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1 . swertisin
C22H22O10 ÏàËƶÈ:96.9%
Molecules 2012 17 7914-7926
Variable-Temperature 1H-NMR Studies on Two C-Glycosylflavones
Julia H. Frank, Yomica L. Powder-George, Russel S. Ramsewak and William F. Reynolds
Structure 13C NMR ̼Æ×Ä£Äâͼ
2 . apigenin-6-C-¦Â-D-glucoside-7-O-methyl ether
ÏàËƶÈ:87.8%
Natural Product Communications 2006 1 457-459
Flavonoid C-glycosides from Pterocephalus sanctus Growingin Egypt
Fahem A. Ahmed and Abdelaaty A. Shahat
Structure 13C NMR ̼Æ×Ä£Äâͼ
3 . luteolin-6-C-¦Â-D-glucoside-7-O-methyl ether
ÏàËƶÈ:84.8%
Natural Product Communications 2006 1 457-459
Flavonoid C-glycosides from Pterocephalus sanctus Growingin Egypt
Fahem A. Ahmed and Abdelaaty A. Shahat
Structure 13C NMR ̼Æ×Ä£Äâͼ
4 . 4'-O-(E)-sinapoyl-7-methoxyisovitexin-2''-O-¦Â-D-glucopyranoside
ÏàËƶÈ:67.6%
Phytochemistry 2010 71 581-589
Metabolic responses of Thellungiella halophila/salsuginea to biotic and abiotic stresses: Metabolite profiles and quantitative analyses
M. Soledade C. Pedras, Qing-An Zheng
Structure 13C NMR ̼Æ×Ä£Äâͼ
5 . 4'-O-(E)-sinapoyl-7-methoxyisovitexin-2''-O-¦Â-D-glucopyranoside
ÏàËƶÈ:67.6%
Phytochemistry 2010 71 581-589
Metabolic responses of Thellungiella halophila/salsuginea to biotic and abiotic stresses: Metabolite profiles and quantitative analyses
M. Soledade C. Pedras, Qing-An Zheng
Structure 13C NMR ̼Æ×Ä£Äâͼ
6 . apigenin-7-O-¦Â-apiofuranosyl-6, 8-di-C-¦Â-glucopyranoside
C32H38O19 ÏàËƶÈ:66.6%
Phytochemistry 2003 449-452
Flavone C-glycosides from Lupinus hartwegii
Mohamed S. Kamel
Structure 13C NMR ̼Æ×Ä£Äâͼ
7 . 6-C-[¦Á-L-arabinopyranosyl-(1¡ú2)-¦Â-D-glucopyranosyl]-7-O-[¦Â-D-glucopyranosyl]-luteolin 3'-methyl ether
C33H40O20 ÏàËƶÈ:66.6%
Natural Product Communications 2011 6 205-208
Secondary Metabolites from the Roots of Paronychia chionaea
Sibel Avunduk, Özgen Alankuş-Çalişkan, Tomofumi Miyamoto, Chiaki Tanaka and Marie-Aleth Lacaille-Dubois
Structure 13C NMR ̼Æ×Ä£Äâͼ
8 . apigenin 6-C-neohesperidoside
ÏàËƶÈ:66.6%
Phytochemistry Letters 2012 5 427-431
Flavonoids from Mimosa xanthocentra (Leguminosae: Mimosoideae) and molecular modeling studies for isovitexin-2¡å-O-¦Á-l-rhamnopyranoside rotamers
Luiza Maria de Magalhães Camargo, Jean-Pierre F¨¦r¨¦zou, Luzineide Wanderley Tinoco, Carlos Roland Kaiser, Sônia Soares Costa
Structure 13C NMR ̼Æ×Ä£Äâͼ
9 . 6'''-feruloylspinosin
C38H40O18 ÏàËƶÈ:63.8%
Tetrahedron 2000 56 8915-8920
Flavonoids from Ziziphus jujuba Mill var. spinosa
Gong Cheng, Yanjing Bai, Yuying Zhao, Jing Tao, Yi Liu, Guangzhong Tu, Libin Ma, Ning Liao, Xiaojie Xu
Structure 13C NMR ̼Æ×Ä£Äâͼ
10 . 6'''-feruloylspinosin
ÏàËƶÈ:63.8%
Korean Journal of Pharmacognosy 2012 43 127-136
Flavonoids from the Seeds of Zizyphus jujuba var. spinosa
Lee, So-Young; Lee, Joo-Young; Kim, Ju-Sun; Lee, Je-Hyun; Kang, Sam-Sik
Structure 13C NMR ̼Æ×Ä£Äâͼ
11 . isovitexin 2''-O-(6'''-(E)-p-coumaroyl)glucoside
C36H36O17 ÏàËƶÈ:63.6%
Phytochemistry 2001 58 167-172
