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²éѯ½á¹û£º¹²²éµ½1426¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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