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»¯ºÏÎï2£º10.5, 13.5, 18.3, 19.6, 20.1, 21.0, 22.9, 25.9, 26.0, 26.9, 29.2, 34.5, 35.9, 36.1, 39.5, 40.1, 47.2, 49.7, 51.2, 58.5, 70.5, 119.0, 122.8, 128.8, 136.6, 138.1, 144.0, 144.9, 147.8, 217.84  (125 MHz, CDCL3)
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wprsahan(¶¹¸ç´ú·¢): ½ð±Ò+20, лл 2013-05-29 15:45:23
1 .     23-hydroxy-8(14¡ú13)-abeo-17,13-fried-3-oxolanosta-8,14(15),24-triene-26,23-olide
C30H42O4     ÏàËÆ¶È:73.3%
Phytochemistry          2013          86          168-175
Lipase inhibitory and LDL anti-oxidative triterpenes from Abies sibirica
Mizuho Handa, Toshihiro Murata, Kyoko Kobayashi, Erdenechimeg Selenge, Toshio Miyase, Javzan Batkhuu, Fumihiko Yoshizaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     compound 5
    ÏàËÆ¶È:70.9%
Chemistry of Natural Compounds          1991          27          444-449
TRITERPENOIDS FROM Abies SPECIES XII. (24Z)- and (24E)-8(14¡ú13)-ABEO-17,13-FRIEDOLANOSTA- 8,14(30),24-TRIENE-3,23-DION-26-OIC ACIDS - NEW TRITERPENOIDS FROM THE NEEDLES OF THE SIBERIAN FIR
V. A. Raldugin, M. M. Shakirov,T. V. Leibyuk, and S. A. Shevtsov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     dyvariabilin H
C30H46O2     ÏàËÆ¶È:66.6%
Journal of Natural Products          2001          64          159-163
New Tirucallane-Type Triterpenes from Dysoxylum variabile
Hongmei Liu, Jörg Heilmann, Topul Rali, and Otto Sticher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     quadrangularic acid J
C31H50O5     ÏàËÆ¶È:64.5%
Journal of Natural Products          2000          63          57-64
Thirteen Novel Cycloartane-Type Triterpenes from Combretum quadrangulare
Arjun H. Banskota,Yasuhiro Tezuka, Kim Qui Tran, Ken Tanaka, Ikuo Saiki,and Shigetoshi Kadota
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     3-oxotirucalla-7,24Z-dien-26-oic acid
C30H46O3     ÏàËÆ¶È:63.3%
Planta Medica          2000          66          463-468
Bioactive Compounds from Celaenodendron mexicanum
Maria del Rayo Camacho,Rachel Mata, Perla Castaneda,Geoffrey C.Kirby,David C.Warhurst,Simon L.Croft,J.David Phillipson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     24,25-Epoxy-tirucall-7-ene-3,23-dione
C30H46O3     ÏàËÆ¶È:63.3%
Acta Botanica Sinica          2004          46          1256-1260
A New Triterpenoid froMamoora dasyclada
WANG Huan, ZHANG Xiao-Feng, YANG Shu-Min, LUO Xiao-Dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     centaurione
C30H44O3     ÏàËÆ¶È:63.3%
Fitoterapia          2000          71          130-133
Two new triterpene lactones from Centaurium pulchellum
Hafsa Bibi, Saeed Anwer, G.A. Miana,Saeed Ahmad, Atta-ur-Rahman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     hispidol B
    ÏàËÆ¶È:63.3%
Chinese Traditional and Herbal Drugs          2009          40          1201-1204
ºìÊ÷ÁÖÖ²Îïľ¹û鬻¯Ñ§³É·ÖµÄÑо¿
ÉòÁ¢Èã;¹ù¶°;Òü±¦Î°;ÕÅÇà;ÕÔÀ×;»ô³¤ºç;ÕÅ‹ Àö;Ê·ÇåÎÄ;ÍõÓÀÀû
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     theonellasterone
C30H48O     ÏàËÆ¶È:63.3%
Marine Drugs          2012          10          2448-2466
Preliminary Structure-Activity Relationship on Theonellasterol, a New Chemotype of FXR Antagonist, from the Marine Sponge Theonella swinhoei
Valentina Sepe, Raffaella Ummarino, Maria Valeria D'Auria, Orazio Taglialatela-Scafati, Simona De Marino, Claudio D'Amore, Barbara Renga, Maria Giovanna Chini, Giuseppe Bifulco, Yoichi Nakao, Nobuhiro Fusetani, Stefano Fiorucci and Angela Zampella
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Lamesticumin D
