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16.6,18.2,20.1,20.4,21.3,28.3,29.5,31.5,34.3,35.2,38.5,39.9,41.3,44.3,47.4,51.6,84.7,121.5,126.7,133.7,134.9,136.8,158.6,189.8,201.6
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1 .     9¦Á,11¦Á-dihydroxyergosta-4,6,8(14),22-tetraen-3-one
C28H40O3     ÏàËÆ¶È:60.7%
Journal of Natural Products          2011          74          1281-1283
A Highly Conjugated Dihydroxylated C28 Steroid from a Myxobacterium
Dnyaneshwar Gawas, Ronald Garcia, Volker Huch, and Rolf M¨¹ller
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     ent-15¦Â-angeloyloxy-9¦Á-hydroxy-kaur-16-en-19-oic acid
    ÏàËÆ¶È:60%
Phytochemistry          2003                   391-396
Studies of ent-kaurane diterpenes from Oyedaea verbesinoides for their inhibitory activity on vascular smooth muscle contraction
Stefan M¨¹ller, Carlos R. Tirapelli, Ana M. de Oliveira, Renato Murillo,Victor Castro, Irmgard Merfort
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     camaldulenic acid
C30H46O4     ÏàËÆ¶È:58.6%
Journal of Natural Products          1997          60          20-23
Triterpenoids from the Leaves of Eucalyptus camaldulensis var. obtusa
Sabira Begum, Farhat, and Bina S. Siddiqui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (23E)-27-Nor-25-oxo-5¦Á-cholest-23-ene-3¦Â,6¦Á,8,14,15¦Á-pentaol 15-O-sulfate,sodium salt
C26H41O9SNa     ÏàËÆ¶È:57.6%
Steroids          2010          75          897-904
Highly hydroxylated steroids of the starfish Archaster typicus from the Vietnamese waters
Natalia V. Ivanchina, Alla A. Kicha, Trinh T.T. Huong, Anatoly I. Kalinovsky, Pavel S. Dmitrenok, Irina G. Agafonova, Pham Q. Long, Valentin A. Stonik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     pittosporatobiraside B
C26H38O5     ÏàËÆ¶È:57.6%
Phytochemistry          1989          28          3085-3091
Sesquiterpene glycosides and other terpene constituents from the flowers of Pittosporum tobira
Kazuhito Ogihara,Kiyotaka Munesada,Takayuki Suga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     24R-and 24S-methyl-3¦Â,6 ¦Á,11-trihydroxy-9,11-seco-5 ¦Á-cholest-7,22E-diene-9-one
    ÏàËÆ¶È:57.1%
Steroids          1998          63          575-578
New 9,11-secosterols from gorgonia Subergorgia suberosa of the Indian Ocean
M. Aknin, V. Costantino, A. Mangoni, E. Fattorusso, E. M. Gaydou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     24,25,26,27-tetranor-apotirucall-6¦Á,22-dihydroxy-7¦Á-acetoxy-1,14,20(21)-trien-3-one-21,23-olide
C28H36O7     ÏàËÆ¶È:57.1%
Journal of Natural Products          2014          77          596-602
Bioactive Limonoids from the Leaves of Azaridachta indica (Neem)
Maria J. Gualtieri, Nicola Malafronte, Antonio Vassallo, Alessandra Braca, Roberta Cotugno, Michele Vasaturo, Nunziatina De Tommasi, and Fabrizio Dal Piaz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     22E-ergosta-4,6,8(14),22-tetraen-3-one
C28H40O     ÏàËÆ¶È:57.1%
Journal of Shenyang Pharmaceutical University          2012          29          678-684
A new disecosteroid from an endolichenic fungal stain Sporormiella irregularis(No.71-11-4-1)
LI Yan-jun; LI Xiao-xia; CHEN Guo-dong; GAO Hao; GUO Liang-dong; YAO Xin-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     camaldulenic acid methyl ester
    ÏàËÆ¶È:56.6%
Journal of Natural Products          1997          60          20-23
Triterpenoids from the Leaves of Eucalyptus camaldulensis var. obtusa
Sabira Begum, Farhat, and Bina S. Siddiqui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     deacetyl-WF11605
C30H48O5     ÏàËÆ¶È:56.6%
The Journal of Antibiotics          1992          45          704-708
WF11605, AN ANTAGONIST OF LEUKOTRIENE B4 PRODUCED BY A FUNGUSII. STRUCTURE DETERMINATION
NOBUHARU SHIGEMATSU, EISAKU TSUJII, NATSUKO KAYAKIRI, SHIGEHIRO TAKASE, HIROKAZU TANAKA, TOSHIJI TADA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 8
C22H34O4     ÏàËÆ¶È:56%
Tetrahedron Letters          2002          43          9043-9046
Stypolactone, an interesting diterpenoid from the brown alga Stypopodium zonale
Enrique Dorta, Mercedes Cueto, Ana R. Dı́az-Marrero, Jos¨¦ Darias
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     2,3-dihydroxy-9(11)-fernen-23-oic acid
    ÏàËÆ¶È:56%
Natural Product Research and Development          2010          22          940-944
Chemical Constituents from Melastoma dodecandrum
YANG Dan;MA Qing-yun; LIU Yu-qing; DING Zhong-tao; ZHOU Jun; ZHAO You-xing;
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     Cholesta-8(14)-en-3¦Â,5¦Á,6¦Á,25-tetrol
C27H50O4N     ÏàËÆ¶È:55.5%
Steroids          2005          70          954-959
Novel polyhydroxysterols from the Red Sea marine sponge Lamellodysidea herbacea
Pierre Sauleau, Marie-Lise Bourguet-Kondracki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     (20R,22S,25S)-veratra-5,13-dien-3¦Â-ol
    ÏàËÆ¶È:55.5%
China Journal of Chinese Materia Medica          2009          34          3039-3042
Steroidal alkaloids of from Veratrum dahuricum
ZHAO Lang, OU Zhiqiang, WANG Kan, FU Hongzheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     (2S,3R,5S,9R,10R,13R,14R,17R)-17-(2-((2R)-5-ethyl-5-methyl-tetrahydrofuran-2-yl)propan-2-yl)-2,3,5,14-tetrahydroxy-10,13,17-trimethyl-1,2,3,4,5,10,11,12,13,15,16,17-dodecahydro-9H-cyclopenta[a]phenanthren-6(14H)-one
C30H48O6     ÏàËÆ¶È:55.5%
Steroids          2011          76          1419-1424
Ecdysteroids from Polypodium vulgare L.
