(7β,8β,10β)-3,4,7,8-Tetramethoxy-17-methyl-8,10-epoxyhasubanan-6-one - Names and Identifiers
Name | Epistephamiersine
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Synonyms | Epistephamiersine 8β,10β-Epoxy-3,4,7β,8-tetramethoxy-17-methylhasubanan-6-one (7S)-8β,10β-Epoxy-3,4,7,8-tetramethoxy-17-methylhasubanan-6-one (7β,8β,10β)-3,4,7,8-Tetramethoxy-17-methyl-8,10-epoxyhasubanan-6-one
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CAS | 52389-15-8
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(7β,8β,10β)-3,4,7,8-Tetramethoxy-17-methyl-8,10-epoxyhasubanan-6-one - Physico-chemical Properties
Molecular Formula | C21H27NO6
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Molar Mass | 389.45 |
Density | 1.31±0.1 g/cm3(Predicted) |
Melting Point | 98℃ |
Boling Point | 532.7±50.0 °C(Predicted) |
Specific Rotation(α) | +64.1 (c, 1.12 in CHCl3) |
pKa | 6?+-.0.60(Predicted) |
Storage Condition | 2-8℃ |
(7β,8β,10β)-3,4,7,8-Tetramethoxy-17-methyl-8,10-epoxyhasubanan-6-one - Introduction
Epistephamiersine(Epistephamiersine) is a natural compound that belongs to the group of alkaloid compounds. It is mainly found in this plant, the epiphytanus (epistepanus sieberi). The following is a description of the nature, use, formulation and safety information of Epistephamiersine:
Nature:
- Epistephamiersine is a colorless crystalline solid with the chemical formula C20H28N2O2.
-It has a special alkaloid skeleton, containing pyrrole ring and piperazine ring.
The solubility of-Epistephamiersine is relatively low, almost insoluble in water, but soluble in organic solvents such as ethanol, chloroform and dimethyl sulfoxide.
Use:
- Epistephamiersine has some potential in the field of pharmacy. Studies have shown that it may have anti-inflammatory, antibacterial, antioxidant and anti-tumor activities.
-At present, although there is no clinical application of Epistephamiersine, scientists are working hard to study its potential pharmacological activity in order to find applications that are beneficial to human health.
Method:
-The preparation method of Epistephamiersine is more complicated, and it usually needs to be extracted from the plant of table Qijinteng.
-The extraction method includes the steps of extraction using an organic solvent, chromatographic separation, and crystallization purification.
-Due to the low content of Epistephamiersine and the cumbersome preparation process, its preparation is relatively difficult.
Safety Information:
-There is a lack of adequate research on the safety and toxicity of Epistephamiersine.
-When using or studying Epistephamiersine, you need to follow the corresponding safety operating procedures.
-Further toxicity and safety studies need to be conducted to ensure its proper use in pharmacy and other fields.
Please note that the above information is for reference only. If more detailed and accurate information is required, it is recommended to consult relevant scientific literature and pharmaceutical materials.
Last Update:2024-04-10 22:29:15