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1 . 2-Hydroxyiminours-12-en-28-oic acid C30H47NO3 ÏàËÆ¶È:76.1% 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 2 . N-(2¦Á,3¦Â,23-Hydroxyurs-12-en-28-oyl)-L-phenylalanine ÏàËÆ¶È:65.8% Chemistry & Biodiversity 2009 6 864-874 Synthesis and Biological Evaluation of Asiatic Acid Derivatives as Inhibitors of Glycogen Phosphorylases Liying Zhang, Jun Chen, Yanchun Gong, Jun Liu, Luyong Zhang, Weiyi Hua, and Hongbin Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Ursolic acid 3-O-caffeate ÏàËÆ¶È:63.4% Archives of Pharmacal Research 2009 32 845-849 Bioactive triterpenoids from Callistemon lanceolatus Wonsik Jeong, Seong Su Hong, Nahyun Kim, Young Taek Yang and Yu Su Shin, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3¦Â-cis-di-O-methylcaffeoyloxy-2¦Á-hyd-roxyurs-12-en-28-oate C42H60O7 ÏàËÆ¶È:61.9% Phytochemistry 1998 49 1119-1122 Ursane triterpenoids from leaves of melaleuca leucadendron Ching-Kuo Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Calotropterpenylester C42H82O2 ÏàËÆ¶È:61.9% Pharmazie 2001 56 175-177 Norditerpenic ester and pentacyclic triterpenoids from root bark of Calotropis procera (Ait) R. Br. S.H. Ansari - M. Ali Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 2-Hydroxyiminoolean-12-en-28-oic acid C30H47NO3 ÏàËÆ¶È:61.3% 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 7 . N-(2¦Á,3¦Â,23-Hydroxyurs-12-en-28-oyl)-L-valine ÏàËÆ¶È:60.9% Chemistry & Biodiversity 2009 6 864-874 Synthesis and Biological Evaluation of Asiatic Acid Derivatives as Inhibitors of Glycogen Phosphorylases Liying Zhang, Jun Chen, Yanchun Gong, Jun Liu, Luyong Zhang, Weiyi Hua, and Hongbin Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . xiongterpene C39H54O5 ÏàËÆ¶È:60.9% China Journal of Chinese Materia Medica 2002 27 519-522 Studies on Chemical Constituents of the Rhizomae of Ligusticum chuangxiong Xiao Yongqng, LI Li, YOU Xiaolin, MASAHIKO TANIGUCHI, KIMIYEBABA Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . methyl 2¦Á,3¦Á,23-trihydroxyurs-12-en-28-oate triacetate ÏàËÆ¶È:60.9% Phytochemistry 1989 28 1703-1710 Configurational studies on hydroxy groups at C-2,3 and 23 or 24 of oleanene and ursene-type triterpenes by NMR spectroscopy Hisashi Kojima,Haruo Ogura Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . N''-[N'-[N-(2¦Á,3¦Â-dihydroxy-12-oleanen-28-oyl)-6-aminohexanoyl]-L-alanyl]-glycine C41H67N3O7 ÏàËÆ¶È:60.9% Bioorganic & Medicinal Chemistry 2009 17 1139-1145 Solution- and solid-phase synthesis and anti-HIV activity of maslinic acid derivatives containing amino acids and peptides Andres Parra, Francisco Rivas, Pilar E. Lopez, Andres Garcia-Granados, Antonio Martinez, Fernando Albericio, Nieves Marquez, Eduardo Muñoz Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . N-{3-[4-(3-(Bis(4-nitrobenzyl)amino)propyl)piper-azinyl]propyl}-3-O-acetylursolamide C56H82N6O7 ÏàËÆ¶È:60.4% Bioorganic & Medicinal Chemistry 2008 16 771-782 Pharmacomodulation on the 3-acetylursolic acid skeleton: Design, synthesis, and biological evaluation of novel N-{3-[4-(3-aminopropyl)piperazinyl]propyl}-3-O-acetylursolamide derivatives as antimalarial agents Simone C.B. Gnoatto, Sophie Susplugas, Luciana Dalla Vechia, Thais B. Ferreira, Alexandra Dassonville-Klimpt, Karine R. Zimmer, Catherine Demailly, Sophie Da Nascimento, Jean Guillon, Philippe Grellier, Hugo Verli, Grace Gosmann, Pascal Sonnet Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . methyl 3¦Â-trans-di-O-methylcaffeoyloxy-2a-hydroxyurs-12-en-28-oate C42H60O7 ÏàËÆ¶È:59.5% Phytochemistry 1998 49 1119-1122 Ursane triterpenoids from leaves of melaleuca leucadendron Ching-Kuo Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . N-{3-[4-(3-(Bis(4-methoxybenzyl)amino)propyl)pip-erazinyl]propyl}-3-O-acetylursolamide C58H88N4O5 ÏàËÆ¶È:59.5% Bioorganic & Medicinal Chemistry 2008 16 771-782 Pharmacomodulation on the 3-acetylursolic acid skeleton: Design, synthesis, and biological evaluation of novel N-{3-[4-(3-aminopropyl)piperazinyl]propyl}-3-O-acetylursolamide derivatives as antimalarial agents Simone C.B. Gnoatto, Sophie Susplugas, Luciana Dalla Vechia, Thais B. Ferreira, Alexandra Dassonville-Klimpt, Karine R. Zimmer, Catherine Demailly, Sophie Da Nascimento, Jean Guillon, Philippe Grellier, Hugo Verli, Grace Gosmann, Pascal Sonnet Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . N-{3-[(4-(3-(4-Nitrobenzyl)amino)propyl)piperazi-nyl]propyl}-3-O-acetyl-ursolamide C49H77N5O5 ÏàËÆ¶È:59.0% Bioorganic & Medicinal Chemistry 2008 16 771-782 Pharmacomodulation on the 3-acetylursolic acid skeleton: Design, synthesis, and biological evaluation of novel N-{3-[4-(3-aminopropyl)piperazinyl]propyl}-3-O-acetylursolamide derivatives as antimalarial agents Simone C.B. Gnoatto, Sophie Susplugas, Luciana Dalla Vechia, Thais B. Ferreira, Alexandra Dassonville-Klimpt, Karine R. Zimmer, Catherine Demailly, Sophie Da Nascimento, Jean Guillon, Philippe Grellier, Hugo Verli, Grace Gosmann, Pascal Sonnet Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 28-hydroxy-12-ursene-3¦Â-yl-caffeate C39H56O5 ÏàËÆ¶È:58.5% Journal of Natural Products 2004 67 1919-1924 Chemical Constituents from the Colombian Medicinal Plant Maytenus laevis Hiroyuki Nakagawa, Yoshihisa Takaishi, Yoshinori Fujimoto, Carmenza Duque, Cristina Garzon, Mitsunobu Sato, Masato Okamoto, Tetsuya Oshikawa, and Sharif Uddin Ahmed Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . oleanolic acid 3-O-(3',3'-tetramethylene)glutarate ÏàËÆ¶È:58.5% Journal of Natural Products 1998 61 1090-1095 Anti-AIDS Agents. 30. Anti-HIV Activity of Oleanolic Acid, Pomolic Acid, and Structurally Related Triterpenoids Yoshiki Kashiwada, Hui-Kang Wang, Tsuneatsu Nagao, Susumu Kitanaka, Ichiro Yasuda, Toshihiro Fujioka, Takashi Yamagishi, L. Mark Cosentino, Mutsuo Kozuka, Hikaru Okabe, Yasumasa Ikeshiro, Chang-Qi Hu, O Eric Yeh, and Kuo-Hsiung Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 3¦Â-[(mmethoxybenzoyl)oxy]urs-12-en-28-oic acid C38H54O5 ÏàËÆ¶È:58.5% Journal of Natural Products 1997 60 1008-1011 Bioactive Constituents of Morus australis and Broussonetia papyrifera Horng-Huey Ko, Sheu-Meei Yu, Feng-Nien Ko, Che-Ming Teng, and Chun-Nan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 2¦Á,3¦Â-dihydroxyup-12-en-28-oic acid 3-(3',4'-dihydroxybenzoyl ester) C37H52O7 ÏàËÆ¶È:58.5% Journal of Natural Products 1996 59 297-300 New Lupane Derivatives from the Leaves of Licania pyrifolia Anna Rita Bilia and Ivano Morelli Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . neriucoumaric acid C30H46O3 ÏàËÆ¶È:58.5% Planta Medica 1987 53 424-427 Isolation and Structure of Neriucoumaric and Isoneriucoumaric Acids from the Leaves of Nerium oleander Salimuzzaman Siddiqui, Bina S. Siddiqui, Farrukh Hafeez, and Sabira Begum Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . isoneriucoumaric acid C30H46O3 ÏàËÆ¶È:58.5% Planta Medica 1987 