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²éѯ½á¹û£º¹²²éµ½6506¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ergosteryl myristate C42H70O2 ÏàËÆ¶È:86.1% Natural Product Sciences 1999 5 93-96 Ergosteryl Myristate, a New Ergosterol Derivative from Unidentified Marine Algicolous Fungus Lee, Dong-Ick; Choi, Jin-Souk; Yang, Mi-Rim; Lee, Won-Kap; Kim, Dong-Soo; Choi, Hong-Dae; Son, Byeng-Wha Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . ergosteryl-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:80.5% Phytochemistry 1999 51 891-898 Antitumor sterols from the mycelia of Cordyceps sinensis Jin Woo Bok, Leonard Lermer, Jeff Chilton, Hans G. Klingeman, G.H. Neil Towers Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . Âó½ÇçÞ´¼ ÏàËÆ¶È:80.5% Chinese Journal of New Drugs 2010 19 2331-2335 Antibacterial metabolites of the endophytic fungus strain BGD22 from the stem of Rhizophora stylosa Griff ZHANG Qing-hua, TIAN Feng, LI Qian, CHANG Min, LI Ming-yue, YE Bo-ping Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 24¦Î-hydroperoxy-24-vinyl-lathosterol C29H48O3 ÏàËÆ¶È:79.4% Planta Medica 2011 77 922-928 Cytotoxic Triterpenoids and Steroids from the Bark of Melia azedarach Shi-BiaoWu, Qiu-Ying Bao,Wen-XuanWang, Yun Zhao, Gang Xia,Zheng Zhao, Huaqiang Zeng, Jin-Feng Hu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-¦Â-O-glucopyranosylergosta-5,7,22-triene C34H54O6 ÏàËÆ¶È:77.7% Phytochemistry 1991 30 4117-4120 Glycosides of ergosterol derivatives from Hericum erinacens Yoshihisa Takaishi, Minoru Uda, Takashi Ohashi, Kimiko Nakano, Koutarou Murakami, Toshiaki Tomimatsu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 2-N'-(1',4'-Diaminophenyl)methylen-19¦Â,28-epoxy-18¦Á-olean-3-one C37H54N2O2 ÏàËÆ¶È:77.7% Chemistry of Natural Compounds 2012 48 75-82 SYNTHESIS OF C2 SYMMETRIC TRITERPENE bis-ENAMINONES L. N. Voronova,I. A. Tolmacheva,V. V. Grishko,and A. G. Tolstikov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 4,4'-Bis-(2-aminomethylen-3-oxo-19¦Â,28-epoxy-18¦Á-oleanyl)diphenylmethane C75H106N2O4 ÏàËÆ¶È:77.7% Chemistry of Natural Compounds 2012 48 75-82 SYNTHESIS OF C2 SYMMETRIC TRITERPENE bis-ENAMINONES L. N. Voronova,I. A. Tolmacheva,V. V. Grishko,and A. G. Tolstikov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . Ergosterol-3-O-(¦Â-D-galactopyranoside) C34H54O6 ÏàËÆ¶È:77.7% Journal of Asian Natural Products Research 2012 14 429-435 Highly efficient synthesis and antitumor activity of monosaccharide saponins mimicking components of Chinese folk medicine Cordyceps sinensis Zhen-Yuan Zhu, Qiang Yao, Yang Liu, Chuan-Ling Si, Jing Chen, Nian Liu,Hong-Yu Lian, Li-Na Ding and Yong-Min Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . ergosta-7,22-dien-3¦Â-O-glucopyranoside C34H56O6 ÏàËÆ¶È:77.7% Phytochemistry 1989 28 945-947 Ergosta-7,22-dien-3¦Â-ol glycoside from Tylopilus neofelleus Yoshihisa Takaishi,Takashi Ohashi,Toshiaki Tomimatsu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . Âó½ÇçÞ-5,7,22-ÈýÏ©-3¦Â-O-¦Â-D-ßÁà«ÆÏÌÑÌÇÜÕ ÏàËÆ¶È:77.7% Chinese Traditional and Herbal Drugs 2007 38 337-339 Chemical constituents of fruiting bodies from basidiomycete Suillus granulatus and their anti-HIV-1 activity DONG Ze-jun; WANG Fei; WANG Rui-rui; YANG Liu-meng; ZHENG Yong-tang; LIU Ji-kai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . ergosta-7,22-dien-3¦Â-ol glycoside ÏàËÆ¶È:77.7% Chinese Traditional and Herbal Drugs 2006 37 1297-1300 Chemical constituents of basidiomycete Coltricium nitidum DU Jian-chang; WANG Xing-na; TAN Ren-xiang; LIU Ji-kai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . Ergosteryl-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:77.7% Archives of Pharmacal Research 2007 30 28-33 Cytotoxic constituents isolated from the fruit bodies of Hypsizigus marmoreus Ming-Lu Xu, Jae-Young Choi, Byeong-Seon Jeong, Gao Li and Kap-Rang Lee, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . ergosteryl-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:77.7% Mycosystema 2010 29 249-253 Steroids from fruiting bodies of Coprinus comatus and their inhibition to tumor cell proliferation FENG Na; ZHANG Jing-Song TANG Qing-Jiu HAO Rui-Xia LIU Yan-Fang YANG Yan JIA Wei ZHOU Shuai TANG Chuan-Hong ZHONG Jian-Jiang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . stigmast-5-en-3¦Â-yl salicylate C36H53O3 ÏàËÆ¶È:77.7% Steroids 2015 94 31−40 Microwave assisted synthesis and biomedical potency of salicyloyloxy and 2-methoxybenzoyloxy androstane and stigmastane derivatives Katarina M. Penov Gaši, Evgenija A. Djurendić, Mih¨¢ly Sz¨¦csi, J¨¢nos Gardi, J¨¢nos J. Csan¨¢di, Olivera R. Klisurić, Sanja V. Dojčinović-Vujašković, Andrea R. Nikolić, Marina P. Savić, Jovana J. Ajduković, Aleksandar M. Oklješa, Vesna V. Kojić, Marija N. Sak Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 24¦Î-hydroperoxy-24-vinyl-cholesterol ÏàËÆ¶È:76.3% Planta Medica 2011 77 922-928 Cytotoxic Triterpenoids and Steroids from the Bark of Melia azedarach Shi-BiaoWu, Qiu-Ying Bao,Wen-XuanWang, Yun Zhao, Gang Xia,Zheng Zhao, Huaqiang Zeng, Jin-Feng Hu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . ergosta-7,11-dien-3¦Â-yl palmitate C44H76O2 ÏàËÆ¶È:76.3% Phytochemistry 1990 29 673-675 A lanostanoid of formosan Ganoderma lucidum Chun-Nan Lin,Whey-Pin Tome,Shen-Jeu Won Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 6a C40H55ClN2O3 ÏàËÆ¶È:76.3% Journal of Medicinal Chemistry 2014 57 4692-4709 Tryptophan Hydroxylase 1 (Tph-1)-Targeted Bone Anabolic Agents for Osteoporosis Hai-Jian Fu, Yu-Ren Zhou, Bei-Hua Bao, Meng-Xuan Jia, Yang Zhao, Lei Zhang, Jian-Xin Li, Hai-Lang He, and Xian-Mei Zhou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . pyrocincholic acid 3¦Â,-O-¦Â-D-fucopyranoside C35H56O7 ÏàËÆ¶È:75% Journal of Natural Products 1996 59 304-307 Triterpenoids from Adina rubella Shi-yue Fang, Zhi-sheng He, and Gao-jun Fan, Hou-ming Wu and Jing-fei Xu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . pyrocincholic acid 3¦Â-O-¦Á-L-rhamnopyranoside C35H56O7 ÏàËÆ¶È:75% Journal of Natural Products 1996 59 304-307 Triterpenoids from Adina rubella Shi-yue Fang, Zhi-sheng He, and Gao-jun Fan, Hou-ming Wu and Jing-fei Xu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . 3¦Â-O-¦Â-xylopyranosylchondrillasterol C34H56O5 ÏàËÆ¶È:75% Planta Medica 2002 68 822-826 Fatty Acid Esters of Triterpenoids and Steroid Glycosides from Gambeya africana Jean Wandji,Francois Tillequin,Dulcie A Mulholland,Jean-Duplex Wansi,Tanee Z.Fomum,Victorine Fuendjiep,Francine Libot,Nole Tsabang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . 3-O-¦Â-D-glucopyranosylchondrillasterol C35H58O6 ÏàËÆ¶È:75% Planta Medica 2002 68 822-826 Fatty Acid Esters of Triterpenoids and Steroid Glycosides from Gambeya africana Jean Wandji,Francois Tillequin,Dulcie A Mulholland,Jean-Duplex Wansi,Tanee Z.Fomum,Victorine Fuendjiep,Francine Libot,Nole Tsabang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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