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14.067,14.456,16.182,16.583,17.726,19.460,19.667,20.295,21.978,23.762,24.761,27.673,27.919,28.234,28.547,28.664,30.151,30.492,30.777,31.565,31.773,33.106,36.144,37.077,38.305,40.024,45.571,50.757,52.034,66.714,79.709,125.774,129.919,130.612,132.387,133.643,135.585,136.077,145.726,169.379,203.471
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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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