| ²é¿´: 630 | »Ø¸´: 3 | ||
cuitianzeng½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖú΢Æ×¡£¡£¡£
|
| 12.20, 12.25, 12.44, 12.78, 18.93, 19.21, 19.26, 20.02, 21.28, 21.38, 21.92, 23.32, 24.24, 24.30, 25.59, 26.35, 28.27, 28.93, 29.42, 29.91, 32.08, 34.10, 36.28, 37.22, 37.61, 38.28, 38.36, 39.53, 39.64, 40.60, 41.48, 43.14, 43.26, 46.07, 46.86, 51.48, 53.76, 56.17, 56.29, 56.87, 56.98, 57.78, 100.09, 129.97, 138.01, 209.28, 211.40, 211.42 |
» ²ÂÄãϲ»¶
293µ÷¼Á
ÒѾÓÐ3È˻ظ´
»úе¹¤³Ì264ѧ˶Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
264Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
22408 266Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
273Çóµ÷¼Á
ÒѾÓÐ43È˻ظ´
307Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
338Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬¸ø30J
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
MestReNovaÎÞ·¨½øÐл¯ºÏÎï½á¹¹ÇâÆ×Ô¤²â
ÒѾÓÐ12È˻ظ´
ÇóÖú΢Æ×Êý¾Ý ÖØ½±
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
ÇóÖú΢Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
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
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
cuitianzeng(¶¹¸ç´ú·¢): ½ð±Ò+10, лл 2013-09-21 11:17:59
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
cuitianzeng(¶¹¸ç´ú·¢): ½ð±Ò+10, лл 2013-09-21 11:17:59
|
²éѯ½á¹û£º¹²²éµ½288¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . daucosterol+stigmasterol-3-O-glucopyranoside ÏàËÆ¶È:70.5% Chinese Traditional and Herbal Drugs 2004 35 608-611 Studies on chemical constituents of Indigofera carlesii SU Yan-fang; ZHANG Xin-xin; YANG Jing; GUO Zeng-jun; L¨¹ Ju-xian; GUO De-an Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (cis)-2-(4-{2-[(ethoxycarbonyl)amino]ethoxy}benzyl)cyclohexyl (3¦Â,22E)-stigmasta-5,22-dien-3-yl butanedioate ÏàËÆ¶È:64.5% Bioorganic & Medicinal Chemistry 2010 18 8194-8203 Steroid conjugates: Synthesis and preliminary biological testing of pro-juvenoids Hana Svobodov¨¢, Hana Ryšav¨¢, Milan Pavl¨ªk, David Šaman, Pavel Drašar, Zden¨§k Wimmer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 5¦Á,14¦Á-cevanin-6-O-20¦Â-hydroxy-3¦Â-yl-3¦Á,7¦Á-dihydroxy-5¦Â-cholan-24-oate C51H81NO6 ÏàËÆ¶È:62.7% Steroids 2009 74 424-434 Structural analysis and antitussive evaluation of five novel esters of verticinone and bile acids Jiu-liang Zhang, Hui Wang, Hui-fang Pi, Han-li Ruan, Peng Zhang, Ji-zhou Wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . lanoscopariol C46H80O3 ÏàËÆ¶È:62.5% Journal of Natural Products 1996 59 181-184 New 9¦Â-Lanostane-Type Triterpenic and 13, 14-seco-Steroidal Esters from the Roots of Artemisia scoparia Surendra Kumar Sharma and Mohammad Ali Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . Sitosteryl oleate C47H82O2 ÏàËÆ¶È:62.5% 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 -------------------------------------------------------------------------------- 6 . 3¦Â-Acetoxy-7¦Â-tert-butyldimethylsilyloxystigma-5-ene C37H66O3Si ÏàËÆ¶È:62.5% 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 . N-(Cholest-5-en-3¦Â-yl)-3¦Â-hydroxyandrost-5-ene-17¦Â-carboxamide C47H75NO2 ÏàËÆ¶È:62.5% Steroids 2009 74 88-94 Steroids linked with amide bond¡ªExtended cholesterol Ivan Černý, Miloš Bud¨§š¨ªnský, Vladim¨ªr Pouzar, Pavel Drašar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . Sitosterol-3-O-12',13'-epoxy-9'-oxo-(10'E)-octadecenoate C47H78O4 ÏàËÆ¶È:62.5% 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 -------------------------------------------------------------------------------- 9 . glucoraphenin ÏàËÆ¶È:62.5% Natural Product Research and Development 2010 22 58-59 Studies on the Chemical Constituents of Cirsium henryi ZHANG Yue; RUAN Han-li; ZHANG Yong-hui; PI Hui-fang; WU Ji-zhou Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (3¦Â,22E)-stigmasta-5,22-dien-3-yl 