| ²é¿´: 179 | »Ø¸´: 1 | ||
gaoaicai123½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
42΢Æ×ÇóÖú
|
| 22.8,30.7,32.9,44.3,44.4,44.6,44.8,44.9,45.1,45.3,119.7,126.5,127.4,132.6,134.1,136.1,137.1,164.5,172.5 |
» ²ÂÄãϲ»¶
0703µ÷¼Á£¬Ò»Ö¾Ô¸Ìì½ò´óѧ319·Ö
ÒѾÓÐ18È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
334·Ö»úеר˶Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
±¾¿ÆÖ£ÖÝ´óѧ£¬Ò»Ö¾Ô¸»ª¶«Ê¦·¶´óѧ282Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
305·ÖÇóµ÷¼Á
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤085600 310·ÖÇóµ÷¼Á
ÒѾÓÐ21È˻ظ´
»¯¹¤Ñ§Ë¶ 285Çóµ÷¼Á
ÒѾÓÐ15È˻ظ´
328Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ9È˻ظ´
081700ѧ˶£¬323·Ö£¬Ò»Ö¾Ô¸Öйúº£Ñó´óѧÇóµ÷¼ÁѧУ
ÒѾÓÐ18È˻ظ´
audreygc
Ìú¸Ëľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 236 (´óѧÉú)
- ½ð±Ò: 5115.1
- ºì»¨: 5
- Ìû×Ó: 519
- ÔÚÏß: 131Сʱ
- ³æºÅ: 1978000
- ×¢²á: 2012-09-05
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
karl2100: ½ð±Ò+1, лл»Ø¸´£¡ 2013-09-11 22:17:39
gaoaicai123: ½ð±Ò+20 2013-09-14 10:00:02
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
karl2100: ½ð±Ò+1, лл»Ø¸´£¡ 2013-09-11 22:17:39
gaoaicai123: ½ð±Ò+20 2013-09-14 10:00:02
|
²éѯ½á¹û£º¹²²éµ½13¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . (-)-ethyl 18-chloro-4,5¦Á-epoxy-3-hydroxy-N-methyl-6¦Á,14¦Á-ethnoisomorphinan-7¦Á-carboxylate C22H24NO4Cl ÏàËÆ¶È:59.0% Recueil des Travaux Chimiques des Pays-Bas 1993 112 113-122 Synthesis and biological activity of new etorphine analogues from 7-chloro-6-demethoxythebaine and 7-chloro-5¦Â-methyl-6-demethoxythebaine (chemistry of opium alkaloids, part XXXVII) R. H. Woudenberg and L. Maat Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (-)-4,5¦Á-Epoxy-6-methoxy-17-methyl-7-propylidene-6¦Á,14¦Á-ethenoisomorphinan-3-ol C22H35NO3 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 1999 7 529-541 chemistry of opium alkaloids. part 44: Synthesis and opioid receptor binding profile of substituted ethenoisomorphinans and ethenomorphinans Leendert Maat, Richard H. Woudenberg, Gerrit J. Meuzelaar, Joannes T.M. Linders Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . (-)-ethyl 18-chloro-4,5¦Á-epoxy-3-hydroxy-¦Á,¦Á,N-trimethyl-6¦Á,14¦Á-ethnoisomorphinan-7¦Á-methanol hydrochloride C22H26NO3Cl ÏàËÆ¶È:54.5% Recueil des Travaux Chimiques des Pays-Bas 1993 112 113-122 Synthesis and biological activity of new etorphine analogues from 7-chloro-6-demethoxythebaine and 7-chloro-5¦Â-methyl-6-demethoxythebaine (chemistry of opium alkaloids, part XXXVII) R. H. Woudenberg and L. Maat Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 5-(4-Methoxyphenyl)-N-{[2-thienylmethylene] amino}-bicyclo[2.2.1]heptane-endo-2,endo-3-dicarboximide C21H20N2O3S ÏàËÆ¶È:52.6% Canadian Journal of Chemistry 2010 88 323-330 Heck-type hydroarylations and 1,3-dipolar cycloaddition reactions of new tricyclic hydrazones Melek Gul and Nuket Ocal Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 2-(4-(Benzyloxy)-3-nitrophenyl)-2-oxoethyl-4-(tertbutoxycarbonylamino)butanoate C24H28N2O8 ÏàËÆ¶È:52.6% Canadian Journal of Chemistry 2011 89 364¨C384 p-Hydroxyphenacyl photoremovable protecting groups ¡ª Robust photochemistry despite substituent diversity Richard S. Givens, Kenneth Stensrud, Peter G. Conrad II, Abraham L. Yousef, Chamani Perera, Sanjeewa N. Senadheera, Dominik Heger, and Jakob Wirz Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . N-(3S-N-L-histidinyl-1,2,3,4-tetrahydroisoquinoline-3-carbonyl)-L-histidine