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thanwen½ð³æ (СÓÐÃûÆø)
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[ÇóÖú]
΢Æ×ÇóÖú 30-H-8-F9 ÒÑÓÐ1È˲ÎÓë
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in DMSO£º 16.07,28.58,42.54,59.88,61.04,61.17,61.31,61.38,65.08,67.61,69.96,70.18,70.21,70.27,71.83,73.49,73.68,75.46,76.45,76.53,76.78,77.09,77.12,77.53,77.56,78.83,79.57,82.93,86.97,95.96,97.05,100.07,100.73,101.68,103.74,104.84,107.75,116.7,128.67,132.14,148.74,158.09,163.09,163.41,165.81,197.5 |
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²éѯ½á¹û£º¹²²éµ½146¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Kaempferol-3-O-(2-O-sinapoyl)-¦Â-D-glucopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside-7-O-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside ÏàËÆ¶È:60.8% Archives of Pharmacal Research 2009 32 1379-1384 Kaempferol glycosides with antioxidant activity from Brassica juncea Hyun Ah Jung, Ju Jung Woo, Mee Jung Jung, Geum-Sook Hwang and Jae Sue Choi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . saxatilisin A C46H62O30 ÏàËÆ¶È:60.8% Phytochemistry 2013 88 85-91 Highly glycosylated flavonols with an O-linked branched pentasaccharide from Iberis saxatilis (Brassicaceae) Thomas A.K. Prescott, Geoffrey C. Kite, Elaine A. Porter, Nigel C. Veitch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . oligosaccharide 2 ÏàËÆ¶È:59.5% Carbohydrate Research 1995 266 103-113 Structure of simusan, a new acidic exopolysaccharide from Arthrobacter sp. Soph'ya N. Senchenkova, Yuriy A. Knirel, Leonid M. Likhosherstov, Aleksander S. Shashkov, Vladimir N. Shibaev, Lyubov' A. Starukhina, Vladimir V. Deryabin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . Quercetin 3-O-[2G-(E)-Coumaroyl-3G-O-¦Â-D-glucosyl-3R-O-¦Â-D-glucosylrutinoside] C48H56O28 ÏàËÆ¶È:58.6% Chemical & Pharmaceutical Bulletin 2008 56 851-853 Structural Determination and DPPH Radical-Scavenging Activity of Two Acylated Flavonoid Tetraglycosides in Oolong Tea (Camellia sinensis) Viola Szu-Yuan Lee, Chiy-Rong Chen, Yun-Wen Liao, Jason Tze-Cheng Tzen, Chi-I Chang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . peonidin 3-O-[6-O-(4-O-(4-O-trans-(¦Â-D-glucopyranosyl)-p-coumaroyl)-¦Á-L-rhamnopyranosyl)-¦Â-D-glucopyranoside]-5-O-[¦Â-D-glucopyranoside] C49H59O27 ÏàËÆ¶È:57.4% Heterocycles 2004 63 509-517 Acylated Peonidin 3-Rutinoside-5-glucosides from Commercial Petunia Cultivars with Pink Flowers Fumi Tatsuzawa, Yukiko Toya, Hitoshi Watanabe, Yuji Hirayama, Koichi Shinoda, Ritsuko Hara, Hiroko Seki, and Toshio Ando* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 28-(O-¦Â-D-galactopyranosyl-(1¡ú4)-O-[¦Â-D-glucopyranosyl-(1¡ú3)]-O-¦Â-D-xylopyranosyl-(1¡ú4)-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-{4-O-[(Z)-4-methoxycinnamoyl]}-¦Â-D-fucopyranosyl) ester C75H112O36 ÏàËÆ¶È:56.5% Helvetica Chimica Acta 2003 Vol. 86 2404 New Acylated Triterpene Saponins from Polygala arenaria Anne-Claire Mitaine-Offer, Tomofumi Miyamoto, V¨¦ronique Laurens, Cl¨¦ment Delaude, and Marie-Aleth Lacaille-Dubois Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 3-O-(¦Â-D-glucopyranosyl)presenegenin 28-(O-¦Â-D-galactopyranosyl-(1¡ú4)-O-[¦Â-D-glucopyranosyl-(1 3)]-O-¦Â-D-xylopyranosyl-(1¡ú4)-O-¦Á-L-rhamnopyranosyl-(1 2)-{4-O-[(Z)-3,4-dimethoxycinnamoyl]}-¦Â-D-fucopyranosyl) ester C76H114O37 ÏàËÆ¶È:56.5% Helvetica Chimica Acta 2003 Vol. 86 2404 New Acylated Triterpene Saponins from Polygala arenaria Anne-Claire Mitaine-Offer, Tomofumi Miyamoto, V¨¦ronique Laurens, Cl¨¦ment Delaude, and Marie-Aleth Lacaille-Dubois Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . (-)-(2R,3S)-1-{4-[¦Â-D-glucopyranosyl-(1¡ú3)-¦Â-D-glucopyranosyloxy]benzyl}-2-O-¦Â-D-glucopyranosyl-4-(4-¦Â-D-glucopyranosyloxybenzyl)- 2-isobutyltartrate C46H66O28 ÏàËÆ¶È:56.5% Journal of Natural Products 2008 71(5) 799-805 Glycosidic Constituents of the Tubers of Gymnadenia conopsea Jiachen Zi, Shuai Li, Mingtao