Abstract
This study presents a novel approach for the regioselective synthesis of a series of alkyl ether analogues of purpurin-18-N-alkylimide. In the purpurinimide series, this is the first example which demonstrates that the presence and position of the substituents in the macrocycle makes a remarkable difference in the in vivo PDT efficacy.
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Antineoplastic Agents / chemistry*
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Antineoplastic Agents / pharmacokinetics
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Antineoplastic Agents / therapeutic use
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Cyanobacteria / chemistry
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Drug Design
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Drug Screening Assays, Antitumor
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Magnetic Resonance Spectroscopy
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Mice
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Molecular Structure
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Neoplasm Transplantation
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Neoplasms, Experimental / drug therapy*
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Neoplasms, Experimental / metabolism
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Photochemotherapy*
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Photosensitizing Agents / chemistry*
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Photosensitizing Agents / pharmacokinetics
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Photosensitizing Agents / therapeutic use*
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Porphyrins / chemical synthesis*
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Structure-Activity Relationship
Substances
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Antineoplastic Agents
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Photosensitizing Agents
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Porphyrins