Acylated flavone C-glycosides from Cucumis sativus
Mamdouh M. Abou-Zaid, Domenic A. Lombardo, Geoffrey C. Kite,Ren¨¦e J. Grayerb, Nigel C. Veitch
Structure 13C NMR ̼Æ×Ä£Äâͼ
12 . embinoidin
ÏàËƶÈ:63.6%
Phytochemistry Letters 2010 3 88-92
Isolation and structure elucidation of flavonoid glycosides from Solanum verbascifolium
Takashi Ohtsuki, Takashi Miyagawa, Takashi Koyano, Thaworn Kowithayakorn, Masami Ishibashi
Structure 13C NMR ̼Æ×Ä£Äâͼ
13 . swertisin 2''-O-rhamnoside-4''-O-glucoside
C34H42O19 ÏàËƶÈ:63.6%
Phytochemistry 1999 51 1395-1399
Novel pigments and copigmentation in the blue marguerite daisy
Stephen J. Bloor
Structure 13C NMR ̼Æ×Ä£Äâͼ
14 . vaccarin(Íõ²»ÁôÐлÆͪÜÕ)
C32H38O19 ÏàËƶÈ:63.6%
Chinese Traditional and Herbal Drugs 2011 42(5) 874-876
Isolation and identification of vaccarin from Vaccariae Semen
MENG He, CHEN Yu-ping, QIN Wen-jie, YE Zu-guang
Structure 13C NMR ̼Æ×Ä£Äâͼ
15 . 2"-O-Glucosyl-isovitexin-7-O-galactosid
ÏàËƶÈ:63.6%
Phytochemistry 1979 18 907-910
Neue flavon-C-O-glykoside aus Melandrium album
Hildebert Wagner, G¨¹nther Obermeier, Otto Seligmann, Vedantha Mohan Chari
Structure 13C NMR ̼Æ×Ä£Äâͼ
16 . 6'''-feruloylspinosin
C38H40O18 ÏàËƶÈ:63.6%
Phytochemistry 1980 19 2791-2793
Acylated flavone-C-glycosides from the seeds of Zizyphus jujuba
Won Sick Woo, Sam Sik Kang, Hildebert Wagner, Otto Seligmann, V.M. Chari
Structure 13C NMR ̼Æ×Ä£Äâͼ
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1 . 6-acetyl-1-[1,3-(4,4'-dihydroxy-3,3'-dimethoxy-¦Â-truxinyl)-¦Â-D-fructofuranosyl]-¦Á-D-glucopyranoside
C34H40O18 ÏàËƶÈ:79.4%
Journal of Asian Natural Products Research 2008 10 299-302
A new lignan glycoside from the rhizomes of Imperata cylindrica
Dae-Young Lee, Kyung-Min Han, Myoung-Chong Song, Do-Gyeong Lee,Yeong-Deok Rho and Nam-in Baek
Structure 13C NMR ̼Æ×Ä£Äâͼ
2 . matairesinol 4'-O-¦Â-D-apiofuranosyl(1¡ú2)-¦Â-D-glucopyranoside
C31H40O15 ÏàËƶÈ:62.5%
Chemical & Pharmaceutical Bulletin 1998 46 1044-1047
New Steroid and Matairesinol Glycosides from Safflower (Carthamus tinctorius L.) Oil Cake
Akito NAGATSU,Hui Li ZHANG,Toshihiro WATANABE,Nari TANIGUCHI,Keiichiro HATANO,Hajime MIZUKAMI and Jinsaku SAKAKIBARA
Structure 13C NMR ̼Æ×Ä£Äâͼ
3 . trigonotin C
C33H38O18 ÏàËƶÈ:60.6%
Journal of Natural Products 2008 71(7) 1178-1181
Identification of Sucrose Diesters of Aryldihydronaphthalene-Type Lignans from Trigonotis peduncularis and the Nature of Their Fluorescence
Hideaki Otsuka, Hidenori Kuwabara, and Hiromi Hoshiyama
Structure 13C NMR ̼Æ×Ä£Äâͼ
4 . viscumneoside
ÏàËƶÈ:58.8%
Acta Pharmaceutica Sinica 1990 Vol 25 608-611
STUDIES ON THE CHEMICAL COMPONENTS OF VISCUMCOLORATUM ¢÷. ISOLATION AND STRUCTURE OF VISCUMNEOSIDE ¢÷
DY Kong; HT Li and SQ Luo
Structure 13C NMR ̼Æ×Ä£Äâͼ
5 . trigonotin A
C35H40O19 ÏàËƶÈ:57.1%
Journal of Natural Products 2008 71(7) 1178-1181
Identification of Sucrose Diesters of Aryldihydronaphthalene-Type Lignans from Trigonotis peduncularis and the Nature of Their Fluorescence
