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O-phosphonatoethanaminium(1-)
"Conjugate base of O-phosphoethanolamine arising from deprotonation of the phosphate OH groups and protonation of the amino group; major species at pH 7.3."


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04. Bioactive Capabilities of Specific Chemicals : Transferases [EC:2] > Transferring one-carbon groups [EC:2.1] > Methyltransferases [EC:2.1.1] > Phosphoethanolamine N-methyltransferase [EC:2.1.1.103] > O-phosphonatoethanaminium(1-) [CHEBI:58190]
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04. Bioactive Capabilities of Specific Chemicals  
04. Bioactive Capabilities of Specific Chemicals
 Transferases [EC:2] (1441) 
 Transferring one-carbon groups [EC:2.1] (318) 
 Methyltransferases [EC:2.1.1] (279) 
 Phosphoethanolamine N-methyltransferase [EC:2.1.1.103] (5) 
 O-phosphonatoethanaminium(1-) [CHEBI:58190] (1)
 Transferring phosphorus-containing groups [EC:2.7] (369) 
 Phosphotransferases with an alcohol group as acceptor [EC:2.7.1] (217) 
 Ethanolamine kinase [EC:2.7.1.82] (5) 
 O-phosphonatoethanaminium(1-) [CHEBI:58190] (1)
 Nucleotidyltransferases [EC:2.7.7] (93) 
 Ethanolamine-phosphate cytidylyltransferase [EC:2.7.7.14] (5) 
 O-phosphonatoethanaminium(1-) [CHEBI:58190] (1)
 Hydrolases [EC:3] (824) 
 Acting on ester bonds [EC:3.1] (313) 
 Phosphoric monoester hydrolases [EC:3.1.3] (102) 
 Phosphoethanolamine/phosphocholine phosphatase [EC:3.1.3.75] (5) 
 O-phosphonatoethanaminium(1-) [CHEBI:58190] (1)
 Phosphoric diester hydrolases [EC:3.1.4] (35) 
 Serine-ethanolaminephosphate phosphodiesterase [EC:3.1.4.13] (5) 
 O-phosphonatoethanaminium(1-) [CHEBI:58190] (1)
 Lyases [EC:4] (743) 
 Carbon-carbon lyases [EC:4.1] (299) 
 Aldehyde-Lyases [EC:4.1.2] (89) 
 Sphinganine-1-phosphate aldolase [EC:4.1.2.27] (3) 
 O-phosphonatoethanaminium(1-) [CHEBI:58190] (1)
 Carbon-oxygen lyases [EC:4.2] (393) 
 Acting on Phosphates [EC:4.2.3] (175) 
 Ethanolamine-phosphate phospho-lyase [EC:4.2.3.2] (4) 
 O-phosphonatoethanaminium(1-) [CHEBI:58190] (1)
08. Chemical Category 
08. Chemical Category
 ion [CHEBI:24870] (4391) 
 anion [CHEBI:22563] (3454) 
 organic anion [CHEBI:25696] (3155) 
 organophosphate oxoanion [CHEBI:58945] (1108) 
 O-phosphonatoethanaminium(1-) [CHEBI:58190] (1)
 organic ion [CHEBI:25699] (3577) 
 organic anion [CHEBI:25696] (3155) 
 organophosphate oxoanion [CHEBI:58945] (1108) 
 O-phosphonatoethanaminium(1-) [CHEBI:58190] (1)
 main group molecular entity [CHEBI:33579] (25650) 
 p-block molecular entity [CHEBI:33675] (25343) 
 pnictogen molecular entity [CHEBI:33302] (10027) 
 phosphorus molecular entity [CHEBI:26082] (2769) 
 phosphorus oxoacids and derivatives [CHEBI:36360] (2691) 
 phosphorus oxoacid derivative [CHEBI:36359] (2628) 
 phosphoric acid derivative [CHEBI:26079] (2611) 
 organophosphate oxoanion [CHEBI:58945] (1108) 
 O-phosphonatoethanaminium(1-) [CHEBI:58190] (1)
 carbon group molecular entity [CHEBI:33582] (23847) 
 organic molecular entity [CHEBI:50860] (23769) 
 organic ion [CHEBI:25699] (3577) 
 organic anion [CHEBI:25696] (3155) 
 organophosphate oxoanion [CHEBI:58945] (1108) 
 O-phosphonatoethanaminium(1-) [CHEBI:58190] (1)
 polyatomic entity [CHEBI:36357] (18777) 
 heteroatomic molecular entity [CHEBI:37577] (13672) 
 oxoacid derivative [CHEBI:33241] (3254) 
 phosphorus oxoacid derivative [CHEBI:36359] (2628) 
 phosphoric acid derivative [CHEBI:26079] (2611) 
 organophosphate oxoanion [CHEBI:58945] (1108) 
 O-phosphonatoethanaminium(1-) [CHEBI:58190] (1)
ChEBI Compound Accession Identifier  [CHEBI:58190]
ChEBI Compound Description  "Conjugate base of O-phosphoethanolamine arising from deprotonation of the phosphate OH groups and protonation of the amino group; major species at pH 7.3."
ChEBI Compound Identification Number  58190
ChEBI InChI Value  InChI=1S/C2H8NO4P/c3-1-2-7-8(4,5)6/h1-3H2,(H2,4,5,6)/p-1
ChEBI InChIKey Value  SUHOOTKUPISOBE-UHFFFAOYSA-M
ChEBI Compound Name  O-phosphonatoethanaminium(1-)
ChEBI SMILES Value  [NH3+]CCOP([O-])([O-])=O
ChEBI Substance ID  103158473
ChEBI URL  ChEBI:58190
ChemSpider ID  5415641
Ontomatica Chemical Accession Key (OnChAKey)  SUHOOTKUPISOBE_UHFFFAOYSA_M_000_000000
PubChem Compound ID  7059434