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Psoralen Derivatives: Recent Advances of Synthetic Strategy and Pharmacological Properties
- Source :
- Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry
- Publication Year :
- 2020
- Publisher :
- Bentham Science Publishers Ltd., 2020.
-
Abstract
- Psoralen or furocoumarin is a linear three ring heterocyclic compound. Psoralens are planar, tricyclic compounds, consisting of a furan ring fused to a coumarin moiety. Psoralen has been known for a wide spectrum of biological activities, spanning from cytotoxic, photosensitizing, insecticidal, antibacterial to antifungal effect. Thus, several structural changes were introduced to explore the role of specific positions with respect to the biological activity. Convenient approaches utilized for the synthesis of psoralen skeleton can be categorized into two parts: (i) the preparation of the tricyclic ring system from resorcinol, (ii) the exocyclic modification of the intact ring system. Furthermore, although psoralens have been used in diverse ways, we mainly focus in this work on their clinical utility for the treatment of psioraisis, vitiligo and skin-related disorder.
- Subjects :
- Immunology
Biological Availability
chemotherapeutic agents
Ring (chemistry)
Skin Diseases
01 natural sciences
Article
chemistry.chemical_compound
Furocoumarins
Furan
Humans
Immunology and Allergy
Moiety
heterocyclic compounds
furan ring
Psoralen
heterocyclic compound
psoralen derivatives
Pharmacology
chemistry.chemical_classification
Photosensitizing Agents
Plants, Medicinal
010405 organic chemistry
Biological activity
Furocoumarin
Ficusin
General Medicine
Coumarin
Combinatorial chemistry
0104 chemical sciences
010404 medicinal & biomolecular chemistry
chemistry
Heterocyclic compound
Dermatologic Agents
pharmacological properties
Tricyclic
Subjects
Details
- ISSN :
- 18715230
- Volume :
- 19
- Database :
- OpenAIRE
- Journal :
- Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry
- Accession number :
- edsair.doi.dedup.....3cee66500ac14694439064f0c7b764e7
- Full Text :
- https://doi.org/10.2174/1871523018666190625170802