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ÓÉÓÚ½Ó´¥²¨Æ×½ÏÉÙ£¬½âÆ×ÃÔ㣬ÏÈÇóÖú¸÷´óÉñÄܸøÓè°ïÖú£¬ÕâЩ¿ÉÄÜÊÇÄÄЩÎïÖÊ£¿·Ç³£¸Ðл 4ºÅ 13C NMR (101 MHz, MeOD) ¦Ä 170.89 (s, 7H), 153.34 (s, 14H), 144.41 (s, 9H), 128.43 (s, 15H), 112.50 (s, 8H), 105.09 (s, 1H), 100.96 (s, 3H), 100.12 (s, 16H), 98.16 (s, 15H), 78.02 (s, 13H), 77.99 ¨C 77.35 (m, 22H), 75.09 ¨C 74.42 (m, 20H), 73.25 (s, 6H), 71.67 ¨C 71.08 (m, 20H), 62.46 (d, J = 8.7 Hz, 21H), 61.27 (s, 16H), 57.33 (s, 1H), 55.49 (s, 3H), 49.87 (s, 1H), 49.74 (d, J = 20.6 Hz, 12H), 49.32 (d, J = 21.5 Hz, 43H), 49.03 (s, 7H), 49.03 (s, 19H), 49.07 ¨C 48.52 (m, 94H), 48.57 (s, 14H), 48.47 (d, J = 21.5 Hz, 23H), 46.78 (s, 16H), 39.52 (s, 15H), 36.37 (s, 15H). 5ºÅ 13C NMR (101 MHz, MeOD) ¦Ä 150.78 (s, 2H), 148.91 (d, J = 26.6 Hz, 3H), 147.32 (t, J = 13.6 Hz, 3H), 137.35 (d, J = 9.5 Hz, 2H), 133.67 (s, 2H), 131.26 (s, 1H), 120.46 ¨C 119.60 (m, 6H), 119.35 (s, 1H), 117.83 (s, 3H), 116.09 (s, 5H), 111.54 (d, J = 5.9 Hz, 3H), 110.97 (s, 3H), 110.53 (s, 1H), 102.68 (s, 3H), 88.92 (s, 1H), 87.36 (s, 3H), 86.98 (s, 2H), 83.43 (s, 1H), 78.04 (s, 4H), 77.69 (s, 5H), 74.80 (s, 5H), 72.60 (d, J = 4.8 Hz, 6H), 71.97 (s, 2H), 71.23 (s, 4H), 70.64 (s, 2H), 62.42 (s, 4H), 56.74 (s, 5H), 56.44 (s, 7H), 55.58 (s, 2H), 55.27 (d, J = 17.6 Hz, 5H), 51.12 (s, 1H), 49.64 (s, 5H), 49.47 (s, 2H), 49.32 (d, J = 21.5 Hz, 41H), 49.00 (s, 32H), 48.83 (s, 4H), 48.68 (d, J = 21.4 Hz, 38H), 48.36 (s, 5H). 6ºÅ 13C NMR (101 MHz, MeOD) ¦Ä 78.04 (s, 2H), 77.72 (s, 2H), 77.39 (s, 2H), 48.59 (s, 1H), 48.37 (s, 3H), 48.16 (s, 5H), 47.95 (s, 6H), 47.74 (s, 5H), 47.52 (s, 3H), 47.31 (s, 1H). 7ºÅ 13C NMR (101 MHz, MeOD) ¦Ä 105.51 (s, 1H), 104.56 (s, 2H), 101.22 (s, 3H), 99.68 (d, J = 5.4 Hz, 3H), 77.86 (s, 8H), 76.10 (s, 2H), 75.00 (s, 10H), 73.39 (d, J = 16.8 Hz, 14H), 71.80 (s, 5H), 71.46 (s, 9H), 69.79 (s, 1H), 67.28 (s, 2H), 62.40 (s, 10H), 57.63 (d, J = 9.2 Hz, 1H), 55.80 (s, 2H), 49.53 (d, J = 21.4 Hz, 15H), 49.42 ¨C 49.40 (m, 4H), 49.12 (d, J = 17.4 Hz, 40H), 49.04 (s, 4H), 48.89 (d, J = 21.5 Hz, 63H), 48.61 (s, 3H), 48.47 (d, J = 21.4 Hz, 18H). 8ºÅ 13C NMR (101 MHz, MeOD) ¦Ä 196.26 (s, 1H), 156.30 (s, 1H), 126.69 (s, 1H), 125.16 (s, 2H), 116.66 (s, 2H), 112.18 (s, 1H), 56.50 (s, 1H), 49.64 (s, 9H), 49.42 (s, 31H), 49.21 (s, 32H), 49.00 (s, 51H), 48.79 (s, 33H), 48.57 (s, 18H), 48.36 (s, 7H). ÔٴθÐл£¡ |
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44 1 . genameside C C23H34O15 ÏàËÆ¶È:57.1% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 10,6'-di-O-(1-methoxy-1-methylethyl)-geniposide C25H40O12 ÏàËÆ¶È:57.1% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . Genipin 1-O-¦Â-D-isomaltoside C23H34O15 ÏàËÆ¶È:57.1% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . genipin-gentiobioside ÏàËÆ¶È:57.1% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . genipin-gentiobioside ÏàËÆ¶È:57.1% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . genameside C