Hideaki Otsuka, Hidenori Kuwabara, and Hiromi Hoshiyama
Structure 13C NMR ̼Æ×Ä£Äâͼ
6 . rupestrin C
C35H40O19 ÏàËƶÈ:57.1%
Journal of Natural Products 2006 69(4) 682-684
Lignan Oligosaccharide Esters from Eritrichium rupestre
Mao-Rong Suo, Jun-Shan Yang, and Qing-Hua Liu
Structure 13C NMR ̼Æ×Ä£Äâͼ
7 . compounds 18
C34H42O13 ÏàËƶÈ:56.2%
Phytochemistry 2004 65 2003-2011
Constituents from the bark of Tabebuia impetiginosa
Tsutomu Warashina, Yoshimi Nagatani, Tadataka Noro
Structure 13C NMR ̼Æ×Ä£Äâͼ
8 . rupestrin B
C32H36O17 ÏàËƶÈ:56.2%
Journal of Natural Products 2006 69(4) 682-684
Lignan Oligosaccharide Esters from Eritrichium rupestre
Mao-Rong Suo, Jun-Shan Yang, and Qing-Hua Liu
Structure 13C NMR ̼Æ×Ä£Äâͼ
9 . glehlinoside D
C34H40O15 ÏàËƶÈ:55.8%
Acta Pharmaceutica Sinica 2008 Vol 43 1036-1039
A new 8-O-4' neolignan from Glehnia littoralis
WANG Li-li; KONG Wei-xue; YUAN Zhong
Structure 13C NMR ̼Æ×Ä£Äâͼ
10 . salsaside E
C32H40O16 ÏàËƶÈ:53.1%
Helvetica Chimica Acta 2007 Vol. 90 79
New Glycosides from Cistanche salsa
Li Lei, Yong Jiang, Xiao-Ming Liu, Peng-Fei Tu, Li-Jun Wu, and Fa-Kui Chen
Structure 13C NMR ̼Æ×Ä£Äâͼ
11 . agastinol
C27H28O8 ÏàËƶÈ:53.1%
Journal of Natural Products 2002 65 414-416
Agastinol and Agastenol, Novel Lignans from Agastache rugosa and Their Evaluation in an Apoptosis Inhibition Assay
Choonghwan Lee, Hyuna Kim, and Yunghee Kho
Structure 13C NMR ̼Æ×Ä£Äâͼ
12 . agastenol
C27H26O8 ÏàËƶÈ:53.1%
Journal of Natural Products 2002 65 414-416
Agastinol and Agastenol, Novel Lignans from Agastache rugosa and Their Evaluation in an Apoptosis Inhibition Assay
Choonghwan Lee, Hyuna Kim, and Yunghee Kho
Structure 13C NMR ̼Æ×Ä£Äâͼ
13 . 9'-methoxyl rutarensin
C32H32O16 ÏàËƶÈ:53.1%
Journal of Asian Natural Products Research 2007 9 59-65
Bioactive coumarins from Boenninghausenia sessilicarpa
Q.-Y. YANG, X.-Y. TIAN and W.-S. FANG
Structure 13C NMR ̼Æ×Ä£Äâͼ
14 . luteolin-7-O-(6''-trans-feruloyl)-¦Â-D-glucopyranoside
ÏàËƶÈ:53.1%
Journal of China Pharmaceutical University 2010 41 120-123
Chemical constituents from the leaves of Callicarpa nudiflora
GAO Fei-peng; WANG Hao; YE Wen-cai; ZHAO Shou-xun
Structure 13C NMR ̼Æ×Ä£Äâͼ
15 . matairesinol-4'-O-¦Â-gentiobioside
C32H42O16 ÏàËƶÈ:53.1%
China Journal of Chinese Materia Medica 2012 37 1581-1585
Trace chemical constituents contained in Trachelospermum jasminoides and structure identification
JING Ling; YU Nengjiang; ZHAO Yimin; LI Yushan
Structure 13C NMR ̼Æ×Ä£Äâͼ
16 . glehlinoside A
C34H43O14 ÏàËƶÈ:52.9%
Chemical & Pharmaceutical Bulletin 2002 50 73-77
Constituents of the Underground Parts of Glehnia littoralis
Zhong Yuan, Yasuhiro Tezuka, Wenzhe Fan, Shigetoshi Kadota and Xian Li
Structure 13C NMR ̼Æ×Ä£Äâͼ
17 . Vanilloylicariside E5
C34H40O14 ÏàËƶÈ:52.9%
Archives of Pharmacal Research 2009 32 1345-1349
Lignans from the fruits of the red pepper (Capsicum annuum L.) and their antioxidant effects
Dae-Young Lee, Do-Gyeong Lee, Jin-Gyeong Cho, Myun-Ho Bang and Ha-Na Lyu, et al.
