47626
Fmoc-Gln-OH
≥95.0% (T)
别名:
Fmoc-L-谷氨酰胺
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关于此项目
经验公式（希尔记法）:
C20H20N2O5
化学文摘社编号:
分子量:
368.38
UNSPSC Code:
12352200
NACRES:
NA.26
PubChem Substance ID:
EC Number:
276-254-3
Beilstein/REAXYS Number:
4722773
MDL number:
InChI key
IZKGGDFLLNVXNZ-KRWDZBQOSA-N
InChI
1S/C20H20N2O5/c21-18(23)10-9-17(19(24)25)22-20(26)27-11-16-14-7-3-1-5-12(14)13-6-2-4-8-15(13)16/h1-8,16-17H,9-11H2,(H2,21,23)(H,22,26)(H,24,25)/t17-/m0/s1
SMILES string
NC(=O)CC[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O
assay
≥95.0% (T)
optical activity
[α]20/D −18.5±1.5°, c = 1% in DMF
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
mp
220 °C (dec.) (lit.)
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-8°C
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存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
C R Wu et al.
International journal of peptide and protein research, 31(1), 47-57 (1988-01-01)
The synthesis of a 37-peptide fragment derived from the carboxyl terminal of the beta-subunit of baboon chorionic gonadotropin has been accomplished by the continuous flow Fmoc-polyamide solid phase method. The use of N alpha-fluorenylmethoxy-carbonyl-glutamine with its sidechain protected by the
Roxana Y P Alta et al.
PloS one, 12(2), e0171729-e0171729 (2017-02-09)
Desferrioxamine (DFO) is a bacterial siderophore with a high affinity for iron, but low cell penetration. As part of our ongoing project focused on DFO-conjugates, we synthesized, purified, characterized and studied new mtDFOs (DFO conjugated to the Mitochondria Penetrating Peptides
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