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²éѯ½á¹û£º¹²²éµ½1574¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . betulinic acid ÏàËÆ¶È:80.5% Natural Product Research and Development 2009 21 438-440 Studies on the Anticancer Constituents in Glycyrrhiza uralensis Fisch YANG Li; CHEN Hai-xia; GAO Wen-yuan; YAN Lu-lu Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . pulsatilla triterpenic acid A C36H52O6 ÏàËÆ¶È:77.7% Heterocycles 2011 83 2365-2371 Three New Triterpenoids from Pulsatilla chinensis (Bunge) Regel and Their Cytotoxic Activities Zhan Shu, Zhong Chen, Xiu-juan Ding, Bing-qian Lu, Chen-jiao Ji, Qiong-Ming Xu,* Xiao-ran Li, and Shi-Lin Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Allyl betulinate C33H52O3 ÏàËÆ¶È:77.7% Bioorganic & Medicinal Chemistry 2006 14 6713-6725 Glycosidation of lupane-type triterpenoids as potent in vitro cytotoxic agents Charles Gauthier, Jean Legault, Maxime Lebrun, Philippe Dufour, Andr¨¦ Pichette Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 28-O-¦Â-D-glucopyranosyl 3¦Â-hydroxy-lup-20(29)-en-28-oate C36H58O8 ÏàËÆ¶È:75% Journal of Natural Products 1999 62 761-763 Glucosidation of Betulinic Acid by Cunninghamella Species Parnali Chatterjee, John M. Pezzuto, and Samir A. Kouzi Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 2¦Á,3¦Á-dihydroxy-lup-20(29)-en-28-oate ÏàËÆ¶È:75% Natural Product Research 2009 23 1218-1230 Chemical composition of the stem bark and leaves of Ficus pandurata Hance M. A. Ramadan; A. S. Ahmad; A. M. Nafady; A. I. Mansour Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . betulinic acid methyl ester ÏàËÆ¶È:75% Tetrahedron Letters 2005 46 2337-2340 Novel biotransformation of pentacyclic triterpenoid acids by Nocardia sp. NRRL 5646 Jian Zhang, Zhi-Hong Cheng, Bo-Yang Yu, Geoffrey A. Cordell, Samuel X. Qiu Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3-O-¦Â-D-Glucopyranoside of betulinic acid C36H58O8 ÏàËÆ¶È:75% Bioorganic & Medicinal Chemistry 2006 14 6713-6725 Glycosidation of lupane-type triterpenoids as potent in vitro cytotoxic agents Charles Gauthier, Jean Legault, Maxime Lebrun, Philippe Dufour, Andr¨¦ Pichette Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3-O-¦Á-D-Arabinopyranoside of betulinic acid C35H56O7 ÏàËÆ¶È:75% Bioorganic & Medicinal Chemistry 2006 14 6713-6725 Glycosidation of lupane-type triterpenoids as potent in vitro cytotoxic agents Charles Gauthier, Jean Legault, Maxime Lebrun, Philippe Dufour, Andr¨¦ Pichette Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3¦Â-O-trans-coumaroyl betulinic acid ÏàËÆ¶È:72.9% Journal of Ethnopharmacology 2012 142 456¨C461 Antiparasitic compounds from Cornus florida L. with activities against Plasmodium falciparum and Leishmania tarentolae Rocky Graziose, Patricio Rojas-Silva, Thirumurugan Rathinasabapathy, Carmen Dekock, Mary H. Grace, Alexander Poulev, Mary Ann Lila, Peter Smith, Ilya Raskin Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3-O-¦Â-D-Glucopyranoside of methyl betulinate C37H60O8 ÏàËÆ¶È:72.9% Bioorganic & Medicinal Chemistry 2006 14 6713-6725 Glycosidation of lupane-type triterpenoids as potent in vitro cytotoxic agents Charles Gauthier, Jean Legault, Maxime Lebrun, Philippe Dufour, Andr¨¦ Pichette Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 2¦Á-hydroxy-3¦Â-O-acetyllup-20(29)-en-28-oic