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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
Comparative study on the rumen microbial populations, hydrolytic enzyme activities and dry matter degradability between different species of ruminant.
2010-12
A new amido phosphonate derivative of carboxymethylcellulose with an osteogenic activity and which is capable of interacting with any Ti surface.
2010-10
Widespread known and novel phosphonate utilization pathways in marine bacteria revealed by functional screening and metagenomic analyses.
2010-01
Seasonal Expression of the Picocyanobacterial Phosphonate Transporter Gene phnD in the Sargasso Sea.
2010
Hydroperoxylation by hydroxyethylphosphonate dioxygenase.
2009-11-11
Structural analysis of O-glycans of mucin from jellyfish (Aurelia aurita) containing 2-aminoethylphosphonate.
2009-11-02
The ethanolamine branch of the Kennedy pathway is essential in the bloodstream form of Trypanosoma brucei.
2009-09
In vitro and in vivo anti-angiogenic activities and inhibition of hormone-dependent and -independent breast cancer cells by ceramide methylaminoethylphosphonate.
2009-06-24
GPIomics: global analysis of glycosylphosphatidylinositol-anchored molecules of Trypanosoma cruzi.
2009
Structures of an alanine racemase from Bacillus anthracis (BA0252) in the presence and absence of (R)-1-aminoethylphosphonic acid (L-Ala-P).
2008-05-01
A review of telavancin in the treatment of complicated skin and skin structure infections (cSSSI).
2008-02
Lipid classes and fatty acid composition of the tropical nudibranch mollusks Chromodoris sp. and Phyllidia coelestis.
2007-12
New ways to break an old bond: the bacterial carbon-phosphorus hydrolases and their role in biogeochemical phosphorus cycling.
2007-10
A sex-specific metabolite identified in a marine invertebrate utilizing phosphorus-31 nuclear magnetic resonance.
2007-08-22
Isolation and characterization of two new microbial strains capable of degradation of the naturally occurring organophosphonate - ciliatine.
2007-04
Detection and identification of Bacteriovorax stolpii UKi2 Sphingophosphonolipid molecular species.
2007-03
Glyco- and sphingophosphonolipids from the medusa Phyllorhiza punctata: NMR and ESI-MS/MS fingerprints.
2007-02
Diversification of function in the haloacid dehalogenase enzyme superfamily: The role of the cap domain in hydrolytic phosphoruscarbon bond cleavage.
2006-12
A role for carbon catabolite repression in the metabolism of phosphonoacetate by Agromyces fucosus Vs2.
2006-08
Identification of cognate ligands for the Escherichia coli phnD protein product and engineering of a reagentless fluorescent biosensor for phosphonates.
2006-07
Inhibition of rabbit brain 4-aminobutyrate transaminase by some taurine analogues: a kinetic analysis.
2006-05-14
GABA-mediated effects of some taurine derivatives injected i.c.v. on rabbit rectal temperature and gross motor behavior.
2006-05
Residue determination of glyphosate, glufosinate and aminomethylphosphonic acid in water and soil samples by liquid chromatography coupled to electrospray tandem mass spectrometry.
2005-07-22
Photoinduced electron transfer between cytochrome c and a novel 1,4,5,8-naphthalenetetracarboxylic diimide with amphiphilic character.
2005-04-04
Sulfoacetaldehyde is excreted quantitatively by Acinetobacter calcoaceticus SW1 during growth with taurine as sole source of nitrogen.
2005-04
Enzymatic synthesis of radiolabeled phosphonoacetaldehyde.
2003-11-15
The phosphonopyruvate decarboxylase from Bacteroides fragilis.
2003-10-17
Cr[(H3N-(CH2)2-PO3)(Cl)(H2O)]: X-ray single-crystal structure and magnetism of a polar organic-inorganic hybrid chromium(II) organophosphonate.
2003-10-06
Sphingophosphonolipid molecular species from edible mollusks and a jellyfish.
2003-09
Properties of phosphoenolpyruvate mutase, the first enzyme in the aminoethylphosphonate biosynthetic pathway in Trypanosoma cruzi.
2003-06-20
High performance carbon-supported catalysts for fuel cells via phosphonation.
2003-04-07
Significance analysis of lexical bias in microarray data.
2003-04-03
Rapid automatic NCS identification using heavy-atom substructures.
2002-12
Degradation pathway of the phosphonate ciliatine: crystal structure of 2-aminoethylphosphonate transaminase.
2002-11-05
Binding of phosphorothioate oligonucleotides to zwitterionic liposomes.
2002-06-13
Structural determinants for ligand binding and catalysis of triosephosphate isomerase.
2001-10
Synthesis of monensin derivatives and their effect on the activity of ricin A-chain immunotoxins.
2001
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:36:09 GMT 2025
Edited
by admin
on Mon Mar 31 19:36:09 GMT 2025
Record UNII
AH00YJQ334
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-133837
Preferred Name English
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
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 Mon Mar 31 19:36:09 GMT 2025 , Edited by admin on Mon Mar 31 19:36:09 GMT 2025
PRIMARY
CHEBI
15573
Created by admin on Mon Mar 31 19:36:09 GMT 2025 , Edited by admin on Mon Mar 31 19:36:09 GMT 2025
PRIMARY
NSC
133837
Created by admin on Mon Mar 31 19:36:09 GMT 2025 , Edited by admin on Mon Mar 31 19:36:09 GMT 2025
PRIMARY
PUBCHEM
339
Created by admin on Mon Mar 31 19:36:09 GMT 2025 , Edited by admin on Mon Mar 31 19:36:09 GMT 2025
PRIMARY
CAS
2041-14-7
Created by admin on Mon Mar 31 19:36:09 GMT 2025 , Edited by admin on Mon Mar 31 19:36:09 GMT 2025
PRIMARY
EPA CompTox
DTXSID10174362
Created by admin on Mon Mar 31 19:36:09 GMT 2025 , Edited by admin on Mon Mar 31 19:36:09 GMT 2025
PRIMARY
FDA UNII
AH00YJQ334
Created by admin on Mon Mar 31 19:36:09 GMT 2025 , Edited by admin on Mon Mar 31 19:36:09 GMT 2025
PRIMARY