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С̹½0018(¶¹¸ç´ú·¢): ½ð±Ò+10, лл 2013-05-29 15:24:18
1 .     Fortisterol
C28H40O3     ÏàËÆ¶È:75%
Journal of Asian Natural Products Research          2006          8          485-489
Fortisterol, a novel steroid with an unusual seven-membered lactone ring B from the Chinese marine sponge Biemna fortis Topsent
X.-C. HUANG, Y.-W. GUO and G.-Q. SONG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     3¦Â,5¦Á,9¦Á-trihydroxy-(22E,24R)-ergosta-7,22-dien-6-one
C28H44O4     ÏàËÆ¶È:71.4%
Chemistry of Natural Compounds          2009          45          759-761
STEROIDS AND OTHER CONSTITUENTS FROMTHE MUSHROOM Armillaria lueo-virens
Hui-Yan Xiong, Dong-Qing Fei, Jin-Song Zhou,Chun-Jiang Yang,and Guo-Liang Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     5, 8-Epidioxy-5¦Á, 8¦Á-ergosta-6, 9, 22E-tien-3¦Â-ol
C28H42O3     ÏàËÆ¶È:67.8%
Acta Botanica Yunnanica          2002          24(4)          525-530
Constituents from Thamnolia vermicularis
J IANGBei,ZHAO Qin-Shi,PENGLi-Yan,LIN Zhong-Wen,SUN Han-Dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (22E,24S)-[26-2H3]-24-Methyl-3¦Á ,5-cyclo-5¦Á -cholest-22-en-6-one
C28H41D3O     ÏàËÆ¶È:67.8%
Steroids          2002          67          587-595
Synthesis of [26-2H3]brassinosteroids
Vladimir A. Khripach, Vladimir N. Zhabinskii, Olga V. Konstantinova, Andrey P. Antonchick, Bernd Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,9¦Á-trihydroxy-6-one
C28H44O4     ÏàËÆ¶È:67.8%
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
6 .     24E-ergosta-7,22-dien-6-one-3¦Â,5¦Á-diol
C28H44O3     ÏàËÆ¶È:67.8%
Natural Product Research and Development          1992          4(2)          44-47
CHEMICAL RESEARCH ON THE METABOLITES OF LACTARIUS HYSGINUS (¢ñ)
Dong Ding* Wang Huaibin Li Guangyi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     Gargalol A
C28H44O3     ÏàËÆ¶È:67.8%
Tetrahedron          2011          67          6576-6581
Osteoclast-forming suppressing compounds, gargalols A, B, and C, from the edible mushroom Grifola gargal
Jing Wu, Jae-Hoon Choi, Miyuki Yoshida, Hirofumi Hirai, Etsuko Harada, Kikuko Masuda, Tomoyuki Koyama, Kazunaga Yazawa, Keiichi Noguchi, Kazuo Nagasawa, Hirokazu Kawagishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (22E,24R)-[26-2H3]-24-methyl-3¦Á,5-cyclo-5¦Á-cholest-22-en-6-one
    ÏàËÆ¶È:67.8%
Chemistry of Natural Compounds          2012          48          601-605
Synthesis of [26-2H3]-6-deoxo-24-epicastasterone
V. A. Khripach, V. N. Zhabinskii, O. V. Gulyakevich and Yu. V. Ermolovich
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     muriflasteroid A
C28H46O4     ÏàËÆ¶È:67.8%
Steroids          2013          78          108-114
3¦Â,5¦Á,6¦Â-Oxygenated sterols from the South China Sea gorgonian Muriceopsis flavida and their tumor cell growth inhibitory activity and apoptosis-inducing function
Tao-Fang Liu, Xin Lu, Hua Tang, Min-Min Zhang, Pan Wang, Peng Sun, Zhi-Yong Liu, Zeng-Lei Wang, Ling Li, Yao-Cheng Rui, Tie-Jun Li, Wen Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     ergosterol
    ÏàËÆ¶È:67.8%
Chinese Traditional and Herbal Drugs          2011          42          251-254
Chemical constituents of Omphalia lapidescens
XU Ming-feng, SHEN Lian-qing, WANG Kui-wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     ergosterol
C28H44O     ÏàËÆ¶È:67.8%
Chinese Traditional and Herbal Drugs          2012          43          1045-1049
Two new triterpenoids from Ganoderma cochlear