acid C32H50O5 ÏàËÆ¶È:72.2% Planta Medica 2008 74 1735-1740 Two Novel Triterpenoids with Antiproliferative and Apoptotic Activities in Human Leukemia Cells Isolated from the Resin of Garcinia hanburyi Li-liWang, Zhan-lin Li, Dan-dan Song, Lin Sun, Yue-hu Pei,Yong-kui Jing, Hui-ming Hua Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 2b ÏàËÆ¶È:72.2% Acta Pharmaceutica Sinica 1996 31 940-944 ISOLATION AND STRUCTURE ELUCIDATION OF CIRENSENOSIDES O AND P FROM THE LEAVES OF OPLOPANAX ELATUS NAKAL GS Wang; YP Chen; JD Xu; T Murayama and J Shoji Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . lupeol-20(29)-en-3-nonadecanoate C39H66O2 ÏàËÆ¶È:72.2% China Journal of Chinese Materia Medica 2009 34 3214-3216 Chemical constituents of Periploca forrestii and their cytotoxicity activity WANG Jin, WANG Cuifang, CHEN Jinxiong, DU Jiang, Qiu Dewen, QIU Minghua Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 3-acetoxyalphitolic acid C32H50O5 ÏàËÆ¶È:72.2% Planta Medica 2010 76 368-371 Anti-HIV©\1 and Anti-Inflammatory Lupanes from the Leaves, Twigs, and Resin of Garcinia hanburyi Reutrakul, Vichai; Anantachoke, Natthinee; Pohmakotr, Manat; Jaipetch, Thaworn; Yoosook, Chalobon; Kasisit, Jittra; Napaswa, Chanita; Panthong, Ampai; Santisuk, Thawatchai; Prabpai, Samran; Kongsaeree, Palangpon; Tuchinda, Patoomratana Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . Acanthosessilioside A C36H56O9 ÏàËÆ¶È:72.2% Journal of Natural Products 2012 75 1138-1144 Bioactive 3,4-seco-Triterpenoids from the Fruits of Acanthopanax sessiliflorus Dae-Young Lee, Kyeong-Hwa Seo, Dong-Sung Lee, Youn-Chul Kim, In-Sik Chung, Gye-Won Kim, Dae-Sung Cheoi, and Nam-In Baek Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 3-O-¦Á-D-Arabinopyranoside of methyl betulinate C36H58O7 ÏàËÆ¶È:72.2% Bioorganic & Medicinal Chemistry 2006 14 6713-6725 Glycosidation of lupane-type triterpenoids as potent in vitro cytotoxic agents Charles Gauthier, Jean Legault, Maxime Lebrun, Philippe Dufour, Andr¨¦ Pichette Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 3-O-¦Á-L-Rhamnopyranoside of betulinic acid C36H58O7 ÏàËÆ¶È:72.2% Bioorganic & Medicinal Chemistry 2006 14 6713-6725 Glycosidation of lupane-type triterpenoids as potent in vitro cytotoxic agents Charles Gauthier, Jean Legault, Maxime Lebrun, Philippe Dufour, Andr¨¦ Pichette Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . pyracrenic acid ÏàËÆ¶È:71.7% China Journal of Chinese Materia Medica 2011 Vol 36,Issue 9 1193-1197 Studies on chemical constituents in roots of Helicteres angustifolia WEI Yingrou,WANG Guocai,ZHANG Xiaoqi,WANG Ying,YE Wencai Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . pyracrenic acid C39H54O6 ÏàËÆ¶È:71.7% Chinese Traditional and Herbal Drugs 2008 39 972-975 Chemical constituents from roots of Millettia speciosa WANG Chun-hua; WANG Ying; WANG Guo-cai; YA Ji; ZHANG Xiao-qi; YE Wen-cai Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . pyracrenic acid ÏàËÆ¶È:71.7% Journal of Chinese Medicinal Materials 2012 35 904-908 Chemical Constituents from the Aerial Roots of Ficus microcarpa JIANG Bei, HAN Wei-li, ZHANG Qing-wen, ZHANG Xiao-qi, YE Wen-cai Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . ÐܹûÐÁõ¥ C38H64O3 ÏàËÆ¶È:71.0% Journal of Plant Resources and Environment 2001 10 1-3 