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13C NMR (75 MHz, MeOD) ¦Ä 13.51, 21.48, 27.89, 29.26, 29.79, 36.48, 38.46, 46.30, 62.71, 69.48, 70.85, 71.49, 73.93, 75.09, 77.78, 77.90, 77.97, 78.00, 96.35, 104.51, 136.36, 137.00, 137.86, 138.35, 167.52, 201.13.
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1 .     6,7-dihydrofoliamenthoic acid 1-O-¦Â-D-glucopyranosyl ester-8-O¦Â-D-glucopyranoside
C22H38O13     ÏàËÆ¶È:65.3%
Phytochemistry          1994          37          461-465
Linarionosides A¨CC and acyclic monoterpene diglucosides from Linaria japonica
Hideaki Otsuka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     jasminoside S
C22H36O12     ÏàËÆ¶È:65.3%
Bioorganic & Medicinal Chemistry Letters          2013          23          1127-1131
Chemical constituents from the fruit of Gardenia jasminoides and their inhibitory effects on nitric oxide production
Kaifeng Peng, Liguo Yang, Shizhe Zhao, Lixia Chen, Feng Zhao, Feng Qiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     ¦Â-gentiobiosyl 2,6,6-trimethylcyclohex-1-ene-1-carboxylate
C22H36O12     ÏàËÆ¶È:65.3%
Chemistry & Biodiversity          2012          9          1490-1499
Melanogenesis Inhibitory Activity of Monoterpene Glycosides from Gardeniae Fructus
Toshihiro Akihisa, Kensuke Watanabe, Ayako Yamamoto, Jie Zhang, Masahiro Matsumoto and Makoto Fukatsu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     platanionoside F
C24H38O11     ÏàËÆ¶È:61.5%
Chemical & Pharmaceutical Bulletin          2002          50(3)          390-394
Platanionosides D¡ªJ: Megastigmane Glycosides from the Leaves of Alangium platanifolium (SIEB. et ZUCC.) HARMS var. platanifolium SIEB. et ZUCC.
Hideaki OTSUKA and Akie TAMAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     platanionoside B
C25H44O12     ÏàËÆ¶È:61.5%
Journal of Natural Products          1999          62          1074-1076
Platanionosides A-C, Megastigmane Diglycosides from the Leaves of Alangium platanifolium
Akie Tamaki, Hideaki Otsuka, and Toshinori Ide
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     3R,7E-9-butoxylmegastigma-3-ol-3-O-¦Â-D-glucopyranoside
C23H40O7     ÏàËÆ¶È:61.5%
Journal of Asian Natural Products Research          2008          10          1109-1115
Three novel compounds from the leaves of Smallanthus sonchifolius
Ying-Kun Qiu, Ting-Guo Kang, De-Qiang Dou, Li Liang and Feng Dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     (1R,4R,5R,8S,9S)-4,5-Epoxycaryophyllane-14-ol 14-O-¦Â-D-glucopyranosyi-(1¡ú6)-¦Â-D-glucopyranoside
     ÏàËÆ¶È:59.2%
Phytochemistry          1994          35          635-639
Biotransformation of caryophyllene oxide by cultured cells of Eucalyptus perriniana
Yutaka Orihara, Kenji Saiki, Tsutomu Furuya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     (3S,5R,6S,7E,9S)-megastigman-7-ene-5,6-epoxy-3,9-diol 3,9-O-¦Â-D-diglucopyranoside
C25H42O13     ÏàËÆ¶È:57.6%
Chemical & Pharmaceutical Bulletin          2007          55(8)          1277-1280
Megastigmane Glucosides from Equisetum debile and E. diffusum
Tripetch KANCHANAPOOM,Hideaki OTSUKA,and Somsak RUCHIRAWAT
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     staphylionoside G
C25H42O12     ÏàËÆ¶È:57.6%
Chemical & Pharmaceutical Bulletin          2005          53(7)          800-807
Staphylionosides A¡ªK: Megastigmane Glucosides from the Leaves of Staphylea bumalda DC.
Qian YU,Katsuyoshi MATSUNAMI,Hideaki OTSUKA,and Yoshio TAKEDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     staphylionoside K
C25H44O12     ÏàËÆ¶È:57.6%
Chemical & Pharmaceutical Bulletin          2005          53(7)          800-807
Staphylionosides A¡ªK: Megastigmane Glucosides from the Leaves of Staphylea bumalda DC.
