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47692

Sigma-Aldrich

Fmoc-Nle-OH

≥98.0% (sum of enantiomers, HPLC)

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Synonym(s):
(S)-2-(Fmoc-amino)caproic acid, (S)-2-(Fmoc-amino)hexanoic acid, N-(9-Fluorenylmethoxycarbonyl)-L-norleucine, Fmoc-L-norleucine
Empirical Formula (Hill Notation):
C21H23NO4
CAS Number:
77284-32-3
Molecular Weight:
353.41
Beilstein:
5305164
MDL number:
MFCD00037537
UNSPSC Code:
12352200
PubChem Substance ID:
57651083
NACRES:
NA.26

Assay

≥98.0% (sum of enantiomers, HPLC)

optical activity

[α]20/D −18±1°, c = 1% in DMF

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

mp

141-144 °C (lit.)

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

CCCC[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O

InChI

1S/C21H23NO4/c1-2-3-12-19(20(23)24)22-21(25)26-13-18-16-10-6-4-8-14(16)15-9-5-7-11-17(15)18/h4-11,18-19H,2-3,12-13H2,1H3,(H,22,25)(H,23,24)/t19-/m0/s1

InChI key

VCFCFPNRQDANPN-IBGZPJMESA-N

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WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Tianliang He et al.
Oncogene (2018-06-22)
The antiviral metabolites from bacterial stress response to bacteriophage infection can maintain homeostasis of host cells, while metabolism disorder is a remarkable characteristic of tumorigenesis. In the aspect of metabolic homeostasis, therefore, the antiviral homeostasis-maintaining metabolites of bacteria may possess

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