C30H46O3     ÏàËÆ¶È:63.3%
Journal of Natural Products          2011          74          1042-1048
Onoceranoid-Type Triterpenoids from Lansium domesticum
Shi-Hui Dong, Chuan-Rui Zhang, Lei Dong, Yan Wu, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     3-Oxo-20-hydroxy-30¦Á-methyl,17(29)¦Á-epoxy-28-norlupane
C29H46O3     ÏàËÆ¶È:63.3%
Chemical & Pharmaceutical Bulletin          2012          60          955-961
Cytotoxic Terpenes from the Stems of Dipterocarpus obtusifolius Collected in Cambodia
Piseth Khiev, Ok-Kyoung Kwon, Hyuk-Hwan Song, Sei-Ryang Oh, Kyung-Seop Ahn, Hyeong-Kyu Lee, Young-Won Chin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     25-methoxy-tirucall-7-23 (trans)-diene-3-one
C31H50O2     ÏàËÆ¶È:61.2%
Phytochemistry          1995          40          1485-1487
Tirucallane triterpenes from the stem bark of Aglaia leucophylla
Abdelilah Benosman, Pascal Richomme, Thierry Sevenet, Guillaume Perromat, A. Hamid A. Hadi, Jean Bruneton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     25-methoxycucurbita-5,23(E)-diene-3¦Â,7¦Â,29-triol
C31H52O4     ÏàËÆ¶È:61.2%
Bioorganic & Medicinal Chemistry          2009          17          6942-6951
New potent P-glycoprotein modulators with the cucurbitane scaffold and their synergistic interaction with doxorubicin on resistant cancer cells
C¨¢tia Ramalhete, Joseph Moln¨¢r, Silva Mulhovo, Virg¨ªlio E. Ros¨¢rio, Maria-Jos¨¦ U. Ferreira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     cornusalterin A
C31H52O2     ÏàËÆ¶È:61.2%
Journal of Natural Products          2011          74          54-59
Tirucallane Triterpenoids from Cornus walteri
Ki Hyun Kim, Sang Un Choi, Young Choong Kim, and Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     cornusalterin H
C31H50O2     ÏàËÆ¶È:61.2%
Journal of Natural Products          2011          74          54-59
Tirucallane Triterpenoids from Cornus walteri
Ki Hyun Kim, Sang Un Choi, Young Choong Kim, and Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     Methyl (13Z,15E,17E,22E)-3¦Â-hydroxy-12-oxomalabarica-13,15,17,22,24-pentaen-28-oate
C31H44O4     ÏàËÆ¶È:61.2%
Australian Journal of Chemistry          1982          35          39-50
Malabaricane triterpenes from a Great Barrier Reef collection of the sponge Jaspis stellifera
BN Ravi and RJ Wells
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     toosendanic acid A
C30H48O4     ÏàËÆ¶È:60%
Journal of Natural Products          2009          72          917-920
Protolimonoids from Melia toosendan
Yi Shu Sang,Chun Yan Zhou, Ai Jun Lu, Xiao Jin Yin,Zhi Da Min,and Ren Xiang Tan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     neoabieslactone A
C30H46O4     ÏàËÆ¶È:60%
Journal of Natural Products          2009          72          1065-1068
Terpenoid Constituents of Abies chensiensis with Potential Anti-inflammatory Activity
Yong-Li Li, Xian-Wen Yang, Su-Mei Li, Yun-Heng Shen, Hua-Wu Zeng, Xiao-Hua Liu, Jian Tang,and Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     neoabieslactone E
C30H42O4     ÏàËÆ¶È:60%
Journal of Natural Products          2009          72          1065-1068
Terpenoid Constituents of Abies chensiensis with Potential Anti-inflammatory Activity
Yong-Li Li, Xian-Wen Yang, Su-Mei Li, Yun-Heng Shen, Hua-Wu Zeng, Xiao-Hua Liu, Jian Tang,and Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     foliasalaci B2
C30H50O2     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          2008          56(7)          915-920
