Fmoc-Aeg(N3)-OH_product_DataBase

Bioactivity	Fmoc-Aeg(N3)-OH is a click chemistry reagent containing an Azide. Alkylating the Nitrogen of an amide bond results in peptoid structures, which leads to conformational restrains, like N-methylation and allows backbone derivatisation. Altering cytotoxicity, bacterial cell selectivity and receptor pharmacology through formation of peptoid derivatives have been published for Cilengitide, Piscidin 1, and MC3, MC4 and MC5 receptor agonist. This building block enables design of macrocycles through intermolecular crosslinking or backbone stabilization through intermolecular ring-closure. This compound is a potential building block for the construction of (customized) peptide nucleic acids (PNAs) and for peptoid synthesis[1].
Name	Fmoc-Aeg(N3)-OH
CAS	1935981-35-3
Formula	C19H18N4O4
Molar Mass	366.37
Transport	Room temperature in continental US; may vary elsewhere.
Storage	Please store the product under the recommended conditions in the Certificate of Analysis.
Reference	[1]. Fernández-Llamazares AI, et al. The backbone N-(4-azidobutyl) linker for the preparation of peptide chimera. Org Lett. 2013 Sep 6;15(17):4572-5. [2]. Kruijtzer JA, et al. Peptoid-peptide hybrids as potent novel melanocortin receptor ligands. J Med Chem. 2005 Jun 30;48(13):4224-30. [3]. Kim JK, et al. Structural flexibility and the positive charges are the key factors in bacterial cell selectivity and membrane penetration of peptoid-substituted analog of Piscidin 1. Biochim Biophys Acta. 2010 Oct;1798(10):1913-25.

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