Andr¨¢s Simon, Attila V¨¢nyol¨®s, Zolt¨¢n B¨¦ni, Mikl¨®s D¨¦k¨¢ny, G¨¢bor T¨®th, M¨¢ria B¨¢thori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     ajugasterone D
C27H42O7     ÏàËÆ¶È:55.5%
Chinese Traditional and Herbal Drugs          2014          45          906-912
Chemical constituents from roots tubers of Serratula chinensis
TANG Hai-jiao, FAN Chun-lin, WANG Gui-yang, WEI Wei, WANG Ying, YE Wen-cai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     24-Methylene-shidasterone
C28H42O6     ÏàËÆ¶È:53.5%
Steroids          2007          72          751-755
Three new steroids from the roots of Serratula wolffii
Andr¨¢s Simon, G¨¢bor T¨®th, Erika Liktor-Busa, Zolt¨¢n Kele, M¨¢ria Tak¨¢cs, Andr¨¢s Gergely, M¨¢ria B¨¢thori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     (20S,22S)-3¦Â,22-dihydroxycucurbita-5(10),24-diene-26,29-dioic acid ¦Ä-lactone
C30H44O5     ÏàËÆ¶È:53.5%
Natural Product Research          2002          16          261-266
New Triterpenoids from the Leaves of Abrus Precatorius
Nam-Cheol Kim; Darrick Kim; A. Douglas Kinghorn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     Clionamine A
C28H45NO3     ÏàËÆ¶È:53.5%
Organic Letters          2008          Vol.10,No.14          2959-2962
Autophagy-Modulating Aminosteroids Isolated from the Sponge Cliona celata
Robert A. Keyzers, Julie Daoust, Michael T. Davies-Coleman,Rob Van Soest,Aruna Balgi,Elizabeth Donohue, Michel Roberge, and Raymond J. Andersen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     5¦Á,6¦Á-Epoxyergosta-8,22-diene-3¦Â,7¦Â-diol
    ÏàËÆ¶È:53.5%
Archives of Pharmacal Research          2008          31          579-586
Cytotoxic constituents of Amanita subjunquillea
Ki Hyun Kim, Sang Un Choi, Ki Moon Park, Soon Ja Seok and Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     22E,24R-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â,9¦Á-tetraol
C28H46O4     ÏàËÆ¶È:53.5%
Chinese Journal of Medicinal Chemistry          2008          18          279-283
Chemical constituents from endophytic fungus S26 of Cephalotaxus hainanensis
CHEN Ping, WU Jiao, DAI Hao-fu, XIE Xiu-chao, MEI Wen-li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     (22E,24R)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Á,9¦Á-tetraol
C32H52O4     ÏàËÆ¶È:53.5%
Natural Product Research and Development          2007          19          436-438
Chemical Constituents of Basidiomycetes Russula subnigricans
GONG Qing-fang; ZHANG Yu-mei; TAN Ning-hua; CHEN Zuo-hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     fomentarol B
C28H46O     ÏàËÆ¶È:53.5%
Phytochemistry          2013          92          137-145
Fomentarols A¨CD, sterols from the polypore macrofungus Fomes fomentarius
Yi Zang, Juan Xiong, Wen-Zhu Zhai, Lei Cao, Sheng-Ping Zhang, Yu Tang, Ji Wang, Jing-Jing Su, Guo-Xun Yang, Yun Zhao, Hui Fan, Gang Xia, Chuan-Gui Wang, Jin-Feng Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     15¦Á-hydroxy-3,11-dione-oleana-12-en-30-oic ac
    ÏàËÆ¶È:53.3%
Journal of Asian Natural Products Research          2008          10          463-466
One new triterpenoid from biotransformation product of glycyrrhizic acid
Li-Ping Kang, Jie Zhang, He-Shui Yua,4 Hong-Zhi Huang, Yong-Ze Wanga and Bai-Ping Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     cucurbita-5,23(E)-diene-3¦Â,7¦Â,25,29-tetraol
C30H50O4     ÏàËÆ¶È:53.3%
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
26 .     2¦Á-hydroxyl-betulinic acid
C30H48O4     ÏàËÆ¶È:53.3%
Lishizhen Medicine and Materia Medica Research          2009          20          122-123
Studies on the Chemical Constituents of Potentilla discolor Bge
LIU Pu; LI Jun-bo; LI Li-ying; YU Hua-ning; QIN Lin-lin; YIN Wei-ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     2¦Á,3¦Â-Dihydroxyolean-11-en-28,13¦Â-olide
C30H46O4     ÏàËÆ¶È:53.3%
Phytochemistry          2013          94          229-237
Biotransformation of oleanolic and maslinic acids by Rhizomucor miehei