ÏàËÆ¶È:57.1% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 6''-O-trans-Sinapoylgenipin gentiobioside C34H44O19 ÏàËÆ¶È:57.1% Chemical & Pharmaceutical Bulletin 2011 59 803-833 Naturally Occurring Iridoids and Secoiridoids. An Updated Review, Part 4 Biswanath DINDA, Sudhan DEBNATH, and Rajarshi BANIK Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . scyphiphorins B C26H38O12 ÏàËÆ¶È:53.5% Helvetica Chimica Acta 2007 Vol. 90 1718 Scyphiphorins A and B, Two New Iridoid Glycosides from the Stem Bark of a Chinese Mangrove Scyphiphora hydrophyllacea Shu-Hong Tao, Jun Wu, Shu-Hua Qi, Si Zhang, Min-Yi Li, and Qing-Xin Li Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 55 1 . Mananthoside K C36H44O15 ÏàËÆ¶È:57.8% Journal of Asian Natural Products Research 2008 10 228-232 Three new lignan glycosides from Mananthes patentiflora Jun-Mian Tian, Hong-Ping He, Ying-Tong Di, Xian-Wen Yang, Zhu-Lin Gao and Xiao-Jiang Hao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . zanthpodocarpin E C41H40O15 ÏàËÆ¶È:56.0% Bioorganic & Medicinal Chemistry Letters 2014 24 4667-4671 Characterization and biological evaluation of six new dimeric lignans with an unusual ¦Á,¦Â-unsaturated ketone motif from Zanthoxylum simulans Jun-Feng Wang, Yi-Hui Deng, Sheng-Hui Yang, Yan-Qun Liu, Yue-Hu Wang, Wei-Wei Pan, Xiao-Jiang Zhou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . pinoresinol O-[6-O-(E)-caffeoyl]-¦Â-D-glucopyranoside C35H38O14 ÏàËÆ¶È:55.2% Chemical & Pharmaceutical Bulletin 2002 50(5) 583-589 Studies on the Constituents from the Aerial Part of Baccharis dracunculifolia DC. II Yoshimi NAGATANI, Tsutomu WARASHINA, and Tadataka NORO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 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II Yoshimi NAGATANI, Tsutomu WARASHINA, and Tadataka NORO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . incanoside D C37H50O20 ÏàËÆ¶È:52.6% Chemical & Pharmaceutical Bulletin 2000 48(7) 1075-1078 Three New Phenylethanoid Glycosides from Caryopteris incana and Their Antioxidative Activity JianJun GAO,Kiharu IGARASHI,and Manabu NUKINA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . chionoside B C36H48O20 ÏàËÆ¶È:52.6% Chemical & Pharmaceutical Bulletin 2010 58 703-711 Phenylethanoid and Iridoid Glycosides in the New Zealand Snow Hebes (Veronica, Plantaginaceae) Rilka M. Taskova, Tetsuo Kokubun, Ken G. Ryan, Phil John Garnock-Jones and Soren Rosendal Jensen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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66 1 . compound 5 C6H13N2O2PS ÏàËÆ¶È:50% Tetrahedron Letters 2000 41 3073-3076 Alkylthiylation of triquinphosphoranes by disulfides: an entry to chiral thiatriquinphosphoranes Caroline Marchi, G¨¦rard Buono Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . (3R,4S,5R)-5-amino-1-(tert-butoxycarbonyl)-3,4-dihydroxypiperidine C10H20O4N2 ÏàËÆ¶È:50% European Journal of Organic Chemistry 2011 2230-2234 Concise Route to (¨C)- and (+)-Aphanorphine Mohamed Medjahdi, Jos¨¦ C. Gonz¨¢lez-G¨®mez, Francisco Foubelo and Miguel Yus Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 39 ÏàËÆ¶È:50% European Journal of Organic Chemistry 2010 5263-5273 An Anomeric Effect Drives the Regiospecific Ring-Opening of 1,3-Oxazolidines under Acetylating Conditions R. Fernando Mart¨ªnez, Mart¨ªn ¨¢valos, Reyes Babiano, Pedro Cintas, Jos¨¦ L. Jim¨¦nez, Mark E. Light, Juan C. Palacios and Esther M. S. P¨¦rez Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 77 1 . compound 5 ÏàËÆ¶È:59.0% Magnetic Resonance in Chemistry 1993 31 599-605 1H and 13C NMR data for 2-O-, 3-O-and 2,3-di-O-glycosylated methyl ¦Á-and ¦Â-D-galactopyranosides Alexander S. Shashkov, Nikolay E. Nifant'ev, Vera Yu. Amochaeva and Nikolay K. Kochetkov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 2,6-dimethoxy-4[(1E)-prop-1-enyl]phenyl O-¦Á-L-rhamnopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside C23H34O12 ÏàËÆ¶È:54.5% Helvetica Chimica Acta 2006 Vol. 89 884 Study on the Chemical Constituents of Daphniphyllum angustifolium Haiyun Bai and Lihong Hu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . rhyncoside D C21H32O13 ÏàËÆ¶È:54.5% Chemical & Pharmaceutical Bulletin 2007 55(8) 1175-1180 Rhyncosides A¡ªF, Phenolic Constituents from the Chinese Mangrove Plant Bruguiera sexangula var. rhynchopetala Shuyun BAO,Yi DING,Zhiwei DENG,Peter PROKSCH,d an Wenhan LIN Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . methyl gentiobioside ÏàËÆ¶È:54.5% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 6'-O-¦Â-D-Glucopyranosyltheviridoside C23H34O16 ÏàËÆ¶È:54.5% Phytochemistry 1995 38 793-794 Minor iridoids from Thevetia peruviana Fumiko Abe, Tatsuo Yamauchi, Shoji Yahara, Toshihiro Nohara Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 5-O-Allosylantirrinoside ÏàËÆ¶È:54.5% Phytochemistry 1993 32 1068-1070 5-O-Allosylantirrinoside from Linaria species Emilia Ilieva, Nedjalka Handjieva, Stefan Spassov, Simeon Popov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 3-O-[¦Â-D-glucopyranosyl (1¡ú3)-¦Á-L-rhamnopyranosyl (1¡ú4)-¦Â-D-xylopyranosyl] hederagenin ÏàËÆ¶È:54.5% Turkish Journal of Chemistry 2002 26 947-954 New Triterpenic Saponins from Cephalaria transsylvanica S¨¹HEYLA KIRMIZIG¨¹L, H¨¹SEYİN ANIL Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 2 ÏàËÆ¶È:54.5% Canadian Journal of Chemistry 1990 68 1238-1250 NMR and conformational study of branched oligosaccharides containing 2,3-disubstituted residues of ¦Á-L-rhamnose Grigory M. Lipkind, Nikolay E. Nifant'ev, Alexander S. Shashkov, Nikolay K. Kochetkov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 8-methoxycarbonyloctyl O-(2-acetamido-2-deoxy-¦Â-D-glucopyranosyl)-(1¡ú2)-O-(3,4-di-O-benzyl-¦Á-L-rhamnopyranosyl)-(1¡ú2)-3,4-di-O-benzyl-¦Á-L-rhamnopyranoside C58H77NO16 ÏàËÆ¶È:54.5% Canadian Journal of Chemistry 1979 57 3073-3079 Artificial carbohydrate antigens: the synthesis of