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Names | |
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IUPAC name
3-Amino-L-alanine
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Systematic IUPAC name
(2S)-2,3-Diaminopropanoic acid | |
Identifiers | |
3D model (
JSmol)
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|
ChEBI | |
ChemSpider | |
KEGG | |
PubChem
CID
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|
UNII | |
CompTox Dashboard (
EPA)
|
|
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Properties | |
C3H8N2O2 | |
Molar mass | 104.109 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
2,3-Diaminopropionic acid (2,3-diaminopropionate, Dpr) [1] is a non-proteinogenic amino acid found in certain secondary metabolites, including zwittermicin A [2] and tuberactinomycin. [3]
2,3-Diaminopropionate is formed by the pyridoxal phosphate (PLP) mediated amination of serine.
![]() | |
Names | |
---|---|
IUPAC name
3-Amino-L-alanine
| |
Systematic IUPAC name
(2S)-2,3-Diaminopropanoic acid | |
Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChemSpider | |
KEGG | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C3H8N2O2 | |
Molar mass | 104.109 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
2,3-Diaminopropionic acid (2,3-diaminopropionate, Dpr) [1] is a non-proteinogenic amino acid found in certain secondary metabolites, including zwittermicin A [2] and tuberactinomycin. [3]
2,3-Diaminopropionate is formed by the pyridoxal phosphate (PLP) mediated amination of serine.