Antonio Martinez, Francisco Rivas, Alberto Perojil, Andres Parra, Andres Garcia-Granados, Antonia Fernandez-Vivas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     12¦Á-bromo-2¦Á,3¦Â-dihydroxyolean-28,13¦Â-olide
C30H47BrO4     ÏàËÆ¶È:53.3%
Phytochemistry          2013          94          229-237
Biotransformation of oleanolic and maslinic acids by Rhizomucor miehei
Antonio Martinez, Francisco Rivas, Alberto Perojil, Andres Parra, Andres Garcia-Granados, Antonia Fernandez-Vivas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     23-Hydroxybetulin
    ÏàËÆ¶È:53.3%
Natural Product Sciences          2013          19          269-274
Chemical Constituents from the Aerial Parts of Aster yomena
Qinglong Jin, Hae Ju Ko, Young-Su Chang, and Eun-Rhan Woo*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     1-hydroxy-20,22-didehydrotaxisterone
C27H42O6     ÏàËÆ¶È:52%
Journal of Natural Products          2007          70          884-886
Ecdysteroids from Serratula wolffii Roots
Erika Liktor-Busa,Andr¨¢s Simon, G¨¢bor T¨®th, G¨¢bor Fekete, Zolt¨¢n Kele, and M¨¢ria B¨¢thori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     compound 19
    ÏàËÆ¶È:52%
Journal of Natural Products          1997          60          959-966
Isolation, Structure Elucidation, and Biological Activity of the Steroid Oligoglycosides and Polyhydroxysteroids from the Antarctic Starfish Acodontaster conspicuus
Simona De Marino, Maria Iorizzi, Franco Zollo, Luigi Minale, Charles D. Amsler, Bill J. Baker, and James B. McClintock
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     10-Acetoxy-18-hydroxy-2,7-dolabelladiene
    ÏàËÆ¶È:52%
Natural Product Sciences          2004          10          253-261
Bioactive Metabolites from the Brittle Star Ophioplocus japonicus
Wang, Wei-Hong; Hong, Jong-Ki; Lee, Chong-Ok; Cho, Hee-Young; Shin, Sook; Jung, Jee-H.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     3R,4S,5S,17R,20R-3,17,20-trihydroxy-4-methylpregn-8-en-7-one
C22H34O4     ÏàËÆ¶È:52%
Journal of Natural Products          2010          73          1294-1300
Homo- and Heptanor-sterols and Tremulane Sesquiterpenes from Cultures of Phellinus igniarius
Xiuli Wu, Sheng Lin, Chenggen Zhu, Zhenggang Yue, Yang Yu, Feng Zhao, Bo Liu, Jungui Dai and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     compound 8
    ÏàËÆ¶È:52%
Journal of the Chemical Society, Perkin Transactions 1          1981                   1773-1778
Cardenolide analogues. Part 12. 13C N.m.r. of semi-synthetic glycosides and side-chain modified genins
H. T. Andrew Cheung, Lindsay Brown, John Boutagy and Richard Thomas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     petrosaspongiolide L
C24H35O2N     ÏàËÆ¶È:52%
Tetrahedron          1997          53          10451-10458
New cytotoxic sesterterpenes from the New Caledonian marine sponge Petrosaspongia nigra (Bergquist)
Luigi Gomez Paloma, Antonio Randazzo, Luigi Minale, C¨¦cile Debitus, Christos Roussakis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     compound 9a
C25H35N3O4     ÏàËÆ¶È:52%
The Journal of Organic Chemistry          2007          72          7190-7198
Spongolactams, Farnesyl Transferase Inhibitors from a Marine Sponge:  Isolation through an LC/MS-Guided Assay, Structures, and Semisyntheses
Daisuke Mori, Yuko Kimura, Shigeyuki Kitamura, Youji Sakagami, Yukio Yoshioka, Tomoaki Shintani, Tetsuji Okamoto, and Makoto Ojika
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     16-acetylkirenol
C22H36O5     ÏàËÆ¶È:52%
Chinese Journal of Natural Medicines          2012          10          13-15
A new carbamate with cytotoxic activity from the aerial parts of Siegesbeckia pubecens
Jia LIU, Rong CHEN, Yu NIE, Lin FENG, Hai-Dao LI, Jing-Yu LIANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     Neosymbioimine
C21H27NO5S     ÏàËÆ¶È:52%
Bioorganic & Medicinal Chemistry          2005          13          5253-5258
Symbioimine and neosymbioimine, amphoteric iminium metabolites from the symbiotic marine dinoflagellate Symbiodinium sp.
