CHEBI:4075 - (R)-(1-aminoethyl)phosphonic acid

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name (R)-(1-aminoethyl)phosphonic acid
ChEBI ID CHEBI:4075
ChEBI ASCII Name (R)-(1-aminoethyl)phosphonic acid
Definition An optically active phosphonic acid having a 1-aminoethyl group attached to the phosphorus.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:42773
Supplier Information
Download Molfile XML SDF
more structures >>
Formula C2H8NO3P
Net Charge 0
Average Mass 125.06360
Monoisotopic Mass 125.02418
InChI InChI=1S/C2H8NO3P/c1-2(3)7(4,5)6/h2H,3H2,1H3,(H2,4,5,6)/t2-/m1/s1
InChIKey UIQSKEDQPSEGAU-UWTATZPHSA-N
SMILES C[C@H](N)P(O)(O)=O
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (R)-(1-aminoethyl)phosphonic acid (CHEBI:4075) has functional parent phosphonic acid (CHEBI:44976)
(R)-(1-aminoethyl)phosphonic acid (CHEBI:4075) is a phosphonic acids (CHEBI:26069)
(R)-(1-aminoethyl)phosphonic acid (CHEBI:4075) is a primary amino compound (CHEBI:50994)
(R)-(1-aminoethyl)phosphonic acid (CHEBI:4075) is enantiomer of (S)-(1-aminoethyl)phosphonic acid (CHEBI:136675)
Incoming (S)-(1-aminoethyl)phosphonic acid (CHEBI:136675) is enantiomer of (R)-(1-aminoethyl)phosphonic acid (CHEBI:4075)
IUPAC Name
[(1R)-1-aminoethyl]phosphonic acid
Synonyms Sources
(1R)-1-aminoethylphosphonic acid ChEBI
(R)-(−)-(1-aminoethyl)phosphonic acid ChEBI
(R)-(1-Aminoethyl)phosphonsäure ChEBI
D-(1-Aminoethyl)phosphonic acid KEGG COMPOUND
D-1-aminoethylphosphonic acid ChEBI
Manual Xrefs Databases
C03782 KEGG COMPOUND
GG7 PDBeChem
View more database links
Registry Numbers Types Sources
3587722 Reaxys Registry Number Reaxys
60687-36-7 CAS Registry Number KEGG COMPOUND
60687-36-7 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
23703726 PubMed citation Europe PMC
3921052 PubMed citation Europe PMC
Last Modified
30 March 2017