| ²é¿´: 599 | »Ø¸´: 4 | ||
summerxkgaoгæ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú»¯ºÏÎï1¸ö£¬Ð»Ð»£¡ ÒÑÓÐ1È˲ÎÓë
|
| 13C NMR (CDCl3): 10.8, 14.5, 20.4, 20.9, 32.5, 34.6, 34.9, 41.8, 48.9, 49.7, 54.0, 81.4, 111.5, 118.9, 119.9, 122.6, 125.9, 130.8, 132.0, 132.5, 138.0, 140.7. |
» ²ÂÄãϲ»¶
ÊÛSCIÒ»ÇøÎÄÕ£¬ÎÒ:8.O.551.O.5.4,¿ÆÄ¿È«,¿ÉÙ¤¼±
ÒѾÓÐ4È˻ظ´
ÊÛSCIÒ»ÇøT0PÎÄÕ£¬ÎÒ:8.O.55.1.O.5.4,¿ÆÄ¿È«,¿É+¼±
ÒѾÓÐ4È˻ظ´
ÊÛSCIÒ»ÇøT0PÎÄÕ£¬ÎÒ:8.O.55.1.O.5.4,¿ÆÄ¿È«,¿É+¼±
ÒѾÓÐ4È˻ظ´
ÊÛSCIÒ»ÇøT0PÎÄÕ£¬ÎÒ:8O.55.1.O.5.4,¿ÆÄ¿ÆëÈ«,¿É+¼±
ÒѾÓÐ4È˻ظ´
2026Äê8ÔÂ25ÈÕ¹ú×ÔÈ»·Å°ñǰͻȻÊÕµ½ÁÐÈëÆÀÉóר¼ÒÓʼþ£¬ÓйØÏµÂð£¿
ÒѾÓÐ20È˻ظ´
½ñÌìÎñί»á¿ªÍêÁË£¬Ã÷Ìì³ö½á¹ûÂð
ÒѾÓÐ22È˻ظ´
ÔÚ¼á±ù»¹¸Ç×ű±º£µÄʱºò£¬ÎÒ¿´µ½ÁËŷŵÄ÷»¨¡£
ÒѾÓÐ9È˻ظ´
Ã÷ÌìÓ¦¸Ã¿É²éÁË£¡£¿
ÒѾÓÐ6È˻ظ´
ÓÐûÓдóÉñ°ïÎÒ¿´¿´»ù½ð´úÂë
ÒѾÓÐ10È˻ظ´
·Å°ñǰµÄ²»µ¶¨
ÒѾÓÐ19È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
·Ç³£¸Ðл£¡Î¢Æ×ÇóÖú
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл¸÷λ
ÒѾÓÐ5È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú1¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý~
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1566 (½²Ê¦)
- ½ð±Ò: 15048.4
- ºì»¨: 21
- Ìû×Ó: 2773
- ÔÚÏß: 261.2Сʱ
- ³æºÅ: 942922
- ×¢²á: 2010-01-15
- ÐÔ±ð: MM
- רҵ: ÌìÈ»Óлú»¯Ñ§
2Â¥2015-01-18 21:46:45
yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1566 (½²Ê¦)
- ½ð±Ò: 15048.4
- ºì»¨: 21
- Ìû×Ó: 2773
- ÔÚÏß: 261.2Сʱ
- ³æºÅ: 942922
- ×¢²á: 2010-01-15
- ÐÔ±ð: MM
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
summerxkgao: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú, лл 2015-01-22 10:54:17
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
summerxkgao: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú, лл 2015-01-22 10:54:17
|
1 . 1-butyl-N-(4-methyl-3-(morpholinosulfonyl)phenyl)-3-(p-tolyl)-1H-pyrazole-4-carboxamide C26H32N4O4S ÏàËÆ¶È:59.0% Bioorganic & Medicinal Chemistry 2014 22 2919-2938 Identification of trisubstituted-pyrazol carboxamide analogs as novel and potent antagonists of farnesoid X receptor Donna D. Yu, Wenwei Lin, Barry M. Forman, Taosheng Chen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . Aza-salicylihalamide analogue C25H32N2O3 ÏàËÆ¶È:56% Organic & Biomolecular Chemistry 2012 10 8147-8153 Synthesis and biological evaluation of a potent salicylihalamide A lactam analogue Dan Balan, Christopher J. Burns, Nicholas G. Fisk, Helmut H¨¹gel, David C. S. Huang, David Segal, Charlotte White, Jörg Wagler and Mark A. Rizzacasa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . flabelliformide B C20H22N2O2 ÏàËÆ¶È:54.5% Helvetica Chimica Acta 2007 Vol. 90 1467 Flabelliformides A and B, Two Novel Indole Alkaloids from Ervatamia flabelliformis Shuang Liang, Hai-Sheng