Masaki Kita, Nao Ohishi, Kazuto Washida, Mikiko Kondo, Tomoyuki Koyama, Kaoru Yamada, Daisuke Uemura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     3¦Â-hydroxy-9(11)-fernen-23-oic acid
C30H48O3     ÏàËÆ¶È:52%
Chinese Traditional and Herbal Drugs          2011          42          1061-1065
Chemical constituents from Osbeckia chinensis
CHEN, Chao, HU, Yu, SUN, Jia-xiang, PI, Hui-fang, ZHANG, Peng, RUAN, Han-li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     topsentisterol A3
C27H40O3     ÏàËÆ¶È:51.8%
Journal of Natural Products          2006          69          1760-1768
26,27-Cyclosterols and Other Polyoxygenated Sterols from a Marine Sponge Topsentia sp.
Xuan Luo, Famei Li, Pramod B. Shinde, Jongki Hong, Chong-O. Lee, Kwang Sik Im, and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     comnostin C
C27H38O5     ÏàËÆ¶È:51.8%
Journal of Natural Products          2000          63          339-343
Novel Extracellular Diterpenoids with Biological Activity from the Cyanobacterium Nostoc commune
B. Jaki, J. Orjala, J. Heilmann, A. Linden, B. Vogler, and O. Sticher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     noscomin
    ÏàËÆ¶È:51.8%
Journal of Natural Products          1999          62          502-503
A Novel Extracellular Diterpenoid with Antibacterial Activity from the Cyanobacterium Nostoc commune
Birgit Jaki, Jimmy Orjala, and Otto Sticher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     compound 18
    ÏàËÆ¶È:51.8%
Journal of Natural Products          1997          60          959-966
Isolation, Structure Elucidation, and Biological Activity of the Steroid Oligoglycosides and Polyhydroxysteroids from the Antarctic Starfish Acodontaster conspicuus
Simona De Marino, Maria Iorizzi, Franco Zollo, Luigi Minale, Charles D. Amsler, Bill J. Baker, and James B. McClintock
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     integristerone A
    ÏàËÆ¶È:51.8%
Helvetica Chimica Acta          2009          92          753-761
Ecdysteroids from Silene viridiflora
Andr¨¢s Simon, No¨¦mi T¨®th, G¨¢bor T¨®th, Zolt¨¢n Kele, Judit Groska, M¨¢ria B¨¢thori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     integristerone A
    ÏàËÆ¶È:51.8%
Steroids          2004          69          389-394
A new ecdysteroid with unique 9¦Â-OH and four other ecdysteroids from Silene italica ssp. nemoralis
Andr¨¢s Simon, Zita Pongr¨¢cz, G¨¢bor T¨®th, Marianna M¨¢k, Imre M¨¢th¨¦, M¨¢ria B¨¢thori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     moniloside C
    ÏàËÆ¶È:51.8%
Journal of Natural Products          1993          Vol 56          99
Brominated Indole Alkaloids from the Marine Tunicate Pseudodistoma arborescens
Mohammed Chbani, Mary Païs, Jean-Marc Delauneux, C¨¦cile Debitus
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     ¦Â-ecdysterone
    ÏàËÆ¶È:51.8%
China Journal of Chinese Materia Medica          2010          35          2994-2998
Flavone and steroid chemical constituents from rhizome of Paris axialis
HUANG Xianxiao; GAO Wenyuan; ZHAO Wanshun; ZHANG Tiejun; XU Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     3¦Â,6¦Á,11-trihydroxy-9,11-seco-5¦Á-cholest-7-ene-9-one
C28H46O4     ÏàËÆ¶È:51.8%
Steroids          1998          63          575-578
New 9,11-secosterols from gorgonia Subergorgia suberosa of the Indian Ocean
M. Aknin, V. Costantino, A. Mangoni, E. Fattorusso, E. M. Gaydou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     3¦Â,5¦Á,6¦Á-trihydroxy-9,11-secocholest-7-en-9-one
C27H44O4     ÏàËÆ¶È:51.8%
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 .     compound 10
C27H42O4     ÏàËÆ¶È:51.8%
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
51 .     25-hydroxydacryhainansterone
C27H42O7     ÏàËÆ¶È:51.8%
Journal of China Pharmaceutical University          2006          37          487-490
Chemical constituents from Asparagus filicinus
WU Jia-jun; WANG Hao; YE Wen-cai; ZUO Xiao-feng; ZHAO Shou-xun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     20¦Â-hydroxy-ecdysone-2-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:51.8%
Natural Product Research and Development          2005          17          125-127
Chemical Constituents of Tinospora craveniana
LI Hong-bo; HU Jun; CHEN Jian-chao; QIU Ming-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     1¦Á,20R-hydroxyecdysone
    ÏàËÆ¶È:51.8%
Natural Product Research and Development          2002          14(1)          9-12
STUDY ON THE CHEMICAL CONSTITUENTS OF LYCHNIS CORONARIA
DAI Hao-fu; LIU Yu-qing; DENG Shi-ming; TAN Ning-hua; ZHOU Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
54 .     polypodingB
    ÏàËÆ¶È:51.8%
Natural Product Research and Development          2002          14(1)          9-12
STUDY ON THE CHEMICAL CONSTITUENTS OF LYCHNIS CORONARIA
DAI Hao-fu; LIU Yu-qing; DENG Shi-ming; TAN Ning-hua; ZHOU Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
55 .     betulinic acid
    ÏàËÆ¶È:51.8%
Journal of Guangdong Phamaceutical University          2012          28          142-144
Studies on chemical constituents from Rubus alceaefolius Poir.
