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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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ 22 . ¶¹çÞ-4-Ï©-3,6-¶þͪ ÏàËÆ¶È:65.5% China Journal of Chinese Materia Medica 2003 28 278-279 ¼Ô¹ûÞ§¹áÖÚ»¯Ñ§³É·ÖµÄÑо¿ Ñî á°, ÕÔÓñÓ¢, ÍÀßÏßÏ Structure 13C NMR ̼Æ×Ä£Äâͼ |

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