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Fmoc-L-Phe(4-CH2-N3)-OH
Nombre químico: N-alpha-(9-Fluorenylmethyloxycarbonyl)-4-azidomethyl-L-phenylalanine // Sinónimos: Fmoc-Phe(4-CH2-N3)-OH, Fmoc-p-azidomethyl-L-phenylalanine, Fmoc-para-methylazido-L-phenylalanine, Fmoc-para-azidomethyl-L-phenylalanine, Fmoc-pN3CH2Phe, Fmoc-pAMF,Fmoc-4-(azidomethyl)-L-phenylalanin e
- Nº Artículo:FAA7740
- Nº CAS:2375587-79-2
- Fórmula:C25H22N4O4
- Storage temperature:2-8°C
- Masa molecular:442,47 g/mol
- Pureza:min. 98%
- Pureza Enantiomérica:min. 99,7%
from 120,00 €
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, 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, Scott H. Brewer;
J. Phys. Chem. B 2013; 117(30): 8987-8993. DOI:10.1021/jp4052598;
Methods of using anti-cd74 antibodies and antibody conjugates in treatment of t-cell lymphoma; Molina, Arturo; PCT Int. Appl. 2019; WO 2019023316 A1.
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