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ľ³æ (ÕýʽдÊÖ)

[ÇóÖú] ΢Æ×Êý¾Ý²éѯÇóÖú£¬¡µ70% ÒÑÓÐ1È˲ÎÓë

¦Ä C (151 MHz, DMSO) 17.86, 42.05, 42.29, 55.66, 66.09, 68.34, 69.57, 70.27, 70.68, 70.71, 72.05, 72.98, 75.50, 76.26, 78.39, 78.46, 95.53, 95.58, 96.36, 99.35, 100.62, 103.33,112.06, 111.98, 114.08, 114.15, 117.79, 117.98, 130.88, 130.96, 146.42, 146.44, 147.91, 147.96, 162.51, 162.55, 163.01, 163.05, 165.08, 165.13, 197.09, 216.88.
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fanqingfei: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2015-02-10 15:57:52
1 .     (¡À)-eriodictyol 7-O-¦Â-D-glucuronide
C21H20O12     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1990          38          3218-3225
Constituents of a Fern, Davallia mariesii MOORE. I. Isolation and Structures of Davallialactone and a New Flavanone Glucuronide
Cheng-Bin CUI,Yasuhiro TEZUKA,Tohru KIKUCHI,Hirofumi NAKANO,Tatsuya TAMAOKI and Jong-Hee PARK
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     hesperidin
    ÏàËÆ¶È:64.2%
Phytochemistry          1977          16          1110-1112
A 13C-NMR study of the structure of an acyl-linarin from Valeriana wallichii
Vedantha Mohan Chari, Madelon Jordan, Hildebert Wagner, Peter W. Thies
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     prainianonide
C22H22O11     ÏàËÆ¶È:57.1%
Canadian Journal of Chemistry          2011          89          461¨C464
Flavanone glucuronides from the leaves of Garcinia prainiana
Saranyoo Klaiklay, Yaowapa Sukpondma, Vatcharin Rukachaisirikul, Nongporn Hutadilok-Towatana, and Kanokphorn Chareonrat
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     scrophuloside B4
C42H48O18     ÏàËÆ¶È:54.7%
Phytochemistry          2005          66          1186-1191
A sugar ester and an iridoid glycoside from Scrophularia ningpoensis
Anh-Tho Nguyen, Jeanine Fontaine, Hugues Malonne, Magda Claeys,Michel Luhmer, Pierre Duez
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     scrophuloside B4
    ÏàËÆ¶È:54.7%
Biochemical Systematics and Ecology          2011          39          902-905
Acylated iridoid glycosides from Scrophularia saharae Batt. & Trab.
Rachid Chebaki, Hamada Haba, Christophe Long, Laurence Marcourt, Mohammed Benkhaled
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     Scrophuloside A4
C43H50O19     ÏàËÆ¶È:54.7%
Chemical & Pharmaceutical Bulletin          2007          55          159-222
Naturally Occurring Iridoids. A Review, Part 1
Biswanath DINDA, Sudhan DEBNATH and Yoshihiro HARIGAYA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     Scrophuloside B4 [6-O-(2''-O-Acetyl-3''-O-cinnamoyl-4''-O-p-methoxycinnamoyl-¦Á-L-rhamnopyranosyl)catalpol]
C42H48O18     ÏàËÆ¶È:54.7%
Chemical & Pharmaceutical Bulletin          2007          55          159-222
Naturally Occurring Iridoids. A Review, Part 1
Biswanath DINDA, Sudhan DEBNATH and Yoshihiro HARIGAYA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     delphinidin 3-[6-O-(¦Á-rhamnopyranosyl)-¦Â-glucopyranoside]-7-O-[6-O-(4-O-(¦Â-glucopyranosyl)-p-hydroxybenzoyl)-¦Â-glucopyranoside]
C53H58O30     ÏàËÆ¶È:54.3%
Heterocycles          2009          77          401-408
7-Acylated Anthocyanins with p-Hydroxybenzoic Acid in the Flowers of Campanula medium
Kenjiro Toki, Norio Saito, Hiroyuki Nishi, Fumi Tatsuzawa, Atsushi Shigihara, and Toshio Honda
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     Kaempferol-3-O-{[¦Â-D-xylopyranosyl(1¡ú3)-¦Á-L-rhamnopyranosyl(1¡ú6)][¦Á-L-rhamnopyranosyl(1¡ú2)]}-¦Â-D-3-trans-p-coumaroylgalactopyranoside
C47H54O25     ÏàËÆ¶È:53.4%
Chemical & Pharmaceutical Bulletin          2002          50(7)          981-984
New Flavonol Tetraglycosides from Astragalus caprinus
Nabil SEMMAR,Bernard FENET,Katia GLUCHOFF-FIASSON,Gilles COMTE,and Maurice JAY
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     scrophuloside A4
C43H50O19     ÏàËÆ¶È:53.4%
Journal of Natural Products          1999          62          1079-1084
Acylated Iridoid and Phenylethanoid Glycosides from the Aerial Parts of Scrophularia nodosa
Toshio Miyase and Ai Mimatsu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     helicioside B
C21H22O12     ÏàËÆ¶È:52.3%
Phytochemistry          2006          67          2681-2685
5-O-glucosyldihydroflavones from the leaves of Helicia cochinchinensis
Ken-Ichi Morimura, Asuka Gatayama, Reiki Tsukimata, Katsuyoshi Matsunami,Hideaki Otsuka, Eiji Hirata, Takakazu Shinzato, Mitsunori Aramoto,Yoshio Takeda
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     MF-1a
    ÏàËÆ¶È:52.3%
Phytochemistry          2003                   589-595
A ¡°flavone-polysaccharide¡± redefined as a mixture of 6-methoxyluteolin penta- and hexa-O-glycosides
Kenneth R. Markham
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     MF-1b
    ÏàËÆ¶È:52.3%
Phytochemistry          2003                   589-595
A ¡°flavone-polysaccharide¡± redefined as a mixture of 6-methoxyluteolin penta- and hexa-O-glycosides
Kenneth R. Markham
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     2''',3'''-diacetyl-O-betonyoside D
C40H52O21     ÏàËÆ¶È:52.3%
Chinese Chemical Letters          2007          18          155-157
Two new phenylethanoid glycosides from the roots of Phlomis umbrosa
Pu Liu, Yoshihisa Takaishi, Hong Quan Duan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     2''', 3'''-di-acetyl-O-betonyoside D
C40H52O21     ÏàËÆ¶È:52.3%
Journal of Asian Natural Products Research          2009          11          69-74
Phenylethanoid glycosides from the roots of Phlomis umbrosa
Pu Liua, Rui-Xue Denga, Hong-Quan Duanb, Wei-Ping Yina and Tian-Zeng Zhaoc
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     Cistansinensose A1/A2
C27H38O17     ÏàËÆ¶È:52.3%
Journal of Asian Natural Products Research          2007          9          79-84
Chemical constituents of Cistanche sinensis
P.-F. TU, H.-M. SHI, Z.-H. SONG, Y. JIANG and Y.-Y. ZHAO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     6-O-¦Á-L-rhamnopyranosylcatalpol
C31H40O17     ÏàËÆ¶È:52.3%
Phytochemistry          1991          30          1917-1920
Iridoid diglycoside monoacyl esters from stems of Premna japonica
Hideaki Otsuka, Naoko Kubo, Yukari Sasaki, Kazuo Yamasaki, Yoshio Takeda, Tarow Seki
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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