Chen, Yun-Heng Shen, Li Jin, and Wei-Dong Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (1¦Â,6¦Á)-1,6-dihydroxy-14-O-[(4- hydroxyphenyl)acetyl]eudesma-3,11(13)-dien-12-oic acid g-lactone C23H26O6 ÏàËÆ¶È:54.5% Helvetica Chimica Acta 2006 Vol. 89 2927 Sesquiterpenoids and Phenylpropane Derivatives from Sonchus uliginosus Zhan-Xin Zhang, Wei-Dong Xie, Ping-Lin Li, Yan-Ping Shi, and Zhong-Jian Jia Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (1S)-N-[2-Methyl-1-(2-phenyl-1H-imidazol-4-yl)propyl]-2-phenyl-1H-imidazole-4-carboxamide C23H23N5O ÏàËÆ¶È:54.5% Molecules 2008 13 2326-2339 Imidazole-based Potential Bi- and Tridentate Nitrogen Ligands: Synthesis, Characterization and Application in Asymmetric Catalysis Roman S¨ªvek, Filip Bureš, Oldřich Pytela and Jiř¨ª Kulh¨¢nek Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . danshenol B C22H26O4 ÏàËÆ¶È:54.5% Chemical & Pharmaceutical Bulletin 1997 45 564-566 DANSHENOLS A AND B, NEW ALDOSE REDUCTASE INHIBITORS FROM THE ROOT OF SALVIA MILTIORHIZA BUNGE Rena KASIMU,Purusotam BASNET,Yasuhiro TEZUKA,Shigetoshi KADOTA and Tsuneo NAMBA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . rhazimanine ÏàËÆ¶È:54.5% Journal of Natural Products 1995 Vol 58 131-133 The Rhazimanine-Bhimberine Enigma Mauri Lounasmaa, Reija Jokela, Pirjo Hanhinen, Jari Miettinen, Jaana Salo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . heteroscyphic acid B C22H32O4 ÏàËÆ¶È:54.5% Phytochemistry 1994 37 1263-1268 Diterpenes of the clerodane-type from cultured cells of Heteroscyphus planus Kensuke Nabeta, Tadashi Oohata, Noriko Izumi, Kenji Katoh Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . heteroscyphic acid B C22H32O4 ÏàËÆ¶È:54.5% Phytochemistry 1994 37 1263-1268 Diterpenes of the clerodane-type from cultured cells of Heteroscyphus planus Kensuke Nabeta, Tadashi Oohata, Noriko Izumi, Kenji Katoh Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . compound 2 C20H32O ÏàËÆ¶È:54.5% Phytochemistry 1988 27 1321-1324 Spatane-type diterpenes with biological activity from the brown alga Dilophus okamurai Kazuya Kurata,Minoru Suzuki,Kazunari Shiraishi,Kazuya Taniguchi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
3Â¥2015-01-18 21:49:00
summerxkgao
гæ (СÓÐÃûÆø)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 140.3
- É¢½ð: 211
- ºì»¨: 1
- Ìû×Ó: 82
- ÔÚÏß: 110.1Сʱ
- ³æºÅ: 1045490
- ×¢²á: 2010-06-22
- רҵ: ÌìÈ»Óлú»¯Ñ§
4Â¥2015-01-19 08:52:14
summerxkgao
гæ (СÓÐÃûÆø)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 140.3
- É¢½ð: 211
- ºì»¨: 1
- Ìû×Ó: 82
- ÔÚÏß: 110.1Сʱ
- ³æºÅ: 1045490
- ×¢²á: 2010-06-22
- רҵ: ÌìÈ»Óлú»¯Ñ§
5Â¥2015-01-19 09:39:11









»Ø¸´´ËÂ¥
20