1296-1305
Stereochemistry of Hydride Reduction of 20-Hydroxyecdysone Derivatives
V. N. Odinokov, R. G. Savchenko, R. V. Shafikov, S. R. Afon'kina and L. M. Khalilov, et al.
Structure 13C NMR ̼Æ×Ä£Äâͼ
9 . 24-hydroxyolean-12-en-3¦Â-yl-¦Â-D-glucopyranoside
C36H60O7 ÏàËÆ¶È:54.0%
Chemical & Pharmaceutical Bulletin 2010 58 1093-1095
Two New Aristolochic Acid Derivatives from the Roots of Aristolochia fangchi and Their Cytotoxicities
Yu Cai and Tian-Ge Cai
Structure 13C NMR ̼Æ×Ä£Äâͼ
10 . (16¦Á,20R,24S)-16,24-epoxy-2,20,25-trihydroxycucurbita-1,5-diene-3,11,22-trione 2-O-¦Â-D-glucopyranoside
C36H52O12 ÏàËÆ¶È:54.0%
Journal of Natural Products 2011 74 2431-2437
Cucurbitane Glucosides from the Root of Machilus yaoshansis
Maoluo Gan, Mingtao Liu, Bo Liu, Sheng Lin, Yanling Zhang, Jiachen Zi, Weixia Song, Fei Ye, Xiaoguang Chen, and Jiangong Shi
Structure 13C NMR ̼Æ×Ä£Äâͼ
11 . (16¦Á,20R,24R)-24N,25-carbamoyloxy-2,16,20-trihydroxycucurbita-1,5-diene-3,11,22-trione 2-O-¦Â-D-glucopyranoside
C37H53NO13 ÏàËÆ¶È:54.0%
Journal of Natural Products 2011 74 2431-2437
Cucurbitane Glucosides from the Root of Machilus yaoshansis
Maoluo Gan, Mingtao Liu, Bo Liu, Sheng Lin, Yanling Zhang, Jiachen Zi, Weixia Song, Fei Ye, Xiaoguang Chen, and Jiangong Shi
Structure 13C NMR ̼Æ×Ä£Äâͼ
12 . (24R)-3¦Â,7¦Â,24,25,30-Pentahydroxy-1-ene-cycloartane24-O-¦Â-D-glucopyranoside
C36H60O10 ÏàËÆ¶È:54.0%
Natural Product Communications 2010 5 1557 - 1560
New Triterpene Glycosides from Camptosorus sibiricus
Ning Li*, Wan Xiao, Bailing Hou and Xian Li
Structure 13C NMR ̼Æ×Ä£Äâͼ
13 . 2,22-dideoxyecdysone 25-O-¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside
C39H64O14 ÏàËÆ¶È:53.8%
Phytochemistry 2009 70 430-436
Ecdysteroids and a sucrose phenylpropanoid ester from Froelichia floridana
Ping Wang, Shiyou Li, Stacy Ownby, Zhizhen Zhang, Wei Yuan, Wanli Zhang, R. Scott Beasley
Structure 13C NMR ̼Æ×Ä£Äâͼ
14 . Machiluside B
ÏàËÆ¶È:52.3%
Organic Letters 2011 Vol.13,No.11 2856-2859
Machilusides A and B: Structurally Unprecedented Homocucurbitane Glycosides from the Stem Bark of Machilus yaoshansis
Mingtao Liu, Maoluo Gan, Sheng Lin, Yanling Zhang, Jiachen Zi,Weixia Song,Xiaona Fan, Ying Liu, Yongchun Yang, and Jiangong Shi
Structure 13C NMR ̼Æ×Ä£Äâͼ
15 . 2¦Á, 19¦Á-dihydroxy-3-oxo-12-en-28-oic acid-28-oic acid-O-¦Á -L-rhamno-pyranosyl-(1¡ú4)-¦Â-D-glucopyranoside
ÏàËÆ¶È:52.3%
Indian Journal of Chemistry Section B 2004 43B 2731-2733