Structure 13C NMR ̼Æ×Ä£Äâͼ
18 . serratumoside A
C36H48O19 ÏàËƶÈ:52.7%
Chinese Chemical Letters 2000 11 323-326
A New Phenylpropanoid Glycoside: Serratumoside A from Clerodendrum serratum
Hui YANG, Ai Jun HOU, Shuang Xi MEI, Li Yan PENG, Han Dong SUN
Structure 13C NMR ̼Æ×Ä£Äâͼ
19 . fraxisecoside
C33H40O20 ÏàËƶÈ:51.5%
Journal of Asian Natural Products Research 2008 10 205-210
Water-soluble constituents of the root barks of Fraxinus rhynchophylla (Chinese drug Qinpi)
KAI XIAO, QING-HONG SONG, SHU-WEI ZHANG and LI-JIANG XUAN
Structure 13C NMR ̼Æ×Ä£Äâͼ
20 . arctigenin-4'-O-¦Â-gentiobioside
ÏàËƶÈ:51.5%
China Journal of Chinese Materia Medica 2012 37 1581-1585
Trace chemical constituents contained in Trachelospermum jasminoides and structure identification
JING Ling; YU Nengjiang; ZHAO Yimin; LI Yushan
Structure 13C NMR ̼Æ×Ä£Äâͼ
21 . glehlinoside F
C35H42O14 ÏàËƶÈ:51.4%
Chinese Chemical Letters 2008 19 1459-1461
New lignan glycosides from Glehnia littoralis
Wei Xue Kong, Zhong Yuan
Structure 13C NMR ̼Æ×Ä£Äâͼ
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1 . ginsenoside Rh1
ÏàËƶÈ:75%
Chinese Traditional and Herbal Drugs 1996 27 647-649
Isolation and Identification of Ginsenoside from the Leaves of Wild Ginseng(Panax ginseng)
Li Jing; Wei Yongdi(Berhune Medical University; Changchun);
Structure 13C NMR ̼Æ×Ä£Äâͼ
2 . 1¦Â,2¦Á,3¦Â,20(R)-Tetrahydroxydammar-24-ene 3-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside
C42H72O13 ÏàËƶÈ:72.7%
Planta Medica 2009 75 541-543
Dammarane-Type Triterpene Glycosides from Oncoba manii Active against Methicillin-Resistant Staphylococcus aureus
Eliane Garo, Chia S. Hung, Russell B.Williams, Krista M. Olson,Jin-Feng Hu, Stephanie M. Rice, Grayson W. Hough,Matt G. Goering, Mark O'Neil-Johnson, Gary R. Eldridge,Courtney M. Starks
Structure 13C NMR ̼Æ×Ä£Äâͼ
3 . ginsenoside Rh
ÏàËƶÈ:72.2%
Planta Medica 1982 44 146-149
Degradation of Ginseng Saponins under Mild Acidic Conditions
B. H. Han, M. H. Park, Y. N. Han, L. K. Woo, U. Sankawa, S. Yahara and 0. Tanaka
Structure 13C NMR ̼Æ×Ä£Äâͼ
4 . ginsenoside-Rh1
ÏàËƶÈ:72.2%
Chemical & Pharmaceutical Bulletin 1979 27 88-92
Further Study on Dammarane-Type Saponins of Roots, Leaves, Flower-Buds, and Fruits of Panax ginseng C. A. MEYER
SHOJI YAHARA,KIYOKO KAJI and OSAMU TANAKA
Structure 13C NMR ̼Æ×Ä£Äâͼ
5 . 20(S)-È˲ÎÔíÜÕ-Rh1
ÏàËƶÈ:72.2%
Chinese Traditional and Herbal Drugs 2009 40 1204-1207
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Structure 13C NMR ̼Æ×Ä£Äâͼ
6 . 20(s)-È˲ÎÔíÜÕ-Rh1
ÏàËƶÈ:72.2%
Chinese Pharmaceutical Journal 2000 35 82-84
Isolation and identification of 20(s)-Ginsenoside Rh_1, Rh_2 and Ginsenoside Rh_3 from the leaves of Panax quinquefolium