Hnew Triterpene Constituents, Foliasalacins A1¡ªA4, B1¡ªB3, and C, from the Leaves of Salacia chinensis
Masayuki YOSHIKAWA,Yi ZHANG, Tao WANG, Seikou NAKAMURA, and Hisashi MATSUDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     ganoderic acid ¦Å
C30H44O7     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          2000          48(7)          1026-1033
Triterpenes from the Spores of Ganoderma lucidum and Their Cytotoxicity against Meth-A and LLC Tumor Cells
Byung-Sun MIN,Jiang-Jing GAO,Norio NAKAMURA and Masao HATTORI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     3,22-dioxo-20-taraxastene
C30H46O2     ÏàËÆ¶È:60%
Phytochemistry          2005          66          495-501
Cytotoxic triterpenes from the aerial roots of Ficus microcarpa
Yi-Ming Chiang, Jang-Yang Chang, Ching-Chuan Kuo,Chi-Yen Chang, Yueh-Hsiung Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     stellettin K
C30H42O4     ÏàËÆ¶È:60%
Journal of Natural Products          2006          69(3)          373-376
Bioactive Isomalabaricane Triterpenoids from Rhabdastrella globostellata that Stabilize the Binding of DNA Polymerase ¦Â to DNA
Jason A. Clement, Mei Li, Sidney M. Hecht, and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     3-oxotirucalla-7,24-dien-21-oic acid
    ÏàËÆ¶È:60%
Journal of Natural Products          2000          63          238-242
Inhibitory Effects on HIV-1 Protease of Constituents from the Wood of Xanthoceras sorbifolia
Chao-mei Ma, Norio Nakamura,Masao Hattori, Hiroko Kakuda,Jun-chan Qiao, and Hai-lan Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     carnosiflogenin C
    ÏàËÆ¶È:60%
Planta Medica          2005          71          983-986
Four New Cucurbitane Glycosides from Hemsleya jinfushanensis
Jian-Chao Chen, Xue-Mei Niu , Zhong-Rong Li , Ming-Hua Qiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     cycloart-23-ene-3, 25-diol
C30H50O2     ÏàËÆ¶È:60%
Acta Botanica Yunnanica          1999          21(2)          260-264
The constituents of Ervatamia divaricata
YU Yang,LIU Ji-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     alisol B
    ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1993          41          2109-2112
Crude Drugs from Aquatic Plants. II. On the Constituents of the Rhizome of Alisma orientale JUZEP. Originating from Japan, Taiwan, and China. Absolute Stereostructures of 11-Deoxyalisols B and B 23-Acetate
Masayuki YOSHIKAWA,Shoko HATAKEYAMA,Nobumitsu TANAKA,Toshiro MATSUOKA,Johji YAMAHARA and Nobutoshi MURAKAMI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     scandenogenin C
C30H50O3     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1988          36          234-243
Glycosides from Chinese Medicinal Plant, Hemsleya panacis-scandens, and Structure-Taste Relationship of Cucurbitane Glycosides
RYOJI KASAI,KAZUHIRO MATSUMOTO,RUI-LIN NIE,JUN ZHOU and OSAMU TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     compound 22
    ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1988          36          234-243
Glycosides from Chinese Medicinal Plant, Hemsleya panacis-scandens, and Structure-Taste Relationship of Cucurbitane Glycosides
RYOJI KASAI,KAZUHIRO MATSUMOTO,RUI-LIN NIE,JUN ZHOU and OSAMU TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     2-cyano-2,3-seco-19¦Â,28-epoxy-18¦Á-oleanan-3-al'
C30H47NO2     ÏàËÆ¶È:60%
Chemistry of Natural Compounds          2008          44          606-611
SYNTHESIS OF LUPANE AND 19¦Â,28-EPOXY-18¦Á-OLEANANE 2,3-seco-DERIVATIVES BASED ON BETULIN
