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H-Aeg-OH
Nom chimique: N-(2-Aminoethyl)glycine // Synonymes: N-beta-Aminoethyl-Gly-OH, Ethylenediamine-N-monoacetic acid, 2-[(2-aminoethyl)amino]acetic acid, Aminoethyl-glycine
- n° Art.:HAA9200
- n° CAS:24123-14-6
- Formule:C4H10N2O2
- Storage temperature:2-8°C
- Masse moléculaire:118,14 g/mol
- Pureté:min. 99%
from 150,00 €
description
Functional building block for the synthesis of peptide nucleic acids and a variety of other reactions, e.g. peptidomimetics, linker with branching functionality. Iris Biotech also offers the Fmoc-protected derivative H-Aeg(Fmoc)-OH*HCl (HAA3180) as well as the double protected Boc-Aeg(Fmoc)-OH (BAA2980) and Fmoc-Aeg(Boc)-OH (FAA1767).
This compound is a potential building block for the construction of (customized) peptide nucleic acids (PNAs) and for peptoid synthesis.
references
PNA hybridizes to complementary oligonucleotides obeying the Watson-Crick hydrogen-bonding rules; M. Egholm, O. Buchardt, L. Christensen, C. Behrens, S. M. Freier, D. A. Driver, R. H. Berg, S. K. Kim, B. Norden, P. E. Nielsen; Nature 1993; 365: 566-568. https://doi.org/10.1038/365566a0.
Peptide nucleic acids rather than RNA may have been the first genetic molecule; K. E. Nelson; M. Levy; S. L. Miller; PNAS 2000; 97(8): 3868-3871. https://doi.org/10.1073/pnas.97.8.3868.
Encoded combinatorial peptide libraries containing non-natural amino acids; J. M. Kerr, S. C. Banville, R. N. Zuckermann; J. Am. Chem. Soc. 1993; 115(6): 2529-2531. https://doi.org/10.1021/ja00059a070.
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Prices and product availability are subject to change and require reconfirmation. Please contact us for further information.
All information contained in our webshop is compiled to the best of our knowledge.
Prices and product availability are subject to change and require reconfirmation. Please contact us for further information.
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