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16.27,16.39,16.83,16.90,16.96,17.07,17.13,18.01,21.03,22.55,22.91,22.95,23.24,23.33,23.76,36.27,37.54,37.62,38.39,38.45,38.67,40.34,40.75,41.31,41.66,45.40,45.65,46.79,46.95,47.03,52.34,54.71,67.11,82.21,83.23,121.39,124.45,138.21,143.87,178.22,178.52
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·ÛÉ«ÓñÃ×(¶¹¸ç´ú·¢): ½ð±Ò+15, лл 2013-05-29 15:35:41
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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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