| ²é¿´: 253 | »Ø¸´: 1 | ||
hejiangboľ³æ (ÖøÃûдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×²éѯ
|
|
ÏàËÆ¶È£º80% ÈܼÁ£ºDMso ºË´ÅÊý¾Ý£º 21.3,23.3,77.9,79.0,79.3,120.3,120.9,121.3,122.8,125.9,126.6,127.2,128.6,131.9,134.7,138.5,147.8,160.2,161.1,170.3,174.6 |
» ²ÂÄãϲ»¶
295·ÖÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
ɽ¶«¸ßУ½Ìʦ¿¼ºË³¬¼¶ÎÞµ×Ïߣ¬Ô±¹¤¹ý²»ÏÂÈ¥À²
ÒѾÓÐ4È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
µ÷¼Á
ÒѾÓÐ19È˻ظ´
²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ10È˻ظ´
307Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
303Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁÏÓ뻯¹¤300Çóµ÷¼Á
ÒѾÓÐ35È˻ظ´
²ÄÁÏרҵ344Çóµ÷¼Á
ÒѾÓÐ21È˻ظ´
Ò»Ö¾Ô¸±±Àí¹¤298Ó¢Ò»Êý¶þÇóµ÷¼Á
ÒѾÓÐ15È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯһ¸ö»¯ºÏÎï~¼±~£¡Ð»Ð»
ÒѾÓÐ3È˻ظ´
¼±ÇóÇóÖú΢Æ×Êý¾Ý¼ìË÷CÆ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²é»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
ÇóÖú΢Æ×²éѯ½âÆ×
ÒѾÓÐ5È˻ظ´
ÇóÖú3¸öÓÃ΢Æ×½âÎöµÄ½á¹¹
ÒѾÓÐ8È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻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
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
jiangchunyong: ½ð±Ò+1, лл 2012-12-03 15:49:46
hejiangbo: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, Ê®·Ö¸Ðл 2012-12-03 15:58:15
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
jiangchunyong: ½ð±Ò+1, лл 2012-12-03 15:49:46
hejiangbo: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, Ê®·Ö¸Ðл 2012-12-03 15:58:15
|
ûÕÒµ½80%µÄ£¬Ö»ÓÐ50%×óÓҵġ£ ²éѯ½á¹û£º¹²²éµ½7¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 2-[2-(2,6-dichlorophenyl)amino]benzyl-6-bromo-3,1-benzoxa-zin-4(H)one C21H13BrCl2N2O2 ÏàËÆ¶È:52.3% Journal of Heterocyclic Chemistry 2010 47 923-931 Synthesis and antimicrobial activity of novel 1,3,4-oxadiazolyl-quinazolin-4(3H)ones Navin B. Patel and Jaymin C. Patel Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 2-Amino-6-(1H-indol-3-yl)-4-(naphthalen-1-yl)4H-pyran-3,5-dicarbonitrile C25H16N4O ÏàËÆ¶È:52.3% Bioorganic & Medicinal Chemistry Letters 2010 20 5054-5061 InCl3 mediated one-pot multicomponent synthesis, anti-microbial, antioxidant and anticancer evaluation of 3-pyranyl indole derivatives Neelakandan Vidhya Lakshmi, Prakasam Thirumurugan, K.M. Noorulla, Paramasivan.T. Perumal Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . N-(6-chlorobenzo[d]thiazol-2-yl)-2-(1H-indol-3-yl)acetamide C17H12ClN3OS ÏàËÆ¶È:52.3% Bioorganic & Medicinal Chemistry 2012 20 6877-6884 Synthesis of retinoid enhancers based on 2-aminobenzothiazoles for anti-cancer therapy Christopher R. Gardner, Belamy B. Cheung, Jessica Koach, David StC. Black, Glenn M. Marshall, Naresh Kumar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 3-aminofluoranthene ÏàËÆ¶È:52.3% Organic Magnetic Resonance 1976 8 161-164 13C NMR spectroscopy of polycyclic aromatics. VIII¡ªamino derivatives of quinoline, isoquinoline, acenaphthene and fluoranthene Ludger Ernst Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . bis(indole-3-yl)-(N-acetylindole-3'-yl)methane C27H21N3O ÏàËÆ¶È:50% Heterocycles 2003 60 1307-1315 Synthesis and Cytotoxic Activity of N-Acetylated Triindolylmethanes Jun Li, Bing Guang, Liangbing Wang, Bogang Li, and Guolin Zhang* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . bis(2-phenylindole-3-yl)-(N-acetylindole-3'-yl)methane C39H29N3O ÏàËÆ¶È:50% Heterocycles 2003 60 1307-1315 Synthesis and Cytotoxic Activity of N-Acetylated Triindolylmethanes Jun Li, Bing Guang, Liangbing Wang, Bogang Li, and Guolin Zhang* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . aspergillamide B C28H34N4P3 ÏàËÆ¶È:50% Tetrahedron 1998 54 13459-13466 Aspergillamides A and B: Modified cytotoxic tripeptides produced by a marine fungus of the genus Aspergillus Steven G. Toske, Paul R. Jensen, Christopher A. Kauffman, William Fenical Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2012-12-03 15:27:05













»Ø¸´´ËÂ¥