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Merck
CN

47472

Fmoc-Phe(4-NO2)-OH

≥96.0% (HPLC)

别名:

Fmoc-4-硝基-L-苯丙氨酸

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关于此项目

经验公式(希尔记法):
C24H20N2O6
化学文摘社编号:
分子量:
432.43
UNSPSC Code:
12352200
NACRES:
NA.26
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5178656
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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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存储类别

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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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