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Merck

911887

Sigma-Aldrich

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl (bromoethyl)carbamate

别名:

Benzyl boronate tag, Bromoethyl boronic acid pinacol ester nuclear tag, Nucleus-targeting probe building block

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100 MG
$374.00

$374.00


预计发货时间2025年7月04日详情


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100 MG
$374.00

About This Item

经验公式(希尔记法):
C16H23BBrNO4
分子量:
384.07
UNSPSC代码:
12352101
NACRES:
NA.22

$374.00


预计发货时间2025年7月04日详情


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表单

liquid

储存温度

2-8°C

应用

This benzyl boronate tag is a synthetic means for the subcellular targeting of cargo to the nucleus. Intracellular targeting can be important for understanding the localization of metabolites, proteins, or chemical probes or to increase therapeutic efficacy by concentrating a drug at its site of action and reducing off-target effects. Localization specifically to the nucleus is typically achieved using peptide localization signals and/or relies on passive diffusion. It was recently demonstrated, however, that nuclear targeting could be accomplished instead with a small-molecule motif benzyl boronic acid via synergistic active and passive transport processes. Tang, et al[1], presented examples using this tag to deliver proteins to the nucleus by the importin α/β pathway, including fluorescent proteins, ribonuclease A (RNase A), and chymotrypsin. The conjugation of this nucleus-targeting building block to other proteins or small molecules will facilitate nuclear localization in varied chemical biology experiments.

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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分析证书(COA)

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Rui Tang et al.
Journal of the American Chemical Society, 139(25), 8547-8551 (2017-06-10)
Active intracellular transport is a central mechanism in cell biology, directed by a limited set of naturally occurring signaling peptides. Here, we report the first nonpeptide moiety that recruits intracellular transport machinery for nuclear targeting. Proteins synthetically modified with a

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