the tetrasaccharide repeating unit of Shigella flexneri O antigen Staffan Josephson, David R. Bundle Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 88 1 . ferulaldehyde C10H10O3 ÏàËÆ¶È:50% Chemistry of Natural Compounds 2009 45 234-236 MONO-AROMATIC CONSTITUENTSOF Dendrobium longicornu Jiang-Tao Li, Ben-Lin Yin, Ying Liu, Li-Qin Wang, and Ye-Gao Chen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . Coniferaldehyde ÏàËÆ¶È:50% Korean Journal of Pharmacognosy 2009 40(4) 326-333 Phytochemical Studies on Lonicera Caulis (2) - Aliphatic and Phenolic Compounds Kim, Ju-Sun; Yean, Min-Hye; Seo, Hyun-Kyu; Lee, Je-Hyun; Kang, Sam-Sik Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . acetovanillone ÏàËÆ¶È:50% Chinese Traditional and Herbal Drugs 2005 36 1604-1607 Effect of phenolic acids isolated from Sambucus williamsii on proliferation and differentiation of rat osteoblastic UMR106 cells YANG Xu-juan; WONG Man-sau; WANG Nai-li; CHAN Sun-chi; YAO Xin-sheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . coniferyl aldehyde ÏàËÆ¶È:50% Chinese Traditional and Herbal Drugs 2011 42 437-439 Chemical constituents of Opuntia milpa (I) LUO Chuan, ZHANG Wan-nian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . coniferyl aldehyde C11H11O3 ÏàËÆ¶È:50% Natural Product Research and Development 2014 26 1780-1784 Chemical Constituents from the Fruits of Capparis masaikai LIAO Jin-hua, HU Xu-jia*, YUAN Chun-mao, HE Hong-ping, DI Ying-tong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 4-Phenylphenol ÏàËÆ¶È:50% Molecules 2012 17 12121-12139 Suzuki-Miyaura Reactions Catalyzed by C2-Symmetric Pd-Multi-Dentate N-Heterocyclic Carbene Complexes Lan Jiang, Fengjun Shan, Zhengning Li and Defeng Zhao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . coniferyl aldehyde ÏàËÆ¶È:50% Chinese Traditional and Herbal Drugs 2012 43 2346-2350 Chemical constituents from fruits of Vitex negundo ZHAO Xiang-xiang; ZHENG Cheng-jian; QIN Lu-ping Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 2-ôÇ»ù-5-¼×Ñõ»ù-±½±ûϩȩ ÏàËÆ¶È:50% China Journal of Chinese Materia Medica 2012 37 2092-2099 Non-anthraquinones constituents from the roots of Knoxia valerianoides ZHAO Feng; WANG Sujuan; WU Xiuli; YU Yang; YUE Zhenggang; LIU Bo; LIN Sheng; ZHU Chenggen; YANG Yongchun; SHI Jiangong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . coniferaldehyde ÏàËÆ¶È:50% Journal of the Korean Society for Applied Biological Chemistry 2012 55 433-437 Cytotoxic Compounds from the Fruits of Vitex rotundifolia against Human Cancer Cell Lines Haejin Kim, Jin-Mu Yi, No Soo Kim, You Jin Lee, Jinhee Kim, Dal-Seok Oh, Se-Mi Oh, Ok-Sun Bang, Jun Lee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . aldehyde ÏàËÆ¶È:50% Chinese Traditional and Herbal Drugs 2014 45 1373-1377 Chemical constituents from Gnaphlium affine LI Sheng-hua Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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