2810-21-1 - Names and Identifiers
Name | (+)-Stepharine
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Synonyms | Stepharine (+)-Stepharine (8'aR)-2',3',8',8'a-Tetrahydro-5',6'-dimethoxyspiro[2,5-cyclohexadiene-1,7'(1'H)-cyclopent[ij]isoquinolin]-4-one (8'aR)-2',3',8',8'a-Tetrahydro-5',6'-dimethoxyspiro[2,5-cyclohexadiene-1,7'(1'H)-cyclopenta[ij]isoquinoline]-4-one Spiro[2,5-cyclohexadiene-1,7'(1'H)-cyclopent[ij]isoquinolin]-4-one, 2',3',8',8'a-tetrahydro-5',6'-dimethoxy-, (8'aR)-
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CAS | 2810-21-1
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2810-21-1 - Physico-chemical Properties
Molecular Formula | C18H19NO3
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Molar Mass | 297.34836 |
Density | 1.27±0.1 g/cm3(Predicted) |
Melting Point | 179-181 °C |
Boling Point | 487.1±45.0 °C(Predicted) |
pKa | 8.08±0.20(Predicted) |
Storage Condition | 2-8℃ |
2810-21-1 - Introduction
()-Stepharine, also known as ()-Stepharine, is an alkaloid found naturally in the Stephania vine plant (Stephania genus). It is a white or yellowish crystalline powder.
Nature:
( )-Stepharine has a high melting point and thermal stability. It is slightly soluble in water and slightly soluble in alcohol and ether solvents.
Use:
( )-Stepharine is widely used in traditional Chinese medicine, mainly for the treatment of rheumatism and gout. This alkaloid has pharmacological effects such as anti-inflammatory, analgesic, cough suppression and cold-repellent.
Method:
( )-Stepharine can be obtained by extracting from the rhizome of the stephanthus plant. The extraction process usually includes the steps of drying, crushing and solvent extraction.
Safety Information:
In normal dosage, Cephaline is generally considered to be relatively safe. However, excessive use or prolonged use may cause adverse reactions such as nausea, vomiting, diarrhea, and allergic reactions. Therefore, it should be used under the guidance of a doctor or professional and follow the appropriate dosage and method of use. During use, safety precautions should be followed to avoid contact with skin, eyes or inhalation. If there is any discomfort or unclear situation, please consult a doctor in time.
Last Update:2024-04-09 20:48:19