Methyl Aminolevulinate Hydrochloride
A hydrochloride form of methyl aminolevulinate with the same therapeutic properties. A photosensitizer for photodynamic therapy of actinic keratoses.
Moleküler Ağırlık
181,6200 g/mol
TPSA
69,40 Ų
Terapötik Alanlar
Etki Mekanizması
Accumulates in target tissues and generates reactive oxygen species upon activation by specific wavelengths of light, causing localized cellular damage and destruction of pathological tissue.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Accumulates in target tissues and generates reactive oxygen species upon activation by specific wavelengths of light, causing localized cellular damage and destruction of pathological tissue.
2D Yapı
Cite this structure
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SMILES
COC(=O)CCC(=O)CN.Cl
InChI
InChI=1S/C6H11NO3.ClH/c1-10-6(9)3-2-5(8)4-7;/h2-4,7H2,1H3;1H
Molecular Formula
C6H12ClNO3
HBD / HBA
2 / 4
Döndürülebilir Bağlar
5
Ağır Atomlar
11
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Sıkça Sorulan Sorular
A hydrochloride form of methyl aminolevulinate with the same therapeutic properties. A photosensitizer for photodynamic therapy of actinic keratoses.
Accumulates in target tissues and generates reactive oxygen species upon activation by specific wavelengths of light, causing localized cellular damage and destruction of pathological tissue.
Yes, Methyl Aminolevulinate Hydrochloride is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1201093. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 157921. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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