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47751

Sigma-Aldrich

Fmoc-Tyr-OH

≥97.0% (HPLC)

Synonym(s):

Nα-Fmoc-L-tyrosine

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About This Item

Empirical Formula (Hill Notation):
C24H21NO5
CAS Number:
92954-90-0
Molecular Weight:
403.43
Beilstein/REAXYS Number:
3573123
MDL number:
MFCD00134890
UNSPSC Code:
12352200
PubChem Substance ID:
57651099
NACRES:
NA.26

assay

≥97.0% (HPLC)

optical activity

[α]20/D −22±2°, c = 1% in DMF

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(O)cc1)NC(=O)OCC2c3ccccc3-c4ccccc24

InChI

1S/C24H21NO5/c26-16-11-9-15(10-12-16)13-22(23(27)28)25-24(29)30-14-21-19-7-3-1-5-17(19)18-6-2-4-8-20(18)21/h1-12,21-22,26H,13-14H2,(H,25,29)(H,27,28)/t22-/m0/s1

InChI key

SWZCTMTWRHEBIN-QFIPXVFZSA-N

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European journal of medicinal chemistry, 44(5), 1933-1940 (2008-12-27)
Twenty-four new dipeptide analogs (1-24) of aurantiamide acetate were designed, synthesized, and assayed for effects on superoxide anion generation and elastase release by human neutrophils in response to fMLP/CB. Among them, seven N-(fluorenyl-9-methoxycarbonyl) (Fmoc)-dipeptides (6, 9, 12, 14, 17, 18
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