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À±±ÊvСÐÂ: ½ð±Ò+1, ¹ÄÀøÓ¦Öú½»Á÷ 2014-04-01 23:01:25
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²éѯ½á¹û£º¹²²éµ½149¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 18f C17H32O3 ÏàËÆ¶È:67.3% Tetrahedron 2012 68 106-113 Structure¨Cactivity relationship of novel juvenile hormone, JHSB3, isolated from the stink bug, Plautia stali Kanako Kaihara, Toyomi Kotaki, Hideharu Numata, Yasufumi Ohfune, Tetsuro Shinada Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 9 C40H80O3 ÏàËÆ¶È:65.9% Tetrahedron 1999 55 167-176 Two terpenoid diepoxides from the green microalga Botryococcus braunii: Their biomimetic conversion to tetrahydrofurans and tetrahydropyrans Pierre Metzger Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 24,26-cyclo-5¦Á-cholest-(22E)-en-3¦Â-ol 4',8',12'-trimethyltridecanoate C43H74O2 ÏàËÆ¶È:63.6% Journal of Natural Products 1991 Vol 54 1119 New Sterol Ester from a Deep Water Marine Sponge, Xestospongia sp. Sarath P. Gunasekera, Susan Cranick, Shirley A. Pomponi Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (2E)-Phyt-2-enyl phytanoate C40H79O2 ÏàËÆ¶È:63.6% Phytochemistry 1996 41 1373-1376 Phytyl esters and phaeophytins from the hornwort Megaceros flagellaris Malcolm S. Buchanan, Toshihiro Hashimoto, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (2E,2'E)-Phyt-2-enyl phyt-2'-enoate C40H76O2 ÏàËÆ¶È:59.0% Phytochemistry 1996 41 1373-1376 Phytyl esters and phaeophytins from the hornwort Megaceros flagellaris Malcolm S. Buchanan, Toshihiro Hashimoto, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 5,6¦Â-Epoxycholesteryl-9,10-di-tertbutyldimethylsilyloxystearate C57H108O5Si2 ÏàËÆ¶È:58.6% Steroids 2008 73 1098-1109 Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1] Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . mixture 5 & 5a C27H45O4N ÏàËÆ¶È:58.6% Tetrahedron 2013 69 2419-2429 Total synthesis of palmyrolide A and its 5,7-epi isomers Gangarajula Sudhakar, Karla Janardhan Reddy, Jagadeesh Babu Nanubolu Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 5,6¦Â-Epoxysitosteryl-9,10-di-tertbutyldimethylsilyloxystearate C59H112O5Si2 ÏàËÆ¶È:58.3% Steroids 2008 73 1098-1109 Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1] Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Sitosterol-3-O-12',13'-epoxy-9'-oxo-(10'E)-octadecenoate C47H78O4 ÏàËÆ¶È:57.4% Journal of Asian Natural Products Research 2003 5 215-221 THE CHEMICAL CONSTITUENTS OF MUNRONIA HENRYI SHU-HUA QI, DA-GANG WU, YUN-BAO MA and XIAO-DONG LUO Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Sinocalycanchinensin C C49H82O4 ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry 2011 19 2790-2796 New 29-nor-cycloartanes with a 3,4-seco- and a novel 2,3-seco-structure from the leaves of Sinocalycanthus chinensis Yoshiki Kashiwada , Kazuya Nishimura, Shin-ichiro Kurimoto, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ¦Á-amyrin hexacosoate ÏàËÆ¶È:56.8% Journal of Chinese Pharmaceutical Sciences 2000 9 131-133 A New Triterpene from Rosemary (Rosmarinus officinalis) Zhou Qunfang, Xu Zhanhui, Tu Pengfei, Li Gansun and Chen Hongming Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 5,6¦Â-Epoxycholesteryl-9,10-dihydroxystearate C45H80O5 ÏàËÆ¶È:56.8% Steroids 2008 73 1098-1109 Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1] Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . atroside C45H78O7 ÏàËÆ¶È:56.8% Fitoterapia 2001 72 712-714 A new acylated