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Details

Stereochemistry ACHIRAL
Molecular Formula C2H8NO3P
Molecular Weight 125.0636
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-AMINOETHYLPHOSPHONIC ACID

SMILES

NCCP(O)(O)=O

InChI

InChIKey=QQVDJLLNRSOCEL-UHFFFAOYSA-N
InChI=1S/C2H8NO3P/c3-1-2-7(4,5)6/h1-3H2,(H2,4,5,6)

HIDE SMILES / InChI

Molecular Formula C2H8NO3P
Molecular Weight 125.0636
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Rapid automatic NCS identification using heavy-atom substructures.
2002 Dec
Binding of phosphorothioate oligonucleotides to zwitterionic liposomes.
2002 Jun 13
High performance carbon-supported catalysts for fuel cells via phosphonation.
2003 Apr 7
A role for carbon catabolite repression in the metabolism of phosphonoacetate by Agromyces fucosus Vs2.
2006 Aug
Diversification of function in the haloacid dehalogenase enzyme superfamily: The role of the cap domain in hydrolytic phosphoruscarbon bond cleavage.
2006 Dec
GABA-mediated effects of some taurine derivatives injected i.c.v. on rabbit rectal temperature and gross motor behavior.
2006 May
Structures of an alanine racemase from Bacillus anthracis (BA0252) in the presence and absence of (R)-1-aminoethylphosphonic acid (L-Ala-P).
2008 May 1
Hydroperoxylation by hydroxyethylphosphonate dioxygenase.
2009 Nov 11
Structural analysis of O-glycans of mucin from jellyfish (Aurelia aurita) containing 2-aminoethylphosphonate.
2009 Nov 2
The ethanolamine branch of the Kennedy pathway is essential in the bloodstream form of Trypanosoma brucei.
2009 Sep
Seasonal Expression of the Picocyanobacterial Phosphonate Transporter Gene phnD in the Sargasso Sea.
2010
Comparative study on the rumen microbial populations, hydrolytic enzyme activities and dry matter degradability between different species of ruminant.
2010 Dec
A new amido phosphonate derivative of carboxymethylcellulose with an osteogenic activity and which is capable of interacting with any Ti surface.
2010 Oct
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:12:24 GMT 2023
Edited
by admin
on Fri Dec 15 19:12:24 GMT 2023
Record UNII
AH00YJQ334
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-AMINOETHYLPHOSPHONIC ACID
Systematic Name English
PHOSPHONIC ACID, (2-AMINOETHYL)-
Common Name English
PHOSPHONIC ACID, P-(2-AMINOETHYL)-
Common Name English
.BETA.-AMINOETHYLPHOSPHONIC ACID
Systematic Name English
NSC-133837
Code English
PHOSPHONOETHYLAMINE
Systematic Name English
CILIATINE
Systematic Name English
2-AMINOETHANEPHOSPHONIC ACID
Systematic Name English
(2-AMINOETHYL)PHOSPHONIC ACID
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
218-043-0
Created by admin on Fri Dec 15 19:12:24 GMT 2023 , Edited by admin on Fri Dec 15 19:12:24 GMT 2023
PRIMARY
CHEBI
15573
Created by admin on Fri Dec 15 19:12:24 GMT 2023 , Edited by admin on Fri Dec 15 19:12:24 GMT 2023
PRIMARY
NSC
133837
Created by admin on Fri Dec 15 19:12:24 GMT 2023 , Edited by admin on Fri Dec 15 19:12:24 GMT 2023
PRIMARY
PUBCHEM
339
Created by admin on Fri Dec 15 19:12:24 GMT 2023 , Edited by admin on Fri Dec 15 19:12:24 GMT 2023
PRIMARY
CAS
2041-14-7
Created by admin on Fri Dec 15 19:12:24 GMT 2023 , Edited by admin on Fri Dec 15 19:12:24 GMT 2023
PRIMARY
EPA CompTox
DTXSID10174362
Created by admin on Fri Dec 15 19:12:24 GMT 2023 , Edited by admin on Fri Dec 15 19:12:24 GMT 2023
PRIMARY
FDA UNII
AH00YJQ334
Created by admin on Fri Dec 15 19:12:24 GMT 2023 , Edited by admin on Fri Dec 15 19:12:24 GMT 2023
PRIMARY