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Details

Stereochemistry ABSOLUTE
Molecular Formula C5H11N3O2
Molecular Weight 145.1597
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLUTAMAMIDE

SMILES

N[C@@H](CCC(N)=O)C(N)=O

InChI

InChIKey=LCGISIDBXHGCDW-VKHMYHEASA-N
InChI=1S/C5H11N3O2/c6-3(5(8)10)1-2-4(7)9/h3H,1-2,6H2,(H2,7,9)(H2,8,10)/t3-/m0/s1

HIDE SMILES / InChI

Molecular Formula C5H11N3O2
Molecular Weight 145.1597
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Site-specific labeling of nucleotides for making RNA for high resolution NMR studies using an E. coli strain disabled in the oxidative pentose phosphate pathway.
2010-05
Architectural underpinnings of the genetic code for glutamine.
2009-02-03
Reactivity of fish and microbial transglutaminases on glutaminyl sites of peptides derived from threadfin bream myosin.
2008-08-27
MSDmotif: exploring protein sites and motifs.
2008-07-17
Nitrogen metabolism of asparagine and glutamate in Vero cells studied by (1)H/ (15)N NMR spectroscopy.
2007-11
L: -Stereoselective amino acid amidase with broad substrate specificity from Brevundimonas diminuta: characterization of a new member of the leucine aminopeptidase family.
2006-04
The role of lysine residues 297 and 306 in nucleoside triphosphate regulation of E. coli CTP synthase: inactivation by 2',3'-dialdehyde ATP and mutational analyses.
2006-02
Glutamine amidotransferase activity of NAD+ synthetase from Mycobacterium tuberculosis depends on an amino-terminal nitrilase domain.
2005-03
Molecular dynamics simulation of the interaction between the complex iron-sulfur flavoprotein glutamate synthase and its substrates.
2004-11
Limited proteolysis of Escherichia coli cytidine 5'-triphosphate synthase. Identification of residues required for CTP formation and GTP-dependent activation of glutamine hydrolysis.
2003-05
Amino acid discrimination by a class I aminoacyl-tRNA synthetase specified by negative determinants.
2003-04-25
Aspartate-107 and leucine-109 facilitate efficient coupling of glutamine hydrolysis to CTP synthesis by Escherichia coli CTP synthase.
2003-02-01
Kinetic characterization of human glutamine-fructose-6-phosphate amidotransferase I: potent feedback inhibition by glucosamine 6-phosphate.
2002-04-26
Determination of the midpoint potential of the FAD and FMN flavin cofactors and of the 3Fe-4S cluster of glutamate synthase.
2001-05-08
A high resolution (1)H magic angle spinning NMR study of a high-M(r) subunit of wheat glutenin.
2001-01
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 22:01:02 GMT 2025
Edited
by admin
on Mon Mar 31 22:01:02 GMT 2025
Record UNII
35L593USSO
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GLUTAMAMIDE
Systematic Name English
GLUTAMINE AMIDE
Preferred Name English
PENTANEDIAMIDE, 2-AMINO-, (S)-
Systematic Name English
L-GLUTAMIC ACID .ALPHA.,.GAMMA.-DIAMIDE
Common Name English
PENTANEDIAMIDE, 2-AMINO-, (2S)-
Systematic Name English
L-GLUTAMINE AMIDE
Common Name English
L-GLUTAMIC ACID 1,5-DIAMIDE
Common Name English
Code System Code Type Description
CHEBI
21309
Created by admin on Mon Mar 31 22:01:02 GMT 2025 , Edited by admin on Mon Mar 31 22:01:02 GMT 2025
PRIMARY
EPA CompTox
DTXSID40173949
Created by admin on Mon Mar 31 22:01:02 GMT 2025 , Edited by admin on Mon Mar 31 22:01:02 GMT 2025
PRIMARY
PUBCHEM
445691
Created by admin on Mon Mar 31 22:01:02 GMT 2025 , Edited by admin on Mon Mar 31 22:01:02 GMT 2025
PRIMARY
CAS
2013-17-4
Created by admin on Mon Mar 31 22:01:02 GMT 2025 , Edited by admin on Mon Mar 31 22:01:02 GMT 2025
PRIMARY
FDA UNII
35L593USSO
Created by admin on Mon Mar 31 22:01:02 GMT 2025 , Edited by admin on Mon Mar 31 22:01:02 GMT 2025
PRIMARY