I. A. Tolmacheva, A. V. Nazarov, O. A. Maiorova, and V. V. Grishko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     compound 17
    ÏàËÆ¶È:60%
Chemistry of Natural Compounds          1985          21          328-332
TRITERPENOIDS FROM THE LEAVES OF THE SIBERIAN SPECIES OF BIRCH Betula nana and B. exilis
N. D. Pokhilo, G. V. Malinovskaya, V. V. Makhan'kov, V. A. Denisenko, and N. I. Uvarova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     compound 11
    ÏàËÆ¶È:60%
Chemistry of Natural Compounds          1984          20          170-173
GLYCOSYLATION OF BETULIN AND ITS ACETATES IN THE PRESENCE OF CADMIUM CARBONATE
L. E. Odinokova, G. I. Oshitok, V. A. Denisenko, V. F. Anufriev, A. M, Tolkach, and N. I. Uvarova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     olean-3-oxo-12-en-28,29-diol acetate
    ÏàËÆ¶È:60%
Acta Pharmaceutica Sinica          1993          28          684-689
STUDIDS ON THE CHEMICAL CONSTITUENTS OF EUONYMUS MUPINENSIS
XL Yah; SX Liao; HQ Liang and P Zhou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     ganoderic acid ¦Å
C30H44O7     ÏàËÆ¶È:60%
Journal of Asian Natural Products Research          2002          4          129-134
A NEW LANOSTANE-TYPE TRITERPENE FROM THE FRUITING BODIES OF GANODERMA LUCIDUM
JUN LUO, YU-YING ZHAO and ZHI-BIN LIN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     7¦Â-hydroxystigmasterol
    ÏàËÆ¶È:60%
China Journal of Chinese Materia Medica          2009          34          1809-1811
Steroids from Monascus purpureus metabolite
SHANG Xiaoya, WANG Ruolan, YI N Suqin, LI Jinjie, JIN Zonglian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     dymacrin K
C30H48O3     ÏàËÆ¶È:60%
Phytochemistry          1999          52          1461-1468
Tirucallane triterpenes from Dysoxylum macranthum
Khalit Mohamad, Marie-Th¨¦r¨¦se Martin, Marc Litaudon, Christiane Gaspard, Thierry S¨¦venet, Mary Païs
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     compound 2
    ÏàËÆ¶È:60%
Journal of Natural Products          1986          Vol 49          148
3-Oxo-28,29-Dihydroxyolean-12-Ene from Orthosphenia mexicana
Antonio G. Gonzalez, Carmen M. Gonzalez, Angel G. Ravelo, Xorge A. Dominguez, Braulio M. Fraga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     penasterone
C30H46O3     ÏàËÆ¶È:60%
Journal of Natural Products          1992          Vol 55          1682
Potent Inhibitors of Histamine Release, Two Novel Triterpenoids from the Okinawan Marine Sponge Penares incrustans
Noboru Shoji, Akemi Umeyama, Setsuko Motoki, Shigenobu Arihara, Toshimasa Ishida, Kyosuke Nomoto, Jun'ichi Kobayashi, Masao Takei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     lupenone
    ÏàËÆ¶È:60%
Natural Product Sciences          2002          8          62-65
Chemical Constituents from Sorbus commixta
Na, Min-Kyun; An, Ren-Bo; Min, Byung-Sun; Lee, Sang-Myung; Kim, Young-Ho; Bae, Ki-Hwan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     carnosiflogenin C
    ÏàËÆ¶È:60%
Phytochemistry          1996          41          1169-1174
Cucurbitane glycosides from Hemsleya panacis-scandens rhizomes
Hideo Kubo, Kazuhiro Ohtani, Ryoji Kasai, Kazuo Yamasaki, Rui-Lin Nie, Osamu Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     13¦Á,14¦Â,17¦Á-1anosta-7,24diene-3¦Â,11¦Â,16¦Á-triol
C30H50O3     ÏàËÆ¶È:60%
Phytochemistry          1994          36          417-419
A tetracyclic triterpenoid from Garuga pinnata
G. Venkatraman, P. S. Thombare, B. K. Sabata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     Alisol B
C30H48O4     ÏàËÆ¶È:60%
