Hexaminolevulinate Hydrochloride
This is the hydrochloride salt form of hexaminolevulinate, a photosensitizing diagnostic agent used to enhance the detection of bladder cancer during fluorescence cystoscopy. Cancer cells absorb and metabolize it more actively than normal cells, making them fluoresce under special blue light. The hydrochloride salt form ensures solubility for bladder instillation.
Masse moléculaire
251,7500 g/mol
TPSA
69,40 Ų
Aires thérapeutiques
Mécanisme d'action
Functions as a diagnostic agent by providing contrast enhancement or radioactive tracer activity that enables visualization of anatomical structures or physiological processes during medical imaging.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Functions as a diagnostic agent by providing contrast enhancement or radioactive tracer activity that enables visualization of anatomical structures or physiological processes during medical imaging.
Structure 2D
Cite this structure
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SMILES
CCCCCCOC(=O)CCC(=O)CN.Cl
InChI
InChI=1S/C11H21NO3.ClH/c1-2-3-4-5-8-15-11(14)7-6-10(13)9-12;/h2-9,12H2,1H3;1H
Molecular Formula
C11H22ClNO3
HBD / HBA
2 / 4
Liaisons Rotatives
10
Atomes Lourds
16
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.
Foire aux questions
This is the hydrochloride salt form of hexaminolevulinate, a photosensitizing diagnostic agent used to enhance the detection of bladder cancer during fluorescence cystoscopy. Cancer cells absorb and metabolize it more actively than normal cells, making them fluoresce under special blue light. The hydrochloride salt form ensures solubility for bladder instillation.
Functions as a diagnostic agent by providing contrast enhancement or radioactive tracer activity that enables visualization of anatomical structures or physiological processes during medical imaging.
Yes, Hexaminolevulinate 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). CHEMBL1201785. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 6433082. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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