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¼±Ç󣡷dz£¸Ðл´óÏÀÃÇ 13C NMR (101 MHz, MeOD) ¦Ä 169.51 (s, 1H), 153.33 (s, 2H), 144.79 (s, 1H), 128.32 (s, 2H), 112.55 (s, 1H), 100.33 (s, 2H), 98.26 (s, 2H), 78.38 (s, 2H), 77.84 (s, 2H), 74.85 (s, 2H), 71.52 (s, 2H), 62.65 (s, 2H), 61.41 (s, 2H), 51.73 (s, 2H), 49.64 (s, 2H), 49.42 (s, 4H), 49.21 (s, 9H), 49.00 (s, 10H), 48.79 (s, 8H), 48.57 (s, 4H), 48.36 (s, 1H), 47.00 (s, 2H), 39.69 (s, 2H), 36.58 (s, 2H). 13C NMR (101 MHz, MeOD) ¦Ä 169.64 (s, 11H), 153.38 (s, 21H), 144.62 (s, 15H), 128.41 (s, 22H), 112.48 (s, 13H), 100.28 (s, 23H), 98.28 (s, 22H), 77.99 (d, J = 51.8 Hz, 47H), 74.76 (s, 23H), 71.42 (s, 24H), 62.55 (s, 23H), 61.34 (s, 23H), 51.85 (s, 20H), 50.22 ¨C 50.04 (m, 1H), 49.96 (s, 8H), 49.90 ¨C 49.42 (m, 41H), 49.21 (s, 42H), 49.12 (s, 5H), 49.00 (s, 41H), 48.68 (d, J = 21.4 Hz, 48H), 48.36 (s, 9H), 46.94 (s, 23H), 39.64 (s, 22H), 36.48 (s, 22H). 13C NMR (101 MHz, MeOD) ¦Ä 101.13 (s, 1H), 98.09 (s, 3H), 93.85 (s, 2H), 78.26 (s, 1H), 78.14 ¨C 76.39 (m, 10H), 76.19 (s, 2H), 75.03 (s, 3H), 74.77 (s, 4H), 73.57 (d, J = 27.8 Hz, 5H), 72.92 (s, 2H), 71.71 (d, J = 11.7 Hz, 9H), 62.70 (d, J = 11.6 Hz, 8H), 55.49 (s, 1H), 49.74 (d, J = 21.0 Hz, 15H), 49.42 (s, 15H), 49.10 (d, J = 21.4 Hz, 71H), 48.82 (s, 4H), 48.82 (s, 4H), 48.82 (s, 9H), 48.81 ¨C 48.07 (m, 55H). |
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1111 1 . 10,6'-di-O-(1-methoxy-1-methylethyl)-geniposide C25H40O12 ÏàËÆ¶È:78.2% Journal of Natural Products 1999 62 1646-1654 Stereoselective Hydrogenation and Ozonolysis of Iridoids. Conversion into Carbocyclic Nucleoside Analogues Henrik Franzyk, and Frank R. Stermitz Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . genameside C C23H34O15 ÏàËÆ¶È:73.9% Chemical & Pharmaceutical Bulletin 2005 53(10) 1342-1344 Iridoid Glucosides from the Fruit of Genipa americana Masateru ONO,Masami UENO,Chikako MASUOKA,Tsuyoshi IKEDA,and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . genipin-gentiobioside ÏàËÆ¶È:73.9% Chemical & Pharmaceutical Bulletin 2005 53(10) 1342-1344 Iridoid Glucosides from the Fruit of Genipa americana Masateru ONO,Masami UENO,Chikako MASUOKA,Tsuyoshi IKEDA,and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Genipin 1-O-¦Â-D-isomaltoside C23H34O15 ÏàËÆ¶È:73.9% Phytochemistry 2009 70 779-784 Iridoid glycosides from Gardeniae Fructus for treatment of ankle sprain Quan Cheng Chen, Wei Yun Zhang, UiJoung Youn, HongJin Kim, IkSoo Lee, Hyun-Ju Jung, MinKyun Na, Byung-Sun Min, KiHwan Bae Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . genipin 1-O-¦Â-D-gentiobioside ÏàËÆ¶È:73.9% Phytochemistry 2009 70 779-784 Iridoid glycosides from Gardeniae Fructus for treatment of ankle sprain Quan Cheng Chen, Wei Yun Zhang, UiJoung Youn, HongJin Kim, IkSoo Lee, Hyun-Ju Jung, MinKyun Na, Byung-Sun Min, KiHwan Bae Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . genipin-1-O-¦Â-D-gentiobioside ÏàËÆ¶È:73.9% China Journal of Chinese Materia Medica 2009 34 1097-1100 A new flavonoid glucoside from Huanglian jiedutang decoction MA Zhaotang, YANG Xiuwei, ZHONG Guoyue Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . genipin-gentiobioside ÏàËÆ¶È:73.9% Chinese Traditional and Herbal Drugs 2014 45 16-22 Chemical constituents