ÊÁÖоßÓС÷12ÐܹûÏ©¹Ç¼ÜµÄÎå»·ÈýÝÆÀ໯ºÏÎï ÁõÑǾý, л½ðÂ× Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 2-O-E-p-Coumaroylalphitolic Acid ÏàËÆ¶È:70.2% Chemical & Pharmaceutical Bulletin 2006 54(4) 535-537 Ceanothane- and Lupane-Type Triterpenes with Antiplasmodial and Antimycobacterial Activities from Ziziphus cambodiana Sunit SUKSAMRARN,Panomwan PANSEETA,Soykam KUNCHANAWATTA,Thanomsin DISTAPORN,Saovaluk RUKTASING,and Apichart SUKSAMRARN Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 3-O-¦Á-L-Rhamnopyranoside of methyl betulinate C37H60O7 ÏàËÆ¶È:70.2% Bioorganic & Medicinal Chemistry 2006 14 6713-6725 Glycosidation of lupane-type triterpenoids as potent in vitro cytotoxic agents Charles Gauthier, Jean Legault, Maxime Lebrun, Philippe Dufour, Andr¨¦ Pichette Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 3¦Â-O-cis-feruloylbetulinic acid C40H56O6 ÏàËÆ¶È:70% Journal of Natural Products 2004 67 994-998 New 3-O-Acyl Betulinic Acids from Strychnos vanprukii Craib Nguyen Quyet Chien, Nguyen Van Hung, Bernard D. Santarsiero, Andrew D. Mesecar,Nguyen Manh Cuong, D. Doel Soejarto, John M. Pezzuto, Harry H. S. Fong, and Ghee T. Tan Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 2a-hydroxy-3¦Â-[(4-hydroxybenzoyl)oxy]taraxer-14-en-28-oate C38H54O6 ÏàËÆ¶È:69.4% Chemistry & Biodiversity 2006 Vol. 3 473 Isolation, DNA Topoisomerase-II Inhibition, and Cytotoxicity of Three New Terpenoids from the Bark of Macaranga tanarius Shun-ichi Wada and Reiko Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . compound II methylate ÏàËÆ¶È:69.4% Chemical & Pharmaceutical Bulletin 1990 38 714-716 Two New Triterpenoid Sulfates from the Leaves of Schefflera octophylla Junichi KITAJIMA,Masami SHINDO and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . glycoside II C44H66O12 ÏàËÆ¶È:69.4% Chemical & Pharmaceutical Bulletin 1989 37 2727-2730 Two New Triterpenoid Glycosides from the Leaves of Schefflera octophylla Junichi KITAJIMA and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . 3-O-¦Â-D-glucopyranosyl 3¦Á,11¦Á-dihydroxylup-20(29)-en-28-oic acid C36H58O9 ÏàËÆ¶È:69.4% Phytochemistry 1999 51 1369-1374 Lupane-triterpene glycosides from leaves of Acanthopanax koreanum Seung-Yeup Chang, Chang-Soo Yook, Toshihiro Nohara Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . 3¦Â-(¦Â-D-glucopyranosyloxy)-20-oxo-30-norlupan-28-oic acid C35H56O9 ÏàËÆ¶È:69.4% Chemistry of Natural Compounds 2011 47 741-748 Synthesis of 3¦Â-hydroxy-20-oxo-30-norlupan-28-oic (platanic) acid and its glycosides M. V. Denisenko, N. F. Samoshina, V. A. Denisenko and P. S. Dmitrenok Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . ¦Â-ÏãÊ÷Ö¬´¼¼ºÃÑ C36H62O ÏàËÆ¶È:69.4% Journal of Plant Resources and Environment 2001 10 1-3 ÊÁÖоßÓС÷12ÐܹûÏ©¹Ç¼ÜµÄÎå»·ÈýÝÆÀ໯ºÏÎï ÁõÑǾý, л½ðÂ× Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . 3¦Â-O-cisferuloylbetulinic acid C39H54O5 ÏàËÆ¶È:69.2% Journal of Natural Products 2004 67 994-998 New 3-O-Acyl Betulinic Acids from Strychnos vanprukii Craib Nguyen Quyet Chien, Nguyen Van Hung, Bernard D. Santarsiero, Andrew D. Mesecar,Nguyen Manh Cuong, D. Doel Soejarto, John M. Pezzuto, Harry H. S. Fong, and Ghee T. Tan Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . 