Diazo Biotin-PEG3-DBCO,二苯并环辛炔PEG3重氮生物素,无铜 Click Chemistry

Diazo Biotin-PEG3-DBCO反应原理:

Diazo Biotin-PEG3-DBCO 是一种点击化学标记生物素,可通过无铜 Click Chemistry 与叠氮化物发生反应。重氮允许使用连二亚硫酸钠 (Na2S2O4) 从链霉亲和素中有效释放捕获的生物素化分子。点击化学生物素标记试剂包含各种点击化学官能团修饰的生物素,适用于各种生物素标记实验。

Diazo Biotin-PEG3-DBCO物理数据:

CAS:N/A | 中文名: 重氮化合物修饰生物素-三聚乙二醇-二苯并环辛炔 |英文名: Diazo Biotin-PEG3-DBCO

结构式:

物理化学相关数据补充:

分子式:C52H60N8O9S

分子量:973.16

纯度标准:95%+,具体的数据可以提供相应的核磁图谱

外形颜色:白色固体

存储条件:阴凉,干燥,通风良好的库房

包装规格:1g、5g、10g等,可进行相应的封装。

注意事项:取用时一定要干燥,避免频繁解冻和冷冻。

溶解性:溶于大部分有机溶剂,溶于水

产品定制:可按照客户的需求进行定制

DBCO同系列产品展示:

CAS:1425485-72-8,DBCO-C6-acid,二苯并环辛炔-C6-酸

CAS:2576471-49-1,DBCO-SS-COOH,二苯并环辛炔-SS-酸

CAS:1353016-71-3,DBCO-NHS ester,二苯并环辛炔-活性酯

CAS:2163772-16-3,DBCO-PEG3-NHS ester,二苯并环辛炔-三聚乙二醇-NHS酯

CAS:1427004-19-0,DBCO-PEG4-NHS ester,二苯基环辛炔-四聚乙二醇-活性酯

CAS:2144395-59-3,DBCO-PEG5-NHS ester,二苯基环辛炔-五聚乙二醇-活性酯

CAS:2093934-94-0,DBCO-PEG12-NHS ester,二苯并环辛炔-十二聚乙二醇-琥珀酰亚胺酯

CAS:1395786-30-7,DBCO-Maleimide,二苯基环辛炔-马来酰亚胺

CAS:2698339-31-8,DBCO-PEG2-Maleimide,二苯并环辛炔-二聚乙二醇-马来酰亚胺

CAS:1480516-75-3,DBCO-PEG4-Maleimide,二苯并环辛炔-四聚乙二醇-马来酰亚胺

CAS:1801863-88-6,(4E)-TCO-PEG4-DBCO,反式环辛烯-四聚乙二醇-二苯并环辛炔

CAS:1854034-70-0,Bis-Sulfone-PEG4-DBCO,双巯基磺酸二苯基

温馨提示:此试剂仅用于科研实验

今日分享的文章包含Diazo Biotin-PEG3-DBCO试剂相关物理数据,化学式,CAS号,反应特点,以及相应的结构式,有相关疑问的朋友,欢迎关注收藏,为大家答疑解惑,进行交流。

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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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