Liu, Maoluo Gan, Sheng Lin, Weixia Song, Yanling Zhang, Xiaona Fan, Yongchun Yang, Jianjun Zhang, Jiangong Shi, and Duolong Di Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 1b ÏàËÆ¶È:56.5% Chemical & Pharmaceutical Bulletin 1998 46 1891-1900 Studies on the Constituents of Clematis Species. VII. Triterpenoid Saponins from the Roots of Clematis terniflora DC. var. robusta TAMURA Yukio KAWATA,Haruhisa KIZU and Tsuyoshi TOMIMORI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 9a ÏàËÆ¶È:56.5% Chemical & Pharmaceutical Bulletin 1998 46 1891-1900 Studies on the Constituents of Clematis Species. VII. Triterpenoid Saponins from the Roots of Clematis terniflora DC. var. robusta TAMURA Yukio KAWATA,Haruhisa KIZU and Tsuyoshi TOMIMORI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 3¦Â-O-[¦Â-D-glucopyranosyl-(1¡ú3)-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Á-L-arabinopyranosyl]olean-12-ene-28-O-[¦Â-D-glucopyranosyl-(1¡ú3)-¦Á-L-rhamnopyranosyl (1¡ú4)-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranosyl]ester C71H116O35 ÏàËÆ¶È:56.5% Journal of Natural Products 2000 63 308-314 Antiproliferative Triterpene Saponins from Trevesia palmata Nunziatina De Tommasi, Giuseppina Autore, Aurora Bellino, Aldo Pinto, Cosimo Pizza,Raffaella Sorrentino, and Pietro Venturella Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . kaempferol 3-O-[¦Â-D-glucopyranosyl-(1¡ú2)-{¦Â-D-glucopyranosyl-(1¡ú3)}-{¦Â-D-glucopyranosyl-(1¡ú4)}-¦Á-L-rhamnopyranoside]-7-O-[¦Á-L-rhamnopyranoside] C45H60O29 ÏàËÆ¶È:56.5% Chemical & Pharmaceutical Bulletin 2009 57 276-279 Two New Flavonol Glycosides from Otostegia limbata BENTH. Afsar Khan, Viqar Uddin Ahmad, Umar Farooq, Sadia Bader and Saima Arshad Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . descaffeoylmontbretin A ÏàËÆ¶È:56.5% Phytochemistry 1988 27 1497-1501 Acylated flavonols from Crocosmia crocosmiiflora Yoshihisa Asada,Yutaka Hirayama,Tsutomu Furuya Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 4''-O-alpha-D-maltosyl stevioside C50H80O28 ÏàËÆ¶È:56.5% Biotechnology Letters 2009 31 1415-1420 Simple and efficient enzymatic transglycosylation of stevioside by ¦Â-cyclodextrin glucanotransferase from Bacillus firmus V. Jaitak, V. Kumar Kaul, Bandna, N. Kumar, B. Singh, L. S. Savergave, V. V. Jogdand, S. Nene Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . I-(2,3)-dihydro-I-7,II-7-di-O-¦Â-D-glucopyranosyl-amentoflavone C42H40O20 ÏàËÆ¶È:56.5% Natural Product Research 2014 28 41-47 Two new dihydroamentoflavone glycosides from Cycas revoluta Abeer Moawad, Mona Hetta, Jordan K. Zjawiony, Daneel Ferreira & Mohamed Hifnawy Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 6''-O-(3R-1-N-¦Â-D-glucopyranosyl-2-oxo-3-hydroxy-indole-3-acetyl)spinosin C44H49NO23 ÏàËÆ¶È:56.5% Fitoterapia 2014 99 48-55 Indoleacetic acid derivatives from the seeds of Ziziphus jujuba var. spinosa Min Li, Yu Wang, Bun Tsoi, Xiao-jie Jin, Rong-Rong He, Xiao-jun Yao, Yi Dai, Hiroshi Kurihara, Xin-Sheng Yao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . Kaempferol 3-O-[2G-(E)-Coumaroyl-3G-O-¦Â-D-glucosyl-3R-O-¦Â-D-glucosylrutinoside] C48H56O27 ÏàËÆ¶È:56.5% Chemical & Pharmaceutical Bulletin 2008 56 851-853 Structural Determination and DPPH Radical-Scavenging Activity of Two Acylated Flavonoid Tetraglycosides in Oolong Tea (Camellia sinensis) Viola Szu-Yuan Lee, Chiy-Rong Chen, Yun-Wen Liao, Jason Tze-Cheng Tzen, Chi-I Chang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-7-[(¦Á-l-rhamnopyranosyl)oxy]-4H-chromen-3-yl b-d-glucopyranosyl-(1¡ú2)-[¦Â-D-glucopyranosyl-(1¡ú4)]-[6-O-[(2E)-3- (4-hydroxyphenyl)prop-2-enoyl]-¦Â-D-glucopyranosyl-(1¡ú3)]-¦Á-L-rhamnopyranoside C54H66O31 ÏàËÆ¶È:56% Helvetica Chimica Acta 2009 92 731-739 Two New Acylated Flavonol Glycosides from the Roots of Otostegia limbata Afsar Khan, Viqar U. Ahmad, Umar Farooq Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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