Substance
ID:182677
Names and Identifiers
IUPAC name
5-amino-4-oxopentanoic acid hydrochloride
IUPAC Traditional name
aminolevulinic acid hydrochloride
Synonyms
ALA5-Amino-4-oxopentanoic acid hydrochloride5-Aminolevulinic acid hydrochlorideδ-Aminolevulinic acid hydrochloride5-Aminolaevulinic acid hydrochloride
Registration numbers
MDL Number
EC Number
Beilstein Number
CAS Number
PubChem SID
Properties
Safety Information
RTECS
OI1640000
Storage Temperature
-20°C
German water hazard class
-
Product Information
Purity
≥98%
Suitability
suitable for cell culture
Physical Property
Apperance
powder
Solubility
H2O: soluble50 mg/mL
Molecule Details
Biochem/physiol Actions
Intermediate in heme biosynthesis.
包装
10 mg in autosmp vl
Application
5-Aminolevulinic acid formed from glycine and succinyl CoA by ALA synthase is the first compound in prophyrin biosynthesis pathway. 5-Aminolevulinic acid is used in photodynamic therapy. This compound may be used to study the effects of photodynamic therapy in vitro.
Intermediate in heme biosynthesis.
包装
10 mg in autosmp vl
Application
5-Aminolevulinic acid formed from glycine and succinyl CoA by ALA synthase is the first compound in prophyrin biosynthesis pathway. 5-Aminolevulinic acid is used in photodynamic therapy. This compound may be used to study the effects of photodynamic therapy in vitro.
Molecular Spectra
No Data Available
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References
No Data Available
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