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hy35855318: ½ð±Ò+15, ¡ïÓаïÖú 2013-09-16 08:28:12
²éѯ½á¹û£º¹²²éµ½28¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     egosterol
    ÏàËÆ¶È:55.1%
Mycosystema          2011          30          464-471
Chemical constituents, biological activities and flourescence quenching of Fomitiporia punctata fruiting body extract
YUAN Bo ZHU Feng CHEN Yong-Qiang HUANG Tian-Zi JU Xiu-Yun WANG Li FENG You-Jian JIANG Ji-Hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (22E,24R) ergosta-5,7,22-trien-3¦Â-ol
    ÏàËÆ¶È:55.1%
Journal of Anhui Agricultural Sciences          2008          36          14614-14616
Study on the Chemical Constituent of Tricholoma giganteum Massee
YAN Min et al
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     erogosterol
    ÏàËÆ¶È:55.1%
Journal of Chinese Medicinal Materials          2011          34          549-551
Studies on the Secondary Metabolites of Coriolopsis sp.G066
SANG Zhi-gao, LI Dong-li, TAO Mei-hua, ZHANG Wei-min, TU Guo-quan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     compound 93
    ÏàËÆ¶È:53.3%
Phytochemistry          1994          37          1517-1575
13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features
Shashi B. Mahato, Asish P. Kundu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     anhydrohirundigenin mono-thevetoside
C28H40O8     ÏàËÆ¶È:51.7%
Planta Medica          2004          70          1075-1079
Steroids from the Roots of Cynanchum stauntonii
Peng Wang,Hai-Lin Qin,Ling Zhang,Zhi-Hong Li,Ying-Hong Wang,Hai-Bo Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     5¦Á ,6 ¦Â-dibromocholest-24-en-3¦Â -yl acetate
C29H46O2Br2     ÏàËÆ¶È:51.7%
Steroids          2009          74          81-87
A facile synthesis of C-24 and C-25 oxysterols by in situ generated ethyl(trifluoromethyl)dioxirane
Shoujiro Ogawa, Genta Kakiyama, Akina Muto, Atsuko Hosoda, Kuniko Mitamura, Shigeo Ikegawa, Alan F. Hofmann, Takashi Iida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     compound 3
    ÏàËÆ¶È:51.7%
Indian Journal of Chemistry          2003          42B          386-389
Triterpenoid saponin from Abrus precatorius (Fabaceae)
Edet M Anam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     3-O-Acetyl-20¦Â-hydroxy- urs-11-en-28,13-olide
C32H48O5     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          2007          55(2)          247-250
Oxyfunctionalization Products of Terpenoids with imethyldioxirane and Their Biological Activity
Shoujiro OGAWA,Keiji HOSOI,Noriaki IKEDA,Mitsuko MAKINO,Yasuo FUJIMOTO,and Takashi IIDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     compound 1
C30H40O5     ÏàËÆ¶È:50%
Journal of Natural Products          1998          61          1328-1331
Isolation of Translactone-containing Triterpenes with Thrombin Inhibitory Activities from the Leaves of Lantana camara
Melanie J. O¡¯Neill, Jane A. Lewis, H. Mary Noble, Susan Holland, Christine Mansat, John E. Farthing, Graham Foster, David Noble, Stephen J. Lane, Philip J. Sidebottom, Sean M. Lynn, Michael V. Hayes, and Clive J. Dix
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     3¦Â-acetoxy-15¦Á,22-dihydroxyhopane
C32H54O4     ÏàËÆ¶È:50%
Planta Medica          2001          67          279-281
A New Antimycobacterial, 3¦Â-Acetoxy-15¦Á,22-dihydroxyhopane,from the Insect Pathogenic Fungus Aschersonia tubulata
Surat Boonphong, Prasat Kittakoop, Masahiko Isaka,Prasit Palittapongarnpim, Amonlaya Jaturapat, Kannawat Danwisetkanjana, Morakot Tanticharoen,Yodhathai Thebtaranonth
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     machaerinic acid lactone