3¦Â-O-cis-coumaroylbetulinic acid C39H54O5 ÏàËÆ¶È:69.2% Journal of Natural Products 2004 67 994-998 New 3-O-Acyl Betulinic Acids from Strychnos vanprukii Craib Nguyen Quyet Chien, Nguyen Van Hung, Bernard D. Santarsiero, Andrew D. Mesecar,Nguyen Manh Cuong, D. Doel Soejarto, John M. Pezzuto, Harry H. S. Fong, and Ghee T. Tan Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . betulinic acid 3,5-dihydroxyl-cinnamate C36H54O6 ÏàËÆ¶È:69.2% Chinese Traditional and Herbal Drugs 1994 25 569-570+574+614 Chemical Components of Mongolian Spirala (Spiraca mongolica) Xie Haihui; Wei Xiaoyi; Wei Biyu (Address: Xie Haihui; South China Institute of Botany; Academy of Military Medical Sciences; Guangzho); Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . 3¦Â-O-trans-feruloylbetulinic acid C40H56O6 ÏàËÆ¶È:67.5% Journal of Natural Products 2004 67 994-998 New 3-O-Acyl Betulinic Acids from Strychnos vanprukii Craib Nguyen Quyet Chien, Nguyen Van Hung, Bernard D. Santarsiero, Andrew D. Mesecar,Nguyen Manh Cuong, D. Doel Soejarto, John M. Pezzuto, Harry H. S. Fong, and Ghee T. Tan Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . quadranoside I C36H58O10 ÏàËÆ¶È:66.6% Journal of Natural Products 2000 63 496-500 Quadranosides I-V, New Triterpene Glucosides from the Seeds of Combretum quadrangulare I Ketut Adnyana, Yasuhiro Tezuka, Arjun H. Banskota, Quanbo Xiong, Kim Qui Tran, and Shigetoshi Kadota Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . notoginsenoside R7 C36H62O8 ÏàËÆ¶È:66.6% Acta Botanica Yunnanica 1993 15(4) 409-412 MINOR COSTITUENTS FROM THE ROOTS OF PANAX NOTOGINSENG(1) ZHAO Ping,LIU Yu-Qing,YANG Chong-Ren Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . compound I methylate ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1990 38 714-716 Two New Triterpenoid Sulfates from the Leaves of Schefflera octophylla Junichi KITAJIMA,Masami SHINDO and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . Quadranoside I ÏàËÆ¶È:66.6% Molecules 2008 13 2717-2728 Bioactive Pentacyclic Triterpenes from the Stems of Combretum laxum Eder Bisoli, Walmir S. Garcez, Lidilhone Hamerski, Caroline Tieppo and Fernanda R. Garcez Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . pulsatilloside A ÏàËÆ¶È:66.6% Phytochemistry 1996 42 799-802 Triterpenoids from Pulsatilla chinensis Wen-Cai Ye, Nine-Ning Ji, Shou-Xun Zhao, Jing-Han Liu, Tao Ye, M. A. McKervey, P. 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Lup-20(29)en-2,28-diol-3-yl caffeate C39H56O6 ÏàËÆ¶È:64.1% Bioorganic & Medicinal Chemistry Letters 2011 21 2906-2910 Antifibrotic constituents of Alnus firma on hepatic stellate cells Mina Lee , Mi Kyeong Lee, Young Choong Kim , Sang Hyun Sung Structure 13C NMR ̼Æ×Ä£Äâͼ 55 . 24¦Î-hydroperoxy-24-vinyl-lathosterol C29H48O3 ÏàËÆ¶È:64.1% Planta Medica 2011 77 922-928 Cytotoxic Triterpenoids and Steroids from the Bark of Melia azedarach Shi-BiaoWu, Qiu-Ying Bao,Wen-XuanWang, Yun Zhao, Gang Xia,Zheng Zhao, Huaqiang Zeng, Jin-Feng Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 56 . 3¦Â-O-cis-coumaroyl betulinic acid ÏàËÆ¶È:64.1% Journal of Ethnopharmacology 2012 142 456¨C461 Antiparasitic compounds from Cornus florida L. with activities against Plasmodium falciparum and Leishmania tarentolae Rocky Graziose, Patricio Rojas-Silva, Thirumurugan Rathinasabapathy, Carmen Dekock, Mary H. 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S. Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 93 . 3¦Â-Hydroxy-olean-30-p-E-hydroxycinnamoyl-12-en-28-oic-acid C39H54O6 ÏàËÆ¶È:61.5% Natural Products and Bioprospecting 2012 2 166-169 Three new triterpenoids from Rubia schumanniana Bin Kuang, Jing Han, Guang-Zhi Zeng, Xiao-Qiang Chen, Wen-Jun He, Ning-Hua Tan Structure 13C NMR ̼Æ×Ä£Äâͼ 94 . compound 8 ÏàËÆ¶È:61.1% Phytochemistry 2003 1201-1205 Further saponins from Taverniera aegyptiaca Zedan Z. Ibraheim, Hashem A. Hassanean, Daoud W. Bishay Structure 13C NMR ̼Æ×Ä£Äâͼ 95 . inerside II C35H56O7 ÏàËÆ¶È:61.1% Phytochemistry 2002 61 379-382 27-Nor-triterpenoid glycosides from Mitragyna inermis Zhi-Hong Cheng, Bo-Yang Yu, Xiu-Wei Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 96 . daedaleanic acid C C34H52O8 ÏàËÆ¶È:61.1% Journal of Natural Products 2005 68 911-914 Cytotoxic Constituents of the Fruit Body of Daedalea dickisii Kazuko Yoshikawa, Kazuaki Kouso, Jyoji Takahashi, Akiko Matsuda, Mina Okazoe, Akemi Umeyama, and Shigenobu Arihara Structure 13C NMR ̼Æ×Ä£Äâͼ 97 . oleanolic acid 3-O-succinate C34H52O6 ÏàËÆ¶È:61.1% 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 98 . rubiarbonol G C32H52O5 ÏàËÆ¶È:61.1% Acta Botanica Yunnanica 1993 15(1) 89-91 NEW ARBORANE TYPE TRITERPENOIDS FROM RUBIA YUNNANENSIS ZOU Cheng,HAO Xiao-Jiang,Chen Chang-Xiang,ZHOU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 99 . liangwanin A C32H50O5 ÏàËÆ¶È:61.1% Acta Botanica Yunnanica 1993 15(3) 311-312 TRITERPENOIDS FROM NOTHOPANAX DAVIDH HONG Hua-Peng,CHENG Guang-Zhong,ZHANG Hong-Jie,SUN Han-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ 100 . chilianthin F C72H100O12 ÏàËÆ¶È:61.1% Chemical & Pharmaceutical Bulletin 1996 44 1669-1675 Chilianthins A-F, Six Triterpene Esters Having Dimeric Structures from Rhoiptelea chiliantha DIELS et HAND.-MAZZ. Zhi-Hong JIANG,Takashi TANAKA and Isao KOUNO Structure 13C NMR ̼Æ×Ä£Äâͼ 101 . compound 14 ÏàËÆ¶È:61.1% Chemical & Pharmaceutical Bulletin 1990 38 375-377 Saponins from Bran of Quinoa, Chenopodium quinoa WILLD. II Fumie MIZUI,Ryoji KASAI,Kazuhiro OHTANI and Osamu TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ |

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Nakai YIN Kai, GAO Hui-yuan, LI Xing-nuo, WU Li-jun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . betulinic acid ÏàËÆ¶È:80.5% Natural Product Research and Development 2009 21 438-440 Studies on the Anticancer Constituents in Glycyrrhiza uralensis Fisch YANG Li; CHEN Hai-xia; GAO Wen-yuan; YAN Lu-lu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 2a ÏàËÆ¶È:80.5% Chemistry Central Journal 2012 6 141 Design, synthesis and biological evaluation ofnovel betulinic acid derivatives Shengjie Yang, Na Liang, Hu Li, Wei Xue, Deyu Hu, Linhong Jin, Qi Zhao, and Song Yang, Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 3a ÏàËÆ¶È:80.5% Chemistry Central Journal 2012 6 141 Design, synthesis and biological evaluation ofnovel betulinic acid derivatives Shengjie Yang, Na Liang, Hu Li, Wei Xue, Deyu Hu, Linhong Jin, Qi Zhao, and Song Yang, Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 3c ÏàËÆ¶È:80.5% Chemistry Central Journal 2012 6 141 Design, synthesis and biological evaluation ofnovel betulinic acid derivatives Shengjie Yang, Na Liang, Hu Li, Wei Xue, Deyu Hu, Linhong Jin, Qi Zhao, and Song