PENG Xing-rong; LIU Jie-qing; XIA Jian-jun; YANG Yong-hong; QIU Ming-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     cerevisterol
C28H46O3     ÏàËÆ¶È:67.8%
Chinese Traditional and Herbal Drugs          2012          43          2356-2360
Chemical constituents from sporophore of Hericium coralloides (¢ñ)
ZHANG Peng; BAO Hai-ying; Tolgor
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     herbarulide
C28H40O3     ÏàËÆ¶È:67.7%
Journal of Natural Products          1999          62          629-630
Herbarulide, a Ketodivinyllactone Steroid with an Unprecedented Homo-6-oxaergostane Skeleton from the Endophytic Fungus Pleospora herbarum1
Karsten Krohn, Carsten Biele, Hans-J¨¹rgen Aust, Siegfried Draeger, and Barbara Schulz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     plakinamine E
C31H50N2O2     ÏàËÆ¶È:66.6%
Journal of Natural Products          2001          64          1474-1476
New Steroidal Alkaloids from an Undescribed Sponge of the Genus Corticium
Hyi-Seung Lee,Youngwan Seo,Jung-Rae Rho, Jongheon Shin,and Valerie J. Paul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     ( 22 E)-3¦Â-Acetoxv-5 ¦Á-hydroxyergosta-7,22-dien-6-one
    ÏàËÆ¶È:66.6%
Steroids          1996          61          540-543
New synthetic strategy for the synthesis of 24-epibrassinolide
Carme Brosa, Rita Puig, Xavier Comas, Cristina Fern¨¢ndez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     stigmast-4-ene-3,6-dione
    ÏàËÆ¶È:65.5%
Journal of Natural Products          2002          65          1857-1862
Antimicrobial Activities of Naphthazarins from Arnebia euchroma
Chien-Chang Shen,Wan-Jr Syu,Shyh-Yuan Li, Chia-Hung Lin, Gum-Hee Lee, and Chang-Ming Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (24R)-24-ethylcholest-4-en-3,6-dione
    ÏàËÆ¶È:65.5%
Chemistry of Natural Compounds          2001          37          351-355
13C NMR SPECTRA OF 6-HYDROXIMINOSTEROIDS OF THE STIGMASTANE SERIES
N. V. Kovganko and Yu. G. Chernov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     compound 8
    ÏàËÆ¶È:65.5%
Chemistry of Natural Compounds          1999          35          646-649
13C NMR SPECTRA OF II-SITOSTEROL DERIVATIVES WITH OXIDIZED RINGS A AND B
N. V. Kovganko, Zh. N. Kashkan,E. V. Borisov, and E. V. Batura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     compound
    ÏàËÆ¶È:65.5%
Biochemical Systematics and Ecology          2000          28          911-913
Stigmast-4-ene-3,6-dione an unusual phytotoxic sterone from the roots of Echium vulgare L.
Fernando Pardo, Fernando Perich, Ren¨¦ Torres, Franco Delle Monache
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     (3E,6E)-Dihydroximino-24-ethylcholest-4-en
    ÏàËÆ¶È:65.5%
Steroids          2009          74          62-72
Synthesis and evaluation of some steroidal oximes as cytotoxic agents: Structure/activity studies (I)
Jian-Guo Cui, Lei Fan, Li-Liang Huang, Hong-Li Liu, Ai-Min Zhou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     (24R)24-ethyl-cholest-6-ene-3¦Â,5¦Á-diol
C29H50O2     ÏàËÆ¶È:65.5%
Natural Product Research          1994          5          7-14
Hydroperoxysterols in Arum italicum
Marina Della Greca; Antonio Fiorentino; Antonio Molinaro; Pietro Monaco; Lucio Previtera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     ¶¹çÞ-4-Ï©-3,6-¶þͪ
    ÏàËÆ¶È:65.5%
China Journal of Chinese Materia Medica          2003          28          278-279
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Ñî á°, ÕÔÓñÓ¢, ÍÀßÏßÏ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
¼èÄÑÀ§¿à£¬ÓñÈêÓڳɡ£
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