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47552

Sigma-Aldrich

Fmoc-Dap-OH

≥97.0% (HPLC)

Synonym(s):

Nα-Fmoc-L-2,3-diaminopropionic acid

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About This Item

Empirical Formula (Hill Notation):
C18H18N2O4
CAS Number:
181954-34-7
Molecular Weight:
326.35
Beilstein/REAXYS Number:
7658592
MDL number:
MFCD00237019
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
57651005
NACRES:
NA.26

assay

≥97.0% (HPLC)

form

solid

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

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

InChI

1S/C18H18N2O4/c19-9-16(17(21)22)20-18(23)24-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15-16H,9-10,19H2,(H,20,23)(H,21,22)/t16-/m0/s1

InChI key

HDSLKWZYHRLRRL-INIZCTEOSA-N

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

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Ahmet Kertmen et al.
Langmuir : the ACS journal of surfaces and colloids, 35(15), 5281-5293 (2019-03-27)
Numerous glutamine analogues have been reported as irreversible inhibitors of the glucosamine-6-phosphate (GlcN-6-P) synthase in pathogenic Candida albicans in the last 3.5 decades. Among the reported inhibitors, the most effective N3-(4-methoxyfumaroyl)-l-2,3-diaminopropanoic acid (FMDP) has been extensively studied in order to

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