New biologically active constituents from Terminalia chebula stem bark
S K Srivastava* & S D Srivastava
Structure 13C NMR ̼Æ×Ä£Äâͼ
16 . Sitosterol-3-O-¦Â-glucoside
ÏàËÆ¶È:51.3%
Chemistry of Natural Compounds 2007 43 614-615
FLAVONOIDS FROM Trifolium resupinatum VAR. microcephalum
Emel Isik, Temine Sabudak, and Sevi Oksuz
Structure 13C NMR ̼Æ×Ä£Äâͼ
17 . prosapogenin
C36H58O8 ÏàËÆ¶È:51.3%
Journal of Asian Natural Products Research 2001 3 213-217
Eclalbatin, a Triterpene Saponin from Eclipta Alba
R. K. UPADHYAY, M. B. PANDEY, R. N. JHA and V. B. PANDEY
Structure 13C NMR ̼Æ×Ä£Äâͼ
18 . momorcharaside B
C36H60O9 ÏàËÆ¶È:51.3%
Acta Pharmaceutica Sinica 1990 Vol 25 898-903
STUDIES ON THE ACTIVE CONSTITUENTS OF MOMORDICA CHARANTIA L.
ZJ Zhu; ZC Zhong; ZY Luo and ZY Xiao
Structure 13C NMR ̼Æ×Ä£Äâͼ
19 . Brainesteroside D
C33H53O10 ÏàËÆ¶È:51.3%
Phytochemistry 2010 71 975-981
Phytoecdysteroids from the rhizomes of Brainea insignis
Ping Wu, Haihui Xie, Wenqin Tao, Shenyu Miao, Xiaoyi Wei
Structure 13C NMR ̼Æ×Ä£Äâͼ
20 . Mogroside I E1
C36H62O9 ÏàËÆ¶È:51.3%
Chinese Journal of Natural Medicines 2010 8 21-24
Chemical Constituents from the Stems and Leaves of Elaeocarpus glabripetalus
ZHANG Sheng; TAO Zheng-Ming; ZHANG Yi; SHEN Zheng-Wu; QIN Guo-Wei
Structure 13C NMR ̼Æ×Ä£Äâͼ
21 . È˲ÎÔíÜÕ Rh1
ÏàËÆ¶È:51.3%
Journal of Shenyang Pharmaceutical University 1992 9 103-105
STUDIES ON THE ANTIARRHYTHMIC CONSTITUENTS FROM THE RHIZOMES OF PANAX GINSENG C.A.MEYER
Zhang Yonghe Lin Jingnan Pei Yuping Chen Yingjie Liu Chongming Xu Shuixu Yao Xinsheng
Structure 13C NMR ̼Æ×Ä£Äâͼ
22 . Cycloccidentaliside I
ÏàËÆ¶È:51.3%
Planta Medica 2012 78 821-827
Li, Shi-Fei; Di, Ying-Tong; Luo, Rong-Hua; Zheng, Yong-Tang; Wang, Yue-Hu; Fang, Xin; Zhang, Yu; Li, Ling; He, Hong-Ping; Li, Shun-Lin; Hao, Xiao-Jiang:
Cycloartane Triterpenoids from Cassia occidentalis
Structure 13C NMR ̼Æ×Ä£Äâͼ
23 . periplocin
ÏàËÆ¶È:51.3%
Natural Product Research and Development 2006 18 772-774
Studies on Chemical Constituents of Periploca omeiensis
ZHANG Yuan-hu; CHEN Dong-lin; WANG Feng-peng
Structure 13C NMR ̼Æ×Ä£Äâͼ
24 . (3S,28S)3-O-acetyl-28-[3-azepan-prop-1-yn-1-yl]lup-20(29)-en-3,28-diol hydrochloride
C41H66NO3Cl ÏàËÆ¶È:51.3%
Bioorganic & Medicinal Chemistry 2013 21 425-435
Cytotoxic betulin-derived hydroxypropargylamines trigger apoptosis
Ren¨¦ Csuk, Ronny Sczepek, Bianka Siewert, Christoph Nitsche
Structure 13C NMR ̼Æ×Ä£Äâͼ
