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23.309,23.520,23.765,25.233,25.683,25.927,27.849,28.199,32.671,37.671,37.974,38.068,39.848,41.081,41.334,41.690,53.718,65.764,72.223,78.710,127.893,138.748,181.234
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µØ¹ÏµØ¹Ï: ½ð±Ò+10, ¡ïÓаïÖú 2014-12-11 12:33:38
1 .     3-benzoxy-(3R,7R,11R)-3,7,11,15-tetramethylhexadec-1-yne
C27H44O     ÏàËÆ¶È:66.6%
Bioorganic & Medicinal Chemistry          2010          18          7628-7638
Design, synthesis, and evaluation of an ¦Á-tocopherol analogue as a mitochondrial antioxidant
Jun Lu, Omar M. Khdour, Jeffrey S. Armstrong, Sidney M. Hecht
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     cholest-5-ene-3¦Â,4¦Â-diol
    ÏàËÆ¶È:66.6%
China Journal of Chinese Materia Medica          2014          39          2284-2288
Chemical constituents of Hyptis rhomboidea and their antifungal acvitity
Tang Lu, Li Xifeng, Yang Shengxiang, Qiu Yan, Yuan Ke
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     23-nor-24-esomethylene-3¦Â,6¦Â,19¦Á-trihydroxyurs-12-en-28 oic acid
    ÏàËÆ¶È:62.9%
Acta Pharmaceutica Sinica          2001          Vol 36          120-122
STUDIES ON THE CHEMICAL CONSTITUENTS OF UNCARIA YUNANENSIS HSIA.C.C
TAO Zhao yang; YI Yang hua; XU Qian zhi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     ursolic acid
C30H48O3     ÏàËÆ¶È:61.5%
Records of Natural Products          2014          8          312-316
Phytochemicals from the Bark of Garcinia hombroniana and Their Biological Activities
Nargis Jamila, Melati Khairuddean, Sadiq Noor Khan , Naeem Khan and Hasnah Osman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (20R)-3¦Â,20-Dihydroxy-5¦Â-pregnane-19-nitrile
C21H33NO2     ÏàËÆ¶È:60.8%
Steroids          2006          71          120-128
Syntheses of 19-[O-(carboxymethyl)oxime] haptens of epipregnanolone and pregnanolone
Ivan Černy, Vladim¨ªr Pouzar, Martin Hill, Helena Havl¨ªkov¨¢, Richard Hampl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     phytenal
    ÏàËÆ¶È:60.8%
Chinese Traditional and Herbal Drugs          2009          40          1198-1201
Chemical constituents of Lobelia chinensis
DENG Ke-zhong; XIONG Ying; GAO Wen-yuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     Ximaosteroid A
C27H40O2     ÏàËÆ¶È:59.2%
Steroids          2009          74          1061-1065
Ximaosteroids A¨CD, new steroids from the Hainan soft coral Scleronephthya sp.
