| ²é¿´: 795 | »Ø¸´: 2 | ||
| ±¾Ìû²úÉú 1 ¸ö ·ÒëEPI £¬µã»÷ÕâÀï½øÐв鿴 | ||
ºìÉ«ÌÒ×Óгæ (СÓÐÃûÆø)
|
[ÇóÖú]
²ËÄñÇóÖú·ÒëÒ»¶Î»°£¡50½ð±Ò
|
|
| º¬ÓÐÛÏ»ùµÄà×ऻ·ÏµÁл¯ºÏÎï¾ßÓп¹°©»îÐÔºÍÃâÒßÔöÇ¿×÷Óã¬ÁòÔ×Ó½ÏÑõÔ×ÓµÄÍâ²ãµç×ӵIJ»Í¬£¬ÁòÔ×ÓµÄ3pµç×ÓÊÜÔ×Ӻ˵ÄÊø¸¿±ÈÑõÔ×ÓµÄ2pµç×ÓС£¬ÀëÓòºóÓë´ó»·Éϵĵç×Ó¹²éʹ¹²éîЧӦÔöÇ¿£»ÁòÔ×ÓÉϵĵç×Ó¿Éͨ¹ý3p¡ú3d ԾǨ£¬ÁòÔ×Ó3p¹ìµÀµÄµç×Ó±ÈÑõÔ×ÓÖÐ2p¹ìµÀµÄµç×ÓµÄÄܼ¶¸ß£¬¶øÁòÔ×ÓµÄ3d¹ìµÀÄܼ¶±ÈôÊ»ùC=OµÄ2¦Ð* ¹ìµÀÌá¸ß²»¶à£¬¹ÊÁòôÊ»ùC=SµÄ3p¡ú3d ԾǨËùÐèÄÜÁ¿Ð¡£¬ÓÐÀûÓÚ3pµç×ӵ路¢£¬º¬ÓÐÁòôÊ»ùµÄºËÜÕÀ໯ºÏÎïÆä4-λôÊ»ùÑõ±»ÁòÈ¡´úºóÎü¹â¶È±ä´ó£¬×î´óÎüÊÕ·åºìÒÆ£¬¶Ô¹â¼«ÆäÃô¸Ð[3]¡£Òò´Ë£¬¶ÔÕý³£Ï¸°ûÎÞº¦µÄµÍ¼ÁÁ¿½ü×ÏÍâ¹â¿ÉÒÔ¼¤·¢ÁòôÊ»ùÖÐÁòÔ×ӵĵç×ÓԾǨ£¬ÆÆ»µÆä»¯ºÏÎïµÄ½á¹¹£¬ºÜÈÝÒ׵ؽ«º¬ÓÐ4-ÁòÐØÜÕµÄDNAµÄÔöÉúϸ°ûɱËÀ¡£ |
» ²ÂÄãϲ»¶
288»·¾³×¨Ë¶,Çóµ÷²ÄÁÏ·½Ïò
ÒѾÓÐ12È˻ظ´
ÇóÉúÎïѧѧ˶µ÷¼Á¡ª¡ª364·Ö
ÒѾÓÐ7È˻ظ´
288Çóµ÷¼Á£¬Ò»Ö¾Ô¸»ªÄÏÀí¹¤´óѧ071005
ÒѾÓÐ4È˻ظ´
11408,335·Ö£¬±¾¿Æ211£¬Çóµ÷¼Á£¬¿Éתרҵ
ÒѾÓÐ5È˻ظ´
0817»¯Ñ§¹¤³ÌÓë¼¼ÊõÇóµ÷¼Á£¬Ò»Ö¾Ô¸Öк£Ñó319
ÒѾÓÐ7È˻ظ´
Äܶ¯µ÷¼Á326ר˶
ÒѾÓÐ4È˻ظ´
295Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
315Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ6È˻ظ´
Î人һÐÄÒ»Òë
¾èÖú¹ó±ö (ÖøÃûдÊÖ)
- ·ÒëEPI: 502
- Ó¦Öú: 8 (Ó×¶ùÔ°)
- ½ð±Ò: 2283.1
- É¢½ð: 5914
- ºì»¨: 32
- Ìû×Ó: 1665
- ÔÚÏß: 321.9Сʱ
- ³æºÅ: 3587652
- ×¢²á: 2014-12-10
- ÐÔ±ð: GG
- רҵ: ¸ß·Ö×Ӻϳɻ¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
É̼ÒÒѾÖ÷¶¯ÉùÃ÷´Ë»ØÌû¿ÉÄܺ¬ÓÐÐû´«ÄÚÈÝ
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
ºìÉ«ÌÒ×Ó: ½ð±Ò+50, ·ÒëEPI+1, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£ÊÜÓã¡ 2015-10-26 19:02:16
ºìÉ«ÌÒ×Ó: ½ð±Ò+50, ·ÒëEPI+1, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£ÊÜÓã¡ 2015-10-26 19:02:16
|
The mercapto group-contained Pyrimidine compounds possess anti-tumor activity and immunological enhancement function. Due to the difference of outer electron structure, the 3p electrons of sulfur atom are bonded with nucleus in less degree as the 2p electrons of oxygen atom are, therefore, after delocalization, the electrons on big ring are conjugatedly distributed, which enhances the conjugated effect. Electrons in sulfur atom may transit from 3p to 3d, the electronic energy level of sulfur atom 3p orbital is higher than that of oxygen atom 2p orbital, which the electronic energy level of sulfur atom 3d orbital is merely higher than that of 2¦Ð* orbital of carbanyl group C=O, therefore, the energy needed for the 3p¡ú3d electron stransition of thiocarbonyl C=S is smaller, which is positive for 3p electron excitation. For the thiocarbonyl-added nucleosides, after the oxgen atom on 4- carbonyl is replaced by sulfur atom, its absorbance will be enlarged, the maximum absorption peak will be red shifted, making it extremely sensitive to light[3]. As a result, the low dosage of near ultraviolet, which creates no harm to normal cells, can stimulate the electron transition of sulfur atom in thiocarbonyl group, thus destroying the compound structure, and easily killing the proliferating cells which contain 4 - sulfur thymidylic DNA. |
2Â¥2015-10-25 19:08:40
ºìÉ«ÌÒ×Ó
гæ (СÓÐÃûÆø)
- Ó¦Öú: 6 (Ó×¶ùÔ°)
- ½ð±Ò: -1.1
- É¢½ð: 1412
- ºì»¨: 7
- Ìû×Ó: 188
- ÔÚÏß: 381.7Сʱ
- ³æºÅ: 2664139
- ×¢²á: 2013-09-18
- רҵ: ·ð½Ì
3Â¥2015-10-26 19:00:22














»Ø¸´´ËÂ¥