橙色固体Diazo Biotin-DBCO,DBCO-Diazo Biotin,叠氮生物素DBCO的化学性质分析

英文名称:Diazo Biotin-DBCO,DBCO-Diazo Biotin

中文名称:重氮-生物素-二苯基环辛炔

外 观:橙色固体

分子式:C52H60N8O9S

分子量:973.15

CAS号: N/A

纯度:>95%

溶解度:DMSO, DMF, DCM, THF, Chloroform

保存条件:-20℃ 12个月

产品描述:重氮生物素DBCO包含通过连二亚硫酸钠(Na2S2O4)可裂解重氮连接剂连接到DBCO基团的生物素部分。捕获的蛋白质靶标可在温和条件下用50 mM连二亚硫酸钠溶液释放,并通过质谱、ELISA、斑点杂交或Western杂交应用进行鉴定。

结构式:

新研博美提供的点击类化学试剂包括:DBCO、TCO、Tetrazine、Azide、Alkyne、Auxiliary reagents等。其中DBCO Reagents又包含了与氨基反应的,与羧基反应的,与生物素交联的,与荧光素交联的,与PEG交联的等等产品。

Copper-free Click Chemistry产品列表:

DBCO-C6-acid                  1425485-72-8

DBCO-PEG1-acid                2228857-38-1

DBCO-PEG4-acid                1537170-85-6

DBCO-PEG5-acid

DBCO-PEG8-acid

DBCO-PEG12-acid

DBCO-NHCO-PEG5-acid           1870899-46-9

DBCO-NHCO-PEG13-acid          1353016-71-3

DBCO-C6-NHS ester             1384870-47-6

DBCO-PEG4-4-Formylbenzoate

DBCO-Sulfo-NHS ester          1400191-52-7

DBCO-NHS ester                1353016-71-3

DBCO-PEG1-NHS ester           2228857-34-7

DBCO-PEG4-NHS ester           1427004-19-0

DBCO-PEG5-NHS ester           2144395-59-3

DBCO-PEG8-NHS ester

DBCO-PEG12-NHS ester

DBCO-C6-NHS ester   

DBCO-NHCO-PEG4-NHS ester     2100306-58-7

DBCO-NHCO-PEG5-NHS ester     1378531-80-6

DBCO-NHCO-PEG13-NHS ester

DBCO-PEG4-PFP ester

DBCO-PEG4-alcohol            1416711-60-8

DBCO-Amine                   1255942-06-3

Sulfo DBCO-amine             2028284-70-8

润色下面英文:The controlled drug delivery systems, due to their precise control of drug release in spatiotemporal level triggered by specific stimulating factors and advantages such as higher utilization ratio of drug, less side-effects to normal tissues and so forth, provide a new strategy for the precise treatment of many serious diseases, especially tumors. The materials that constitute the controlled drug delivery systems are called “smart materials” and they can respond to the stimuli of some internal (pH, redox, enzymes, etc.) or external (temperature, electrical/magnetic, ultrasonic and optical, etc.) environments. Before and after the response to the specific stimulus, the composition or conformational of smart materials will be changed, damaging the original balance of the delivery systems and releasing the drug from the delivery systems. Amongst them, the photo-controlled drug delivery systems, which display drug release controlled by light, demonstrated extensive potential applications, and received wide attention from researchers. In recent years, photo-controlled drug delivery systems based on different photo-responsive groups have been designed and developed for precise photo-controlled release of drugs. Herein, in this review, we introduced four photo-responsive groups including photocleavage groups, photoisomerization groups, photo-induced rearrangement groups and photocrosslinking groups, and their different photo-responsive mechanisms. Firstly, the photocleavage groups represented by O-nitrobenzyl are able to absorb the energy of the photons, inducing the cleavage of some specific covalent bonds. Secondly, azobenzenes, as a kind of photoisomerization groups, are able to convert reversibly between the apolar trans form and the polar cis form upon different light irradiation. Thirdly, 2-diazo-1,2-naphthoquinone as the representative of the photo-induced rearrangement groups will absorb specific photon energy, carrying out Wolff rearrangement reaction. Finally, coumarin is a promising category photocrosslinking groups that can undergo [2+2] cycloaddition reactions under light irradiation. The research progress of photo-controlled drug delivery systems based on different photo-responsive mechanisms were mainly reviewed. Additionally, the existing problems and the future research perspectives of photo-controlled drug delivery systems were proposed.
02-06
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