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xp¡ªflyÌú¸Ëľ³æ (ÖøÃûдÊÖ)
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΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
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| 13C NMR (151 MHz, MeOD) ¦Ä 15.32, 17.85, 25.86, 26.96, 36.49, 36.55, 39.21, 61.44, 61.72, 70.18, 70.52, 74.91, 76.31, 76.49, 76.95, 77.11, 78.79, 79.02, 79.09, 79.16, 79.66, 79.74, 89.90, 103.12, 104.01, 126.80, 128.48, 135.64, 142.49. |
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²éѯ½á¹û£º¹²²éµ½138¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . soldanellic acid B C40H72O21 ÏàËÆ¶È:70% European Journal of Organic Chemistry 2001 2001 369-373 Soldanelline B − The First Acylated Nonlinear Tetrasaccharide Macrolactone from the European Convolvulaceae Calystegia soldanella Elvira Maria M. Gaspar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . yinxiancaoside B C25H44O14 ÏàËÆ¶È:68.9% Chemistry & Biodiversity 2008 Vol. 5 1736 Sesquiterpene Glucosides from Chloranthus japonicus Sieb. Haixue Kuang, Yonggang Xia, Bingyou Yang, Qiuhong Wang, and Shaowa L Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 7,11-dimethyl-3-methylene-1,6-dodecadien-10,11-diol 10-O-¦Â-D-glucopyranosyl-(1¡ú4)-O-¦Â-D-glucopyranoside ÏàËÆ¶È:68.9% Chemical & Pharmaceutical Bulletin 2007 55(4) 551-556 Two New Steroid Glycosides and a New Sesquiterpenoid Glycoside from the Underground Parts of Trillium kamtschaticum Masateru ONO,Chika TAKAMURA,Fumie SUGITA,Chikako MASUOKA,Hitoshi YOSHIMITSU,Tsuyoshi IKEDA,and Toshihiro NOHARAc Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . dendronobiloside C C27H44O12 ÏàËÆ¶È:68.9% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 6 C45H73NO15 ÏàËÆ¶È:68.9% Phytochemistry 1982 21 187-192 Basic steroid saponins from aerial parts of Fritillaria Thunbergii Junichi Kitajima, Tetsuya Komori, Toshio Kawasaki, Hans-rolf Schulten Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . Ts-x ÏàËÆ¶È:68.9% Phytochemistry 1983 22 1249-1251 A flavonol glycoside and A sesquiterpene cellobioside from Trillium tschonoskii K. Nakano, A. Maruhashi, T. Nohara, T. Tomimatsu, N. Imamura, T. Kawasaki Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 3-O-¦Â-D-glucopyranosylalbicanol-11-O-¦Â-D-glucopyranoside ÏàËÆ¶È:68.9% Molecules 2014 19 507-513 Characterization of a New Sesquiterpene and Antifungal Activities of Chemical Constituents from Dryopteris fragrans (L.) Schott Yu-Hong Huang, Wei-Min Zeng, Guo-Yu Li, Guo-Qing Liu, Dan-Dan Zhao, Jing Wang and Yan-Long Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . (-)-curcuhydroquinone 2,5-di-O-¦Â-D-glucopyranoside C27H42O12 ÏàËÆ¶È:68.9% Helvetica Chimica Acta 2014 97 438-446 New Bisabolane Sesquiterpenes from the Rhizomes of Curcuma xanthorrhiza Roxb. and Their Inhibitory Effects on UVB-Induced MMP-1 Expression in Human Keratinocytes (pages 438¨C446) Ji-Hae Park, Ye-Jin Jung, Mohamed Antar Aziz Mohamed, Tae Hoon Lee, Chang-Ho Lee, Daeseok Han, Myung-Chong Song, Jiyoung Kim and Nam-In Baek Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . Microtropioside C C32H56O14 ÏàËÆ¶È:68.7% Phytochemistry 2010 71 675-681 Microtropiosides A¨CF: ent-Labdane diterpenoid glucosides from the leaves of Microtropis japonica (Celastraceae) Yuka Koyama, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Yoshio Takeda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . Microtropioside D C32H56O14 ÏàËÆ¶È:68.7% Phytochemistry 2010 71 675-681 Microtropiosides A¨CF: ent-Labdane diterpenoid glucosides from the leaves of Microtropis japonica (Celastraceae) Yuka Koyama, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Yoshio Takeda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . Microtropioside E C32H54O13 ÏàËÆ¶È:68.7% Phytochemistry 2010 71 675-681 Microtropiosides A¨CF: ent-Labdane diterpenoid glucosides from the leaves of Microtropis japonica (Celastraceae) Yuka Koyama, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Yoshio Takeda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . lyciumoside III ÏàËÆ¶È:68.7% Bulletin of the Korean Chemical Society 2008 29 2267-2269 A New Acyclic Diterpene from Trigonotis peduncularis Myoung Chong Song, Hye Joung Yang, Dae Keun Kim, Nam In Baek* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . frehmaglutoside G C31H48O18 ÏàËÆ¶È:67.7% Natural Product Research 2015 29 59-63 Two new ionone glycosides from the roots of Rehmannia glutinosa Libosch. Wei-Sheng Feng, Meng Li, Xiao-Ke Zheng, Na Zhang, Kai Song, Jian-Chao Wang & Hai-Xue Kuang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . cussoside B C32H54O13 ÏàËÆ¶È:65.6% Phytochemistry 2002 60 339-343 Clerodane and labdane diterpene glycosides from a Malagasy endemic plant, Cussonia racemosa R.R. Harinantenaina Liva, Ryoji Kasai, Kazuo Yamasaki Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . leucasperoside B C32H51O12 ÏàËÆ¶È:65.6% Journal of Natural Products 2006 69 988-994 Diterpenes from Leucas aspera Inhibiting Prostaglandin-Induced Contractions Samir Kumar Sadhu, Emi Okuyama, Haruhiro Fujimoto, and Masami Ishibashi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . lyciumoside III C32H56O13 ÏàËÆ¶È:65.6% Chemical & Pharmaceutical Bulletin 1993 41 703-709 Cyclic Peptides, Acyclic Diterpene Glycosides and Other Compounds from Lycium chinense MILL Shoji YAHARA,Choko SHIGEYAMA,Takeshi URA,Kaori WAKAMATSU,Tadashi YASUHARA and Toshihiro NOHARA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . phlomisoside-II C32H50O12 ÏàËÆ¶È:65.6% Chemical & Pharmaceutical Bulletin 1985 33 4275-4280 Sweet and Bitter Principles of the Chinese Plant Drug, Bai-Yun-Shen : Revision of the Assignment of the Source Plant and Isolation of Two New Diterpene Glycosides TAKASHI TANAKA,OSAMU TANAKA,ZHONGWEN LIN and JUN ZHOU Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . alangicadinoside B C32H50O17 ÏàËÆ¶È:65.6% Phytochemistry 1996 41 1351-1355 Alangicadinosides A-E: Sesquiterpene glycosides from leaves of Alangium premnifolium Hideaki Otsuka, Masami Yao, Eiji Hirata, Anki Takushi, Yoshio Takeda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . phlomisoside II ÏàËÆ¶È:65.6% Phytochemistry 1994 35 439-442 Diterpenoid glycosyl esters from Phlomis younghusbandii and P. medicinalis roots Masako Katagiri, Kazuhiro Ohtani, Ryoji Kasai, Kazuo Yamasaki, Chong-Ren Yang, Osamu Tanaka Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . goshonoside-F5 ÏàËÆ¶È:65.6% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . Microtropioside F C32H54O13 ÏàËÆ¶È:65.6% Phytochemistry 2010 71 675-681 Microtropiosides A¨CF: ent-Labdane diterpenoid glucosides from the leaves of Microtropis japonica (Celastraceae) Yuka Koyama, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Yoshio Takeda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . Goshonoside-F5 ÏàËÆ¶È:65.6% Chemistry of Natural Compounds 2013 49 49-53 A new ent-labdane diterpene saponin from the fruits of Rubus chingii Nan Sun, Yan Wang, Yun Liu, Mei-Li Guo, Jun Yin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . lucihirtin A C32H48O15 ÏàËÆ¶È:65.6% Chemistry of Natural Compounds 2014 50 288-290 Chemical Constituents of the Aerial Parts of Lycopus lucidus var. hirtus Chao Li, Zhen-Lin Li, Tao Wang, Shi-Hui Qian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 24 . cichorioside L C26H40O13 ÏàËÆ¶È:65.5% Chemical & Pharmaceutical Bulletin 2008 56(10) 1445-1451 Sesquiterpenes from the Roots of Cichorium endivia Tsutomu WARASHINA,and Toshio MIYASE Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 25 . staphylionoside K C25H44O12 ÏàËÆ¶È:65.5% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 26 . platanionoside D C25H44O12 ÏàËÆ¶È:65.5% 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. |

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