| Catalogue number: | PA 27 0032375 |
| Chemical name: | Fmoc-Aeg(N3)-OH |
CAS Number: |
1935981-35-3 |
| Category: | miscellaneous compounds,Antibody Drug Conjugate |
| Synonyms: | N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N-(2-azidoethyl)glycine; Glycine, N-(2-azidoethyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-; N-(2-Azidoethyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]glycine; |
| Molecular form: | C19H18N4O4 |
| Appearance: | NA |
| Mol. Weight: | 366.38 |
| Storage: | 2-8°C Refrigerator |
| Shipping Conditions: | Ambient |
| Applications: | 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]. Fmoc-Aeg(N3)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. |
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