XU Dan-dan, ZHOU Hong-bo, FANG Zhi-jian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
56 .     polypodine B
C27H44O8     ÏàËÆ¶È:51.8%
Chinese Traditional and Herbal Drugs          2014          45          906-912
Chemical constituents from roots tubers of Serratula chinensis
TANG Hai-jiao, FAN Chun-lin, WANG Gui-yang, WEI Wei, WANG Ying, YE Wen-cai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
57 .     25-hydroxydacryhainansterone
    ÏàËÆ¶È:51.8%
Chinese Traditional and Herbal Drugs          2012          43          1716-1720
Steroids from tubers of Asparagus filicinus
TAO Hua-ming; WANG Li-shu; ZHAO Da-qing; ZHU Quan-hong; YIN Yong-guan; LIU Yong-hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
58 .     20-Hydroxyecdysone
C27H44O7     ÏàËÆ¶È:51.8%
Monatshefte f¨¹r Chemie          2000          131          195-204
Three Saponins, a Steroid, and a Flavanol Glycoside from Achyrantes aspera
Olaf Kunert, Ernst Haslinger, Martin G. Schmid, Josef Reiner, Franz Bucar, Efrem Mulatu, Dawit Abebe, and Asfaw Debella
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
59 .     Ë®Áú¹ÇçÞͪB
C27H44O8     ÏàËÆ¶È:51.8%
Journal of Tropical and Subtropical Botany          2013          21          57-62
Chemical Constituents from Roots of Achyranthes bidentata
TANG Xin, PEI Gang, ZHOU Zhong-yu, TAN Jian-wen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
60 .     compound 4
    ÏàËÆ¶È:51.8%
The Journal of Organic Chemistry          1991          56          1146-1153
Novel marine polyhydroxylated steroids from the starfish Myxoderma platyacanthum
Ester Finamore, Luigi Minale, Raffaele Riccio, Gaetano Rinaldo, Franco Zollo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
61 .     songarosaponin A
C54H88O21     ÏàËÆ¶È:51.7%
Phytochemistry          1991          30          3395-3400
Triterpene saponins from Verbascum songaricum
Karlheiz Seifert, Alfred Preiss, Siegfried Johne, J¨¹rgen Schmidt, Nguyen T. Lien, Catherine Lavaud, Georges Massiot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
62 .     crustulinol
C30H50O6     ÏàËÆ¶È:51.7%
Tetrahedron letters          1983          24          1635-1638
Fungal metabolites XIII: New cytotoxic triterpene from Hebeloma species (basidiomycetes)
M. De Bernardi, G. Fronza, M.P. Gianotti, G. Mellerio, G. Vidari, P. Vita-Finzi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
63 .     5¦Á-stigmasta-7,9(11),24(28)Z-triene-3¦Â,26,29-triol
C29H46O3     ÏàËÆ¶È:51.7%
Phytochemistry          2013          96          288-298
Steroids with anti-inflammatory activity from Vernonia nigritiana Oliv. & Hiern.
Antonio Vassallo, Nunziatina De Tommasi, Irmgard Merfort, Rokia Sanogo, Lorella Severino, Marco Pelin, Roberto Della Loggia, Aurelia Tubaro, Silvio Sosa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
64 .     sarcsteroid C
    ÏàËÆ¶È:51.7%
Steroids          2013          78          1353-1358
Bioactive polyhydroxylated sterols from the marine sponge Haliclona crassiloba
Zhong-Bin Cheng, Han Xiao, Cheng-Qi Fan, Ya-Nan Lu, Ge Zhang, Sheng Yin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
65 .     Rubrajaleelic acid
C29H46O4     ÏàËÆ¶È:51.7%
Phytochemistry Letters          2013          6          291-298
Isolation and characterization of the chemical constituents from Plumeria rubra
Nasim Akhtar, Muhammad Saleem, Naheed Riaz, M. Shaiq Ali, Asma Yaqoob, Faiz-ul-Hassan Nasim, Abdul Jabbar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
66 .     3¦Â-Hydroxy-4,4-dimethylcholesta-8,24-dien-23-one 3-¦Â-D-Xyloside
    ÏàËÆ¶È:51.7%
The Journal of Organic Chemistry          1988          53          5941-5947
Sarasinoside A1: a saponin containing amino sugars isolated from a sponge
Francis J. Schmitz, Mohamad B. Ksebati, Sarath P. Gunasekera, Santosh Agarwal
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
67 .     serrulatin E
C30H50O6     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2008          Vol. 91          665
Triterpenoids from the Edible Leaves of Photinia serrulata
Ya-Ling Song, Yue-Hu Wang, Qing Lu, Hui-Jun Qiao, and Yong-Xian Cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
68 .     cylindrictone C
C28H46O4     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2008          Vol. 91          1578
Six New Dammarane Triterpenoids from Viburnum cylindricum
Lin Tu, Yu Zhao, Zu-Yin Yu, Yu-Wen Cong, Gang Xu, Li-Yan Peng, Peng-Tao Zhang, Xiao Cheng, and Qin-Shi Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
69 .     topsentisterol B4
C28H44O3     ÏàËÆ¶È:50%
Journal of Natural Products          2006          69          1760-1768
26,27-Cyclosterols and Other Polyoxygenated Sterols from a Marine Sponge Topsentia sp.