Cong Dengli (Cong DL), Song Changchun (Song CC), Xu Jingda (Xu JD)
Structure 13C NMR ̼Æ×Ä£Äâͼ
7 . 20(S)-Rh1
ÏàËƶÈ:72.2%
Chinese Journal of Medicinal Chemistry 1992 2(2) 31-35
STUDIES ON THE CHEMICAL CONSTITUENTS OF FLOWER-BUDS OF PANAX GINSENG C A MEYER
Wang Hongyan Pei Yuping Chen Yingjie
Structure 13C NMR ̼Æ×Ä£Äâͼ
8 . ginsenoside Rh1
ÏàËƶÈ:69.4%
Chinese Chemical Letters 2001 12 59-62
A Novel Hexanordammarane Glycoside from the Roots of Panax notoginseng
Hai Zhou LI, Rong Wei TENG, Chong Ren YANG
Structure 13C NMR ̼Æ×Ä£Äâͼ
9 . notoginsenoside R9
C36H622O10 ÏàËƶÈ:69.4%
Phytochemistry 1996 41 1419-1422
Minor dammarane saponins from Panax notoginseng
Ping Zhao, Yu-Qing Liu, Chong-Ren Yang
Structure 13C NMR ̼Æ×Ä£Äâͼ
10 . ginsenoside Rh1
ÏàËƶÈ:69.4%
Phytochemistry 1996 41 1419-1422
Minor dammarane saponins from Panax notoginseng
Ping Zhao, Yu-Qing Liu, Chong-Ren Yang
Structure 13C NMR ̼Æ×Ä£Äâͼ
11 . ginsenoside Rh1
ÏàËƶÈ:69.4%
Journal of Natural Medicines 2006 60 135-137
New dammarane-type saponin from roots of Panax notoginseng
Nozomi Komakine, Mamoru Okasaka, Yoshihisa Takaishi, Kazuyoshi Kawazoe and Kotaro Murakami, et al.
Structure 13C NMR ̼Æ×Ä£Äâͼ
12 . 20(S)-ginsenoside-Rh1
ÏàËƶÈ:69.4%
Magnetic Resonance in Chemistry 2002 40 483-488
Complete assignment of 1H and 13C NMR data for nine protopanaxatriol glycosides
Rongwei Teng, Haizhou Li, Jiangtao Chen, Dezu Wang, Yineng He and Chongren Yang
Structure 13C NMR ̼Æ×Ä£Äâͼ
13 . 20 (R)-È˲ÎÔíÜÕ-Rh1
C36H62O9 ÏàËƶÈ:69.4%
Chinese Traditional and Herbal Drugs 2009 40 1204-1207
Î÷Ñó²Î×ÜÔíÜÕÒÒËáË®½â²úÎïµÄ»¯Ñ§³É·ÖÑо¿(¢ñ)
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Structure 13C NMR ̼Æ×Ä£Äâͼ
14 . ginsenoside Rh1
ÏàËƶÈ:69.4%
Chinese Traditional and Herbal Drugs 2005 36 499-503
·¢½ÍÈýÆßÖеÄÔíÜճɷÖÑо¿
Àî¹úºì,ÉòÔÂë,ÍõÆô·½,ÕÅ¿ËÇÚ
Structure 13C NMR ̼Æ×Ä£Äâͼ
15 . 20(S)-ginsenoside Rh1
ÏàËƶÈ:69.4%
Chinese Pharmaceutical Journal 2008 43 412-415
Study on Isolation and Structural Elucidation of Ginsenosides from Transgenic Crown Gall of Panax quinquefolium
ZHU Jian-hua YU Rong-min YAN Chun-yan SONG Li-yan ZHAO Yu
Structure 13C NMR ̼Æ×Ä£Äâͼ
16 . compound III
ÏàËƶÈ:69.4%
Chinese Journal of Medicinal Chemistry 1992 2(2) 31-35
STUDIES ON THE CHEMICAL CONSTITUENTS OF FLOWER-BUDS OF PANAX GINSENG C A MEYER
Wang Hongyan Pei Yuping Chen Yingjie
Structure 13C NMR ̼Æ×Ä£Äâͼ
17 . pisumosides B
C32H52O16 ÏàËƶÈ:66.6%
Chemical & Pharmaceutical Bulletin 2001 49(1) 73-77
Medicinal Foodstuffs. XXII.1) Structures of Oleanane-Type Triterpene Oligoglycosides, Pisumsaponins I and II, and Kaurane-Type Diterpene Oligoglycosides, Pisumosides A and B, from Green Peas, the Immature Seeds of Pisum sativum L.
