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Products
Pharmacology
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- Technical support
- Resources
(NLysNpheNphe)2-NH2
Cat. No. PT-103
Structure:
Activity:
Chongsiriwatana et al (2008) Peptoids that mimic the structure, function, and mechanism of helical antimicrobial peptides. Proc. Natl. Acad. Sci 105(8) 2794 DOI: 10.1073/pnas.0708254105
Zuckermann (2011) Peptoid origins. Biopolymers, 96 545 doi:10.1002/bip.21573
Sun and Zuckermann (2013) Peptoid Polymers: A Highly Designable Bioinspired Material. ACS Nano 7(6) 4715 https://doi.org/10.1021/nn4015714
Huang et al (2014) Learning from Host-Defense Peptides: Cationic, Amphipathic Peptoids with Potent Anticancer Activity. PLoS ONE 9(2) e90397. https://doi.org/10.1371/journal.pone.0090397
Eggimann et al (2015) Investigating the Anti‐leishmanial Effects of Linear Peptoids. ChemMedChem. 10 233 doi:10.1002/cmdc.201402416
Related areas
Technical Data
Structure | NLys-Nphe-Nphe-NLys-Nphe-Nphe-NH2 |
Molecular Weight | 862.1 |
Formula | C48H63N9O6 |
Sequence | NLys-Nphe-Nphe-NLys-Nphe-Nphe-NH2 |
Modifications | NLys is the N-(4-aminobutyl)glycine peptoid monomer and Nphe is the N-(phenylmethyl)glycine peptoid monomer For more information about peptoids and their nomenclature please refer to the peptide resources page |
Solubility and Storage
Solubility | Soluble in dilute acid |
Appearance | Freeze dried solid |
Storage | Store desiccated, frozen and in the dark |
Batch Specific Data
Purity | >90% by HPLC |
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Recent citations
A new publication from the University of Ljubljana uses MCA-AVLQSGFR-Lys(Dnp)-Lys-NH2, the FRET substrate for the severe acute respiratory syndrome coronavirus main protease (SARS-CoV Mpro), to determine the inhibitory potential of plant polyphenols
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