Phytochemistry          1994          36          119-127
Terpenoids of Alisma orientale rhizome and the crude drug alismatis rhizoma
Yoshijiro Nakajima, Yohko Satoh, Masumi Katsumata (nee Ohtsuka), Kazuko Tsujiyama (nee Mikoshiba), Yoshiteru Ida, Junzo Shoji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     Alisol C
C30H46O5     ÏàËÆ¶È:60%
Phytochemistry          1994          36          119-127
Terpenoids of Alisma orientale rhizome and the crude drug alismatis rhizoma
Yoshijiro Nakajima, Yohko Satoh, Masumi Katsumata (nee Ohtsuka), Kazuko Tsujiyama (nee Mikoshiba), Yoshiteru Ida, Junzo Shoji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     6¦Â-hydroxy-lup-20(30)-en-3-one
    ÏàËÆ¶È:60%
Phytochemistry          1991          30          3490-3493
11,11-dimethyl-1,3,8,10-tetrahydroxy-9-methoxypeltogynan and three pentacyclic triterpenes from Cassine transvaalensis
Siegfried E. Drewes, M. Jeffrey Mashimbye, John S. Field, Niyum Ramesar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     (5R,20R)-23-hydroxyl-8(14¡ú13R)-abeo-17,13-friedo-3-oxolanosta-8,14(30),24-triene-26,23-olide
C30H42O4     ÏàËÆ¶È:60%
Phytochemistry          2011          72          2197-2204
Miscellaneous terpenoid constituents of Abies nephrolepis and their moderate cytotoxic activities
Dan-Wei Ou-Yang, Liang Wu, Yong-Li Li, Pei-Ming Yang, De-Yun Kong, Xian-Wen Yang, Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     3¦Â-hydroxy-5¦Á,6¦Á-epoxy-9-oxo-9,11-secogorgostan-11-ol
C30H50O4     ÏàËÆ¶È:60%
Tetrahedron Letters          2000          41          6035-6040
New antiproliferative epoxysecosterols from Pseudopterogorgia americana
Samina Naz, Russell G. Kerr, Ramaswamy Narayanan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     compound 9
C30H50O3     ÏàËÆ¶È:60%
Phytochemistry          1987          26          1371-1376
Sweet and bitter cucurbitane glycosides from hemsleya carnosiflora
Ryoji Kasai,Kazuhiro Matsumoto,Rui-Lin Nie,Toshinobu Morita,Akimi Awazu,Jun Zhou,Osamu Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     3-oxoolean-12-ene-20¦Á-carboxylic acid
C30H46O3     ÏàËÆ¶È:60%
Phytochemistry          1990          29          3259-3261
Friedelane and oleanane triterpenoids from bark wood ofAustroplenckia populnea
Jost R. De Sousa,Gracia D.F. Silva,Jose¡äL. Pedersoli,Ricardo J Alves
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     3¦Â,5¦Á,6¦Á-trihydroxy-9,11-secocholest-7-en-9-one
C27H44O4     ÏàËÆ¶È:60%
Steroids          1995          60          666-673
New cytotoxic steroids from the marine sponge Dysidea fragilis coming from the lagoon of Venice
Anna Aiello, Ernesto Fattorusso, Marialuisa Menna, Rosa Carnuccio, Teresa Iuvone
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     16,23-oxidoalisol B
C30H46O4     ÏàËÆ¶È:60%
Chinese Traditional and Herbal Drugs          2008          39          1788-1790
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ºúÑ©ÑÞ;³Âº£Ï¼;¸ßÎÄÔ¶;ÁõÐÂÇÅ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     piscidinol A
    ÏàËÆ¶È:60%
Chinese Journal of Natural Medicines          2009          7          31-33
Triterpenes from the Fruits of Phellodendron chinense Schneid var. glabriusculum Schneid
YAN Chen; WANG Ye; HAO Xiao-Jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     stigmast-5,22-dien-3¦Â,7¦Â-diol
    ÏàËÆ¶È:60%
Journal of Shenyang Pharmaceutical University          2011          28          120-123
Isolation and identification of chemical constituents from whole plant of Saussurea involucrata Kar. et kir.
