4H-1-Benzopyran-4-one, 2,3-dihydro-3,5,7-trihydroxy-8-(3-methyl-2-buten-1-yl)-2-phenyl-, (2R,3R)-
Glepidotin B
CAS: 87440-56-0
Molecular Formula: C20H20O5
4H-1-Benzopyran-4-one, 2,3-dihydro-3,5,7-trihydroxy-8-(3-methyl-2-buten-1-yl)-2-phenyl-, (2R,3R)- - Names and Identifiers
4H-1-Benzopyran-4-one, 2,3-dihydro-3,5,7-trihydroxy-8-(3-methyl-2-buten-1-yl)-2-phenyl-, (2R,3R)- - Physico-chemical Properties
| Molecular Formula | C20H20O5 |
| Molar Mass | 340.37 |
| Density | 1.321±0.06 g/cm3(Predicted) |
| Melting Point | 172-173℃ |
| Boling Point | 592.5±50.0 °C(Predicted) |
| Solubility | Methanol; Chloroform |
| pKa | 7.53±0.60(Predicted) |
| Storage Condition | 2-8℃ |
4H-1-Benzopyran-4-one, 2,3-dihydro-3,5,7-trihydroxy-8-(3-methyl-2-buten-1-yl)-2-phenyl-, (2R,3R)- - Introduction
Glepidotin B (Glepidotin B) is a natural organic compound that belongs to the class of flavonoids. It can be extracted from the broad-leaved Southern Aegilops (Glebionis scaposa) plant.
The chemical structure of Glepidotin B contains an aromatic ring and multiple hydroxyl functional groups. It has anti-inflammatory, antioxidant and antibacterial activities, so it has certain application potential in the field of medicine.
At present, the main use of Glepidotin B is as a natural medicine or food additive for research and development. It is considered to have potential therapeutic effects in the field of medicine and can be used in the treatment of inflammatory diseases, such as rheumatoid arthritis and inflammatory bowel disease.
regarding the preparation method, the extraction of Glepidotin B is mainly obtained by alcohol extraction, separation and purification of the broad-leaved Southern Ao chrysanthemum plant. The specific extraction method may vary depending on the experimental conditions and the purpose of the study.
In terms of safety, there are relatively few studies on Glepidotin B, and its clinical application is also limited. Therefore, its safety and toxicity are not fully understood. When using or studying Glepidotin B, the relevant specifications and safety guidelines for chemical laboratory operations should be followed to ensure the safety of the operator. In addition, in any use other than the experimental use, the impact on human health should be carefully evaluated and the corresponding regulations and guidance should be followed. If necessary, please use it under the guidance of professionals.
The chemical structure of Glepidotin B contains an aromatic ring and multiple hydroxyl functional groups. It has anti-inflammatory, antioxidant and antibacterial activities, so it has certain application potential in the field of medicine.
At present, the main use of Glepidotin B is as a natural medicine or food additive for research and development. It is considered to have potential therapeutic effects in the field of medicine and can be used in the treatment of inflammatory diseases, such as rheumatoid arthritis and inflammatory bowel disease.
regarding the preparation method, the extraction of Glepidotin B is mainly obtained by alcohol extraction, separation and purification of the broad-leaved Southern Ao chrysanthemum plant. The specific extraction method may vary depending on the experimental conditions and the purpose of the study.
In terms of safety, there are relatively few studies on Glepidotin B, and its clinical application is also limited. Therefore, its safety and toxicity are not fully understood. When using or studying Glepidotin B, the relevant specifications and safety guidelines for chemical laboratory operations should be followed to ensure the safety of the operator. In addition, in any use other than the experimental use, the impact on human health should be carefully evaluated and the corresponding regulations and guidance should be followed. If necessary, please use it under the guidance of professionals.
Last Update：2024-04-09 21:49:45
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Product Name: Glepidotin B Visit Supplier Webpage Request for quotation
CAS: 87440-56-0
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
CAS: 87440-56-0
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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