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rootulyssesгæ (СÓÐÃûÆø)
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΢Æ×ÇóÖú
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| 13C NMR (CD3OD) ¦Ä 153.07, 134.52, 133.91, 129.84, 128.57, 104.08, 77.02, 76.48, 74.39,69.99, 62.25, 61.24, 55.67 |
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1 . syringin ÏàËÆ¶È:81.2% China Journal of Chinese Materia Medica 2008 33 1032-1035 Studies on chemical constituents of Saussurea laniceps DAWA Zhuoma, ZHOU Yan, BAI Yang, GESANG Suolang, XIE Ping, DING Lisheng Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . cis-syringin ÏàËÆ¶È:78.5% Acta Pharmaceutica Sinica 2007 Vol 42 757-761 The chemical constituents of Polygala hongkongensis Hemsl WU Jian-feng;; CHEN Si-bao; CHEN Shi-lin; TU Peng-fei Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . syringin ÏàËÆ¶È:75% Acta Pharmaceutica Sinica 1999 Vol 34 839-841 STUDIES ON CHEMICAL CONSTITUENTS FROM ACANTHOPANAX SENTICOSUS (RUPR.ET MAXIM.) HARMS Wu Lijun(Wu LJ); Ruan Lijun(Ruan LJ); Zheng Jian(Zheng J); Wang Feifei(Wang FF); Ding Fuli(Ding FL) and Gong Haiping(Gong HP) Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . glucoacetosyringone ÏàËÆ¶È:69.2% Bioorganic & Medicinal Chemistry 2010 18 7052-7057 Chalcone glycosides isolated from aerial parts of Brassica rapa L. ¡®hidabeni¡¯ suppress antigen-stimulated degranulation in rat basophilic leukemia RBL-2H3 cells Tomohiro Itoh, Masayuki Ninomiya, Yoshinori Nozawa, Mamoru Koketsu Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 4-ôǼ׻ù-2,6-¼×Ñõ»ù±½·Ó-1-O-¦Â-D-ÆÏÌÑÌÇÜÕ ÏàËÆ¶È:69.2% China Journal of Chinese Materia Medica 2012 37 1782-1787 Phenolic components from Petasites tricholobus ZHANG Yong; GUO Fujiang; ZENG Peng; JIA Qi; LI Yiming; ZHU Weiliang; CHEN Kaixian Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 2 ÏàËÆ¶È:64.2% Chemical & Pharmaceutical Bulletin 1988 36 2726-2729 TANGHENOSIDES I AND II FROM CHUAN-DANGSHEN, THE ROOT OF CODONOPSIS TANGSHEN OLIV. Kenji Mizutani,Masamichi Yuda,Osamu Tanaka,Yuh-ichiro Saruwatari,Ming-Ru Jia,Yi-Kui Ling and Xui-Feng Pu Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 4-Allyl-2,6-dimethoxyphenyl glucoside ÏàËÆ¶È:64.2% Archives of Pharmacal Research 2007 30 1067-1074 Lignan and terpene constituents from the aerial parts of saussurea pulchella Sang Un Choi, Min Cheol Yang, Kyu Ha Lee, Ki Hyun Kim and Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 2,6-dimethoxy-4-hydroxyphenol-1-O-¦Â-D-glucopyranoside ÏàËÆ¶È:64.2% Journal of Shenyang Pharmaceutical University 2009 26 530-535 Chemical constituents from stem of Cratoxylon cochinchinensis Bl. YU Hai-yang, WANG Nai-li, ZHANG Xue, JIN San-lin, YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . syringin ÏàËÆ¶È:61.5% China Journal of Chinese Materia Medica 2008 33 1641-1643 Study on Chemical Constituents from Juniperus sabina L. ZHAO Jun, YAN Ming, HUANG Yi, LIU Tao, ZHAO Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ëÁøÜÕ ÏàËÆ¶È:61.5% Chinese Traditional and Herbal Drugs 2010 41 867-870 ´óѪÌٵĻ¯Ñ§³É·ÖÑо¿(¢ò) ³ÂÖÇÏÉ;¸ßÎÄÔ¶;Áõá·ÁÕ;ÕÅÌú¾ü Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ¶¡ÏãËáÆÏÌÑÌÇÜÕ C15H20O10 ÏàËÆ¶È:61.5% Chinese Traditional and Herbal Drugs 2010 41 867-870 ´óѪÌٵĻ¯Ñ§³É·ÖÑо¿(¢ò) ³ÂÖÇÏÉ;¸ßÎÄÔ¶;Áõá·ÁÕ;ÕÅÌú¾ü Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . syringin ÏàËÆ¶È:61.5% Chinese Pharmaceutical Journal 2008 43 1461-1463 Study on Chemical Constituents from Juniperus sabina L. ZHAO Jun, YAN Ming, HUANG Yi, LIU Tao, ZHAO Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (1S)-1,5-anhydro-D-glucitol-spiro[1.5]-3-(4-cyanophenyl)-1,4,2-oxathiazole C14H14N2O6S ÏàËÆ¶È:61.5% Bioorganic & Medicinal Chemistry 2009 17 5696-5707 Glucose-based spiro-heterocycles as potent inhibitors of glycogen phosphorylase