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zhiwu1983: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-07-01 08:19:46
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zhiwu1983: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-07-01 08:19:46
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²éѯ½á¹û£º¹²²éµ½28319¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 3¦Á,16 ,20,22-tetrahydroxyergosta-5,24(28)-diene C28H46O4 ÏàËÆ¶È:96.4% Journal of Natural Products 2010 73 693-697 Sterols and Terpenoids from Melia azedarach Qin-Gang Tan, Xiao-Ning Li, Hao Chen, Tao Feng, Xiang-Hai Cai and Xiao-Dong Luo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . suberoretisteroide B C29H44O6 ÏàËÆ¶È:86.2% Helvetica Chimica Acta 2005 Vol. 88 87 Suberoretisteroids A-E, Five New Uncommon Polyoxygenated Steroid 24-Ketals from the Hainan Gorgonian Suberogorgia reticulata Wen Zhang, Yue-Wei Guo, Margherita Gavagnin, Ernesto Mollo, Guido Cimino Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . crassarosterol A C28H46O3 ÏàËÆ¶È:85.7% Marine Drugs 2012 10 439-450 Steroids from the Soft Coral Sinularia crassa Chih-Hua Chao, Kuei-Ju Chou, Chiung-Yao Huang, Zhi-Hong Wen, Chi-Hsin Hsu, Yang-Chang Wu, Chang-Feng Dai and Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . guggulsterol Y C27H46O4 ÏàËÆ¶È:81.4% Phytochemistry 2003 213-218 Inhibition of LPS-induced NO production by the oleogum resin of Commiphora wightii and its constituents Meselhy R. Meselhy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (20R,22R)-Cholest-5-ene-3¦Â,20,22-triol C27H46O3 ÏàËÆ¶È:81.4% Steroids 2004 69 483-493 Stereoselective synthesis of (22R)- and (22S)-castasterone/ponasterone A hybrid compounds and evaluation of their molting hormone activity Bunta Watanabe, Yoshiaki Nakagawa, Takehiko Ogura, Hisashi Miyagawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (25R)-Cholest-5-en-3¦Â,16¦Â,27-triol ÏàËÆ¶È:81.4% Steroids 2006 71 599-602 Short synthesis of 16¦Â-hydroxy-5¦Á-cholestane-3,6-dione a novel cytotoxic marine oxysterol Mickaël Denanc¨¦, Mich¨¨le Guyot, Mohammad Samadi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (20R,22R)-20,22-Dihydroxycholest-5-ene C27H46O3 ÏàËÆ¶È:81.4% Steroids 2008 73 1452-1464 Synthesis of ponasterone A derivatives with various steroid skeleton moieties and evaluation of their binding to the ecdysone receptor of Kc cells Hirokazu Arai, Bunta Watanabe, Yoshiaki Nakagawa, Hisashi Miyagawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 3,22,25-trihydroxy-16-24,20-24-bisepoxy-(3¦Â,16¦Á,20S,22R,24S )-cholest-5-ene ÏàËÆ¶È:81.4% Natural Product Research 2003 17 149-152 A New Spiroketal Steroid from Gorgonella Umbraculum Ammanamanchi S. R. Anjaneyulu; Vadali Lakshmana Rao; Vedula Girija Sastry Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 22-acetoxy-3,25-dihydroxy-16-24,20-24-bisepoxy-(3¦Â,16¦Á,20S,22R,24S)-cholest-5-ene ÏàËÆ¶È:81.4% Natural Product Research 2003 17 149-152 A New Spiroketal Steroid from Gorgonella Umbraculum Ammanamanchi S. R. Anjaneyulu; Vadali Lakshmana Rao; Vedula Girija Sastry Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 15,16-seco-22¦ÁH,25¦ÂH-Solanida-5,14-dien-3¦Â-ol ÏàËÆ¶È:81.4% Phytochemistry 1995 40 979-981 Steroidal alkaloids of Fritillaria maximowiczii Zhong-Zhi Qian, Toshihiro Nohara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . Schubertoside B ÏàËÆ¶È:81.4% Phytochemistry 