53 424-427 Isolation and Structure of Neriucoumaric and Isoneriucoumaric Acids from the Leaves of Nerium oleander Salimuzzaman Siddiqui, Bina S. Siddiqui, Farrukh Hafeez, and Sabira Begum Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . jacoumaric acid ÏàËÆ¶È:58.5% China Journal of Chinese Materia Medica 2009 34 3225-3228 Chemical constituents of Periploca forrestii GAN Xiuhai, ZHOU Xin, CHEN Huaguo, GONG Xiaojian, ZHAO Chao Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . methyl 3¦Â-(cis-p-methoxycinnamoyloxy)-12-ursen-28-oate ÏàËÆ¶È:58.5% Phytochemistry 1997 44 1309-1312 Terpenoids and other constituents of Eucalyptus globulus Gabriela G. Santos, João C. N. Alves, Jesus M. L. Rodilla, A. Paula Duarte, Anna M. Lithgow, Julio G. Urones Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . compound 6 ÏàËÆ¶È:58.5% Phytochemistry 1994 37 1139-1142 Icacinic acid, a triterpenoid from Poraqueiba guianensis Mar¨ªlia O.F. Goulart, Antônio E.G. Sant'ana, Ricardo J. Alves, Jos¨¦ D. de Souza Filho, Jos¨¦ G.S. Maia, Geovane G. de Oliveira, La¨ªde B. de Oliveira Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . methyl 2¦Á,3¦Á,24-trihydroxyurs-12-en-28-oate triacetate C57H56O8 ÏàËÆ¶È:58.5% Phytochemistry 1987 26 1107-1111 Pentacyclic triterpenoids from Prunella vulgaris Hisashi Kojima,Hideo Tominaga,Shigeki Sato,Haruo Ogura Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . ´¨ÜºÈýÝÆ ÏàËÆ¶È:58.5% Modern Chinese Medicine 2010 12(3) 22-25 Study on Chemical Constituents of Ligusticum chuanxiong Hort1 Hao Shujuan, Zhang Zhenxue, Tian Yang, Ma Yueping, Pengqing, Shenshuo, Zhanglei, Wang Jinhui Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . hexyl 3¦Â-hydroxyurs-12-en-28-oate C36H60O3 ÏàËÆ¶È:58.5% Bioorganic & Medicinal Chemistry 2009 17 7265-7274 Ursolic acid derivatives induce cell cycle arrest and apoptosis in NTUB1 cells associated with reactive oxygen species Huang-Yao Tu, A-Mei Huang, Bai-Luh Wei, Kim-Hong Gan, Tzyh-Chyuan Hour, Shyh-Chyun Yang, Yeong-Shiau Pu, Chun-Nan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . benzyl 3-O-¦Â-(3-ferrocenylpropanoyl) ursolate C50H66FeO4 ÏàËÆ¶È:58.5% European Journal of Medicinal Chemistry 2008 43 1865-1877 Evaluation of ursolic acid isolated from Ilex paraguariensis and derivatives on aromatase inhibition Simone C.B. Gnoatto, Alexandra Dassonville-Klimpt, Sophie Da Nascimento, Philippe Gal¨¦ra, Karim Boumediene, Grace Gosmann, Pascal Sonnet, Safa Moslemi Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . N-{3-[4-(3-(Bis(4-bromobenzyl)amino)propyl)piper-azinyl]propyl}-3-O-acetylursolamide C56H82N4O3Br2 ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry 2008 16 771-782 Pharmacomodulation on the 3-acetylursolic acid skeleton: Design, synthesis, and biological evaluation of novel N-{3-[4-(3-aminopropyl)piperazinyl]propyl}-3-O-acetylursolamide derivatives as antimalarial agents Simone C.B. Gnoatto, Sophie Susplugas, Luciana Dalla Vechia, Thais B. Ferreira, Alexandra Dassonville-Klimpt, Karine R. Zimmer, Catherine Demailly, Sophie Da Nascimento, Jean Guillon, Philippe Grellier, Hugo Verli, Grace Gosmann, Pascal Sonnet Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . aesculioside IVa C57H90O23 ÏàËÆ¶È:56.0% Phytochemistry 2006 67 784-794 Triterpenoid saponins from the fruits of Aesculus pavia Zhizhen Zhang, Shiyou Li, Shanmin Zhang, David Gorenstein Structure 13C NMR ̼Æ×Ä£Äâͼ |

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