Xuan Luo, Famei Li, Pramod B. Shinde, Jongki Hong, Chong-O. Lee, Kwang Sik Im, and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
70 .     topsentisterol B5
C28H44O3     ÏàËÆ¶È:50%
Journal of Natural Products          2006          69          1760-1768
26,27-Cyclosterols and Other Polyoxygenated Sterols from a Marine Sponge Topsentia sp.
Xuan Luo, Famei Li, Pramod B. Shinde, Jongki Hong, Chong-O. Lee, Kwang Sik Im, and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
71 .     topsentisterol D3
C28H42O2     ÏàËÆ¶È:50%
Journal of Natural Products          2006          69          1760-1768
26,27-Cyclosterols and Other Polyoxygenated Sterols from a Marine Sponge Topsentia sp.
Xuan Luo, Famei Li, Pramod B. Shinde, Jongki Hong, Chong-O. Lee, Kwang Sik Im, and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
72 .     mahureone D
32H48O6     ÏàËÆ¶È:50%
Journal of Natural Products          2005          68          979-984
Acylphloroglucinol Derivatives from Mahurea palustris
Georges Massiot, Christophe Long, Bruno David, Marie-Jeanne Serrano, Florence Daubi, Frdric Alby, Frdric Ausseil, Martine Knibiehler, Christian Moretti, Jean-Sbastien Hoffmann, Christophe Cazaux, and Catherine Lavaud
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
73 .     plakinamine J
C30H50N2     ÏàËÆ¶È:50%
Journal of Natural Products          2003          66          1536-1539
New Cytotoxic Steroidal Alkaloids from the Philippine Sponge Corticium niger
Christian P. Ridley and D. John Faulkner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
74 .     20,22-didehydrotaxisterone
C27H42O5     ÏàËÆ¶È:50%
Journal of Natural Products          2007          70          884-886
Ecdysteroids from Serratula wolffii Roots
Erika Liktor-Busa,Andr¨¢s Simon, G¨¢bor T¨®th, G¨¢bor Fekete, Zolt¨¢n Kele, and M¨¢ria B¨¢thori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
75 .     (22E)-2¦Á-Fluoro-5¦Á-stigmasta-22-en-3,6-dione
C29H45O2F     ÏàËÆ¶È:50%
Steroids          2009          74          435-440
Synthesis and biological activity of brassinosteroids fluorinated at C-2
Sof¨ªa L. Acebedo, Javier A. Ram¨ªrez, Lydia R. Galagovsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
76 .     22E,4R-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â,9¦Á,14¦Á-pentol
C28H46O5     ÏàËÆ¶È:50%
Natural Product Research          2008          22          1137-1142
Sterols and triterpenoids from the spores of Ganoderma lucidum
Chuan-Rui Zhang; Sheng-Ping Yang; Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
77 .     5¦Á-ergosta-7,22-diene-3¦Â,5,6¦Â-triol
    ÏàËÆ¶È:50%
Journal of Natural Products          1988          Vol 51          1098
Polar Steroids from the Marine Scallop Patinopecten yessoensis
Maria Iorizzi, Luigi Minale, Raffaele Riccio, Jong-Soo Lee, Takeshi Yasumoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
78 .     6-oxotingenol
C28H36O4     ÏàËÆ¶È:50%
Journal of Natural Products          1994          Vol 57          1675
Cytotoxic Aromatic Triterpenes from Maytenus ilicifolia and Maytenus chuchuhuasca
Osamu Shirota, Hiroshi Morita, Koichi Takeya, Hideji Itokawa, Yoichi Iitaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
79 .     (22E,24R,25S)-24-methyl-5¦Á-cholesta-22-en-3¦Â,5,6¦Â,15¦Á,26-pentaol 26-sulfate
    ÏàËÆ¶È:50%
Journal of Natural Products          1995          Vol 58          653-671
Chemical and Biological Investigation of the Polar Constituents of the Starfish Luidia clathrata, Collected in the Gulf of Mexico
Maria Iorizzi, Patrick Bryan, James McClintock, Luigi Minale, Elio Palagiano, Stefano Maurelli, Raffaele Riccio, Franco Zollo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
80 .     (22E,24R)-3¦Â,5¦Á,9¦Á-trihydroxyergosta-7,22-dien-6-one
    ÏàËÆ¶È:50%
Chinese Journal of Marine Drugs          2009          28(5)          11-16
Cytotoxic metabolites from symbiotic fungus Penicilliom sp.HK13-8 with Rhizophora stylosa
HAN Xiu-li, LIN Zhen-jian, TAO Hong-wen, LIU Pei-pei, WANG Yi, ZHU Wei-ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
81 .     compound 1a
    ÏàËÆ¶È:50%
