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1 .     3-O-(3',3'-dimethylsuccinyl)-ursolic acid
C36H56O6     ÏàËÆ¶È:72.2%
Journal of Natural Products          2000          63          1619-1622
Anti-AIDS Agents 38. Anti-HIV Activity of 3-O-Acyl Ursolic Acid Derivatives1
Yoshiki Kashiwada,Tsuneatsu Nagao, Ayumi Hashimoto, Yasumasa Ikeshiro, Hikaru Okabe,L. Mark Cosentino, and Kuo-Hsiung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     N-{3-[4-(3-aminopropyl)piperazinyl]propyl}-3-O-acetylursolamide
C42H72N4O3     ÏàËÆ¶È:70.2%
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
3 .     N-{3-[4-(3-aminopropyl)piperazinyl]propyl}-3-O-acetylursolamide
C42H72N4O3     ÏàËÆ¶È:70.2%
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
4 .     2',2'-dimethylsuccinyl-ursolic acid
C36H56O6     ÏàËÆ¶È:69.4%
Journal of Natural Products          2000          63          1619-1622
Anti-AIDS Agents 38. Anti-HIV Activity of 3-O-Acyl Ursolic Acid Derivatives1
Yoshiki Kashiwada,Tsuneatsu Nagao, Ayumi Hashimoto, Yasumasa Ikeshiro, Hikaru Okabe,L. Mark Cosentino, and Kuo-Hsiung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     3-O-¦Â-D-glucopyranosyl-23-hydroxyursolic acid
    ÏàËÆ¶È:69.4%
Chinese Journal of Natural Medicines          2009          7          206-209
Triterpene Saponins from the Leaves of Ilex pernyi
XIE Guang-Bo; JIANG Yong; LEI Lian-Di; TU Peng-Fei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     2¦Á,3¦Â,27-trihydroxylup-12-en-28-oic acid 3-(3',4'-dihydroxybenzoyl ester)
C37H52O8     ÏàËÆ¶È:67.5%
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
7 .     guajanoic acid
C40H56O6     ÏàËÆ¶È:67.5%
Natural Product Research          2004          18          135-140
Chemical constituents from the leaves of Psidium guajava
Sabira Begum; Syed Imran Hassan; Syed Nawazish Ali; Bina S. Siddiqui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     3-O-(¦Â-D-glucopyranosyl)-23-hydroxyursolic acid
C36H58O9     ÏàËÆ¶È:66.6%
Journal of Natural Products          2003          66          1266-1269
Saponins from Cussonia bancoensis and Their Inhibitory Effects on Nitric Oxide Production
Leon A. Tapondjou, David Lontsi, Beibam L. Sondengam, Fazarna Shaheen, Mohammad I. Choudhary,Atta-ur-Rahman, Fanie R. van Heerden, Hee-Juhn Park, and Kyung-Tae Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     3-O-(3',3'-dimethylglutaryl)-ursolic acid
C37H56O6     ÏàËÆ¶È:66.6%
Journal of Natural Products          2000          63          1619-1622
Anti-AIDS Agents 38. Anti-HIV Activity of 3-O-Acyl Ursolic Acid Derivatives1
Yoshiki Kashiwada,Tsuneatsu Nagao, Ayumi Hashimoto, Yasumasa Ikeshiro, Hikaru Okabe,L. Mark Cosentino, and Kuo-Hsiung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     3-O-isovalaryl-ursolic acid
C35H56O4     ÏàËÆ¶È:66.6%
Journal of Natural Products          2000          63          1619-1622
Anti-AIDS Agents 38. Anti-HIV Activity of 3-O-Acyl Ursolic Acid Derivatives1
Yoshiki Kashiwada,Tsuneatsu Nagao, Ayumi Hashimoto, Yasumasa Ikeshiro, Hikaru Okabe,L. Mark Cosentino, and Kuo-Hsiung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     3-O-tert-butylacetyl-ursolic acid
C36H58O4     ÏàËÆ¶È:66.6%
Journal of Natural Products          2000          63          1619-1622
Anti-AIDS Agents 38. Anti-HIV Activity of 3-O-Acyl Ursolic Acid Derivatives1
Yoshiki Kashiwada,Tsuneatsu Nagao, Ayumi Hashimoto, Yasumasa Ikeshiro, Hikaru Okabe,L. Mark Cosentino, and Kuo-Hsiung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     N-(2¦Á,3¦Â,23-Hydroxyurs-12-en-28-oyl)-L-alanine
    ÏàËÆ¶È:66.6%
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
13 .     N-(2¦Á,3¦Â,23-Hydroxyurs-12-en-28-oyl)-L-valine
    ÏàËÆ¶È:66.6%
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
14 .     Glycoside B 2
    ÏàËÆ¶È:66.6%
Chemistry of Natural Compounds          2000          36          173-176
TRITERPENE GLYCOSIDES OF Scheffleropsis angkae.I. STRUCTURE OF GLYCOSIDES L-B1, L-B2, L-H1, AND L-H 2
A. S. StolyarenkoJ V. I. Grishkovets, 1 N. N. Arnautov, S. V. Iksanova, and V. Ya. Chirva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     2¦Á,3¦Â-dihydroxyurs-12-en-28-oic acid-(28¡ú1)-¦Â-D-glucopyranosyl ester
