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47703

Sigma-Aldrich

Fmoc-Glu(OAll)-OH

≥96.0% (HPLC)

Synonym(s):

Fmoc-L-glutamic acid 5-allyl ester

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About This Item

Empirical Formula (Hill Notation):
C23H23NO6
CAS Number:
133464-46-7
Molecular Weight:
409.43
Beilstein/REAXYS Number:
6670846
MDL number:
MFCD00190879
UNSPSC Code:
12352209
PubChem Substance ID:
57651087
NACRES:
NA.26

Quality Level

100

assay

≥96.0% (HPLC)

optical activity

[α]20/D −16.5±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](CCC(=O)OCC=C)NC(=O)OCC1c2ccccc2-c3ccccc13

InChI

1S/C23H23NO6/c1-2-13-29-21(25)12-11-20(22(26)27)24-23(28)30-14-19-17-9-5-3-7-15(17)16-8-4-6-10-18(16)19/h2-10,19-20H,1,11-14H2,(H,24,28)(H,26,27)/t20-/m0/s1

InChI key

LRBARFFNYOKIAX-FQEVSTJZSA-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)

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG6308
BCCF2799
BCBV9951
BCBV3751
BCBT0096

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Lorna A Farrelly et al.
Nature, 567(7749), 535-539 (2019-03-15)
Chemical modifications of histones can mediate diverse DNA-templated processes, including gene transcription1-3. Here we provide evidence for a class of histone post-translational modification, serotonylation of glutamine, which occurs at position 5 (Q5ser) on histone H3 in organisms that produce serotonin

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