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À±±ÊvСÐÂ: ½ð±Ò+1, ¹ÄÀøÓ¦Öú½»Á÷ 2014-04-01 23:01:25
swj19900601: ½ð±Ò+10 2014-04-02 08:17:01
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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
24 .     ¦Â-Sitosteryl-3-O-¦Â-D-glucopyranosyl-6'-O-palmitate
2Â¥2014-04-01 20:39:56
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swj19900601

½ð³æ (ÕýʽдÊÖ)

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2Â¥: Originally posted by Ц¶à»á»³ÔÐ at 2014-04-01 20:39:56
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 ju ...

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