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JINQH1982: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-06-11 09:18:08
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½4151¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 2¦Á,3¦Á,24-ÈýôÇ»ù-12-Ï©-28-Æë¶Õ¹ûËá C30H48O5 ÏàËÆ¶È:83.8% Chinese Pharmaceutical Journal 2001 36 445-447 Studies on the chemical constituents of Callicarpa bodinieri (¢ò) REN Feng zhi, LUAN Xin hui, QU Hui hua, ZHAO Yi min Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 2¦Á,3¦Â,24-trihydroxyolean-12-en-28-oate C31H50O5 ÏàËÆ¶È:83.8% The Journal of Organic Chemistry 2007 72 3500-3509 Remote Hydroxylation of Methyl Groups by Regioselective Cyclopalladation. Partial Synthesis of Hyptatic Acid-A Andr¨¦s Garc¨ªa-Granados, Pilar E. L¨®pez, Enrique Melguizo, Andr¨¦s Parra, and Yolanda Sime¨® Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . methyl 2¦Á,3¦Â,24-trihydroxy-olean-12-en-28-oate ÏàËÆ¶È:83.8% Indian Journal of Chemistry 2002 41B 234-236 Triterpene and triterpene glycosides from Salvia tricupis Zhen-Fu Hou, Zhi-Xiang Xie, Yong-Qiang Tu & Yu Li Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . olean-12-en-28-oic acid 3¦Â,24-diol ÏàËÆ¶È:80.6% Chemical & Pharmaceutical Bulletin 1982 30 3340-3346 Studies on the Constituents of Clematis Species. V. On the Saponins of the Root of Clematis chinensis OSBECK. (5) HARUHISA KIZU and TSUYOSHI TOMIMORI Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Maslinic acid C30H48O4 ÏàËÆ¶È:80.6% Chemistry of Natural Compounds 2009 45 921-924 ISOPRENOIDS OF Euphorbia sororia. I. TRITERPENOIDS Y. Huang,H. A. Aisa, and M. I. Isaev Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 4-epihederagenin ÏàËÆ¶È:80.6% Chemistry of Natural Compounds 1992 28 1-23 13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES A. I. Kalinovskii Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 2¦Á,3¦Á,24-trihydroxyolean-12-en-28-oic acid ÏàËÆ¶È:80.6% Journal of Chinese Pharmaceutical Sciences 2000 9 128-130 A New Phenylpropanoid and Triterpenoids from Prunella vulgaris Wang Zhuju, Zhao Yuying, Wang Bin, Li Jiexiu, Ai Tiemin and Chen Yayan Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3¦Â,16¦Á,24-OH oleanlic acid ÏàËÆ¶È:80.6% Acta Pharmaceutica Sinica 1999 Vol 34 679-681 STUDIES ON THE CHEMICAL CONSTITUENTS FROM PRUNELLA VULGARIS Wang Zhuju (Wang ZJ); Zhao Yuying (Zhao YY); Tu Guangzhong (Tu GZ); Hong Shaoliang (Hong SL) and Chen Yayan (Chen YY) Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . epihedaragenin ÏàËÆ¶È:80.6% Phytochemistry 1994 37 1517-1575 13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features Shashi B. Mahato, Asish P. Kundu Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 4-epi-hederagenin ÏàËÆ¶È:80.6% Korean Journal of Pharmacognosy 1987 18(3) 151-167 13C NMR Spectroscopy of Amyrins Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 2¦Á,3¦Â,24-ÈýôÇ»ù-12-Ï©-28-Æë¶Õ¹ûËá(2¦Á,3¦Â,24-trihydroxy-olea-12-en-28-oic acid) ÏàËÆ¶È:80.6% Chinese Traditional and Herbal Drugs 2011 42(5) 859-862 Chemical constituents of Salvia plebaia LU Ru-mei, YANG Chang-shui, WEI Jian-hua Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . maslinatic acid C30H48O4 ÏàËÆ¶È:80.6% Chinese Traditional and Herbal Drugs 2000 31 409-412 Triterpenes from Butter-and-Eggs (Linaria vulgaris) Shenyang Pharmaceutical University (Shenyang )Hua Huiming; Hou Bailing; Li Wen and Li Xian Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 2¦Á,3¦Â,24-trihydroxy olean-12-en-28-oic acid ÏàËÆ¶È:80.6% Chinese Journal of Natural Medicines 2009 7 421-424 Triterpenes from Prunella vulgaris QI Jin; HU Zheng-Fang; LIU Zhi-Jun; YU Bo-Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 2¦Á,3¦Â,24-Trihydroxyolea-12en-28oic acid ÏàËÆ¶È:80.6% Archives of Pharmacal Research 2008 31 1578-1583 Triterpenoic acids of Prunella vulgaris var. lilacina and their cytotoxic activities In Vitro Il Kyun Lee, Do Hoon Kim, Seung Young Lee, Kyung Ran Kim and Sang Un Choi, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . maslinic acid ÏàËÆ¶È:80.6% Chinese Pharmaceutical Journal 2003 38 752-757 Studies on constituents of triterpene acids from Eriobotrya japonica and their anti-inflammatory and antitussive effects JU Jian-hua, ZHOU Liang, LIN Geng, LIU Dong, WANG Li-wei, YANG