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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:
Molecular Weight:
409.43
Beilstein:
6670846
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.26

Quality Level

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Ashley E Lepack et al.
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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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