Toshiyuki MURAKAMI, Kentarou KOHNO, Hisashi MATSUDA, and Masayuki YOSHIKAWA
Structure 13C NMR ̼Æ×Ä£Äâͼ
18 . ginsenoside-Rh6
C36H62O11 ÏàËƶÈ:66.6%
Chemical & Pharmaceutical Bulletin 2001 49(4) 442-446
Six New Dammarane-type Triterpene Saponins from the Leaves of Panax ginseng
De-Qiang DOU,Ying-Jie CHEN,Li-Hong LIANG,Fa-Gen PANG,Noriko SHIMIZU, and Tadahiro TAKEDA
Structure 13C NMR ̼Æ×Ä£Äâͼ
19 . vina-ginsenoside-R10
C36H62O10 ÏàËƶÈ:66.6%
Chemical & Pharmaceutical Bulletin 1994 42 634-640
Saponins from Vietnamese Ginseng, Panax vietnamensis HA et GRUSHV. Collected in Central Vietnam. III
NGUYEN Minh Duc,Ryoji KASAI,Kazuhiro OHTANI,Aiko ITO,Thoi Nham NGUYEN,Kazuo YAMASAKI and Osamu TANAKA
Structure 13C NMR ̼Æ×Ä£Äâͼ
20 . lyciumoside III
C32H56O13 ÏàËƶÈ:66.6%
Chemical & Pharmaceutical Bulletin 1993 41 703-709
Cyclic Peptides, Acyclic Diterpene Glycosides and Other Compounds from Lycium chinense MILL
Shoji YAHARA,Choko SHIGEYAMA,Takeshi URA,Kaori WAKAMATSU,Tadashi YASUHARA and Toshihiro NOHARA
Structure 13C NMR ̼Æ×Ä£Äâͼ
21 . ginsenoside Rh1
ÏàËƶÈ:66.6%
Acta Pharmaceutica Sinica 1987 Vol 22 750-755
STUDIES ON THE CHEMICAL CONSTITUENTS OF PANAX QUINQUEFOLIUS LINN
XU Sui-Xu; CHEN Ying-Jie; CAI Zhong-Oin and YAO Xin-Sheng
Structure 13C NMR ̼Æ×Ä£Äâͼ
22 . Ginsenoside Rh1
ÏàËƶÈ:66.6%
Molecules 2010 15 399-406
Isolation, Synthesis and Structures of Ginsenoside Derivatives and Their Anti-Tumor Bioactivity
Mei Han, Jin-Gang Hou, Cheng-Ming Dong, Wei Li, Hao-Lun Yu, Yi-Nan Zheng and Li Chen
Structure 13C NMR ̼Æ×Ä£Äâͼ
23 . 20(R)-Rh1
ÏàËƶÈ:66.6%
Chinese Journal of Medicinal Chemistry 1992 2(2) 31-35
STUDIES ON THE CHEMICAL CONSTITUENTS OF FLOWER-BUDS OF PANAX GINSENG C A MEYER
Wang Hongyan Pei Yuping Chen Yingjie
Structure 13C NMR ̼Æ×Ä£Äâͼ
24 . È˲ÎÔíÜÕ Rh1
ÏàËƶÈ:66.6%
Journal of Shenyang Pharmaceutical University 1992 9 217-218
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
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1 . Chrysoeriol 7-glucoside
ÏàËƶÈ:84%
Journal of Chinese Pharmaceutical Sciences 2000 9 119-121
Flavone Glycosides from the Leaves of Ginkgo biloba
Tang Yuping, Zheng Weiping, Lou Fengchang, Li Yanfang and Wang Jinghua
Structure 13C NMR ̼Æ×Ä£Äâͼ
2 . chrysoeriol-7-O-¦Â-D-glucoside
C22H22O11 ÏàËƶÈ:84%
Natural Product Sciences 2006 12 89-93
Chemical Constituents of Gomphrena globosa. II
Dinda, Biswanath; Ghosh, Biplab; Achari, Basudev; Arima, Shiho; Sato, Nariko; Harigaya, Yoshihiro
Structure 13C NMR ̼Æ×Ä£Äâͼ
3 . chrysoeriol-7-O-¦Â-D-glucoside
ÏàËƶÈ:84%
China Journal of Chinese Materia Medica 2010 35 869-871
Chemical constituents from Lagotis brevituba
CHI Feng; DENG Jun; WANG Yanhan
Structure 13C NMR ̼Æ×Ä£Äâͼ
4 . ½ðÊ¥²Ý»ÆËØ-7-O-¦Â-D-ÆÏÌÑÌÇÈ©ËáÜÕ
ÏàËƶÈ:84%
Chinese Traditional and Herbal Drugs 2009 40 1715-1719
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½âЦè¤;ËÕÑÞ·¼;²ñÐÀ;ÖÜάÒå;µËС¾ê;¹ùÀöƼ;¸ßÐã÷;ÕŲ®Àñ
Structure 13C NMR ̼Æ×Ä£Äâͼ
5 . ½ðÊ¥²ÝËØ-7-O-¦Â-D-ßÁà«ÆÏÌÑÌÇÜÕ
C22H22O11 ÏàËƶÈ:84%
Chinese Traditional and Herbal Drugs 2008 39 1635-1636+1720