4-(12-amino-4,9-diazadodecylamino)-4-oxobutanoate C43H76N4O3 ÏàËÆ¶È:62.5% Steroids 2012 77 1212-1218 Polyamine conjugates of stigmasterol Norbert Vida, Hana Svobodov¨¢, Lucie R¨¢rov¨¢, Pavel Drašar, David Šaman, Josef Cvačka, Zden¨§k Wimmer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . (6R,E)-6-((3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-(palmitoyloxy)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-3-ethyl-2-methylhept-4-enoic acid C45H78O4 ÏàËÆ¶È:62.5% Life Sciences 2013 92 202-210 Antiulcer and antioxidant activities of a new steroid from Morus alba Aftab Ahmad, Gaurav Gupta, Muhammad Afzal, Imran Kazmi, Firoz Anwar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . compound 16a+17a ÏàËÆ¶È:62.2% Steroids 2012 77 780-790 A new approach to the side chain formation of 24-alkyl-22-hydroxy steroids: Application to the preparation of early brassinolide biosynthetic precursors Alaksiej L. Hurski, Vladimir N. Zhabinskii, Vladimir A. Khripach Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 3-Oxo-5¦Â-cholan-24-oic acid (cholan-24-oic acidmethyl ester)-3-yl ester C49H79O5 ÏàËÆ¶È:61.2% Steroids 2003 68 1157-1161 Synthesis of ester-linked lithocholic acid dimers Lutfun Nahar, Alan B. Turner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 5¦Á,14¦Á-cevanin-6-O-20¦Â-hydroxy-3¦Â-yl-3¦Á,7¦Â-dihydroxy-5¦Â-cholan-24-oate C51H81NO6 ÏàËÆ¶È:60.7% Steroids 2009 74 424-434 Structural analysis and antitussive evaluation of five novel esters of verticinone and bile acids Jiu-liang Zhang, Hui Wang, Hui-fang Pi, Han-li Ruan, Peng Zhang, Ji-zhou Wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 5¦Á,14¦Á-cevanin-6-O-20¦Â-hydroxy-3¦Â-yl-3¦Á,6¦Á-dihydroxy-5¦Â-cholan-24-oate C51H81NO6 ÏàËÆ¶È:60.7% Steroids 2009 74 424-434 Structural analysis and antitussive evaluation of five novel esters of verticinone and bile acids Jiu-liang Zhang, Hui Wang, Hui-fang Pi, Han-li Ruan, Peng Zhang, Ji-zhou Wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . ¦Â-sitosterol-¦Â-D-ghcopyranoside ÏàËÆ¶È:60.4% Phytochemistry 1991 30 1026-1029 A butyrolactone lignan disaccharide from Flacourtia ramontchi V. Satyanarayana, G.L.David Krupadanam, G. Srimannarayana Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . Lobophytone B C43H66O10 ÏàËÆ¶È:60.4% Organic Letters 2010 Vol.12,No.11 2484-2487 Lobophytones A-G, New Isobiscembranoids from the Soft Coral Lobophytum pauciflorum Pengcheng Yan, Yang Lv, Leen van Ofwegen, Peter Proksch,and Wenhan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . ¦Â-sitosterol linoleate ÏàËÆ¶È:60.4% Chinese Pharmaceutical Journal 2007 42 661-663 Studies on Chemical Constituents of Paeonia veitchii L. WANG Rui, CHOU Gui-xin, ZHU En-yuan, WANG Zheng-tao, BI Kai-shun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . methyl N-{5-oxo-5-[(3¦Â,22E)-stigmasta-5,22-dien-3-yloxy]-3,3-dimethylpentanoyl}-L-phenylalanine C46H69NO5 ÏàËÆ¶È:60.4% Molecules 2011 16 9357-9367 Stigmasterol-Based Novel Low Molecular Weight/Mass Organic Gelators Jana Šustekov¨¢, Pavel Drašar, David Šaman and Zden¨§k Wimmer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . ¦Â-Sitosteryl linoleate ÏàËÆ¶È:60.4% Zeitschrift f¨¹r Naturforschung C 2012 67 172-180 Anti-Helicobacter pylori Activity of the Methanolic Extract of Geum iranicum and its Main Compounds Somayeh Shahani, Hamid R. Monsef-Esfahani, Soodabeh Saeidnia, Parastoo Saniee, Farideh Siavoshi, Alireza Foroumadi, Nasrin Samadi, and Ahmad R. Gohari Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-09-18 08:21:47
cuitianzeng
½ð³æ (СÓÐÃûÆø)
- Ó¦Öú: 30 (СѧÉú)
- ½ð±Ò: 193.8
- É¢½ð: 927
- ºì»¨: 3
- Ìû×Ó: 225
- ÔÚÏß: 350.3Сʱ
- ³æºÅ: 1624600
- ×¢²á: 2012-02-18
- רҵ: ÌìȻҩÎﻯѧ
3Â¥2013-09-18 11:07:55
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
4Â¥2013-09-18 14:34:03














»Ø¸´´ËÂ¥
Ö±½Ó·¢¸øÎҾͺÃÁËÈö