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Details

Stereochemistry ACHIRAL
Molecular Formula C10H14N2O
Molecular Weight 178.231
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLYCINEXYLIDIDE

SMILES

CC1=CC=CC(C)=C1NC(=O)CN

InChI

InChIKey=IXYVBZOSGGJWCW-UHFFFAOYSA-N
InChI=1S/C10H14N2O/c1-7-4-3-5-8(2)10(7)12-9(13)6-11/h3-5H,6,11H2,1-2H3,(H,12,13)

HIDE SMILES / InChI

Molecular Formula C10H14N2O
Molecular Weight 178.231
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Quantitative analysis of lignocaine and metabolites in equine urine and plasma by liquid chromatography-tandem mass spectrometry.
2010-07-15
[Determination of lidocaine and its metabolites in human plasma by liquid chromatography in combination with tandem mass spectrometry].
2010-07
Serum concentrations of lidocaine and its metabolites after prolonged infusion in healthy horses.
2008-06
Effect of erythromycin and rifampicin on monoethylglycinexylidide test.
2008-03
Determination of lidocaine and its two N-desethylated metabolites in dog and horse plasma by high-performance liquid chromatography combined with electrospray ionization tandem mass spectrometry.
2007-06-01
Differential effect of chronic renal failure on the pharmacokinetics of lidocaine in patients receiving and not receiving hemodialysis.
2006-12
Thrombosis as a conformational disease.
2005-02
Effect of lidocaine on the minimum alveolar concentration of isoflurane in dogs.
2004-10
Propofol does not inhibit lidocaine metabolism during epidural anesthesia.
2004-10
Cytochrome P450 1A2 is a major determinant of lidocaine metabolism in vivo: effects of liver function.
2004-01
Utility of nonaqueous capillary electrophoresis for the determination of lidocaine and its metabolites in human plasma: a comparison of ultraviolet and mass spectrometric detection.
2004
Free lidocaine concentrations during continuous epidural anesthesia in geriatric patients.
2003-05-29
Effect of the CYP3A4 inhibitor erythromycin on the pharmacokinetics of lignocaine and its pharmacologically active metabolites in subjects with normal and impaired liver function.
2003-01
Chromatographic determination of free lidocaine and its active metabolites in plasma from patients under epidural anesthesia.
2002-11
Involvement of liver carboxylesterases in the in vitro metabolism of lidocaine.
2002-06
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 22:59:21 GMT 2025
Edited
by admin
on Mon Mar 31 22:59:21 GMT 2025
Record UNII
D2D932W316
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GLYCINEXYLIDIDE
Common Name English
ASTRA-6204
Preferred Name English
GLYCYLXYLIDIDE
Common Name English
N-GLYCYL-2,6-XYLIDINE
Systematic Name English
W-49167
Code English
GX
Common Name English
GLYCYL XYLIDIDE
Common Name English
N-(2,6-DIMETHYLPHENYL)GLYCINAMIDE
Systematic Name English
.OMEGA.-AMINO-2,6-DIMETHYLACETANILIDE
Systematic Name English
N-(2,6-DIMETHYLPHENYL)-2-AMINOACETAMIDE
Systematic Name English
2-AMINO-2',6'-DIMETHYLACETOANILIDE
Systematic Name English
Code System Code Type Description
FDA UNII
D2D932W316
Created by admin on Mon Mar 31 22:59:21 GMT 2025 , Edited by admin on Mon Mar 31 22:59:21 GMT 2025
PRIMARY
CAS
18865-38-8
Created by admin on Mon Mar 31 22:59:21 GMT 2025 , Edited by admin on Mon Mar 31 22:59:21 GMT 2025
PRIMARY
CHEBI
357241
Created by admin on Mon Mar 31 22:59:21 GMT 2025 , Edited by admin on Mon Mar 31 22:59:21 GMT 2025
PRIMARY
PUBCHEM
87833
Created by admin on Mon Mar 31 22:59:21 GMT 2025 , Edited by admin on Mon Mar 31 22:59:21 GMT 2025
PRIMARY
EPA CompTox
DTXSID40876064
Created by admin on Mon Mar 31 22:59:21 GMT 2025 , Edited by admin on Mon Mar 31 22:59:21 GMT 2025
PRIMARY
Related Record Type Details
BINDER->LIGAND
Related Record Type Details
PARENT -> METABOLITE LESS ACTIVE
PLASMA