| ²é¿´: 326 | »Ø¸´: 1 | ||
н´77Òø³æ (СÓÐÃûÆø)
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[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý
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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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н´77: ½ð±Ò+5, ¡ï¡ï¡ïºÜÓаïÖú 2013-09-22 16:47:19
н´77: ½ð±Ò+5, ¡ï¡ï¡ïºÜÓаïÖú 2013-09-22 16:47:19
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²éѯ½á¹û£º¹²²éµ½150¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ |
2Â¥2013-09-22 08:26:38














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