| ²é¿´: 722 | »Ø¸´: 3 | ||
| ±¾Ìû²úÉú 1 ¸ö ·ÒëEPI £¬µã»÷ÕâÀï½øÐв鿴 | ||
ÑÌÔÆÌýÓêÌú¸Ëľ³æ (ÕýʽдÊÖ)
½ð³æ
|
[ÇóÖú]
·ÒëÒ»¶ÎÎÄÏ×£¨Óлú»¯Ñ§£©
|
|
|
In addition to the scaffold bearing the ethyl side chain of stenine and neostenine, a collection of nonnatural Stemonalike ketoamide scaffolds were constructed via this route, which then served as the substrates for the preparation of six sets of functionalized analogues. These bore core changes that could not be readily accomplished by modification of the natural product itself. Representative examples of the various pathways of these initial efforts are shown in Scheme 2. Almost exclusively, these analogues displayed ring systems or functional groups substantially different from those of the natural products, including carbamates, amides, aryl groups, and heterocyclic moieties (e.g., indole and quinoline) (39). At the outset, it was unknown whether these analogues would possess any significant binding activity. |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸»ª¶«Ê¦·¶´óѧÓлú»¯Ñ§×¨Òµ£¬³õÊÔ351·Ö£¬¸´ÊÔ±»Ë¢Çóµ÷¼Á!
ÒѾÓÐ4È˻ظ´
298Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
²ÄÁÏѧ˶333Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
0856Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
356Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
332Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
348Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
305Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤´óѧ²ÄÁÏÓ뻯¹¤£¨085600£©296Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
µ÷¼Á310
ÒѾÓÐ9È˻ظ´

8814402
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- ·ÒëEPI: 509
- Ó¦Öú: 18 (СѧÉú)
- ¹ó±ö: 0.381
- ½ð±Ò: 12916.1
- É¢½ð: 47
- ºì»¨: 16
- Ìû×Ó: 4183
- ÔÚÏß: 357.8Сʱ
- ³æºÅ: 1184404
- ×¢²á: 2011-01-06
- רҵ: Ò©ÎïѧÆäËû¿ÆÑ§ÎÊÌâ
2Â¥2011-07-13 09:55:18
fmmuboy
Òø³æ (ÕýʽдÊÖ)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 246.8
- ºì»¨: 1
- Ìû×Ó: 411
- ÔÚÏß: 18.1Сʱ
- ³æºÅ: 1343536
- ×¢²á: 2011-07-12
- ÐÔ±ð: GG
- רҵ: ¹Ç¡¢¹Ø½Ú¡¢Èí×éÖ¯ÍËÐÐÐÔ²¡

3Â¥2011-07-13 10:14:00
8814402
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- ·ÒëEPI: 509
- Ó¦Öú: 18 (СѧÉú)
- ¹ó±ö: 0.381
- ½ð±Ò: 12916.1
- É¢½ð: 47
- ºì»¨: 16
- Ìû×Ó: 4183
- ÔÚÏß: 357.8Сʱ
- ³æºÅ: 1184404
- ×¢²á: 2011-01-06
- רҵ: Ò©ÎïѧÆäËû¿ÆÑ§ÎÊÌâ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï
ÑÌÔÆÌýÓê(½ð±Ò+15, ·ÒëEPI+1): ·Ç³£¸Ðл£¬·ÒëµÄºÜºÃ£¬ÑöĽ£¡ÄÜ·ñÔÙ°ï·Ò룿лл 2011-07-13 12:36:15
Mally89(½ð±Ò+2): ¸ÐлӦÖú£¡~ 2011-07-18 20:09:23
ÑÌÔÆÌýÓê(½ð±Ò+15, ·ÒëEPI+1): ·Ç³£¸Ðл£¬·ÒëµÄºÜºÃ£¬ÑöĽ£¡ÄÜ·ñÔÙ°ï·Ò룿лл 2011-07-13 12:36:15
Mally89(½ð±Ò+2): ¸ÐлӦÖú£¡~ 2011-07-18 20:09:23
| In addition to the scaffold bearing the ethyl side chain of stenine and neostenine, a collection of nonnatural Stemonalike ketoamide scaffolds were constructed via this route, which then served as the substrates for the preparation of six sets of functionalized analogues. ³ýÁË´øÓÐË¹ÌæÄþ¼îºÍÐÂË¹ÌæÄþ¼îµÄÒÒÍé»ù²àÁ´µÄÖ§¼Ü£¬Ò»ÏµÁзÇÌìÈ»°Ù²¿Ñù°±»ù֧ͪ¼Üͨ¹ýÕâһ·Ïß¹¹½¨¡£These bore core changes that could not be readily accomplished by modification of the natural product itself. Õâ²úÉúµÄºËÐı仯²»Ò×ÓÚͨ¹ý¶ÔÌìÈ»²úÎï×ÔÉíµÄÐÞÊζøÊµÏÖ¡£Representative examples of the various pathways of these initial efforts are shown in Scheme 2. ÕâЩ¿ª´´ÐÔŬÁ¦µÄ²»Í¬Â·¾¶µÄ´ú±íÐÔÀý×ÓÏÔʾÓÚʾÒâͼ2ÖС£Almost exclusively, these analogues displayed ring systems or functional groups substantially different from those of the natural products, including carbamates, amides, aryl groups, and heterocyclic moieties (e.g., indole and quinoline) (39). ¼¸ºõÊÇÎÞÒ»ÀýÍâµÄ£¬ÕâЩÀàËÆÎï¶¼ÏÔʾÁËÓëÌìÈ»²úÎïÏ൱²»Í¬µÄ»·ÏµÍ³ºÍ¹ÙÄÜÍÅ£¬°üÀ¨°±»ù¼×Ëá¡¢õ£°·¡¢·¼»ù¼¯Íź;ֲ¿ÔÓ»·½á¹¹£¨ÈçßÅßáºÍàßø£©¡£At the outset, it was unknown whether these analogues would possess any significant binding activity.Æð³õ£¬ÕâЩÀàËÆÎïÊÇ·ñ¾ßÓÐÓÐЧµÄ½áºÏ»îÐÔÉв»µÃ¶øÖª¡£ |
4Â¥2011-07-13 10:20:27














»Ø¸´´ËÂ¥