from root tubers of Rehmannia glutinosa LIU Yan-fei, LIANG Dong, LUO Huan, HAO Zhi-you, WANG Yan, ZHANG Chun-lei, CHEN Ruo-yun, YU De-quan Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . genameside C ÏàËÆ¶È:73.9% Chinese Traditional and Herbal Drugs 2014 45 16-22 Chemical constituents from root tubers of Rehmannia glutinosa LIU Yan-fei, LIANG Dong, LUO Huan, HAO Zhi-you, WANG Yan, ZHANG Chun-lei, CHEN Ruo-yun, YU De-quan Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . genipin-1-gentiobioside ÏàËÆ¶È:73.9% Lishizhen Medicine and Materia Medica Research 2013 24 1599-1603 »ÆÁ¬½â¶¾ÌÀ»¯Ñ§³É·Ö¼°ÆäÉñ¾Ï¸°û±£»¤×÷ÓÃÑо¿ ÑîÑô, ÕÔº£Óþ, Ëν¨·¼, Íõºê½à, Ñ, ˾ÄÏ, ÁõÇìɽ, ±ß±¦ÁÖ* Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . genipin 1-O-¦Â-D-apiofuranosyl(1¡ú6)-¦Â-D-glucopyranoside C22H32O14 ÏàËÆ¶È:69.5% 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 222 1 . 10,6'-di-O-(1-methoxy-1-methylethyl)-geniposide C25H40O12 ÏàËÆ¶È:73.9% Journal of Natural Products 1999 62 1646-1654 Stereoselective Hydrogenation and Ozonolysis of Iridoids. Conversion into Carbocyclic Nucleoside Analogues Henrik Franzyk, and Frank R. Stermitz Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . genameside C C23H34O15 ÏàËÆ¶È:69.5% Chemical & Pharmaceutical Bulletin 2005 53(10) 1342-1344 Iridoid Glucosides from the Fruit of Genipa americana Masateru ONO,Masami UENO,Chikako MASUOKA,Tsuyoshi IKEDA,and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . genipin-gentiobioside ÏàËÆ¶È:69.5% Chemical & Pharmaceutical Bulletin 2005 53(10) 1342-1344 Iridoid Glucosides from the Fruit of Genipa americana Masateru ONO,Masami UENO,Chikako MASUOKA,Tsuyoshi IKEDA,and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 2',3':4',6'-di-O-isopropylidene-geniposide C23H32O10 ÏàËÆ¶È:69.5% Journal of Natural Products 1999 62 1646-1654 Stereoselective Hydrogenation and Ozonolysis of Iridoids. Conversion into Carbocyclic Nucleoside Analogues Henrik Franzyk, and Frank R. Stermitz Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Genipin 1-O-¦Â-D-isomaltoside C23H34O15 ÏàËÆ¶È:69.5% Phytochemistry 2009 70 779-784 Iridoid glycosides from Gardeniae Fructus for treatment of ankle sprain Quan Cheng Chen, Wei Yun Zhang, UiJoung Youn, HongJin Kim, IkSoo Lee, Hyun-Ju Jung, MinKyun Na, Byung-Sun Min, KiHwan Bae Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . genipin-1-O-¦Â-D-gentiobioside ÏàËÆ¶È:69.5% China Journal of Chinese Materia Medica 2009 34 1097-1100 A new flavonoid glucoside from Huanglian jiedutang decoction MA Zhaotang, YANG Xiuwei, ZHONG Guoyue Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . genipin 1-O-¦Á-D-xylopyranosyl (1¡ú6)-¦Â-D-glucopyranoside C22H32O14 ÏàËÆ¶È:69.5% 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 8 . genipin-gentiobioside ÏàËÆ¶È:69.5% Chinese Traditional and Herbal Drugs 2014 45 16-22 Chemical constituents from root tubers of Rehmannia glutinosa LIU Yan-fei, LIANG Dong, LUO Huan, HAO Zhi-you, WANG Yan, ZHANG Chun-lei, CHEN Ruo-yun, YU De-quan Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . genameside C ÏàËÆ¶È:69.5% Chinese Traditional and Herbal Drugs 2014 45 16-22 Chemical constituents from root tubers of Rehmannia glutinosa LIU Yan-fei, LIANG Dong, LUO Huan, HAO Zhi-you, WANG Yan, ZHANG