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Details

Stereochemistry ABSOLUTE
Molecular Formula C13H16N2O4
Molecular Weight 264.2771
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHENYLACETYLGLUTAMINE

SMILES

NC(=O)CC[C@H](NC(=O)CC1=CC=CC=C1)C(O)=O

InChI

InChIKey=JFLIEFSWGNOPJJ-JTQLQIEISA-N
InChI=1S/C13H16N2O4/c14-11(16)7-6-10(13(18)19)15-12(17)8-9-4-2-1-3-5-9/h1-5,10H,6-8H2,(H2,14,16)(H,15,17)(H,18,19)/t10-/m0/s1

HIDE SMILES / InChI

Molecular Formula C13H16N2O4
Molecular Weight 264.2771
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 17:53:51 UTC 2023
Edited
by admin
on Fri Dec 15 17:53:51 UTC 2023
Record UNII
92358I79RG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PHENYLACETYLGLUTAMINE
Systematic Name English
ANTINEOPLASTON AS2-1 COMPONENT PHENYLACETYLGLUTAMINE
Common Name English
PHENYLACETYL-L-GLUTAMINE
Systematic Name English
Phenylacetylglutamine [WHO-DD]
Common Name English
NSC-203800
Code English
PHENYLACETYLGLUTAMINE [MI]
Common Name English
L-GLUTAMINE, N2-(PHENYLACETYL)-
Systematic Name English
ASTUGENAL COMPONENT PHENYLACETYLGLUTAMINE
Common Name English
ANTINEOPLASTON AS 2-1 COMPONENT PHENYLACETYLGLUTAMINE
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 189804
Created by admin on Fri Dec 15 17:53:51 UTC 2023 , Edited by admin on Fri Dec 15 17:53:51 UTC 2023
FDA ORPHAN DRUG 267408
Created by admin on Fri Dec 15 17:53:51 UTC 2023 , Edited by admin on Fri Dec 15 17:53:51 UTC 2023
Code System Code Type Description
CHEBI
17884
Created by admin on Fri Dec 15 17:53:51 UTC 2023 , Edited by admin on Fri Dec 15 17:53:51 UTC 2023
PRIMARY
NCI_THESAURUS
C1613
Created by admin on Fri Dec 15 17:53:51 UTC 2023 , Edited by admin on Fri Dec 15 17:53:51 UTC 2023
NO STRUCTURE GIVEN
CHEBI
8087
Created by admin on Fri Dec 15 17:53:51 UTC 2023 , Edited by admin on Fri Dec 15 17:53:51 UTC 2023
PRIMARY
FDA UNII
92358I79RG
Created by admin on Fri Dec 15 17:53:51 UTC 2023 , Edited by admin on Fri Dec 15 17:53:51 UTC 2023
PRIMARY
NSC
203800
Created by admin on Fri Dec 15 17:53:51 UTC 2023 , Edited by admin on Fri Dec 15 17:53:51 UTC 2023
PRIMARY
EPA CompTox
DTXSID90182324
Created by admin on Fri Dec 15 17:53:51 UTC 2023 , Edited by admin on Fri Dec 15 17:53:51 UTC 2023
PRIMARY
MERCK INDEX
m11916
Created by admin on Fri Dec 15 17:53:51 UTC 2023 , Edited by admin on Fri Dec 15 17:53:51 UTC 2023
PRIMARY
WIKIPEDIA
PHENYLACETYLGLUTAMINE
Created by admin on Fri Dec 15 17:53:51 UTC 2023 , Edited by admin on Fri Dec 15 17:53:51 UTC 2023
PRIMARY
CAS
28047-15-6
Created by admin on Fri Dec 15 17:53:51 UTC 2023 , Edited by admin on Fri Dec 15 17:53:51 UTC 2023
PRIMARY
PUBCHEM
92258
Created by admin on Fri Dec 15 17:53:51 UTC 2023 , Edited by admin on Fri Dec 15 17:53:51 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> METABOLITE
Formed in the liver and excreted in the urine responsible for the reduction of ammonia in the blood.
MAJOR
URINE
Related Record Type Details
ACTIVE MOIETY