Aminolevulinic acid hydrochlorideProduct ingredient for Aminolevulinic acid

Show full entry for Aminolevulinic acid
Name
Aminolevulinic acid hydrochloride
Drug Entry
Aminolevulinic acid

A compound produced from succinyl-CoA and glycine as an intermediate in heme synthesis. It is used as a photochemotherapy for actinic keratosis. [PubChem]

See full entry for Aminolevulinic acid
Accession Number
DBSALT000934
Structure
Similar Structures
Synonyms
5-aminolevulinic acid hydrochloride / Aminolevulinic acid HCl
UNII
V35KBM8JGR
CAS Number
5451-09-2
Weight
Average: 167.59
Monoisotopic: 167.0349209
Chemical Formula
C5H10ClNO3
InChI Key
ZLHFONARZHCSET-UHFFFAOYSA-N
InChI
InChI=1S/C5H9NO3.ClH/c6-3-4(7)1-2-5(8)9;/h1-3,6H2,(H,8,9);1H
IUPAC Name
5-amino-4-oxopentanoic acid hydrochloride
SMILES
Cl.NCC(=O)CCC(O)=O
PubChem Compound
123608
ChemSpider
110200
ChEBI
132969
ChEMBL
CHEMBL1200582
Wikipedia
Aminolevulinic_acid
Predicted Properties
PropertyValueSource
Water Solubility173.0 mg/mLALOGPS
logP-2.8ALOGPS
logP-3.3Chemaxon
logS0.12ALOGPS
pKa (Strongest Acidic)4.05Chemaxon
pKa (Strongest Basic)7.84Chemaxon
Physiological Charge0Chemaxon
Hydrogen Acceptor Count4Chemaxon
Hydrogen Donor Count2Chemaxon
Polar Surface Area80.39 Å2Chemaxon
Rotatable Bond Count4Chemaxon
Refractivity30.45 m3·mol-1Chemaxon
Polarizability12.56 Å3Chemaxon
Number of Rings0Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterNoChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleNoChemaxon