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²éѯ½á¹û£º¹²²éµ½899¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . fomitoside I C36H58O8 ÏàËÆ¶È:63.4% Journal of Natural Products 2005 68 69-73 Lanostane Triterpenoids and Triterpene Glycosides from the Fruit Body of Fomitopsis pinicola and Their Inhibitory Activity against COX-1 and COX-2 Kazuko Yoshikawa, Megumi Inoue, Yuki Matsumoto, Chika Sakakibara,Hideki Miyataka, Hitoshi Matsumoto, and Shigenobu Arihara Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . euphol 3-O-cinnamate C39H56O2 ÏàËÆ¶È:63.4% Phytochemistry 1990 29 1625-1628 Constituents of the latex of Euphorbia antiquorum Mohan B. Gewali,Masao Hattori,Yasuhiro Tezuka,Tohru Kikuchi,Tsuneo Namba Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 21,22:24,25-di-O-isopropylidene derivative C36H60O5 ÏàËÆ¶È:63.4% Tetrahedron 2013 69 3536-3542 Terresterol, a polyoxygenated lanostanoid, isolated from the oomycete Saprolegnia terrestris, and its innate immune-promoting activity Haruhisa Kikuchi, Yuichi Sato, Shoichiro Kurata, Yasuhiro Katou, Yoshiteru Oshima Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 7¦Â-Methoxymultiflor-8-ene-3¦Á,29-diol 3,29-dibenzoate C45H60O5 ÏàËÆ¶È:63.4% Molecules 2014 19 4802-4813 Three New Triterpene Esters from Pumpkin (Cucurbita maxima) Seeds Takashi Kikuchi, Shinsuke Ueda, Jokaku Kanazawa, Hiroki Naoe, Takeshi Yamada and Reiko Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 11 ,12 :13 ,28-diepoxyoleanan-3 -yl (9Z)-hexadec-9-enoate C46H76O4 ÏàËÆ¶È:63.0% Helvetica Chimica Acta 2004 Vol. 87 46 Palmitoleate (=(9Z)-Hexadeca-9-enoate) Esters of Oleanane Triterpenoids from the Golden Flowers of Tagetes erecta: Isolation and Autoxidation Products Shaheen Faizi and Aneela Naz Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (3¦Â,5¦Á,6¦Â,22E)-ergosta-7,22-diene-3,5,6-triol 6-oleate ÏàËÆ¶È:62.2% Helvetica Chimica Acta 2007 Vol. 90 1165 New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (3¦Â,5¦Á,6¦Â,22E)-ergosta-7,22-diene-3,5,6-triol 6-linoleate ÏàËÆ¶È:62.2% Helvetica Chimica Acta 2007 Vol. 90 1165 New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (3¦Â,5¦Á,6¦Â,22E)-ergosta-7,22-diene-3,5,6-triol 6-palmitate C44H76O4 ÏàËÆ¶È:60.9% Helvetica Chimica Acta 2007 Vol. 90 1165 New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (3¦Â,5¦Á,6¦Â,22E)-ergosta-7,22-diene-3,5,6-triol 6-stearate C46H80O4 ÏàËÆ¶È:60.9% Helvetica Chimica Acta 2007 Vol. 90 1165 New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . fomitoside F C37H58O8 ÏàËÆ¶È:60.9% Journal of Natural Products 2005 68 69-73 Lanostane Triterpenoids and Triterpene Glycosides from the Fruit Body of Fomitopsis pinicola and Their Inhibitory Activity against COX-1 and COX-2 Kazuko Yoshikawa, Megumi Inoue, Yuki Matsumoto, Chika Sakakibara,Hideki Miyataka, Hitoshi Matsumoto, and Shigenobu Arihara Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 5¦Á,8¦Á-epidioxy- 24-hydroperoxycholesta-6,28(29)-dien-3¦Â-ol(a/b) C29H46O5 ÏàËÆ¶È:60.9% Journal of Natural Products 1999 62 152-154 A New Epidioxy Sterol as an Antifouling Substance from a Palauan Marine Sponge, Lendenfeldia chondrodes Yutaka Sera, Kyoko Adachi, and Yoshikazu Shizuri Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 3¦Á-acetoxy-5¦Á-lanosta-8,24-dien-21-oic acid ester ¦Â-D-glucoside C38H60O9 ÏàËÆ¶È:60.9% Journal of Natural Products 1998 61 485-487 Mediation of the Cytotoxicity of Lanostanoids and Steroids of Ganoderma tsugae through Apoptosis and Cell Cycle Kim-Hong Gan, Yih-Fen Fann, Shu-Hui Hsu, Kou-Wha Kuo, and Chun-Nan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 5,20-O-diacetylingenol 3-O-(2'E,4'Z)-tetradecadienoate C39H54O9 ÏàËÆ¶È:60.9% Planta Medica 1996 62 260-262 Ingenane Diterpenes from Euphorbia petiolata Yan-Ping Shi, Zhong-Jian Jia, Bin Ma, Sadiq Saleh, and Jamil Lahham Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Methyl Ester of N-[3-Hydroxyimino-20(29)-lupen-28-oyl]-9-amino acid ÏàËÆ¶È:60.9% Chemistry of Natural Compounds 2002 38 331-339 SYNTHESIS OF BETULONIC ACID DERIVATIVES CONTAINING AMINO-ACID FRAGMENTS N. I. Petrenko, N. V. Elantseva, V. Z. Petukhova,M. M. Shakirov, E. E. Shul'ts, and G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 3,29-O-Dibenzoylmultiflor-8-en-3¦Á,7¦Â,29-triol ÏàËÆ¶È:60.9% Phytochemistry Letters 2009 2 130-133 Phenolic glycosides from Cucumis melo var. inodorus seeds Simona De Marino, Carmen Festa, Franco Zollo, Maria Iorizzi Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 3¦Â-phalmitoyl-panaxdiol C46H82O4 ÏàËÆ¶È:60.9% Chemical Research in Chinese Universities 2007 23 176-182 Synthesis and Primary Research on Antitumor Activity of Three New Panaxadiol Fatty Acid Esters ZHANG Chun-hong, LIXiang-gao,GAO Yu-gang,ZHANG Lian-xue and FU Xue-qi Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 7 ÏàËÆ¶È:60.9% Phytochemistry 1988 27 2199-2204 Sesquiterpenoid glycosides and an acetogenin glucoside from Lessingia glandulifera Shivanand D. Jolad,Barbara N. Timmermann,Joseph J. Hoffmann,Robert B. Bates,Fernando A. Camou,Teruna J. Siahaan Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . carboxyacetylquercinic acid methyl ester C36H56O7 ÏàËÆ¶È:60.9% Phytochemistry 1990 29 923-928 Malonate half-esters of homolanostanoid from an asian Ganoderma fungus Chairul,Takashi Tokuyama,Mugio Nishizawa,Motoo Shiro,Harukuni Tokuda,Yuji Hayashiji Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . multiflora-7,9(11)-diene-3¦Á,29-diol 3-p-hydroxybenzoate-29-benzoate C44H56O5 ÏàËÆ¶È:60.9% Molecules 2013 18 5568-5579 Three New Multiflorane-Type Triterpenes from Pumpkin (Cucurbita maxima) Seeds Takashi Kikuchi, Mika Takebayashi, Mayumi Shinto, Takeshi Yamada and Reiko Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 28-hydroxy-11-oxoolean-12-en-3 -yl (9Z)-hexadec-9-enoate C46H76O4 ÏàËÆ¶È:60.8% Helvetica Chimica Acta 2004 Vol. 87 46 Palmitoleate (=(9Z)-Hexadeca-9-enoate) Esters of Oleanane Triterpenoids from the Golden Flowers of Tagetes erecta: Isolation and Autoxidation Products Shaheen Faizi and Aneela Naz Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 5,6¦Â-Epoxysitosteryl oleate C47H82O3 ÏàËÆ¶È:60% Steroids 2008 73 1098-1109 Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1] Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . N-[3¦Â-acetoxy-20(29)-lupen-28-oyl]-9-amino acid Methyl Ester ÏàËÆ¶È:59.5% Chemistry of Natural Compounds 2002 38 331-339 SYNTHESIS OF BETULONIC ACID DERIVATIVES CONTAINING AMINO-ACID FRAGMENTS N. I. Petrenko, N. V. Elantseva, V. Z. Petukhova,M. M. Shakirov, E. E. Shul'ts, and G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . compound 2b ÏàËÆ¶È:59.5% Phytochemistry 1999 51 1021-1026 Multiflorane triterpenoid esters from pumpkin. An unexpected extrafolic source of PABA Giovanni Appendino, Jasmin Jakupovic, Emanuela Belloro, Augusto Marchesini Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 3¦Â-stearoyl-panaxdiol C48H86O4 ÏàËÆ¶È:59.5% Chemical Research in Chinese Universities 2007 23 176-182 Synthesis and Primary Research on Antitumor Activity of Three New Panaxadiol Fatty Acid Esters ZHANG Chun-hong, LIXiang-gao,GAO Yu-gang,ZHANG Lian-xue and FU Xue-qi Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . Stigmastanol-3¦Â-p-butanoxydihydrocoumaroate C42H68O3 ÏàËÆ¶È:59.5% Phytochemical Analysis 2006 17 36-45 Chemical constituents of rice (Oryza sativa) hulls and their herbicidal activity against duckweed (Lemna paucicostata Hegelm 381) Ill Min Chung, Mohd Ali, Ateeque Ahmad, Jung Dae Lim, Chang Yeon Yu and Jin Seog Kim Structure 13C NMR ̼Æ×Ä£Äâͼ |

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