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13C NMR (101 MHz, MeOD)
¦Ä 15.83, 17.56, 17.64, 17.99,21.11,21.20, 22.10, 23.80, 24.96, 25.34, 28.08, 29.07, 29.23, 31.90, 32.10, 33.08, 37.15, 37.87, 39.69, 40.09, 44.36, 44.76, 45.51, 47.13, 67.34, 70.11, 78.49, 85.24, 97.27, 97.83, 104.48, 109.19, 112.35, 112.90, 113.43, 115.10, 116.78, 131.15, 141.56, 145.37, 148.88, 149.92, 162.81, 165.14, 165.85, 173.14, 173.22,195.89
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1 .     [3-(4-Fluoro)cinnamamidoolean-12-en-28-yl][4-(4-fluoro)cinnamamidopiperazin-1-yl]methanone
C52H67F2N3O3     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          2011          59(8)          1051-1056
Synthesis of New a-Glucosidase Inhibitors Based on Oleanolic Acid Incorporating Cinnamic Amides
Wei NIE, Jian-Guang LUO, Xiao-Bing WANG, Hong YIN, Hong-Bin SUN, He-Quan YAO, and Ling-Yi KONG
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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2 .     [3-(4-Methoxyl)cinnamamidoolean-12-en-28-yl][4-(4-methoxyl)cinnamamidopiperazin-1-yl]mthanone
C54H73N3O5     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          2011          59(8)          1051-1056
Synthesis of New a-Glucosidase Inhibitors Based on Oleanolic Acid Incorporating Cinnamic Amides
Wei NIE, Jian-Guang LUO, Xiao-Bing WANG, Hong YIN, Hong-Bin SUN, He-Quan YAO, and Ling-Yi KONG
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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3 .     desfontainic acid
     ÏàËÆ¶È:66.6%
Phytochemistry          1986          25          1907-1912
Iridoids, iridoid-triterpenoid congeners and lignans from Desfontainia spinosa
Peter J. Houghton, Lu Ming Lian
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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4 .     ganosinensin C
C51H74O8     ÏàËÆ¶È:64.7%
Journal of Natural Products          2009          72          958-961
Triterpene-Farnesyl Hydroquinone Conjugates from Ganoderma sinense
Naoto Sato, Chao-Mei Ma, Katsuko Komatsu, and Masao Hattori
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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5 .     Ganosinensin C
     ÏàËÆ¶È:64.7%
Molecules          2014          19          17478-17535
A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp.
Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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6 .     gymnasterone A
C45H67NO5     ÏàËÆ¶È:64.5%
Journal of Natural Products          2007          70          1731-1740
Variation in Cytostatic Constituents of a Sponge-Derived Gymnascella dankaliensis by Manipulating the Carbon Source
Taro Amagata,Makoto Tanaka,Takeshi Yamada, Mitsunobu Doi, Katsuhiko Minoura, Hirofumi Ohishi,Takao Yamori, and Atsushi Numata
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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7 .     myriceric acid C
C48H60O10     ÏàËÆ¶È:64.5%
Chemical & Pharmaceutical Bulletin          1996          44          343-351
Endothelin Receptor Antagonist Triterpenoid, Myriceric Acid A, Isolated from Myrica cerifera, and Structure Activity Relationships of Its Derivatives
Kensuke SAKURAWI,Fumio YASUDA,Takehiko TOZYO,Miharu NAKAMURA,Tomohiro SATO,Junko KIKUCHI,Yoshihiro TERUI,Yuji IKENISHI,Tsuyoshi IWATA,Kazuhiro TAKAHASHI,Toshiro KONOIKE,Shin-ichi MIHARA and Masafumi FUJIMOTO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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8 .     methylation of asprellic acid A
C51H66O8     ÏàËÆ¶È:64.5%
Journal of Natural Products          1993          Vol 56          2077
Antitumor Agents, 145. Cytotoxic Asprellic Acids A and C and Asprellic Acid B, New p-Coumaroyl Triterpenes, from Ilex asprella
Yoshiki Kashiwada, De-Cheng Zhang, Yuh-Pan Chen, Chang-Ming Cheng, Hsien-Tsung Chen, Hsien-Chang Chang, Jer-Jang Chang, Kuo-Hsuing Lee
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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9 .     11-deoxyisochiisanoside
C48H76O19     ÏàËÆ¶È:64.5%
Natural Product Sciences          2006          12          119-121
Studies on the Constituents of the Leaves of Acanthopanax divaricatus forma flavi-flos
Nam, Sang-Gil; Yook, Chang-Soo; Kim, In-Seon; Choi, Hyun-Sik; Park, Sang-Yong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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10 .     1-hydroxy-7-((2S,3R,4R,5S)-2'',3'',4''-trihydroxy-5''-(hydroxymethyl)tetrahydro-2H-pyran-1-yloxy)anthracen-2-yl 3',7',11',15',19'-pentamethyltricosanoate
C48H74O9     ÏàËÆ¶È:64.5%