Yang, Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 3e ÏàËÆ¶È:80.5% Chemistry Central Journal 2012 6 141 Design, synthesis and biological evaluation ofnovel betulinic acid derivatives Shengjie Yang, Na Liang, Hu Li, Wei Xue, Deyu Hu, Linhong Jin, Qi Zhao, and Song Yang, Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 3f ÏàËÆ¶È:80.5% Chemistry Central Journal 2012 6 141 Design, synthesis and biological evaluation ofnovel betulinic acid derivatives Shengjie Yang, Na Liang, Hu Li, Wei Xue, Deyu Hu, Linhong Jin, Qi Zhao, and Song Yang, Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 3g ÏàËÆ¶È:80.5% Chemistry Central Journal 2012 6 141 Design, synthesis and biological evaluation ofnovel betulinic acid derivatives Shengjie Yang, Na Liang, Hu Li, Wei Xue, Deyu Hu, Linhong Jin, Qi Zhao, and Song Yang, Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 3i ÏàËÆ¶È:80.5% Chemistry Central Journal 2012 6 141 Design, synthesis and biological evaluation ofnovel betulinic acid derivatives Shengjie Yang, Na Liang, Hu Li, Wei Xue, Deyu Hu, Linhong Jin, Qi Zhao, and Song Yang, Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 3j ÏàËÆ¶È:80.5% Chemistry Central Journal 2012 6 141 Design, synthesis and biological evaluation ofnovel betulinic acid derivatives Shengjie Yang, Na Liang, Hu Li, Wei Xue, Deyu Hu, Linhong Jin, Qi Zhao, and Song Yang, Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 3l ÏàËÆ¶È:80.5% Chemistry Central Journal 2012 6 141 Design, synthesis and biological evaluation ofnovel betulinic acid derivatives Shengjie Yang, Na Liang, Hu Li, Wei Xue, Deyu Hu, Linhong Jin, Qi Zhao, and Song Yang, Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . methyl betulinate ÏàËÆ¶È:80.5% Journal of Agricultural and Food Chemistry 2000 48 3437-3439 Identification of Three Triterpenoids in Almond Hulls Gary Takeoka, Lan Dao, Roy Teranishi, Rosalind Wong, Stephan Flessa, Leslie Harden, and Richard Edwards Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 3-O-¦Â-D-Glucosyl betulinic amide C36H59NO7 ÏàËÆ¶È:80.5% Natural Product Research 2013 27 2033-2038 New natural compounds from Rhododendron lepidotum Shakeel-u-Rehman, Shahnawaz Nabi Sofi, Mohammad Akbar Khuroo, Subhash Chandra Taneja, Khursheed Ahmad Bhat & Ram Vishwakarma Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 1-(9-oximino-1-isopropenyl-5a,5b,8,8,11a-pentamethylperhydrocyclopenta[a]chrysen-3-ylcarbonylhydroxymethyl)perhydroquinolizine ÏàËÆ¶È:78.3% Chemistry of Natural Compounds 2004 40 569-570 SYNTHESIS OF THE LUPININE ESTER OF BETULONIC ACID F. Z. Galin, V. G. Kartsev, O. B. Flekhter,G. V. Giniyatullina, and G. A. Tolstikov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . compound 3k ÏàËÆ¶È:78.3% Chemistry Central Journal 2012 6 141 Design, synthesis and biological evaluation ofnovel betulinic acid derivatives Shengjie Yang, Na Liang, Hu Li, Wei Xue, Deyu Hu, Linhong Jin, Qi Zhao, and Song Yang, Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . 3¦Â-N-(t-butoxycarbonyl)-3-deoxybetulinate C36H59NO4 ÏàËÆ¶È:77.7% Chemistry of Natural Compounds 2008 44 603-605 EFFECTIVE SYNTHESIS OF METHYL 3¦Â-AMINO-3-DEOXYBETULINATE G. V. Giniyatullina, O. B. Flekhter, I. P. Baikova,Z. A. Starikova, and G. A. Tolstikov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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