25 . neomacroin
C32H48O6 ÏàËÆ¶È:51.3%
Phytochemistry 2014 102 189-196
Cycloartane triterpenes from the leaves of Neoboutonia macrocalyx L. Original Research Article
Jane Namukobe, Bernard T. Kiremire, Robert Byamukama, John M. Kasenene, Vincent Dumontet, Françoise Gu¨¦ritte, Sabrina Krief, Isabelle Florent, John D. Kabasa
Structure 13C NMR ̼Æ×Ä£Äâͼ
26 . including periplocin
ÏàËÆ¶È:51.3%
China Pharmacy 2010 21 4463-4465
Study on Chemical Constituents of Periploca calophylla
TAN Xiao-hong, ZHANG Yuan-hu, ZHOU Lan, TAN Ming-chun, SUN Qian-yun, HAO Xiao-jiang
Structure 13C NMR ̼Æ×Ä£Äâͼ
27 . periplocin
ÏàËÆ¶È:51.3%
China Pharmaceuticals 2009 18 24-26
Study on Chemical Constituents of Periploca Omeiensis
Wu Bin
Structure 13C NMR ̼Æ×Ä£Äâͼ
28 . 3¦Â-(¦Â-D-glucosyloxy)-16¦Á,23¦Á-epoxycucurbita-5,24-diene-11-one
ÏàËÆ¶È:51.3%
Zeitschrift f¨¹r Naturforschung C 2000 55 141-145
A New Cucurbitacin Glycoside from Kageneckia oblonga (Rosaceae)
O. Munñoz, C. Delporte, N. Backhouse, S. Erazo, R. Negrete, S. Maldonado, J. L. L¨®pez-P¨¦rez, and A. S. Feliciano
Structure 13C NMR ̼Æ×Ä£Äâͼ
29 . cauloside C
C41H66O13 ÏàËÆ¶È:51.2%
Journal of Agricultural and Food Chemistry 2001 49 5969-5974
Characterization of the Triterpene Saponins of the Roots and Rhizomes of Blue Cohosh (Caulophyllum Thalictroides)
Jin-Woo Jhoo, Shengmin Sang, Kan He, Xiaofang Cheng, Nanqun Zhu, Ruth E. Stark, Qun Yi Zheng, Robert T. Rosen, and Chi-Tang Ho
Structure 13C NMR ̼Æ×Ä£Äâͼ
30 . daphcalycinosidine C
C38H49NO12 ÏàËÆ¶È:50%
Journal of Natural Products 2004 67 1094-1099
New Alkaloids from Daphniphyllum calycinum
Hoda El Bitar, Van Hung Nguyen, Anthony Gramain, Thierry Svenet, and Bernard Bodo
Structure 13C NMR ̼Æ×Ä£Äâͼ
31 . picfeltarraenin IB
C42H64O14 ÏàËÆ¶È:50%
Journal of Natural Products 1998 61 757-761
Complement-Inhibiting Cucurbitacin Glycosides from Picria fel-terrae
Ying Huang, Tess De Bruyne, Sandra Apers, Yuliang Ma, Magda Claeys, Dirk Vanden Berghe, Luc Pieters, and Arnold Vlietinck
Structure 13C NMR ̼Æ×Ä£Äâͼ
32 . Machiluside A
C42H62O17 ÏàËÆ¶È:50%
Organic Letters 2011 Vol.13,No.11 2856-2859
Machilusides A and B: Structurally Unprecedented Homocucurbitane Glycosides from the Stem Bark of Machilus yaoshansis
Mingtao Liu, Maoluo Gan, Sheng Lin, Yanling Zhang, Jiachen Zi,Weixia Song,Xiaona Fan, Ying Liu, Yongchun Yang, and Jiangong Shi
Structure 13C NMR ̼Æ×Ä£Äâͼ |
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