Bulletin of the Korean Chemical Society          2006          27          995-1000
Novel Anthracene Derivatives Isolated from Rice Hulls of Oryza sativa and Their Growth Inhibitory Activity of Radish Seed
Ill-Min Chung, Yoong-Ho Lim, Mohd Ali, Shahnaz Sultana, Ateeque Ahmad*
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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11 .     Orbiculamide A
     ÏàËÆ¶È:64.5%
Journal of the American Chemical Society          1991          113          7811-7812
Orbiculamide A: a novel cytotoxic cyclic peptide from a marine sponge Theonella sp
Nobuhiro Fusetani, Takeo Sugawara, Shigeki Matsunaga, Hiroshi Hirota
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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12 .     compound 1a
     ÏàËÆ¶È:63.2%
Chemistry of Natural Compounds          2005          41          436-441
TRITERPENE GLYCOSIDES FROM Cussonia paniculata.II. ACETYLATED GLYCOSIDES FROM LEAVES
V. I. Grishkovets, I. I. Dovgii, V. V. Kachala,and A. S. Shashkov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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13 .     compound 2a
     ÏàËÆ¶È:63.2%
Chemistry of Natural Compounds          2005          41          436-441
TRITERPENE GLYCOSIDES FROM Cussonia paniculata.II. ACETYLATED GLYCOSIDES FROM LEAVES
V. I. Grishkovets, I. I. Dovgii, V. V. Kachala,and A. S. Shashkov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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14 .     TE2
     ÏàËÆ¶È:63.2%
Bioorganic & Medicinal Chemistry Letters          1994          4          1375-1380
Synthesis of ¦Â-estradiol-3-benzoate-17-(succinyl-12A-tetracycline): A potential bone-seeking estrogen
Mark W. Orme, Virender M. Labroo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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15 .     3¦Â-L-Tryptophan ester olean-12-en-28-oic acid-3,5,6-trimethylpyrazin-2-methyl ester
C49H68N4O4     ÏàËÆ¶È:63.2%
Molecules          2014          19          18215-18231
Amino Acid Derivatives of Ligustrazine-Oleanolic Acid as New Cytotoxic Agents
Fuhao Chu, Xin Xu, Guoliang Li, Shun Gu, Kuo Xu, Yan Gong, Bing Xu, Mina Wang, Huazheng Zhang, Yuzhong Zhang, Penglong Wang and Haimin Lei
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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16 .     3'-azido-3'-deoxythymidine-5'-yl 3-O-(3',3'-dimethylsuccinyl)-lup-20(29)en-28-yl glutarate
C51H75N5O11     ÏàËÆ¶È:62.7%
Bioorganic & Medicinal Chemistry          2010          18          6451-6469
Conjugates of betulin derivatives with AZT as potent anti-HIV agents
Juan Xiong, Yoshiki Kashiwada, Chin-Ho Chen, Keduo Qian, Susan L. Morris-Natschke, Kuo-Hsiung Lee, Yoshihisa Takaishi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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17 .     bidentatoside I
C47H70O20     ÏàËÆ¶È:62.5%
Journal of Natural Products          2001          64          243-245
Bidentatoside I, a New Triterpene Saponin from Achyranthes bidentata
Anne-Claire Mitaine-Offer,Abderrazak Marouf, Cosimo Pizza, Trân Cong Khanh,Bruno Chauffert, and Marie-Aleth Lacaille-Dubois
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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18 .     ulmicin C
C45H60O8     ÏàËÆ¶È:62.5%
Journal of Natural Products          2001          64          328-331
Five Novel Neuroprotective Triterpene Esters of Ulmus davidiana var. japonica
Mi Kyeong Lee and Young Choong Kim
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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19 .     3-O-¦Á-L-arabinopyranosyl-(1¡ú3)-¦Â-D-glucuropyranosyl-oleanolic acid-28-O-¦Â-D-glucopyranoside
C47H74O18     ÏàËÆ¶È:62.5%
Acta Botanica Yunnanica          2003          25(2)          235-240
New Triterpenoid Glycosides from Hemsleya penxianensis var. gulinensis
LIN Yu-Ping,QIU Ming-Hua, LI Zhong-Rong,GAO Xu-Hong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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20 .     betavulgaroside I
C47H70O20     ÏàËÆ¶È:62.5%
Chemical & Pharmaceutical Bulletin          1996          44          1212-1217
Medicinal Foodstuffs. III. Sugar Beet. (1) : Hypoglycemic Oleanolic Acid Oligoglycosides, Betavulgarosides, I, II, III, and IV, from the Root of Beta vulgaris L. (Chenopodiaceae)
Masayuki YOSHIKAWA,Toshiyuki MURAKAMI,Masashi KADOYA,Hisashi MATSUDA,Osamu MURAOKA,Johji YAMAHARA and Nobutoshi MURAKAMI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-01-26 15:25:31
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