| ²é¿´: 386 | »Ø¸´: 1 | |||
×ÏÒÂÇáÆïľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
΢Æ×Êý¾ÝÇóÖú»¯ºÏÎï ÒÑÓÐ1È˲ÎÓë
|
|
ÈܼÁΪDMSO Êý¾ÝÈçÏ£º 55.7,62.4,111.4,113.4,115.5,121.4,123.6,125.4,127.5,139.9,146.9,147.9,149.3,149.8,165.5 |
» ²ÂÄãϲ»¶
»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´
326·Ö£¬Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬Ð»Ð» £¨TE1-1£©
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý4¸ö
ÒѾÓÐ6È˻ظ´
΢Æ×ÇóÖú3¸ö»¯ºÏÎï
ÒѾÓÐ4È˻ظ´
΢Æ×Êý¾ÝÇóÖú¡ª¡ªÈý¸ö»¯ºÏÎï лл£¡
ÒѾÓÐ8È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
Çó΢Æ×Êý¾Ý лл
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
¡¾·ÖÏí¡¿Ãâ·ÑµÄ20¸öÆ×ͼÊý¾Ý¿â
ÒѾÓÐ13È˻ظ´
cjpballack
Ìú¸Ëľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 328 (´óѧÉú)
- ½ð±Ò: 6551.4
- ºì»¨: 8
- Ìû×Ó: 663
- ÔÚÏß: 88.5Сʱ
- ³æºÅ: 2433043
- ×¢²á: 2013-04-23
- ÐÔ±ð: GG
- רҵ: ÖÐҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
×ÏÒÂÇáÆï: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-06-12 15:06:44
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
×ÏÒÂÇáÆï: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-06-12 15:06:44
|
²éѯ½á¹û£º¹²²éµ½35¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . S-benzo[d]oxazol-2-yl O-2-methoxyphenyl carbonimidothioate ÏàËÆ¶È:73.3% Organic Magnetic Resonance 1979 12 95−97 ¨¹ber Zuordnungsprobleme von 13C-Signalen in den NMR-Spektren von Benzheteroazolen E. Gr¨¹ndemann, D. Martin and A. Wenzel Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 3-(3,4-dimethoxyphenyl)-5-(pyridin-4-yl)-1H-pyrrolo[2,3-b]-pyridine C20H17N3O2 ÏàËÆ¶È:70.5% Journal of Medicinal Chemistry 2014 57 6428−6443 Development and Biological Evaluation of Potent and Selective c-KITD816V Inhibitors Soyoung Lee, Hyunseung Lee, Jinhee Kim, Suhyun Lee, Soo Jung Kim, Byong-Seok Choi, Soon-Sun Hong, and Sungwoo Hong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . N,N'-[2,2'-(5,5'-dihydroxy-4,4'-bi-1H-indol-3,3'-yl)diethyl]-diferulamide ÏàËÆ¶È:65% Chemical & Pharmaceutical Bulletin 1997 45 1910-1914 Antioxidative Compounds Isolated from Safflower (Carthamus tinctorius L.) Oil Cake Hui Li ZHANG,Akito NAGATSU,Toshihiro WATANABE,SAKAKIBARA and Harumi OKUYAMA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 7,8-dihydroxy-3',4',-dimethoxyisoflavone C17H14O6 ÏàËÆ¶È:64.7% Chemical & Pharmaceutical Bulletin 2009 57 346-360 Synthesis of Various Kinds of Isoflavones, Isoflavanes, and Biphenyl-Ketones and Their 1,1-Diphenyl-2-picrylhydrazyl Radical-Scavenging Activities Hideyuki Goto, Yoshiyasu Terao and Shuji Akai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (13R,13aR)-13,13a-dihydro-13-hydroxy-2,3-dimethoxy-6H,8H-[2.7]naphthyridino[2.3-c][1,3]benzothiazino-8-one C17H16N2O4S ÏàËÆ¶È:64.7% Canadian Journal of Chemistry 1987 65 636-638 Isomeric 6H,8H-naphthyridino-1,3-benzothiazin-8-ones Lajos Fodor, David B. MacLean Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 4,4''-bis(N-feruloyl)serotonin ÏàËÆ¶È:63.1% Chemical & Pharmaceutical Bulletin 1996 44 874-876 NOVEL ANTIOXIDANTS FROM SAFFLOWER (CARTHAMUS TINCTORIUS L.) OIL CAKE Hui Li ZHANG,Akito NAGATSU and Jinsaku SAKAKIBARA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 1-O-feruloyl-¦Â-D-glucopyranoside ÏàËÆ¶È:62.5% Phytochemistry 1992 31 2477-2480 Two glycosides from roots of Asiasarum sieboldi Kazunori Hashimoto, Takao Katsuhara, Kazuaki Niitsu, Yukinobu Ikeya, Minoru Okada, Hiroshi Mitsuhashi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 3-(3,4-dimethoxyphenyl)-2-thioxoquinazoline-4-one C16H14N2O3S ÏàËÆ¶È:62.5% Chemical & Pharmaceutical Bulletin 2014 62 979-988 Development of 2-Thioxoquinazoline-4-one Derivatives as Dual and Selective Inhibitors of Dynamin-Related Protein 1 (Drp1) and Puromycin-Sensitive Aminopeptidase (PSA) Akiyoshi Numadate, Yusuke Mita, Yotaro Matsumoto, Shinya Fujii, Yuichi Hashimoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 3-(1H-Benzimidazol-2-ylthio)-2-phenylquinoline-4-carboxylic acid C23H15N3O2S ÏàËÆ¶È:61.1% Zeitschrift f¨¹r Naturforschung B 2009 64 826-830 A New Aspect of the Pfitzinger Reaction: Microwave-assisted Synthesis of the New Heterocyclic Ring System 6-Arylbenzo[4,5]imidazolo[2,1-b]quino[4,3-e]-1,3-thiazin-14-one H. A. Abdel-Aziz and S. M. Gomha Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 3-(1H-Benzimidazol-2-ylthio)-2-(4-bromophenyl)quinoline-4-carboxylic acid C23H14BrN3O2S ÏàËÆ¶È:61.1% Zeitschrift f¨¹r Naturforschung B 2009 64 826-830 A New Aspect of the Pfitzinger Reaction: Microwave-assisted Synthesis of the New Heterocyclic Ring System 6-Arylbenzo[4,5]imidazolo[2,1-b]quino[4,3-e]-1,3-thiazin-14-one H. A. Abdel-Aziz and S. M. Gomha Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-06-12 12:18:47














»Ø¸´´ËÂ¥