Xiao-Hong Yan, Hai-Li Liu, Yue-Wei Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     2¦Á,3¦Â-(22R )-trihydrosycholestan-6-one
C27H46O4     ÏàËÆ¶È:59.2%
Phytochemistry          1999          51          453-456
A steroidal glycoside from Lepisorus ussuriensis
Young Hae Choi, Jinwoong Kim, Young-Hee Choi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     Cholest-5-ene-1¦Â,3¦Á,21-triol,3,21-disulfate
C27H44O9S2Na2     ÏàËÆ¶È:59.2%
Journal of Natural Products          1994          Vol 57          1591
Inhibitors of Protein Tyrosine Kinase pp60v-src: Sterol Sulfates from the Brittle Star Ophiarachna incrassata
Xiong Fu, Francis J. Schmitz, Rita H. Lee, Jacqueline S. Papkoff, Doris L. Slate
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     rotundioic acid
    ÏàËÆ¶È:59.2%
Natural Product Research and Development          2009          21          593-599
Chemical Constituents of Osmanthus yunnanensis
MA Xiao-li;LIN Wen-bing; ZHANG Guo-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     urs-2¦Á,3,19,23-tetrahydroxy-12-en-28-oic acid
C30H48O6     ÏàËÆ¶È:59.2%
Chinese Journal of Pharmaceuticals          2007          38          221-226
Two New Compounds from Picrorhiza scrophulariiflora
XIE Zhi-yong, HU Hong-xia, KONG De-yun, YANG Pei-ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     tormentic acid
C30H48O5     ÏàËÆ¶È:57.6%
Chemical & Pharmaceutical Bulletin          1993          41          2007-2009
Constituents of Prunus zippeliana Leaves and Branches
Junichi KITAJIMA and Yasuko TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     ursolic acid
    ÏàËÆ¶È:57.6%
Food Chemistry          2011          124          468-475
Analysis of the anti-inflammatory properties of Rosmarinus officinalis L. in mice
Juc¨¦lia Pizzetti Beninc¨¢, Juliana Bastos Dalmarco, Moacir Geraldo Pizzolatti, Tania Silvia Fröde
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     rotundic acid
    ÏàËÆ¶È:57.1%
Journal of Natural Products          1999          62          1379-1384
Activity of Triterpenoid Glycosides from the Root Bark of Mussaenda macrophylla against Two Oral Pathogens
Nam-Cheol Kim, Anne E. Desjardins, Christine D. Wu, and A. Douglas Kinghorn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     ursolic acid
    ÏàËÆ¶È:57.1%
Phytochemistry          1992          31          3909-3914
Triterpenoids from plants of the sanguisorbeae
Gesa Reher, Miloš Bud¨§š¨ªnsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     2¦Á,3¦Â,19¦Á-trihydroxyurs-12-en-28-oic acid
    ÏàËÆ¶È:57.1%
Journal of the Chinese Chemical Society          1995          42          573-577
Chemical Constituents from the Root and Aerial Parts of Rosa taiwanensis
—î„Ù¿¡(Shen-Chyun Yang);·½¿¡Ãñ(Jim-Min Fang);à?Óñè¦(Yu-Shia Cheng)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     axinyssine C
C16H29NO3     ÏàËÆ¶È:57.1%
Tetrahedron          2014          70          3576-3583
Formamidobisabolene-based derivatives from a sponge Axinyssa sp. Original Research Article
Wei Cheng, Dong Liu, Fengying Zhang, Qingying Zhang, Patchara Pedpradab, Peter Proksch, Hong Liang, Wenhan Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     tetraol-1
C22H37O4N     ÏàËÆ¶È:56.5%
Acta Botanica Yunnanica          1997          19(4)          429-432
DITERPENE ALKALOIDS FROM SPIRAEA JAPONICA VAR. ACUTA
Nie Jinglei,¡¡Hao Xiaojiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     tetraol-2
C22H37O4N     ÏàËÆ¶È:56.5%
Acta Botanica Yunnanica          1997          19(4)          429-432
DITERPENE ALKALOIDS FROM SPIRAEA JAPONICA VAR. ACUTA
Nie Jinglei,¡¡Hao Xiaojiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     compound 26b
    ÏàËÆ¶È:56.5%
Chemical & Pharmaceutical Bulletin          1982          30          3932-3941
Studies on the Constituents of Asclepiadaceae Plants. LI. Oxidation at the 18-Methyl Group of C/D-cis-Pregnane Type Steroids and 13C-Nuclear Magnetic Resonance Spectra of 18-Oxygenated Pregnanes and Related Compounds
MASAHIKO KIMURA,KOJI HAYASHI,HIROSHI NARITA and HIROSHI MITSUHASHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     7¦Á-hydroxycholesterol
C27H46O2     ÏàËÆ¶È:56.5%
Steroids          2005          70          907-912
Synthesis and antifungal activity of oxygenated cholesterol derivatives
Jean Michel Brunel, C¨¦line Loncle, Nicolas Vidal, Michel Dherbomez, Yves Letourneux
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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