HOU Peng-yi, HUANG Jian, SUN Bo-hang, WU Li-jun, GAO Hui-yuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     (22E,24S)-3¦Á,5-cyclo-stigmast-22-en-6-one
    ÏàËÆ¶È:60%
Steroids          2012          77          91-99
Brassinosteroids and analogs as neuroprotectors: Synthesis and structure¨Cactivity relationships
Jihane Ismaili, Martin Boisvert, Fanny Longpr¨¦, Julie Carange, C¨¦line Le Gall, Maria-Grazia Martinoli, Benoit Daoust
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
54 .     dyvariabilin H
C30H48O3     ÏàËÆ¶È:60%
Organic & Biomolecular Chemistry          2011          9          7685-7696
Protolimonoids and norlimonoids from the stem bark of Toona ciliata var. pubescens
Jian-Rong Wang, Hai-Li Liu, Tibor Kurt¨¢n, Attila M¨¢ndi, S¨¢ndor Antus, Jia Li, Hai-Yan Zhang and Yue-Wei Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
55 .     alisol C
    ÏàËÆ¶È:60%
Natural Product Research and Development          2001          13(4)          1-4
TERPENOIDS OF ALISMA ORIENTALIS JUZEP.
PENG Guo ping; LOU Feng chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
56 .     sodwanone R
C30H46O4     ÏàËÆ¶È:60%
Tetrahedron          1999          55          5555-5566
Several new isoprenoids from two marine sponges of the family Axinellidae
Amira Rudi, Tesfamariam Yosief, Michael Schleyer, Yoel Kashman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
57 .     alisol B
    ÏàËÆ¶È:60%
Bioorganic & Medicinal Chemistry Letters          2012          22          4787-4792
Triterpenes from Alisma orientalis act as farnesoid X receptor agonists
Hsiang-Ru Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
58 .     (24S)-24-ethyl-4¦Â-methyl-5¦Á-cholestan-3-one
C30H50O     ÏàËÆ¶È:60%
Marine Drugs          2012          10          2448-2466
Preliminary Structure-Activity Relationship on Theonellasterol, a New Chemotype of FXR Antagonist, from the Marine Sponge Theonella swinhoei
Valentina Sepe, Raffaella Ummarino, Maria Valeria D'Auria, Orazio Taglialatela-Scafati, Simona De Marino, Claudio D'Amore, Barbara Renga, Maria Giovanna Chini, Giuseppe Bifulco, Yoichi Nakao, Nobuhiro Fusetani, Stefano Fiorucci and Angela Zampella
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
59 .     alisol B
C30H48O4     ÏàËÆ¶È:60%
Biological and Pharmaceutical Bulletin          2012          35          1581-1587
The Rhizomes of Alisma orientale and Alisol Derivatives Inhibit Allergic Response and Experimental Atopic Dermatitis
Je Hyeong Lee, Oh Song Kwon, Hong-Guang Jin, Eun-Rhan Woo, Yeong Shik Kim, Hyun Pyo Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
60 .     11¦Á-Hydroxy-¦Â-boswellic acid
C30H48O4     ÏàËÆ¶È:60%
Natural Product Communications          2008          3          21-26
Boswellic Acids with Acetylcholinesterase InhibitoryProperties from Frankincense
Masahiro Ota and Peter J. Houghton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
61 .     17¦Á-Hydroxy-28-nor-18¦Á(H)-lupan-3-one
C29H48O2     ÏàËÆ¶È:60%
Natural Product Communications          2008          3          1569-1574
Oxidative Decarboxylation of Triterpene C-28 Acids ofLupane Series
Nataliya G. §¬omissarova, Nataliya G. Belenkova, Olga V. Shitikova, Leonid V. Spirikhin andMarat S. Yunusov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
62 .     3-Hydroxymogrol
C30H52O4     ÏàËÆ¶È:60%
