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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½1940¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . hymenosetin C23H33NO4 ÏàËÆ¶È:65.3% Phytochemistry 2014 100 86-91 Hymenosetin, a 3-decalinoyltetramic acid antibiotic from cultures of the ash dieback pathogen, Hymenoscyphus pseudoalbidus Sandra Halecker, Frank Surup, Eric Kuhnert, Kathrin I. Mohr, Nelson L. Brock, Jeroen S. Dickschat, Corina Junker, Barbara Schulz, Marc Stadler Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 14-epi-pre-1a C28H46O3 ÏàËÆ¶È:64.2% Bioorganic & Medicinal Chemistry Letters 2009 19 5397-5400 Synthesis of 2¦Á-substituted-14-epi-previtamin D3 and its genomic activity Daisuke Sawada, Tomoyuki Katayama, Yuya Tsukuda, Nozomi Saito, Masashi Takano, Hiroshi Saito, Ken-ichiro Takagi, Eiji Ochiai, Seiichi Ishizuka, Kazuya Takenouchi, Atsushi Kittaka Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (22E,24R)-ergosta-5,22-dien-3¦Â-hydroxyl-7-one ÏàËÆ¶È:64.2% Natural Product Research and Development 2007 19 605-609 Study on the Chemical Constitutes of Hydnellum concrescens YANG Xiao-long;WANG Fei; SHAO Hong-jun; DONG Ze-jun; DING Zhi-hui; YANG Wan-qiu; LIU Ji-kai Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3¦Â-hyohoxy-ergosta-5,22-dien-7-one C28H44O2 ÏàËÆ¶È:64.2% Natural Product Research and Development 2004 16 204-206 THE CHEMICAL CONSTITUENTS OF BASIDIOMYCETE CALODON SUAVEOLENS WANG Fei; LIU Ji-kai * Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (22E,24R)-3¦Â-hydroxy-24-methylcholesta-5,22-dien-7-one ÏàËÆ¶È:64.2% Acta Botanica Boreali-Occidentalia Sinica 2012 32 600-603 Chemical constituents from the fruiting bodies of Hydnellum sp. No.2 liu Han-wei, Gao Jin-min Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . indioside N C27H42O4 ÏàËÆ¶È:62.9% Bioorganic & Medicinal Chemistry Letters 2013 23 2738-2742 Spirostanoids with 1,4-dien-3-one or 3¦Â,7¦Á-diol-5,6-ene moieties from Solanum violaceum Fang-Rong Chang, Chiao-Ting Yen, Mohamed El-Shazly, Cheng-Ying Yu, Ming-Hong Yen, Yuan-Bin Cheng, Shu-Li Chen, Yang-Chang Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . sesterterpenoic acid C25H40O3 ÏàËÆ¶È:61.5% Journal of Natural Products 2002 65 1749-1753 Isolation and Structure Elucidation of an Isoflavone and a Sesterterpenoic Acid from Henriettella fascicularis Angela I. Calder¨®n,Christian Terreaux, Kurt Schenk,Phil Pattison, Joanna E. Burdette,John M. Pezzuto, Mahabir P. Gupta,and K. Hostettmann Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 4¦Â,5¦Â-Epoxy-6-cholesten-3¦Â-ol ÏàËÆ¶È:61.5% Steroids 2005 70 245-250 Epoxidation and reduction of cholesterol, 1,4,6-cholestatrien-3-one and 4,6-cholestadien-3¦Â-ol Eunsook Ma, Haksoon Kim, Eunjeong Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . coniosetin C25H35NO4 ÏàËÆ¶È:61.5% The Journal of Antibiotics 2003 56 114-122 Coniosetin, a Novel Tetramic Acid Antibiotic from Coniochaeta ellipsoidea DSM 13856 MARIAN PAUL SEGETH,ALAIN BONNEFOY,MARK BRÖNSTRUP,MARTIN KNAUF,DIETMAR SCHUMMER,LUIGI TOTI,L¨¢SZL¨® V¨¦RTESY,MARIE-C¨¦CILE WETZEL-RAYNAL,JOACHIM WINK and GERHARD SEIBERT Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Ergosta-8(9),22-diene-3,5,6,7-tetraol (30,5¦Á,6¦Â,7¦Á,22E) C28H46O4 ÏàËÆ¶È:60.7% Chinese Chemical Letters 2004 15 419-422 A New Cytotoxic Sterol Produced by an Endophytic Fungus from Castaniopsis fissa at the South China Sea Coast Hou Jin LI, Yong Cheng LIN, L. L. P. VRIJMOED , E. B. G. JONES Structure 13C NMR ̼Æ×Ä£Äâͼ |

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