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Details

Stereochemistry RACEMIC
Molecular Formula C5H12NO5P
Molecular Weight 197.1262
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-AMINO-5-PHOSPHONOVALERATE

SMILES

NC(CCCP(O)(O)=O)C(O)=O

InChI

InChIKey=VOROEQBFPPIACJ-UHFFFAOYSA-N
InChI=1S/C5H12NO5P/c6-4(5(7)8)2-1-3-12(9,10)11/h4H,1-3,6H2,(H,7,8)(H2,9,10,11)

HIDE SMILES / InChI

Molecular Formula C5H12NO5P
Molecular Weight 197.1262
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 05:27:22 UTC 2023
Edited
by admin
on Sat Dec 16 05:27:22 UTC 2023
Record UNII
39PJ29YY8Z
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-AMINO-5-PHOSPHONOVALERATE
Systematic Name English
AP 5 (AMINO ACID)
Common Name English
AP 5 (±)-
Common Name English
2-APV
Common Name English
NORVALINE, 5-PHOSPHONO- (±)-
Systematic Name English
(±)-AMINO-5-PHOSPHONOPENTANOIC ACID
Systematic Name English
DL-2-AMINO-5-PHOSPHONOVALERIC ACID
Common Name English
DL-2-AMINO-5-PHOSPHONOPENTANOIC ACID
Common Name English
5-PHOSPHONO-DL-NORVALINE
Systematic Name English
DL-AP-5
Code English
APV (±)-
Common Name English
DL-NORVALINE, 5-PHOSPHONO-
Systematic Name English
(±)-2-AMINO-5-PHOSPHONOVALERIC ACID
Systematic Name English
AP-5 (±)-
Code English
2-AMINO-5-PHOSPHONOVALERIC ACID
Systematic Name English
2-AMINO-5-PHOSPHONOPENTANOIC ACID
Systematic Name English
Classification Tree Code System Code
WIKIPEDIA NMDA receptor antagonist
Created by admin on Sat Dec 16 05:27:22 UTC 2023 , Edited by admin on Sat Dec 16 05:27:22 UTC 2023
Code System Code Type Description
PUBCHEM
1216
Created by admin on Sat Dec 16 05:27:22 UTC 2023 , Edited by admin on Sat Dec 16 05:27:22 UTC 2023
PRIMARY
CAS
76326-31-3
Created by admin on Sat Dec 16 05:27:22 UTC 2023 , Edited by admin on Sat Dec 16 05:27:22 UTC 2023
PRIMARY
WIKIPEDIA
2-Amino-5-phosphonovalerate
Created by admin on Sat Dec 16 05:27:22 UTC 2023 , Edited by admin on Sat Dec 16 05:27:22 UTC 2023
PRIMARY
MESH
D015763
Created by admin on Sat Dec 16 05:27:22 UTC 2023 , Edited by admin on Sat Dec 16 05:27:22 UTC 2023
PRIMARY
CHEBI
138644
Created by admin on Sat Dec 16 05:27:22 UTC 2023 , Edited by admin on Sat Dec 16 05:27:22 UTC 2023
PRIMARY
FDA UNII
39PJ29YY8Z
Created by admin on Sat Dec 16 05:27:22 UTC 2023 , Edited by admin on Sat Dec 16 05:27:22 UTC 2023
PRIMARY
EPA CompTox
DTXSID90893701
Created by admin on Sat Dec 16 05:27:22 UTC 2023 , Edited by admin on Sat Dec 16 05:27:22 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
Binds to glutamate site
COMPETITIVE INHIBITOR
ACTIVE ENANTIOMER->RACEMATE
Related Record Type Details
ACTIVE MOIETY