Peptides & Peptide Synthesis Products

Boc-Gln-ONp

Boc-Gln-ONp

$29.00
$29.00
Boc-Gln-ONp, Catalog No: 48042
(4-nitrophenyl) 5-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxopentanoate, CAS: 15387-45-8, MW: 367.35, Formula: C16H21N3O7
Catalog No: 48042
(4-nitrophenyl) 5-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxopentanoate, CAS: 15387-45-8, MW: 367.35, Formula: C16H21N3O7
Description

Details

(4-nitrophenyl) 5-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxopentanoate
Additional Information

Additional Information

Catalog Number 48042
CAS 15387-45-8
M.W. 367.35
Formula C16H21N3O7
IUPAC Name (4-nitrophenyl) 5-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxopentanoate
Synonym No
Also Known As
  • (4-nitrophenyl) 5-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxopentanoate
  • (4-nitrophenyl) 5-amino-2-(tert-butoxycarbonylamino)-5-oxo-pentanoate
  • 5-amino-2-[(tert-butoxy-oxomethyl)amino]-5-oxopentanoic acid (4-nitrophenyl) ester
  • 5-amino-2-(tert-butoxycarbonylamino)-5-keto-valeric acid (4-nitrophenyl) ester
  • (4-nitrophenyl) 5-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxo-pentanoate
  • 15387-45-8
  • N2-((1,1-Dimethylethoxy)carbonyl)-L-glutamine, 4-nitrophenyl ester
  • N.alpha.-(tert-butoxycarbonyl)glutamine 4-nitrophenyl ester
  • L-Glutamine, N2-((1,1-dimethylethoxy)carbonyl)-, 4-nitrophenyl ester
InChIKey HJMMCTZLXOVMFB-UHFFFAOYSA-N
InChI InChI=1S/C16H21N3O7/c1-16(2,3)26-15(22)18-12(8-9-13(17)20)14(21)25-11-6-4-10(5-7-11)19(23)24/h4-7,12H,8-9H2,1-3H3,(H2,17,20)(H,18,22)
SMILES CC(C)(C)OC(=O)NC(CCC(=O)N)C(=O)OC1=CC=C(C=C1)[N+](=O)[O-]
Cited Uses

Details

1. Polgár L et al, "Metalloendopeptidase QG. Isolation from Escherichia coli and characterization.", Biochemical Journal, 273(Pt 3) pp.725-731 (1991 Feb 1).
2. Yamaoka Y et al, "Purification and Characterization of a Cysteine Endopeptidase in Cotyledons of Germinated Mung Bean Seeds", Plant Physiology, 94(2) pp.561-566 (1990 Oct).
3. Csoma C et al, "Proteinase from germinating bean cotyledons. Evidence for involvement of a thiol group in catalysis.", Biochemical Journal, 222(3) pp.769-776 (1984 Sep 15).
4. Folkers K et al, "Synthesis and activities of neurotensin, and its acid and amide analogs: possible natural occurrence of [Gln4]-neurotensin.", Proceedings of the National Academy of Sciences of the United States of America, 73(11) pp.3833-3837 (1976 Nov).
5. Meienhofer J et al, "Solid-Phase Synthesis with Attachment of Peptide to Resin through an Amino Acid Side Chain: [8-Lysine]-Vasopressin", Proceedings of the National Academy of Sciences of the United States of America, 68(5) pp.1006-1009 (1971 May).
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