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Merck

806005

Sigma-Aldrich

APN-Amine HCl

95%

别名:

3-(4-(4-(Aminomethyl)-1H-1,2,3-triazol-1-yl)phenyl)propiolonitrile hydrochloride

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About This Item

经验公式(希尔记法):
C12H10N5Cl
分子量:
259.69
UNSPSC代码:
12352200
PubChem化学物质编号:

质量水平

方案

95%

表单

powder

反应适用性

reagent type: cross-linking reagent

储存温度

2-8°C

SMILES字符串

N#CC#CC1=CC=C(N2C=C(CN)N=N2)C=C1.[H]Cl

InChI

1S/C12H9N5.ClH/c13-7-1-2-10-3-5-12(6-4-10)17-9-11(8-14)15-16-17;/h3-6,9H,8,14H2;1H

InChI key

JZGAUVVBWJHLGN-UHFFFAOYSA-N

应用

APN-Amine is a bifunctional crosslinker for thiol-to-carboxyl coupling. The coupling can be performed with high selectivity in biological medium using mild reaction conditions. The amino group readily reacts with activated carboxylic acids (e.g. NHS-esters) in basic conditions to produce stable amide bonds. The APN group can be used for coupling with free thiols (e.g. labeling of free cysteines in proteins).

其他说明

Standard protein labeling procedure (cysteine labeling):
  • Dissolve the protein in the appropriate buffer* with pH 6.5-9.0 (e.g. PBS) at 1-10 mg/mL concentration.
  • Apply the appropriate amount of the stock solution of the reagent (1-5 molar eq. per free cysteine residue).
  • Incubate at room temperature for 2 hours.
  • If necessary, purify the protein conjugate using size exclusion chromatography or ultrafiltration.
*Note: avoid thiol-containing buffers.

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Sergii Kolodych et al.
Bioconjugate chemistry, 26(2), 197-200 (2015-01-24)
Amine-to-thiol coupling is the most common route for the preparation of antibody-drug conjugates (ADC). It is usually achieved by using heterobifunctional reagents possessing an activated ester at one end and a maleimide group at the other. However, maleimide-based conjugates were

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