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About This Item
Empirical Formula (Hill Notation):
C24H20N2O6
CAS Number:
Molecular Weight:
432.43
UNSPSC Code:
12352200
NACRES:
NA.26
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5178656
Quality Level
assay
≥96.0% (HPLC)
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-8°C
SMILES string
OC(=O)[C@H](Cc1ccc(cc1)[N+]([O-])=O)NC(=O)OCC2c3ccccc3-c4ccccc24
InChI
1S/C24H20N2O6/c27-23(28)22(13-15-9-11-16(12-10-15)26(30)31)25-24(29)32-14-21-19-7-3-1-5-17(19)18-6-2-4-8-20(18)21/h1-12,21-22H,13-14H2,(H,25,29)(H,27,28)/t22-/m0/s1
InChI key
RZRRJPNDKJOLHI-QFIPXVFZSA-N
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Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Rosa Bellavita et al.
Journal of enzyme inhibition and medicinal chemistry, 35(1), 1751-1764 (2020-09-23)
The rapid development of antimicrobial resistance is pushing the search in the discovering of novel antimicrobial molecules to prevent and treat bacterial infections. Self-assembling antimicrobial peptides, as the lipidated peptides, are a novel and promising class of molecules capable of