    ÏàËÆ¶È:50%
Acta Pharmaceutica Sinica          1997          32          144-147
STUDIES ON THE TRITERPENE SAPOGENINS FROM ALBIZZIAE CORTEX
SP Chen and RY Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     2¦Á-,3¦Â-,19¦Á-trihydroxy-urs-12-ene-23,28-dioic acid
    ÏàËÆ¶È:50%
Journal of Asian Natural Products Research          2000          2          81-86
A New Triterpenoid from Stelmatocrypton khasianum
QING-YING ZHANG, YU-YING ZHAO, TIE-MING CHENG,YU-XIN CUI and XUE-HUI LIU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     2¦Á,3¦Â,7¦Â-trihydroxyurs-11-en-28,13¦Â-olide
C30H44O4     ÏàËÆ¶È:50%
Phytochemistry          2000          54          861-865
Triterpenoidal constituents from Eucalyptus camaldulensis var. obtusa leaves
Bina S. Siddiqui, Ishrat Sultana, Sabira Begum
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     polystachin
    ÏàËÆ¶È:50%
Phytochemistry          1999          51          927-930
Limonoids from Aphanamixis polystacha
Dulcie A. Mulholland, Nesan Naidoo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     glaucinoic acid
C16H24O3     ÏàËÆ¶È:50%
Zeitschrift f¨¹r Naturforschung B          2005          60b          347-350
Some Chemical Constituents of Terminalia glaucescens and their Enzymes Inhibition Activity
Atta-ur-Rahman, Seema Zareen, M. Iqbal Choudhary, M. Nadeem Akhtar, Shahida Shujaat, and F. N. Ngounou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     Rohituka-3
C32H40O11     ÏàËÆ¶È:50%
Magnetic Resonance in Chemistry          2007          45          189-192
Complete assignments of 1H and 13C NMR data for rings A, B-seco limonoids from the seed of Aphanamixis polystachya (pages 189¨C192)
Huaping Zhang, Feng Chen, Xi Wang, Dagang Wu and Qing Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     3¦Â,22¦Â-dihydroxy-olean-12-en-29-oic acid (22-epi-maytenfolic acid)
C30H48O4     ÏàËÆ¶È:50%
Magnetic Resonance in Chemistry          2002          40          366-370
Epikatonic acid from Austroplenckia populnea: structure elucidation by 2D NMR spectroscopy and X-ray crystallography
G. D. F. Silva, L. P. Duarte, S. A. Vieira Filho, A. C. Doriguetto, Y. P. Mascarenhas, J. Ellena, E. E. Castellano and A. B. Cota
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     1¦Â-ôÇ»ùÓðÉȶ¹´¼
    ÏàËÆ¶È:50%
Journal of Shenyang Pharmaceutical University          2008          25          286-289
Chemical constitunts from Sonneratia ovata
ZHENG Zhe, PEI Yue-hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     (3S,20R)-20-[(E)-2-(pyridin-2-yl)-ethenyl]-pregn-7-en-3-yl acetate
    ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2009          17          8123-8137
Side chain azasteroids and thiasteroids as sterol methyltransferase inhibitors in ergosterol biosynthesis
Delphine Renard, Johann Perruchon, Martin Giera, Jörg M¨¹ller, Franz Bracher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     methyl 5-(2-{2-[N-(1-methoxycarbonyl-3-methylsulfanylpropyl)-N-(¦¥)-(crotonyl)amino-methyl]furan-3-yl}ethyl)-1,4a-dimethyl-6-methyl-enedecahydronaphthalene-1-carboxylate {methyl(1S,5S,9S,10R)-16-[N-(1-methoxycarbonyl-3-methylsulfanyl)-N-(¦¥)-(crotonyl)amino
C32H47NO6S     ÏàËÆ¶È:50%
Russian Journal of Organic Chemistry          2009          45          637-649
Synthetic transformations of higher terpenoids: XIX. Synthesis of 1,7-epoxyisoindolones and 7,9a-epoxythiazolo[2,3-a]isoindolones from terpenoids
Yu. V. Kharitonov, E. E. Shults, M. M. Shakirov and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-09-12 20:29:42
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