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ÇóÎÊorthogonal reactionÏê½â
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aircraftvip
ר¼Ò¹ËÎÊ (ÕýʽдÊÖ)
-

ר¼Ò¾Ñé: +40 - BM-EPI: 10
- Ó¦Öú: 232 (´óѧÉú)
- ¹ó±ö: 0.06
- ½ð±Ò: 7345.7
- É¢½ð: 24
- ºì»¨: 28
- Ìû×Ó: 987
- ÔÚÏß: 487.4Сʱ
- ³æºÅ: 1007878
- ×¢²á: 2010-04-28
- ÐÔ±ð: GG
- רҵ: ¸ß·Ö×Ӻϳɻ¯Ñ§
- ¹ÜϽ: ÉúÎï²ÄÁÏ
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fool_proof: ½ð±Ò+1, ר¼Ò¿¼ºË, ¸Ðл»ØÌûÓ¦Öú£¬»¶Ó³£À´ÉúÎï²ÄÁϰæ¿é½»Á÷~ 2013-03-17 10:05:36
°×Íõ·µ°: ½ð±Ò+2, ¡ï¡ï¡ïºÜÓаïÖú 2013-03-17 10:22:39
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
fool_proof: ½ð±Ò+1, ר¼Ò¿¼ºË, ¸Ðл»ØÌûÓ¦Öú£¬»¶Ó³£À´ÉúÎï²ÄÁϰæ¿é½»Á÷~ 2013-03-17 10:05:36
°×Íõ·µ°: ½ð±Ò+2, ¡ï¡ï¡ïºÜÓаïÖú 2013-03-17 10:22:39
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Orthogonal reactions are based on orthogonal chemistry. Here you could more information. http://en.wikipedia.org/wiki/Bioorthogonal_chemistry ''The term bioorthogonal chemistry refers to any chemical reaction that can occur inside of living systems without interfering with native biochemical processes.The term was coined by Carolyn R. Bertozzi in 2003. Since its introduction, the concept of the bioorthogonal reaction has enabled the study of biomolecules such as glycans, proteins,and lipids in real time in living systems without cellular toxicity. A number of chemical ligation strategies have been developed that fulfill the requirements of bioorthogonality, including the 1,3-dipolar cycloaddition between azides and cyclooctynes (also termed copper-free click chemistry),between nitrones and cyclooctynes,oxime/hydrazone formation from aldehydes and ketones, the tetrazine ligation, the isonitrile-based click reaction, and most recently, the quadricyclane ligation.'' |

2Â¥2013-03-17 01:31:59
yuanliu1work
½ð³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 17 (СѧÉú)
- ½ð±Ò: 1328.3
- ºì»¨: 2
- Ìû×Ó: 1463
- ÔÚÏß: 176.1Сʱ
- ³æºÅ: 1331402
- ×¢²á: 2011-06-26
- ÐÔ±ð: MM
- רҵ: µç»¯Ñ§

3Â¥2013-03-17 02:38:04
aircraftvip
ר¼Ò¹ËÎÊ (ÕýʽдÊÖ)
-

ר¼Ò¾Ñé: +40 - BM-EPI: 10
- Ó¦Öú: 232 (´óѧÉú)
- ¹ó±ö: 0.06
- ½ð±Ò: 7345.7
- É¢½ð: 24
- ºì»¨: 28
- Ìû×Ó: 987
- ÔÚÏß: 487.4Сʱ
- ³æºÅ: 1007878
- ×¢²á: 2010-04-28
- ÐÔ±ð: GG
- רҵ: ¸ß·Ö×Ӻϳɻ¯Ñ§
- ¹ÜϽ: ÉúÎï²ÄÁÏ

4Â¥2013-03-18 01:05:27
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5Â¥2014-11-20 14:58:22













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