Veronika Nagy, Mahmoud Benltifa, S¨¦bastien Vidal, Eszter Berzs¨¦nyi, Cathie Teilhet, Katalin Czifr¨¢k, Gyula Batta, Tibor Docsa, P¨¢l Gergely, L¨¢szl¨® Soms¨¢k, Jean-Pierre Praly Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . prunasin ÏàËÆ¶È:61.5% Natural Product Sciences 2012 18 200-203 Chemical Constituents from the Fruits of Prunus mume Jin, Qinghao; Lee, Chul; Lee, Jin-Woo; Lee, In-Sun; Lee, Mi-Kyeong; Jeon, Won-Kyung; Hwang, Bang-Yeon Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . juniperoside C18H26O9 ÏàËÆ¶È:60% Planta Medica 1996 62 88-89 Phenyipropane Glycosides from Jun iperus pharnicea Glues C'omte, AlbertJ. Ghulia. Joseph Vercauteren,and Daovy P. Allais Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . liriodenrin C34H46O18 ÏàËÆ¶È:57.1% Chinese Journal of Natural Medicines 2010 8 199-201 Chemical Constituents from the Aerial Part of Peganum nigellastrum YANG Fei; CHEN Rong; FENG Lin; LI Hai-Dao; ZHANG Hua; LIANG Jing-Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . syringin ÏàËÆ¶È:57.1% Chinese Pharmaceutical Journal 2009 44 1137-1140 Studies on Chemical Constituents of Acanthopanax brachypus(¢ò) HU Hao-bin, FAN Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . dihydrosyringin ÏàËÆ¶È:57.1% Chinese Pharmaceutical Journal 2010 45 975-979 Phenolic Components and Flavanones from Dendrobium candidum LI Yan, WANG Chun-lan, WANG Fang-fei, DONG Hai-ling, GUO Shun-xing, YANG Jun-shan, XIAO Pei-gen Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . liriodendrin ÏàËÆ¶È:57.1% Turkish Journal of Chemistry 2009 33 561-568 A novel naphthoquinone glycoside from Rubia peregrina L. UFUK ÖZGEN, CAVİT KAZAZ, HASAN SEÇEN, İHSAN ÇALIŞ, MAKSUT COŞKUN, PETER J. HOUGHTON Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . liriodendrin ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 1985 33 1452-1457 Studies on the Constituents of Cistanchis Herba. V. Isolation and Structures of Two New Phenylpropanoid Glycosides, Cistanosides E and F HIROMI KOBAYASHI,HIROKO KARASAWA,TOSHIO MIYASE and SEIGO FUKUSHIMA Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . coniferine C16H22O8 ÏàËÆ¶È:56.2% Turkish Journal of Chemistry 2009 33 667-675 Secondary metabolites from Nepeta heliotropifolia ZÜHAL GÜVENALP, HİLAL ÖZBEK, AYŞE KURUÜZÜM-UZ, CAVİT KAZAZ, L. ÖMÜR DEMİREZER Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 4-(1,2,3-trihydroxypropyl)-2,6-dimethoxyphenyl-1-O-¦Â-D-glucopyranoside C17H26O11 ÏàËÆ¶È:56.2% Chinese Traditional and Herbal Drugs 2012 43 1462-1470 Studies on chemical constituents from Aidi Injection ZHANG Miao-miao; LIU Yan-li; CHEN Zhong; LI Xiao-ran; XU Qiong-ming; YANG Shi-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . viridoside ÏàËÆ¶È:53.8% Phytochemistry 2006 67 2380-2391 Comparative phytochemical characterization of three Rhodiola species Gad G. Yousef, Mary H. Grace, Diana M. Cheng, Igor V. Belolipov,Ilya Raskin, Mary Ann Lila Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . benzyl alcohol glucoside C13H18O6 ÏàËÆ¶È:53.8% Phytochemistry 2002 60 873-882 Cyanogenic allosides and glucosides from Passiflora edulis and Carica papaya David S. Seigler, Guido F. Pauli, Adolf Nahrstedt, Rosemary Leen Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . cirsiumoside C13H20O9 ÏàËÆ¶È:53.8% Planta Medica 1990 56 472-474 New Furans from Cirsium chiorolepis Yue-mao Shen and Quan-zhang Mu Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . compound 9a C20H26O14 ÏàËÆ¶È:53.8% Journal of Asian Natural Products Research 2009 11 172-176 The synthesis of analogs of shuangkangsu, a novel natural cycloperoxide glucoside from Lonicera japonica Thunb Yan-Bo Tang, Long-Jiang Huang, Di-Zao Li, Qing-Jian Zhang, Ruo-Yun Chen and De-Quan Yu Structure 13C NMR ̼Æ×Ä£Äâͼ |

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