1992 31 3969-3973 Acylated cholestane glycosides from the bulbs of Ornithogalum saundersiae Satoshi Kubo, Yoshihiro Mimaki, Miki Terao, Yutaka Sashida, Tamotsu Nikaido, Taichi Ohmoto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . (20R,22R)-Cholest-5-ene-3¦Â,20,22-triol ÏàËÆ¶È:81.4% Steroids 1999 64 385-395 An improved synthesis of(20R,22R)-cholest-5-ene-3¦Â,20,22-triol, an intermediate in steroid hormone formation and an activator of nuclear orphan receptor LXR¦Á Benfang Ruan, William K. Wilson, George J. SchroepferJr. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . (20S,22S)-cholest-5-ene-3¦Â,20,22-triol ÏàËÆ¶È:81.4% Steroids 1999 64 385-395 An improved synthesis of(20R,22R)-cholest-5-ene-3¦Â,20,22-triol, an intermediate in steroid hormone formation and an activator of nuclear orphan receptor LXR¦Á Benfang Ruan, William K. Wilson, George J. SchroepferJr. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . glycoside E ÏàËÆ¶È:81.4% Chinese Traditional and Herbal Drugs 2005 36 350-351 ÇàÉßÌٵĻ¯Ñ§³É·ÖÑо¿(¢ò) ¹ùºìÀö,ÖܽðÔÆ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . ¡÷5-22-cyclopentyloxil-22-deisopenty-3¦Â-hydroxyl-furanstanol C27H42O3 ÏàËÆ¶È:81.4% Chinese Traditional and Herbal Drugs 1998 29 505-507 Studies on the Structures and Antitumor Activities of Two New Compounds Isolated from Fig (Ficus carica) Yin Weiping (Institute of Chemical Research; Henan Academy of Sciences; Zhengzhou )Chen Hongming; Wang Tianxin; Cai Mengshen (College of Pharmacy; Beijing University of Medical Sciences)Yan Fulin; Wu Biao; Xi Rongying (Xinxiang Medical College); Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . veraflorizine ÏàËÆ¶È:81.4% Tetrahedron letters 1979 20 3737-3740 13C-NMR studies on the cevanine alkaloids : the application of 13C-NMR spectrum for structure elucidation of new alkaloids, baimonidine and isoverticine Kô Kaneko, Mikako Tanaka, Kimiaki Haruki, Nobuaki Naruse, Hiroshi Mitsuhashi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . compound 20 ÏàËÆ¶È:81.4% Journal of the Chemical Society, Perkin Transactions 1 1984 467-474 Studies on Indian medicinal plants. Part 77. Structure and stereochemistry of some new steroidal alkaloids from Solanum pseudocapsicum and Solanum giganteum by nuclear magnetic resonance spectroscopy Ajit K. Chakravarty, Binayak Das, Esahak Ali and Satyesh C. Pakrashi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 3,22,25-Trihydroxy-16-24,20-24-bisepoxy-3¦Â,16¦Â, 20S,22R,24S-cholest-5-ene C27H42O5 ÏàËÆ¶È:81.4% Chinese Journal of Chemistry 2005 23 1218-1222 Three Polyoxygenated Steroids from the South China Sea Gorgonian Coral Subergorgia reticulata Jin Yang, Shu-Hua Qi, Si Zhang, Jun Wu and Zhi-Hui Xiao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 3,22,25-trihydroxy-16-24,20-24-bisepoxy-(3¦Â,16¦Á,20S,22R,24S)-cholest-5-ene C27H42O5 ÏàËÆ¶È:81.4% Journal of Chemical Research 2000 24 182-183 A new polyoxygenated steroid from the gorgonian Gorgonella umbraculum Subrahmanyam, Chitti; Kumar, Sreekantha Ratna Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . Gracillin ÏàËÆ¶È:81.4% Magnetic Resonance in Chemistry 2012 50 813-817 Steroidal saponins and pregnane glycosides from Smilax microphylla Tao Lin, Hui-Lian Huang, Rong-Hua Liu, Ji-Cheng Shu, Gang Ren, Feng Shao and Li-sha Liu Structure 13C NMR ̼Æ×Ä£Äâͼ |
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