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Structure 13C NMR ̼Æ×Ä£Äâͼ
6 . chrysoeriol-7-O-¦Â-D-g lucoside
C22H22O11 ÏàËƶÈ:84%
Chinese Traditional and Herbal Drugs 2005 36 819-820
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Structure 13C NMR ̼Æ×Ä£Äâͼ
7 . chrysoeriol-7-O-¦Â-D-glucopyranoside
ÏàËƶÈ:84%
Chinese Journal of Natural Medicines 2005 3 86-89
Acetylenes and Flavonoids from Artemisia scoparia¢ò
XIE Tao; LIU Jing; LIANG Jing-Yu; ZHANG Zhi-Ming; WEI Xiu-Li
Structure 13C NMR ̼Æ×Ä£Äâͼ
8 . ¿ÂÒÁÀûËØ-7-O-¦Â-D-ÆÏÌÑÌÇÜÕ
ÏàËƶÈ:84%
Chinese Pharmaceutical Journal 2009 44 336-338
Study on Five Flavanoids in Barks of Quercus pannosa Hand.-Mazz.
LI Qin SHEN Yue-mao LI Ping~
Structure 13C NMR ̼Æ×Ä£Äâͼ
9 . chrysoeriol-7-O-¦Â-D-glucoside
ÏàËƶÈ:84%
Chinese Pharmaceutical Journal 2009 44 1475-1477
Studies on Flavonoids from Galium aparine
CAI Xiao-mei, YANG Juan, RAO Qiong-juan
Structure 13C NMR ̼Æ×Ä£Äâͼ
10 . chrysoeriol-7-O-glucoside
ÏàËƶÈ:84%
Journal of China Pharmaceutical University 2005 36 402-404
Chemical Constituents of Dendranthema nankingense
YANG Nian-Yun; REN Ai-Nong; HU Wan-Chun; QIAN Shi-Hui; DUAN Jin-Ao; TIAN Li-Juan
Structure 13C NMR ̼Æ×Ä£Äâͼ
11 . chrysoeriol-7-O-glucopyranoside
C22H22O11 ÏàËƶÈ:84%
Turkish Journal of Chemistry 2006 30 383-390
Secondary Metabolites from Phlomis syriaca and Their Antioxidant Activities
¨¹. ŞEBNEM HARPUT, İHSAN ÇALIŞ, İCLAL SARACOĞLU, ALİ ARSLAN DÖNMEZ, AKITO NAGATSU
Structure 13C NMR ̼Æ×Ä£Äâͼ
12 . chrysoeriol 7-O-glucoside
ÏàËƶÈ:84%
Chemistry & Biodiversity 2012 9 2096-2158
Flavonoids in Subtribe Centaureinae (Cass.) Dumort. (Tribe Cardueae, Asteraceae): Distribution and 13C-NMR Spectral Data
Carmen Formisano, Daniela Rigano, Felice Senatore, Svetlana Bancheva, Antonella Maggio, Sergio Rosselli and Maurizio Bruno
Structure 13C NMR ̼Æ×Ä£Äâͼ
13 . 5,7,4'-Trihydroxy-3'-methoxyflavone-7-O-¦Â-D-glucopyranoside
ÏàËƶÈ:84%
Phytochemistry Letters 2011 4 151-157
Phenolic constituents of the inflorescences of Sorbus torminalis (L.) Crantz
Monika A. Olszewska, Joanna Marta Roj
Structure 13C NMR ̼Æ×Ä£Äâͼ
14 . chrysoeriol-7-O-¦Â-D-glucoside
ÏàËƶÈ:84%
China Journal of Chinese Materia Medica 2012 37 1581-1585
Trace chemical constituents contained in Trachelospermum jasminoides and structure identification
JING Ling; YU Nengjiang; ZHAO Yimin; LI Yushan
Structure 13C NMR ̼Æ×Ä£Äâͼ
15 . thermopsoside
ÏàËƶÈ:80%
Chemistry of Natural Compounds 1989 25 303-308
FLAVONOIDS OF Thermopsisalterniflora. CROTONOYLTHERMOPSOSIDE AND CROTONOYLCOSMOSIIN - NEW ACYLATED FLAVONE GLYCOSIDES
M. P. Yuldashev, E. Kh. Batirov, A. D. Vdovin,V. M. Malikov, and M. R. Yagudaev
Structure 13C NMR ̼Æ×Ä£Äâͼ
16 . chrysoerin-7-O-¦Â-D-glucoside
ÏàËƶÈ:80%
China Journal of Chinese Materia Medica 2006 31 395-397
Studies on the flavones in of Chrozophora sabulosa
Shi Xinhong, LIU Youqiang, KONG Lingyi
Structure 13C NMR ̼Æ×Ä£Äâͼ
17 . O-(6''-O-Acetyl-)-¦Â-glucopyranosylchrysoeriol
C24H24O12 ÏàËƶÈ:80%
Fitoterapia 2009 80 51-53
An iridoid and a flavonoid from Sideritis lanata L.
