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li7yanÌú³æ (СÓÐÃûÆø)
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[ÇóÖú]
΢Æ×²éѯ
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| 13C NMR: 11.98, 17,46, 18.19, 19.61, 24.08, 26.06, 27.29, 27.68, 28.30, 28.83, 29.86, 30.05, 32.96, 38.70, 38.96, 39.44, 40.82, 46.55, 47.18, 51.78, 56.58, 57.97, 61.34, 65.89, 66.72, 72.20, 212.24 |
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lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
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li7yan: ½ð±Ò+15, ¡ïÓаïÖú 2013-11-14 12:29:09
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li7yan: ½ð±Ò+15, ¡ïÓаïÖú 2013-11-14 12:29:09
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²éѯ½á¹û£º¹²²éµ½4995¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 3¦Â-propionoxyimperialine C30H47NO4 ÏàËÆ¶È:76.6% Planta Medica 1998 64 172-174 Structure-Activity Relationships of Imperialine Derivatives and their Anticholinergic Activity AttaurRahma, M. lqbal Choudhary, Afgan Farooq,Shazia Anjum, Jesse Baumgold, and Bilge Sener Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 12¦Á-Chloro-9¦Á,11¦Á-epoxy-5¦Á-stigmastan-3¦Â-ol C29H49ClO2 ÏàËÆ¶È:71.4% European Journal of Organic Chemistry 1993 1993 657-663 Pheromone Synthesis, CLI. Synthesis of Chlorinated Steroids Related to the Structures Proposed for Blattellastanosides A and B, the Aggregation Pheromone of the German Cockroach, Blattella germanica L. Kenji Mori, Kunio Fukamatsu and Masaru Kido Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 3¦Â-butyroxyimperialine C31H49NO4 ÏàËÆ¶È:70.9% Planta Medica 1998 64 172-174 Structure-Activity Relationships of Imperialine Derivatives and their Anticholinergic Activity AttaurRahma, M. lqbal Choudhary, Afgan Farooq,Shazia Anjum, Jesse Baumgold, and Bilge Sener Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . compound 4 ÏàËÆ¶È:70% Chemistry of Natural Compounds 1985 21 605-612 13C NMR SPECTRA OF A NUMBER OF PENTA- AND HEXACYCLIC TRITERPENOIDS DERIVED FROM GLYCYRRHETIC ACID G. A. Tolstikov, L. M. Khalilov, L. A. Baltina, R. M. Kondratenko, A. A. Panasenko, and E. V. Vasil'eva Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 24¦Î-methylcholestane-3¦Â,5¦Á,6¦Â,25-tetrol C28H50O4 ÏàËÆ¶È:67.8% Acta Scientiarum Naturalium Universitatis Sunyatseni 1994 33(1) 123-126 Studies on the Marine Soft Coral Lobiphytum caledonense Tix Dur¢ò, Polyhydroxysteriods Meng Yanhui, Su Jingyu, Zeng Longmei, Cui Yusheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 6¦Á-acetoxy-16¦Â,22-dihydroxy-3-ketoisohopane C32H52O5 ÏàËÆ¶È:66.6% Fitoterapia 2002 73 363-368 Triterpenes from Adiantum lunulactum G. Brahmachari , D. Chatterjee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (3¦Â,18¦Â,20¦Â)-3-amino-11-oxo-olean-12-en-29-oic acid hyd-rochloride ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 2010 18 7522-7541 Synthesis of novel 3-amino and 29-hydroxamic acid derivatives of glycyrrhetinic acid as selective 11¦Â-hydroxysteroid dehydrogenase 2 inhibitors Christian Stanetty, Laszlo Czollner, Iris Koller, Priti Shah, Rawindra Gaware, Thierry Da Cunha, Alex Odermatt, Ulrich Jordis, Paul Kosma, Dirk Claßen-Houben Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . Epoxyinonotsudiol C30H48O3 ÏàËÆ¶È:66.6% Phytochemistry Letters 2012 5 480-485 Four new lanostane-type triterpenoids from Inonotus obliquus Noriko Handa, Takeshi Yamada, Reiko Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . cyclopholidone ÏàËÆ¶È:65.5% China Journal of Chinese Materia Medica 2004 29 47-49 Studies on chemical constituents of Pholidaota yunnanensid BI Zhiming, WANG Zhengtao, XU Luoshan, XU Guojun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . imperialine ¦Â-N-oxide C27H43O4N ÏàËÆ¶È:64.2% Planta Medica 1998 64 448-450 Isolation and Structure Elucidation of Alkaloids from the Bulb of Fritillaria wabuensis Anjiang Zhang, Huayuan Wang, Xinyao Tang, Yong Zheng, Xiaohui Yi, and Kaibei Yu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . (1'S,5R/S) 7-Butyl-8,8-dimethyl-3-(1',2'-di-O-isopropylidene-1',2'-dihydroxyethyl)-6-oxo-1-oxa-2,7-diazaspiro-[4,4]non-2-ene ÏàËÆ¶È:64.2% Molecules 1997 2 57-61 Synthesis of Spiroisoxazolines by 1, 3-Dipolar Cycloaddition Peter Micuch, Lubor Fisera, Vladimir Ondrus and Peter Ertl Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . compound 2 ÏàËÆ¶È:64.2% Acta Pharmaceutica Sinica 1993 28 192-196 ISOLATION AND IDENTIFICATION OF YIBEINOSlDE B YJ Xu DM Xu; DB Cui; EX Huang; XQ Jin; SY Liu and MM Yan Structure 13C NMR ̼Æ×Ä£Äâͼ |
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