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Nom chimique: Azido-L-valine cyclohexylammonium salt // Synonymes: N3-Val-OH*CHA, (S)-2-Azido isovaleric acid cyclohexylammonium salt, (S)-2-Azido-3-methylbutyric acid cyclohexylammonium salt, (S)-2-Azido-3-methylbutanoic acid cyclohexylammonium salt, 40224-47-3 net
from 119,00 €
Valine derivative bearing an azide moiety suitable for Click chemistry. Furthermore, this building block is reported as Valaciclovir (Valacyclovir) synthesis intermediate.
References:
Expansion of Phosphane Treasure Box for Staudinger Peptide Ligation; K. Bajaj, G. G. Pillai, R. Sakhuja, D. Kumar; J. Org. Chem. 2020; 85(19): 12147-12159. https://doi.org/10.1021/acs.joc.0c01319.
Synthesis, antibacterial properties and 2D-QSAR studies of quinolone-triazole conjugates; H. M. Faidalah, A. S. Girgis, A. D. Tiwari, H. H. Honkanadavar, S. J. Thomas, A. Samir, A. Kalmouch, K. A. Alamry, K. A. Khan, T. S. Ibrahim, A. M. M. Al-Mahmoudy, A. M. Asiri, S. S. Panda; Eur. J. Med. Chem. 2018; 143: 1524-1534. https://doi.org/10.1016/j.ejmech.2017.10.042.
Reenginering Antibiotics to Combat Bacterial Resistance: Click Chemistry [1,2,3]-Triazole Vancomycin Dimers with Potent Activity against MRSA and VRE; Chem. Eur. J. 2016; 23(1): 79-83.