Zeitschrift f¨¹r Naturforschung B          2011          66b          624-628
Dialiumoside, an Olean-18-ene Triterpenoid from Dialium excelsum
Angelbert F. Awantu, Bruno N. Lenta, Tobias Bogner, Yanick F. Fongang,Silv¨¨re Ngouela, Jean D. Wansi, Etienne Tsamo, and Norbert Sewald
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
82 .     7¦Á,21¦Á-dihydroxyfriedelane-3-one
C30H50O3     ÏàËÆ¶È:50%
Zeitschrift f¨¹r Naturforschung B          2010          65b          1284-1288
Study on Chemical Constituents and Cytotoxic Activities of Salacia chinensis Growing in Vietnam
Tran Thi Minh, Nguyen Thi Hoang Anh, Vu Dao Thang, and Tran Van Sung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
83 .     2¦Á,3¦Â-dihydroxylup-20(29)-en-28-oic acid
C30H48O4     ÏàËÆ¶È:50%
Phytochemistry Letters          2011          4          259-266
Seven new triterpene glycosides from the pericarps of Stryphnodendron fissuratum
Akihito Yokosuka, Sachiko Kawakami, Mitsue Haraguchi, Yoshihiro Mimaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
84 .     (24R)-24-Hydroxymethyl-24-bydroxycholesterol
    ÏàËÆ¶È:50%
Journal of Natural Products          1995          58          653-671
Chemical and Biological Investigation of the Polar Constituents of the Starfish Luidia clathrata, Collected in the Gulf of Mexico
Maria Iorizzi, Patrick Bryan, James McClintock, Luigi Minale, Elio Palagiano, Stefano Maurelli, Raffaele Riccio, Franco Zollo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
85 .     compound 12
    ÏàËÆ¶È:50%
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
86 .     betulinic acid
    ÏàËÆ¶È:50%
Chinese Traditional and Herbal Drugs          2009          40          1039-1042
ɽ·¯µÄ»¯Ñ§³É·ÖÑо¿
»ô³¤ºç;Áººè;ÕÅÇìÓ¢;Íõß“;ÕÔÓñÓ¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
87 .     3¦Â,11-dihydroxy-24-methyl-9,11-secocholest-5-en-9-one
    ÏàËÆ¶È:50%
Chinese Journal of Natural Medicines          2010          8          186-188
Cytotoxic 9,11-Secosterols from the Marine Soft Coral Sinularia robusta
HE Xi-Xin; ZHANG Cui-Xian; ZENG Long-Mei; YANG Xiao-Ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
88 .     25-Epi-pseudolarolide Q
C30H42O7     ÏàËÆ¶È:50%
Planta Medica          2011          77          1924-1931
Antimicrobial, Cytotoxic Lignans and Terpenoids from the Twigs of Pseudolarix kaempferi
He, Wen-Jun; Chu, Hong-Biao; Zhang, Yu-Mei; Han, Hong-Jin; Yan, He; Zeng, Guang-Zhi; Fu, Zhao-Hui; Olubanke, Ogunlana; Tan, Ning-Hua:
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
89 .     balsaminol E
C30H48O3     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2010          18          5254-5260
New antimalarials with a triterpenic scaffold from Momordica balsamina
C¨¢tia Ramalhete, Dinora Lopes, Silva Mulhovo, Joseph Moln¨¢r, Virg¨ªlio E. Ros¨¢rio, Maria-Jos¨¦ U. Ferreira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
90 .     (22E,24R)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
C28H46O3     ÏàËÆ¶È:50%
Natural Product Research and Development          2007          19          620-622
Chemical Constituents of Piper pedicellatum C. DC
LI Jun-zhu; LIU Hai-yang; DONG Qiu; CHEN Chang-xiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
91 .     betulinic acid
    ÏàËÆ¶È:50%
Natural Product Research and Development          2006          18          58-60
Chemical Constituents from Euphorbia latifolia
ZHANG Lei-hong; ZHANG Xian-tao; YE Wen-cai; YIN Zhi-qi; ZHENG Dan; ZHAO Shou-xun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
92 .     simiarenol
    ÏàËÆ¶È:50%
Natural Product Research and Development          2004          16          131-132
STUDIES ON CHEMICAL CONSTITUENTS OF GENDARUSSA VENTRICOSA
ZHANG Xiao-li;YU Zheng-wen;GUO Fang-qin; YANG Xiao-sheng *; HAO Xiao-jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
93 .     parathiosteroid B
C26H39NO3S     ÏàËÆ¶È:50%
The Journal of Organic Chemistry          2008          73          7978-7984
Isolation, Biological Significance, Synthesis, and Cytotoxic Evaluation of New Natural Parathiosteroids A−C and Analogues from the Soft Coral Paragorgia sp.