C22H25N7O4 ÏàËÆ¶È:52.6% Bioorganic & Medicinal Chemistry 2010 18 1536-1554 2, 3-Diamino acid modifying 3S-tetrahydroisoquinoline-3-carboxylic acids: Leading to a class of novel agents with highly unfolded conformation, selective in vitro anti-platelet aggregation and potent in vivo anti-thrombotic activity Xiaoyi Zhang, Wei Wang, Shenling Cheng, Ming Zhao, Meiqing Zheng, Heng Wei Chang, Jianhui Wu, Shiqi Peng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . methyl N-4-(4-acetoxymethylbenzamidyl)benzyl-4-aminobutanoate C22H26N2O5 ÏàËÆ¶È:52.6% Bioorganic & Medicinal Chemistry 2010 18 7291-7301 Design and preparation of sterol mimetics as potential antiparasitics Federica Gigante, Marcel Kaiser, Reto Brun, Ian H. Gilbert Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . N-(8-dimethylamino-4-(4-methylphenylsulfonamido)-3-nitronaphthalen-1-yl)-N-methylformamide C21H22N4O5S ÏàËÆ¶È:52.6% Tetrahedron 2013 69 1919-1929 ¡®Proton sponge¡¯ amides: unusual chemistry and conversion into superbasic 6,7-bis(dimethylamino)perimidines Valery A. Ozeryanskii, Marina P. Vlasenko, Alexander F. Pozharskii Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (-)-4,5¦Á-Epoxy-6-methoxy-7,17¦Á-dimethyl-6¦Á,14-ethenoisomorphinan-3-ol ÏàËÆ¶È:52.3% Bioorganic & Medicinal Chemistry 1999 7 529-541 chemistry of opium alkaloids. part 44: Synthesis and opioid receptor binding profile of substituted ethenoisomorphinans and ethenomorphinans Leendert Maat, Richard H. Woudenberg, Gerrit J. Meuzelaar, Joannes T.M. Linders Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . N-Hydroxy-3-[1-(3-naphthalen-2-yl-propyl)-2-oxo-2,5-dihydro-1H-pyrrol-3-yl]-propionamide ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry Letters 2011 21 1218-1221 Structure and property based design, synthesis and biological evaluation of ¦Ã-lactam based HDAC inhibitors Eunhyun Choi, Chulho Lee, Jung Eun Park, Jeong Jea Seo, Misun Cho, Jong Soon Kang,Hwan Mook Kim, Song-Kyu Park, Kiho Lee, Gyoonhee Han Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 3-(5-3-methyl-5-[(3-methyl-7-5-[2-(4-methylphenyl)-4-oxo-1,3-thia-zolan-3-yl]-1,3,4-thiadiazol-2-ylbenzofuran-5-yl)methyl]benzo- C43H34N4O4S4 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2010 58 805-810 Synthesis, Nematicidal and Antimicrobial Activity of 3-(5-3-Methyl-5-[(3-methyl-7-5-[2-(aryl)-4-oxo-1,3-thiazolan-3-yl]-1,3,4-thiadiazol-2-ylbenzofuran-5-yl)methyl]benzofuran-7-yl-1,3,4-thiadiazol-2-yl)-2-(aryl)-1,3-thiazolan-4-one Cherkupally Sanjeeva Reddy, Dasari Chandrashekar Rao, Vookanti Yakub and Adki Nagaraj Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 6¦Á-isovaleryloxy-1-hydroxy-4¦ÁH-1,10-secoeudesma-5(10),11(13)-dien-12,8¦Â-olide C20H30O5 ÏàËÆ¶È:50% Tetrahedron 2010 66 9379-9388 New sesquiterpenes from Inula japonica Thunb. with their inhibitory activities against LPS-induced NO production in RAW264.7 macrophages Jiang-Jiang Qin, Hui-Zi Jin, Jia-Xian Zhu, Jian-Jun Fu, Qi Zeng, Xiang-Rong Cheng, Yan Zhu, Lei Shan, Shou-De Zhang, Yue-Xing Pan, Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . neodidennilactone C30H30O3 ÏàËÆ¶È:50% Tetrahedron 1994 50 7385-7400 Didemnilactones A and B and neodidemnilactone three new fatty acid metabolites isolated from the tunicate Didemnum moseleyi (Herdman) Haruki Niwa, Masaru Watanabe, Hideaki Inagaki, Kiyoyuki Yamada Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-09-11 14:56:32














»Ø¸´´ËÂ¥