Jun-shan Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . maslinic acid C30H48O4 ÏàËÆ¶È:80.6% Natural Product Research and Development 2009 21 608-611 Chemical Constituents of Clerodendranthus spicatus TAN Jun-jie; TAN Chang-heng; CHEN Yi-lei; JIANG Shan-hao; ZHU Da-yuan Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . ÐܹûËáÒÒõ¥ ÏàËÆ¶È:80.6% Natural Product Research and Development 2007 19 51-54 Study on Nonirodoids from Fruits of Lonicera maackii WANG Yu-li; YANG Li; LUO Guo-an; WANG Yi-ming* Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 2¦Á,3¦Á,24-trihydroxyolean-12-en-28-oic acid C30H48O5 ÏàËÆ¶È:80.6% Academic Journal of Second Military Medical University 2011 32 749-753 Anti-tumor constituents from the roots of Actinidia valvata XU Yi-xin, XIANG Zhao-bao, CHEN Xiao-jing, CHEN Hai-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 2¦Á,3¦Á,24-trihydroxy-olea-12-en-28-oic acid ÏàËÆ¶È:80.6% Chinese Traditional and Herbal Drugs 2012 43 861-865 Chemical constituents from whole herb of Hedyotis scandens DENG Fang-ye; WANG Guo-cai; WANG Chun-hua; YE Wen-cai Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 2¦Á,3¦Â-dihydroxyolean-12-ene-24,28-dioic acid dimethyl ester C32H50O6 ÏàËÆ¶È:78.1% Planta Medica 2003 69 327-331 A New in vitro Tissue Factor Inhibitory Triterpene from the Fruits of Chaenomeles sinensis Ming Hong Lee,Yong Nam Han Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 2¦Á-Hydroxyolean-12-en-28-oic acid C30H48O3 ÏàËÆ¶È:77.4% Journal of Natural Products 2009 72 1414-1418 Synthesis of 3-Deoxypentacyclic Triterpene Derivatives as Inhibitors of Glycogen Phosphorylase Pu Zhang,Jia Hao,Jun Liu,Qian Lu, Huaming Sheng, Luyong Zhang, and Hongbin Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . methyl arjunolate ÏàËÆ¶È:77.4% Planta Medica 1990 56 287-289 Further Triterpenoids of Musanga cecropioides:The Structure of Cecropic Acid D. Lontsi, B. L. Sondengam, J. F. Ayafor, M G. Tsoupras, andR. Tabacchi Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . Hedera ÏàËÆ¶È:77.4% Acta Botanica Yunnanica 2000 22(2) 201-208 Triterpenoid Glycosides from the Lonicera japonica CHEN Chang-Xiang,WANGWei-Wei,NI Wei,CHEN Neng-Yu,ZHOU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . compound 2b ÏàËÆ¶È:77.4% Chemical & Pharmaceutical Bulletin 1992 40 401-405 Studies on Differentiation-Inducing Activities of Triterpenes Kaoru UMEHARA,Rieko TAKAGI,Masanori KUROYANAGI,Akira UENO,Takao TAKI and Ying-Jie CHEN Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . compound 2 ÏàËÆ¶È:77.4% Chemical & Pharmaceutical Bulletin 1989 37 1770-1775 Studies on the Constituents of Actinostemma lobatum MAXIM. IV. Structures of Lobatosides C, D and H, the Dicrotalic Acid Esters of Bayogenin Bisdesmosides Isolated from the Herb Toshihiro FUJIOKA,Masayo IWAMOTO,Yukiko IWASE,Shizuko HACHIYAMA,Hikaru OKABE,Tatsuo YAMAUCHI and Kunihide MIHASHI Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . oleanolic acid acid 3-O-sulfate ÏàËÆ¶È:77.4% Chemical & Pharmaceutical Bulletin 1985 33 3715-3723 Sulfated Triterpenoid Saponins from the Leaves of Bupleurum rotundifolium L. ERIKO AKAI,TADAHIRO TAKEDA,YOSHIMASA KOBAYASHI and YUKIO OGIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . compound 7 C30H47O6S-0.5Ca-3.5H2O ÏàËÆ¶È:77.4% Chemical & Pharmaceutical Bulletin 1985 33 3715-3723 Sulfated Triterpenoid Saponins from the Leaves of Bupleurum rotundifolium L. ERIKO AKAI,TADAHIRO TAKEDA,YOSHIMASA KOBAYASHI and YUKIO OGIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . ST-D2 ÏàËÆ¶È:77.4% Chemistry of Natural Compounds 1997 33 316-319 TRITERPENE GLYCOSIDES OF Hedera taurica XVI. STRUCTURES OF GLYCOSIDES St-A, St-B 1, St-B 2, St-C,St-D1, St-D2, St-E, St-F 1, AND St-F 2 FROM THE STEMS OF CRIMEAN IVY V. I. GriShkovets, S. V. Godin, O. Ya. Tsvetkov,A. S. Shamhkov, and V. Ya. Chirva Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-06-10 18:37:40
JINQH1982
½ð³æ (СÓÐÃûÆø)
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- ½ð±Ò: 1052.5
- É¢½ð: 60
- ºì»¨: 2
- Ìû×Ó: 278
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3Â¥2013-06-11 09:26:10
JINQH1982
½ð³æ (СÓÐÃûÆø)
- Ó¦Öú: 11 (СѧÉú)
- ½ð±Ò: 1052.5
- É¢½ð: 60
- ºì»¨: 2
- Ìû×Ó: 278
- ÔÚÏß: 167.8Сʱ
- ³æºÅ: 459216
- ×¢²á: 2007-11-14
- ÐÔ±ð: GG
- רҵ: ÌìȻҩÎﻯѧ
4Â¥2013-06-11 10:19:44













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