Javier Jesus Poza, Rogelio Fernandez, Fernando Reyes, Jaime Rodriguez and Carlos Jimenez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
94 .     (20R,22R)-2¦Â,3¦Â,20,22,25-pentahydroxy-5¦Â-cholest-8(14)-en-6-one
    ÏàËÆ¶È:50%
Russian Journal of Organic Chemistry          2010          46          1735-1740
¦¤8(14)-14¦Á-deoxy- and 14¦Á-deoxy-14¦Á-hydroperoxyecdysteroids
A. Sh. Ibragimova, N. A. Ves¡¯kina, I. V. Galyautdinov and V. N. Odinokov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
95 .     andrastin C
    ÏàËÆ¶È:50%
The Journal of Antibiotics          1996          49          1278-1280
Andrastin D, Novel Protein Farnesyltransferase Inhibitor Produced by Penidllium sp. FO-3929
RYUJI UCHIDA, KAZURO SHIOMI, JUNJI INOKOSHI, HARUO TANAKA, YUZURU IWAI, SATOSHI OMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
96 .     andrastin D
C26H36O5     ÏàËÆ¶È:50%
The Journal of Antibiotics          1996          49          1278-1280
Andrastin D, Novel Protein Farnesyltransferase Inhibitor Produced by Penidllium sp. FO-3929
RYUJI UCHIDA, KAZURO SHIOMI, JUNJI INOKOSHI, HARUO TANAKA, YUZURU IWAI, SATOSHI OMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
97 .     12-O-¦Â-D-glucopyranosyl-3,11,16-trihydroxyabieta-8,11,13-triene
    ÏàËÆ¶È:50%
Phytotherapy Research          2010          24          1720-1723
Anti-complement activity of isolated compounds from the roots of Clerodendrum bungei Steud.
Soo-Ki Kim, Sang-Buem Cho and Hyung-In Moon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
98 .     ergosta-7,22-diene-3¦Â,5¦Á,6¦Â,9¦Á-tetraol
C28H46O4     ÏàËÆ¶È:50%
Natural product sciences          2011          17          85-89
Cytotoxicity of Ergosterol Derivatives from the Fruiting Bodies of Hygrophorus russula
Lee, Ik-Soo; Kim, Jin-Pyo; Na, Min-Kyun; Jung, Hyun-Ju; Min, Byung-Sun; Bae, Ki-Hwan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
99 .     2,3-acetonide-24-hydroxyecdysone
C30H48O7     ÏàËÆ¶È:50%
Planta Medica          2013          79          52-59
Phytoecdysteroids from the Stem Bark of Vitex doniana and Their Anti-Inflammatory Effects
Ochieng, Charles O.; Ishola, Ismail O.; Opiyo, Sylvia A.; Manguro, Lawrence A.O.; Owuor, Philip O.; Wong, Keng-Chong:
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
100 .     ergosterolperoxide
    ÏàËÆ¶È:50%
Journal of Guangdong Phamaceutical University          2011          27          256-259
Chemical constituents of the mycelia of Guignardia mangiferae,an endophyte from Smilax glabra
LIANG Fa-liang, LI Dong-li, TAO Mei-hua, ZHANG De-zhi, ZHANG Wei-min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
101 .     (22E,24R)-5¦Á,8¦Á,-epidioxyergosta-6,9,22-triene-3¦Â-ol
    ÏàËÆ¶È:50%
Journal of Guangdong Phamaceutical University          2011          27          256-259
Chemical constituents of the mycelia of Guignardia mangiferae,an endophyte from Smilax glabra
LIANG Fa-liang, LI Dong-li, TAO Mei-hua, ZHANG De-zhi, ZHANG Wei-min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
102 .     monacolin O acetone ketal
C28H44O8     ÏàËÆ¶È:50%
Journal of Asian Natural Products Research          2013          15          600-609
Cytotoxic monacolin analogs from Monascus purpureus-fermented rice
Ming-Tao Liu, A-Li Wang, Zhen Sun, Jin-Jie Li, Xiu-Li Wu, Yan-Xia Liu & Xiao-Ya Shang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
103 .     fomentarol A
C28H44O     ÏàËÆ¶È:50%
Phytochemistry          2013          92          137-145
Fomentarols A¨CD, sterols from the polypore macrofungus Fomes fomentarius
Yi Zang, Juan Xiong, Wen-Zhu Zhai, Lei Cao, Sheng-Ping Zhang, Yu Tang, Ji Wang, Jing-Jing Su, Guo-Xun Yang, Yun Zhao, Hui Fan, Gang Xia, Chuan-Gui Wang, Jin-Feng Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
104 .     24,25,26,27-tetranor-apotirucall-6¦Á-hydroxy-7¦Á-acetoxy-14-en-3-one-21,24-anhydride
C28H38O7     ÏàËÆ¶È:50%
Journal of Natural Products          2014          77          596-602
Bioactive Limonoids from the Leaves of Azaridachta indica (Neem)
Maria J. Gualtieri, Nicola Malafronte, Antonio Vassallo, Alessandra Braca, Roberta Cotugno, Michele Vasaturo, Nunziatina De Tommasi, and Fabrizio Dal Piaz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
105 .     (22E,22R)-ergost-7,22-diene-3¦Â,5¦Á,6¦Â,9¦Á-tetraol
    ÏàËÆ¶È:50%
Chinese Journal of Marine Drugs          2013          32          8-12
Secondary metabolites from the fungus Engyodontium album associated with the South China Sea starfish Anthenea pentagonula
E Heng-chao, ZHOU Wei, LIU Bao-shu, TANG Hua, SUN Peng, LI Ling, ZHANG Wen*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
106 .     (22E,24R)-3¦Â-ôÇ»ùÂó½ÇçÞ-5,8,22-ÈýÏ©-7-ͪ
C28H42O2     ÏàËÆ¶È:50%
Journal of Chinese Medicinal Materials          2008          31          1343-1347
Studies on the Anti-tumor Activity Principles of a Marine-derived Fungus BZYT-21
GAO Zong-hua, MA Li-ying, SHEN Yun-xiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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