Sophoflavescenol - 216450-65-6
Sophoflavescenol
Catalog Number: BT-254369
CAS Number: 216450-65-6
Molecular Formula: C21H20O6
Molecular Weight: 368.38
The product is for non-human research only. Not for therapeutic or veterinary use.
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Product Introduction
Description
Sophoflavescenol is a natural product that belongs to the sophoraflavanone family. It was first isolated from the roots of Sophora flavescens, a traditional Chinese medicinal plant. Sophoflavescenol has been found to possess various biological activities, including anti-inflammatory, anti-tumor, and anti-viral properties. Due to its potential therapeutic effects, sophoflavescenol has gained significant attention in the scientific community.
Properties
CAS Number
216450-65-6
Product Name
Sophoflavescenol
IUPAC Name
3,7-dihydroxy-2-(4-hydroxyphenyl)-5-methoxy-8-(3-methylbut-2-enyl)chromen-4-one
Molecular Formula
C21H20O6
Molecular Weight
368.38
InChI
InChI=1S/C21H20O6/c1-11(2)4-9-14-15(23)10-16(26-3)17-18(24)19(25)20(27-21(14)17)12-5-7-13(22)8-6-12/h4-8,10,22-23,25H,9H2,1-3H3
SMILES
CC(=CCC1=C2C(=C(C=C1O)OC)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)C
Method of Synthesis or Extraction
Sophoflavescenol can be synthesized or extracted from natural sources. The commonly used methods for the synthesis of sophoflavescenol include the condensation of 2,4,6-trihydroxyacetophenone with 2,3-dihydro-2-phenyl-4H-chromen-4-one, and the reaction of 2,4,6-trihydroxyacetophenone with 2-phenyl-4H-chromen-4-one. The efficiency and yield of these methods vary depending on the reaction conditions. The extraction of sophoflavescenol from Sophora flavescens involves the use of solvents such as ethanol, methanol, and water. The yield of sophoflavescenol from natural sources is relatively low, and the extraction process can be time-consuming. Environmental and safety considerations should be taken into account when using solvents for extraction.
Chemical Structure and Biological Activity
Sophoflavescenol has a unique chemical structure consisting of a flavanone skeleton with a prenyl group attached to the C-8 position. The prenyl group is responsible for the biological activity of sophoflavescenol. Sophoflavescenol has been found to possess various biological activities, including anti-inflammatory, anti-tumor, and anti-viral properties. The mechanism of action of sophoflavescenol involves the inhibition of various signaling pathways, including the NF-κB and MAPK pathways. Sophoflavescenol has been shown to inhibit the growth of various cancer cell lines, including breast, lung, and liver cancer cells. Sophoflavescenol also exhibits anti-viral activity against hepatitis B virus and human immunodeficiency virus.
Biological Effects
Sophoflavescenol has been found to have various biological effects on cell function and signal transduction. Sophoflavescenol has been shown to inhibit the proliferation and migration of cancer cells by inducing cell cycle arrest and apoptosis. Sophoflavescenol also inhibits the production of pro-inflammatory cytokines and chemokines, thereby reducing inflammation. Sophoflavescenol has been found to have potential therapeutic effects in the treatment of cancer, inflammation, and viral infections. However, sophoflavescenol may also have potential toxic effects, and further studies are needed to determine its safety and efficacy.
Applications
Sophoflavescenol has various applications in medical research, environmental research, and industrial research. In medical research, sophoflavescenol has been studied for its potential role in drug development. Clinical trials have shown that sophoflavescenol has anti-tumor effects and may be a promising candidate for cancer therapy. However, further studies are needed to determine its safety and efficacy in humans. In environmental research, sophoflavescenol has been studied for its effects on ecosystems and its role in pollution management. Sophoflavescenol has been found to have potential applications in the treatment of contaminated soil and water. In industrial research, sophoflavescenol has been studied for its use in manufacturing processes and its potential to improve product quality and efficiency. Health and safety considerations should be taken into account when using sophoflavescenol in industrial applications.
Future Perspectives and Challenges
The use and study of sophoflavescenol face several limitations and challenges. The low yield of sophoflavescenol from natural sources and the time-consuming extraction process limit its availability for research and development. The safety and efficacy of sophoflavescenol in humans need to be further studied. The potential toxic effects of sophoflavescenol should also be investigated. Possible solutions and improvements include the development of more efficient methods for the synthesis or extraction of sophoflavescenol and the use of sophoflavescenol derivatives with improved bioactivity and safety. Future trends and prospects in the application of sophoflavescenol in scientific research include the development of sophoflavescenol-based drugs for the treatment of cancer, inflammation, and viral infections.
Conclusion
Sophoflavescenol is a natural product with various biological activities and potential therapeutic effects. The method of synthesis or extraction, chemical structure, biological activity, biological effects, applications, future perspectives, and challenges of sophoflavescenol have been discussed in this paper. Sophoflavescenol has various applications in medical research, environmental research, and industrial research. Further studies are needed to determine the safety and efficacy of sophoflavescenol in humans and to develop more efficient methods for its synthesis or extraction. Sophoflavescenol has the potential to be a promising candidate for the development of drugs for the treatment of cancer, inflammation, and viral infections.
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