Chun-lei, CHEN Ruo-yun, YU De-quan Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . genipin-1-gentiobioside ÏàËÆ¶È:69.5% Lishizhen Medicine and Materia Medica Research 2013 24 1599-1603 »ÆÁ¬½â¶¾ÌÀ»¯Ñ§³É·Ö¼°ÆäÉñ¾Ï¸°û±£»¤×÷ÓÃÑо¿ ÑîÑô, ÕÔº£Óþ, Ëν¨·¼, Íõºê½à, Ñ, ˾ÄÏ, ÁõÇìɽ, ±ß±¦ÁÖ* Structure 13C NMR ̼Æ×Ä£Äâͼ 33 1 . maltose ÏàËÆ¶È:63.1% Canadian Journal of Chemistry 1975 53 1030-1037 A Carbon-13 Nuclear Magnetic Resonance Study of Chlorinated and Polyol Analogs of Glucose and Related Oligomers Pierre Colson, Keith N. Slessor, H. J. Jennings, Ian C. P. Smith Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . methyl gentiobioside ÏàËÆ¶È:57.8% Chemical & Pharmaceutical Bulletin 1989 37 2727-2730 Two New Triterpenoid Glycosides from the Leaves of Schefflera octophylla Junichi KITAJIMA and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . K-red ÏàËÆ¶È:57.8% Chemical & Pharmaceutical Bulletin 1982 30 4334-4340 Studies on the Constituents of Momordica charantia L. IV. Characterization of the New Cucurbitacin Glycosides of the Immature Fruits. (2) Structures of the Bitter Glycosides, Momordicosides K and L HIKARU OKABE,YUMI MIYAHARA and TATSUO YAMAUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ajureptaside C C16H26O10 ÏàËÆ¶È:57.8% Chemical & Pharmaceutical Bulletin 2011 59(8) 1065-1068 Four New Iridoid Glucosides from Ajuga reptans Masateru ONO, Chisato FURUSAWA,Takumi OZONO, Keisuke ODA, Shin YASUDA,Masafumi OKAWA, Junei KINJO, Tsuyoshi IKEDA, Hiroyuki MIYASHITA,Hitoshi YOSHIMITSU, and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ¦Â-D-ßÁà«ÆÏÌÑÌÇ»ù-(1¡ú6)-¦Â-D-ßÁà«ÆÏÌÑÌÇ»ù(1¡ú4)2¦Â2D2ßÁà«ÆÏÌÑÌÇ ÏàËÆ¶È:57.8% Chinese Pharmaceutical Journal 2003 38 836-838 Studies on chemical constituents of Lysimachia davurica TIAN Jing kui, ZOU Zhong mei, XU Li zhen, Liu Jian xin, ZHANG Hong wu, YANG Shi lin Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 6'-chloro-6'-deoxymaltose ÏàËÆ¶È:57.8% Canadian Journal of Chemistry 1975 53 1030-1037 A Carbon-13 Nuclear Magnetic Resonance Study of Chlorinated and Polyol Analogs of Glucose and Related Oligomers Pierre Colson, Keith N. Slessor, H. J. Jennings, Ian C. P. Smith Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 2 ÏàËÆ¶È:57.8% Magnetic Resonance in Chemistry 1997 35 414-419 1H and 13C NMR Data for 3-O-, 4-O- and 3,4-Di- 1O-glycosylated Methyl ¦Á-L-Rhamnopyranosides Elena A. Khatuntseva, Alexander S. Shashkov and Nikolay E. Nifant¡¯ev Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . N-Trisaccharide C12H33O15N ÏàËÆ¶È:57.8% Phytomedicine 2014 21 624−630 Anti-diabetic effect of a novel N-Trisaccharide isolated from Cucumisprophetarum on streptozotocin¨Cnicotinamide induced type 2 diabeticrats G.B. Kavishankar, N. Lakshmidevi Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . tecomosid ÏàËÆ¶È:52.6% Planta Medica 1985 51 229-232 Further Iridoid Glucosides from Penstemon strictus Peter Junior Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3-epiphlomurin C18H28O11 ÏàËÆ¶È:52.6% Phytochemistry 2000 55 353-357 Iridoid and megastigmane glycosides from Phlomis aurea Mohamed S. Kamel, Khaled M. Mohamed, Hashim A. Hassanean, Kazuhiro Ohtani, Ryoji Kasai, Kazuo Yamasaki Structure 13C NMR ̼Æ×Ä£Äâͼ |

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