steroid glucoside from Pero skia atriplicifolia M.S. Alia, M. Saleema, A.W. Erian Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 3¦Á-Tetrahydropyranyloxy-5¦Â-cholan-24-ol C29H50O3 ÏàËÆ¶È:56.8% Steroids 2011 76 291-300 Synthesis and olfactory activity of unnatural, sulfated 5-bile acid derivatives in the sea lamprey (Petromyzon marinus) Aaron C. Burns, Peter W. Sorensen, Thomas R. Hoye Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 20 C16H30O3 ÏàËÆ¶È:56.8% Tetrahedron 2012 68 106-113 Structure¨Cactivity relationship of novel juvenile hormone, JHSB3, isolated from the stink bug, Plautia stali Kanako Kaihara, Toyomi Kotaki, Hideharu Numata, Yasufumi Ohfune, Tetsuro Shinada Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 32,33,34-trimethyl-bacteriohopan-16-ene 3-O-¦Â-D-glucopyranoside C44H76O6 ÏàËÆ¶È:56.8% Journal of Ethnopharmacology 2011 135 78-87 Chemical constituents from the stem bark of Symplocos paniculata Thunb. with antimicrobial, analgesic and anti-inflammatory activities Ruchi Badoni Semwal, Deepak Kumar Semwal, Ravindra Semwal, Randhir Singh, Mohan Singh Maniyari Rawat Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . N,N-dimethyl-(3¦Â-acetate-cholest-5-ene)-N-decylammonium bromide C41H73NO2Br2 ÏàËÆ¶È:56.8% Molecules 2013 18 14961-14976 Synthesis, Spectroscopic and Semiempirical Studies of New Quaternary Alkylammonium Conjugates of Sterols Bogumił Brycki, Hanna Koenig, Iwona Kowalczyk and Tomasz Pospieszny Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . cholestery 9,12-octadecadienoate ÏàËÆ¶È:55.5% Chinese Pharmaceutical Journal 2011 46 17-20 Studies on Chemical Constituents of Sarcopyramis nepdensis ZHANG Jin-wen, CHEN Hua-dong, LIAO Mei, ZHANG Yong-hui Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 21-benzoxy-1-tert-butyldiphenylsilyloxy-(2R,6S,10R,14R,18S)-2,6,10,14,18-pentamethyl-8-(E/Z)-8-henei-cosene C49H76O2Si ÏàËÆ¶È:55.3% The Journal of Organic Chemistry 2013 78 5970-5986 Highly Stereocontrolled Total Synthesis of ¦Â-d-Mannosyl Phosphomycoketide: A Natural Product from Mycobacterium tuberculosis Nan-Sheng Li, Louise Scharf, Erin J. Adams, and Joseph A. Piccirilli Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . ¦Â-sitosteryl-3-O-¦Â-D-glucopyranoside-2'-O-palmitate C51H90O7 ÏàËÆ¶È:54.5% Phytochemistry 2008 69 2627-2633 Non-cannabinoid constituents from a high potency Cannabis sativa variety Mohamed M. Radwan, Mahmoud A. ElSohly, Desmond Slade, Safwat A. Ahmed, Lisa Wilson,Abir T. El-Alfy, Ikhlas A. Khan, Samir A. Ross Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . compound 4 ÏàËÆ¶È:54.5% Phytochemistry 1993 34 751-753 Diterpenoid constituents of the liverwort Nardia subclavata Masao Toyota, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . Tagalsin I C40H60O2 ÏàËÆ¶È:54.5% Organic Letters 2005 Vol. 7, No. 14 3037-3040 Tagalsins I and J, Two Novel Tetraterpenoids from the Mangrove Plant, Ceriops tagal Yan Zhang, Yang Lu, Li Mao, Peter Proksch, and Wenhan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . stigmast-5-en-3¦Â-ol-3-O-¦Â-D-(2'-n-triacontanoyl) glucopyranoside C65H118O7 ÏàËÆ¶È:54.5% Journal of Asian Natural Products Research 2012 14 301-307 New steroidal glycoside ester and aliphatic acid from the fruits of Lycium chinense Woo-Suk Jung,Ill-Min Chung,Mohd Ali and Ateeque Ahmad Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . ¦Â-Sitosteryl-3-O-¦Â-D-glucopyranosyl-6'-O-palmitate |
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