Bioorganic & Medicinal Chemistry          2011          19          5776-5781
Potential AMPK activators of cucurbitane triterpenoids from Siraitia grosvenorii Swingle
Xu-bing Chen, Jing-jing Zhuang, Jun-hua Liu, Min Lei, Lei Ma, Jing Chen, Xu Shen, Li-hong Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
63 .     compound 2a
    ÏàËÆ¶È:60%
Chemistry of Natural Compounds          2012          48          821-826
Preparation and nitration of allobetulin seco-derivatives
A. V. Shernyukov , I. Ya. Mainagashev, D. V. Korchagina, Yu. V. Gatilov, N. F. Salakhutdinov, G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
64 .     2,2-dinitrobetulone
    ÏàËÆ¶È:60%
Chemistry of Natural Compounds          2012          48          821-826
Preparation and nitration of allobetulin seco-derivatives
A. V. Shernyukov , I. Ya. Mainagashev, D. V. Korchagina, Yu. V. Gatilov, N. F. Salakhutdinov, G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
65 .     Alisol B
    ÏàËÆ¶È:60%
Archives of Pharmacal Research          2012          35          1919-1926
A new triterpenoid from Alisma orientale and their antibacterial effect
Hong-Guang Jin, Qinglong Jin, A. Ryun Kim, Hyemin Choi, Je Hyun Lee, Yeong Shik Kim, Dong Gun Lee, Eun-Rhan Woo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
66 .     alisol A
    ÏàËÆ¶È:60%
Chinese Traditional and Herbal Drugs          2012          43          841-843
A new triterpene in rhizome of Alisma orientale
XU Nan; ZHANG Hong-da; XIE Xue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
67 .     25-methoxy-cyc loart-23E-en-3¦Â-ol
    ÏàËÆ¶È:60%
Chinese Journal of Applied & Environmental Biology          2005          11          265-270
CHEMICAL STUDY OF STREPTOCAULON GRIFFITHII
MA Chunhui; HUANG Tianfang; QI Huayi; LI Bogang; ZHANG Guolin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
68 .     29-O-acetyl-3-oxotirucalla-7,24-dien-21-oic acid
    ÏàËÆ¶È:59.3%
Journal of Natural Products          2000          63          238-242
Inhibitory Effects on HIV-1 Protease of Constituents from the Wood of Xanthoceras sorbifolia
Chao-mei Ma, Norio Nakamura,Masao Hattori, Hiroko Kakuda,Jun-chan Qiao, and Hai-lan Yu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
69 .     acetoxyketone
    ÏàËÆ¶È:59.3%
Chemistry of Natural Compounds          2007          43          153-158
REACTION OF 3-ACETOXY-(2,3),(19b,28)-DIEPOXYOLEANANE WITH CYCLIC AND LINEAR AMINES
I. A. Tolmacheva, L. N. Shelepen'kina, A. S. Shashkov,V. V. Grishko, V. A. Glushkov, and A. G. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
70 .     23(E)-cycloart-23-en-25-ethoxy-3¦Â-ol
C32H54O2     ÏàËÆ¶È:59.3%
Journal of the Chinese Chemical Society          2007          54          1565-1572
Triterpenoids and Other Constituents from Euphorbia humifusa
Ying-Ge Pei, Quan-Xiang Wu and Yan-Ping Shi*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
71 .     quadrangularate N
C31H48O4     ÏàËÆ¶È:58.0%
Chemical & Pharmaceutical Bulletin          2000          48(4)          496-504
Methyl Quadrangularates A-D and Related Triterpenes from Combretum quadrangulare
Arjun Hari BANSKOTA,Yasuhiro TEZUKA,Kim Qui TRAN,Ken TANAKA, Ikuo SAIKI and Shigetoshi KADOTA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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