Padeliporfin Potassium
A potassium salt of padeliporfin (WST11), a photosensitizer used in vascular-targeted photodynamic therapy for localized low-risk prostate cancer. When activated by near-infrared laser light, it generates reactive oxygen species that destroy tumor-associated blood vessels.
Molekularmasse
916,4000 g/mol
TPSA
240,00 Ų
Wirkmechanismus
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.
SMILES
CC[C@@H]1[C@H](C2=CC\3=NC(=C(/C3=C(\C)/[O-])C)C=C4[C@H]([C@@H](C(=N4)C(=C5C(=C(C(=N5)C=C1N2)C)C(=NCCS(=O)(=O)[O-])[O-])CC(=O)OC)CCC(=O)[O-])C)C.[K+].[K+].[Pd+2]
InChI
InChI=1S/C37H45N5O9S.2K.Pd/c1-8-22-17(2)25-16-30-33(21(6)43)19(4)27(40-30)14-26-18(3)23(9-10-31(44)45)35(41-26)24(13-32(46)51-7)36-34(37(47)38-11-12-52(48,49)50)20(5)28(42-36)15-29(22)39-25;;;/h14-18,22-23,39,43H,8-13H2,1-7H3,(H,38,47)(H,44,45)(H,48,49,50);;;/q;2*+1;+2/p-4/b25-16?,26-14?,29-15?,33-21-,36-24?;;;/t17-,18+,22-,23+;;;/m1.../s1
Molecular Formula
C37H41K2N5O9PdS
HBD / HBA
1 / 14
Rotierbare Bindungen
9
Schwere Atome
55
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.
Häufig gestellte Fragen
A potassium salt of padeliporfin (WST11), a photosensitizer used in vascular-targeted photodynamic therapy for localized low-risk prostate cancer. When activated by near-infrared laser light, it generates reactive oxygen species that destroy tumor-associated blood vessels.
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, Padeliporfin Potassium 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). CHEMBL4594285. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 135391044. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
Medizinischer Haftungsausschluss
This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.
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