    ÏàËÆ¶È:66.6%
Journal of Natural Products          1994          Vol 57          333
New Triterpenoid Saponins from the Roots of Potentilla tormentilla
A. R. Bilia, E. Palme, S. Catalano, G. Flamini, I. Morelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     methyl 2¦Á-methoxyursolate
    ÏàËÆ¶È:66.6%
Phytochemistry          1991          30          3383-3387
Steroids and triterpenoids from Rosa laevigata
Jim-Min Fang, Kuang-Chaun Wang, Yu-Shia Cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     methyl 2¦Á,3¦Á,23-trihydroxyurs-12-en-28-oate
    ÏàËÆ¶È:66.6%
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
18 .     obtusinin
C30H46O4     ÏàËÆ¶È:66.6%
Phytochemistry          1990          29          3615-3620
Pentacyclic triterpenoids from Plumeria obtusa
Salimuzzaman Siddiqui,Bina Shaheen Siddiqui,Sabira Begum,Akhtar Naeed
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     methyl nepetoate
C32H52O4     ÏàËÆ¶È:66.6%
Phytochemistry          1990          29          3956-3958
Ursane triterpenoids from Nepeta eriostachia
S.P.S. Bhandari,H.S. Garg,P.K. Agrawal,D.S. Bhakuni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     ursolic acid
    ÏàËÆ¶È:66.6%
Natural Product Research and Development          1994          6(2)          49-51
THE CHEMICAL CONSTITUENTS OF THE FRUITS OF CRATAEGUS SCABRIFOLIA
Si Jianyong; Gau Guangyao; Chen Dihua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     N'-[N-(2¦Á,3¦Â-dihydroxy-12-oleanen-28-oyl)-L-alanyl]-glycine
C35H56N2O6     ÏàËÆ¶È:66.6%
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
22 .     benzyl ursolate
C37H54O3     ÏàËÆ¶È:66.6%
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
23 .     2¦Á,3¦Â-dihydroxyup-12-en-28-oic acid 3-(3',4'-dihydroxybenzoyl ester)
C37H52O7     ÏàËÆ¶È:64.8%
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
24 .     2¦Á,3-dihydroxy-3¦Â-(trans-p-coumaroyloxy)-urs-12-en-28-oic acid
    ÏàËÆ¶È:64.8%
Phytochemistry          1992          31          2801-2804
Triterpenoids from the fruit galls of Actinidia polygama
Yutaka Sashida, Kazunori Ogawa, Noriaki Mori, Tsuyoshi Yamanouchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     compound 1
C39H54O6     ÏàËÆ¶È:64.1%
Chemical & Pharmaceutical Bulletin          2002          50(8)          1124-1125
A New Acylated Triterpene from the Roots of Chaenomeles japonica
Yong Nan XU,Ju Sun KIM,Sam Sik KANG,Kun Ho SON,Hyun Pyo KIM, Hyeun Wook CHANG,and KiHwan BAE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     guavacoumaric acid
C39H54O7     ÏàËÆ¶È:64.1%
Phytochemistry          2002          61          399-403
Triterpenoids from the leaves of Psidium guajava
Sabira Begum, Syed Imran Hassan, Bina S. Siddiqui, Farhana Shaheen,M. Nabeel Ghayur, Anwar H. Gilani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     2¦Á-hydroxy-3¦Â-(trans-p-coumaroyloxy)-urs-12-en-28-oic acid
C39H54O6     ÏàËÆ¶È:64.1%
Acta Botanica Yunnanica          2008          30(1)          121-124
Triterpenoids from Saurauia napaulensis (Saurauiaceae)
WANGQiong,JU Peng,WANG Yi-Fen,LUO Shi-De
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     N-(2¦Á,3¦Â,23-Hydroxyurs-12-en-28-oyl)-L-phenylalanine
    ÏàËÆ¶È:64.1%
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
29 .     jacoumaic acid
    ÏàËÆ¶È:64.1%
Chemical & Pharmaceutical Bulletin          1989          37          648-651
Cytotoxic Triterpenes from a Chinese Medicine, Goreishi
Atsushi NUMATA,Peiming YANG,Chika TAKAHASHI,Ryoko FUJIKI,Michiko NABAE and Eiichi FUJITA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     jacoumaric acid
    ÏàËÆ¶È:64.1%
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
31 .     jacoum-aric acid
    ÏàËÆ¶È:64.1%
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
32 .     guavanoic acid
C32H50O6     ÏàËÆ¶È:63.8%
Phytochemistry          2002          61          399-403
Triterpenoids from the leaves of Psidium guajava
Sabira Begum, Syed Imran Hassan, Bina S. Siddiqui, Farhana Shaheen,M. Nabeel Ghayur, Anwar H. Gilani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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