H-L-Phe(4-CH2-N3)*HCl

Nombre químico: 4-azidomethyl-L-phenylalanine hydrochloride // Sinónimos: H-Phe(4-CH2-N3)*HCl, para-methylazido-L-phenylalanine hydrochloride, para-azidomethyl-L-phenylalanine hydrochloride, pAMF*HCl, pN3CH2Phe*HCl,(S)-2-amino-3-(4-(azidomethyl)phenyl)propanoic acid hydro chloride, CAS 2517638-29-6

  • Nº Artículo:HAA4090
  • Nº CAS:1446772-80-0
  • Fórmula:C10H12N4O2*HCl
  • Storage temperature:2-8°C
  • Masa molecular:220,23*36,45 g/mol
  • Pureza:min. 98%
  • Pureza Enantiomérica:min. 99,7%

from 84,00 €

Grouped product items
Cantidad Unidad de venta Precio Unidad de almacenamiento de stock (SKU) Disponibilidad
100 mg
84,00 €
HAA4090.0100
<10 días laborables
250 mg
140,00 €
HAA4090.0250
<10 días laborables
500 mg
252,00 €
HAA4090.0500
<10 días laborables
1 g
392,00 €
HAA4090.1000
<10 días laborables
5 g
1.400,00 €
HAA4090.5000
<10 días laborables
Hoja de seguridad
description

This material is used in antibody drug conjugates as a superior SPAAC reaction partner in comparison to H-Phe(4-N3). It can serve as a vibrational reporter of local protein environments after genetic incorporation into proteins.


references

Production of Site-Specific Antibody–Drug Conjugates Using Optimized Non-Natural Amino Acids in a Cell-Free Expression System; Erik S. Zimmerman, Tyler H. Heibeck, Avinash Gill, Xiaofan Li, Christopher J. Murray, Mary Rose Madlansacay, Cuong Tran, Nathan T. Uter, Gang Yin, Patrick J. Rivers, Alice Y. Yam, Willie D. Wang, Alexander R. Steiner, Sunil U. Bajad, Kalyani Penta, Wenjin Yang, Trevor J. Hallam, Christopher D. Thanos, and Aaron K. Sato; Bioconjugate Chem. 2014; 25(2): 351–361. DOI: 10.1021/bc400490z.

Sensitive, Site-Specific, and Stable Vibrational Probe of Local Protein Environments: 4-Azidomethyl-l-Phenylalanine; Christopher G. Bazewicz, Melanie T. Liskov, Kevin J. Hines, and Scott H. Brewer; J. Phys. Chem. B 2013; 117(30): 8987–8993. DOI: 10.1021/jp4052598.

Molina, Arturo PCT Int. Appl. 2019; WO 2019023316 A1.


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