Qian YU,Katsuyoshi MATSUNAMI,Hideaki OTSUKA,and Yoshio TAKEDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     5-methyl-2-(1-methylethyl)phenyl 6-O-(¦Â-D-glucopyranosyl)-¦Â-D-glucopyranoside
C22H34O11     ÏàËÆ¶È:57.6%
Phytochemistry          2006          67          2256-2261
Biotransformation of thymol, carvacrol, and eugenol by cultured cells of Eucalyptus perriniana
Kei Shimoda, Yoko Kondo, Tomohisa Nishida, Hatsuyuki Hamada,Nobuyoshi Nakajima, Hiroki Hamada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     eriojaposide A
C24H38O11     ÏàËÆ¶È:57.6%
Journal of Natural Products          2001          64          737-740
Megastigmane Glycosides and an Acylated Triterpenoid from Eriobotrya japonica
Hideyuki Ito,Eri Kobayashi, Shu-Hua Li, Tsutomu Hatano, Daigo Sugita, Naoki Kubo, Susumu Shimura, Yoshio Itoh, and Takashi Yoshida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     12¦Â,16¦Á,19-trihydroxy-ent-kaurane 19-O-¦Â-D-glucopyranoside
     ÏàËÆ¶È:57.6%
Chemical & Pharmaceutical Bulletin          1983          31          3865-3871
Chemical and Chemotaxonomical Studies on Filices. XLIII. Chemical Studies on the Constituents of Lindsaea javanensis BL., L. japonica (BAK.) DIELS and Tapeinidium pinnatum (CAV.) C. CHR.
TOSHIKO SATAKE,TAKAO MURAKAMI,YASUHISA SAIKI and CHIUMING CHEN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     Jasminoside M
C21H34O11     ÏàËÆ¶È:57.6%
Helvetica Chimica Acta          2010          93          763-771
Monoterpenoids from the Fruit of Gardenia jasminoides
Yang Yu, Hao Gao, Yi Dai, Ying Wang, He-Ru Chen and Xin-Sheng Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     goshonoside-F2
     ÏàËÆ¶È:57.6%
Phytochemistry          1984          23          615-621
Ent-labdane-type diterpene glucosides from leaves of Rubus chingii
Takashi Tanaka, Keiko Kawamura, Takumi Kitahara, Hiroshi Kohda, Osamu Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     genipin-gentiobioside
     ÏàËÆ¶È:57.6%
Journal of Chinese Medicinal Materials          2012          35          1950-1952
Study on the Chemical Constituents of Fructus Gardeniae
HUANG Tao, MU Shu-zhen, HAO Xiao-jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     staphylionoside K
     ÏàËÆ¶È:57.6%
Acta Pharmaceutica Sinica          2010          45          1527-1532
Two new phenolic glycosides from the stems of Clematis parviloba
YAN Li-hua, XU Li-zhen *, WANG Zhi-min, ZHANG Qi-wei, YANG Shi-lin *
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     nonioside R
C22H40O12     ÏàËÆ¶È:57.6%
Chemistry & Biodiversity          2012          9          1172-1187
Melanogenesis-Inhibitory Saccharide Fatty Acid Esters and Other Constituents of the Fruits of Morinda citrifolia (Noni)
Toshihiro Akihisa, Shun Tochizawa, Nami Takahashi, Ayako Yamamoto, Jie Zhang, Takashi Kikuchi, Makoto Fukatsu, Harukuni Tokuda and Nobutaka Suzuki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     3,9-dihydroxymegastigmast-5-ene-3-O-[¦Â-D-glucopyranosyl-(1¡ú6)]-¦Â-D-glucopyranoside
     ÏàËÆ¶È:57.6%
Journal of Agricultural and Food Chemistry          2006          54          9592-9597
Spectroscopic Identification and Antioxidant Activity of Glucosylated Carotenoid Metabolites from Cydonia vulgaris Fruits
Antonio Fiorentino, Brigida D'Abrosca, Severina Pacifico, Claudio Mastellone, Vincenzo Piscopo, and Pietro Monaco
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     dendronobiloside C
C27H44O12     ÏàËÆ¶È:55.5%
Planta Medica          2002          68          723-729
New Alloaromadendrane,Cadinene and Cyclocopacamphane Type Sesquiterpene Derivatives and Bibenzyls from Dendrobium nobile
Qinghua Ye,Weimin Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-09-22 08:26:38
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