Psoralen: A Biologically Important Coumarin with Emerging Applications
Language English Country Netherlands Media print
Document type Journal Article, Review
PubMed
32348216
DOI
10.2174/1389557520666200429101053
PII: MRMC-EPUB-106216
Knihovny.cz E-resources
- Keywords
- DNA, Psoralens, anti-inflammatory agents, antidiabetic, breast cancer, furocoumarins,
- MeSH
- Analgesics chemistry pharmacology MeSH
- Anti-Infective Agents chemistry pharmacology MeSH
- Antitubercular Agents chemistry pharmacology MeSH
- Ficusin chemistry pharmacology MeSH
- Hypoglycemic Agents chemistry pharmacology MeSH
- Humans MeSH
- Molecular Structure MeSH
- Neuroprotective Agents chemistry pharmacology MeSH
- Antineoplastic Agents chemistry pharmacology MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
- Names of Substances
- Analgesics MeSH
- Anti-Infective Agents MeSH
- Antitubercular Agents MeSH
- Ficusin MeSH
- Hypoglycemic Agents MeSH
- Neuroprotective Agents MeSH
- Antineoplastic Agents MeSH
Coumarin belongs to a class of lactones that are fundamentally comprised of a benzene ring fused to an α-pyrone ring; these lactones are known as benzopyrones. Similarly, coumarin has a conjugated electron-rich framework and good charge-transport properties. Plants produce coumarin as a chemical response to protect themselves from predation. Coumarins are used in different products, such as cosmetics, additives, perfumes, aroma enhancers in various tobaccos and some alcoholic drinks, and they play a relevant role in natural products and in organic and medicinal chemistry. In addition, as candidate drugs, many coumarin compounds have strong pharmacological activity, low toxicity, high bioavailability and better curative effects and have been used to treat various types of diseases. Various endeavors were made to create coumarin-based anticoagulant, antimicrobial, antioxidant, anticancer, antidiabetic, antineurodegenerative, analgesic and anti-inflammatory agents. A class of chemical compounds called furocoumarins has phototoxic properties and is naturally synthesized via the fusion of coumarin to a furan ring in different plant species. Psoralens belong to the furocoumarin class and occur naturally in various plants, e.g., lemons, limes, and parsnips. Angelicin is an isomer of psoralens, and most furocoumarins, e.g., xanthotoxin, bergapten, and nodekenetin, are derivatives of psoralens or angelicin. The present work demonstrated that psoralen molecules exhibit anti-tumoral activity against breast cancer and influence different intracellular signals to maintain the high survival of breast cancer cells. Psoralens perform different functions, e.g., antagonize metabolic pathways, protease enzymes, and cell cycle progression and even interfere in the crosslinking between receptors and growth factor mitogenic signaling.
Department of Chemistry S M D R S D College of Education Pathankot 145001 India
PG Department of Zoology DAV College Jalandhar 144008 Punjab India
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