Kalina I. Alipieva , Emanuela P. Kostadinova , Ljuba N. Evstatieva ,Marina Stefova , Vassya S. Bankova
Structure 13C NMR ̼Æ×Ä£Äâͼ
18 . chrysoeriol-7-O-¦Â-D-glucopyranoside
ÏàËƶÈ:80%
Chinese Journal of Natural Medicines 2005 3 357-358
Chemical Constituents from Lithospermum zollingeri
ZHANG Xian-Tao; YIN Zhi-Qi; YE Wen-Cai; NI Li; ZHAO Shou-Xun
Structure 13C NMR ̼Æ×Ä£Äâͼ
19 . chrysoerid-7-O-¦Â-D-glucoside
ÏàËƶÈ:80%
Chinese Pharmaceutical Journal 2005 40 1778-1780
Study on chemical constituents from Artemisia selengensis leaves
ZHANG Jian, KONG Ling-yi
Structure 13C NMR ̼Æ×Ä£Äâͼ
20 . crotonoylthermopsoside
C26H26O12 ÏàËƶÈ:76.9%
Chemistry of Natural Compounds 1989 25 303-308
FLAVONOIDS OF Thermopsisalterniflora. CROTONOYLTHERMOPSOSIDE AND CROTONOYLCOSMOSIIN - NEW ACYLATED FLAVONE GLYCOSIDES
M. P. Yuldashev, E. Kh. Batirov, A. D. Vdovin,V. M. Malikov, and M. R. Yagudaev
Structure 13C NMR ̼Æ×Ä£Äâͼ
21 . chrysoeriol 4'-O-¦Â-D-glucopyranoside
ÏàËƶÈ:76%
Phytochemistry 2000 55 67-75
Phenolic glycosides of forage legume Onobrychis viciifolia
Yinrong Lu, Yan Sun, L. Yeap Foo, W.C. McNabb, A.L. Molan
Structure 13C NMR ̼Æ×Ä£Äâͼ
22 . chrysoeriol-4'-O-glucoside
ÏàËƶÈ:76%
China Journal of Chinese Materia Medica 2001 26 841-844
Studies on Flavonoids from Leaves of Callicarpa bodinieri Levl.
REN Fengzhi, LUAN Xianhui, ZHAO Yimin, QU Huihua
Structure 13C NMR ̼Æ×Ä£Äâͼ
23 . tricin-7-O-¦Â-D-glucopyranoside
ÏàËƶÈ:76%
China Journal of Chinese Materia Medica 1998 23 614-616
Studies on Flavonoids from Fenugreek (Trigonella foenumgraecum L.)
Shang Mingying , Cai Shaoqing , Han Jian , Li Jun , Zhao Yuying and Zheng Junhua
Structure 13C NMR ̼Æ×Ä£Äâͼ
24 . Tricin 7-glucoside
ÏàËƶÈ:76%
Records of Natural Products 2008 2 76-82
Anti-ulcerogenic Activity of Extract and Some Isolated Flavonoids from Desmostachia bipinnata (L.) Stapf
Amani S. Awaad, Nawal H. Mohamed, Derek J. Maitland and
Structure 13C NMR ̼Æ×Ä£Äâͼ
25 . Chrysoeriol-7-O-glucoside
ÏàËƶÈ:76%
Natural Product Sciences 2007 13 186-189
Phytochemical and Biological Studies on Verbascum sinaiticum Growing in Egypt
Mahmoud, Samia M.; Abdel-Azim, Nahla S.; Shahat, Abdelaaty A.; Ismail, Shams I.; Hammouda, Faiza M.
Structure 13C NMR ̼Æ×Ä£Äâͼ |
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