47378
Fmoc-D-Phe-OH
≥98.0%
Synonym(s):
Fmoc-D-phenylalanine
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About This Item
Empirical Formula (Hill Notation):
C24H21NO4
CAS Number:
Molecular Weight:
387.43
NACRES:
NA.26
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
MDL number:
Beilstein/REAXYS Number:
4767931
Quality Level
assay
≥98.0%
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](Cc1ccccc1)NC(=O)OCC2c3ccccc3-c4ccccc24
InChI
1S/C24H21NO4/c26-23(27)22(14-16-8-2-1-3-9-16)25-24(28)29-15-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h1-13,21-22H,14-15H2,(H,25,28)(H,26,27)/t22-/m1/s1
InChI key
SJVFAHZPLIXNDH-JOCHJYFZSA-N
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Charles A Galea et al.
Biochemistry, 56(4), 657-668 (2017-01-11)
Polymyxins remain one of the few antibiotics available for treating antibiotic resistant bacteria. Here we describe polymyxin B thioesterase which performs the final step in polymyxin B biosynthesis. Isolated thioesterase catalyzed cyclization of an N-acetylcystamine polymyxin B analogue to form
Oliver John V Belleza et al.
MedChemComm, 9(10), 1673-1678 (2018-11-16)
Nobilamide B, a TRPV1 antagonist, and a series of Ala-substituted analogues were synthesized and their neuroactivity was assessed in a primary culture of dorsal root ganglion (DRG) neurons. Analogues 4, 6, and 7 showed comparable activity, affecting capsaicin response in
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 47378-5G | 04061832360966 |