Eichlerianic acid - Names and Identifiers
Name | Eichlerianic acid
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Synonyms | Eichlerianic acid (20S,24S)-20,24-Epoxy-25-hydroxy-3,4-secodammar-4(28)-en-3-oic acid (20S,24S)-20,24-Epoxy-25-hydroxy-3,4-seco-5α-dammar-4(28)-en-3-oic acid 1H-Benz[e]indene-6-propanoic acid, dodecahydro-6,9a,9b-trimethyl-7-(1-methylethenyl)-3-[(2S,5S)-tetrahydro-5-(1-hydroxy-1-methylethyl)-2-methyl-2-furanyl]-, (3S,3aR,5aR,6S,7S,9aR,9bR)-
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CAS | 56421-13-7
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Eichlerianic acid - Physico-chemical Properties
Molecular Formula | C30H50O4
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Molar Mass | 474.72 |
Melting Point | 109-110℃ |
Specific Rotation(α) | +37.6 (c, 0.8 in CHCl3) |
Storage Condition | 2-8℃ |
Eichlerianic acid - Introduction
Eichlerianic acid is a natural product, belonging to the class of caffeic acid derivatives. It is mainly found in certain plants, such as Eichlerianthus sieberi and Pandanus candelabrum.
The chemical structure of Eichlerianic acid includes a benzene ring and a cyclopropane ring, with a carboxylic acid functional group. Its chemical formula is C16H20O6.
Eichlerianic acid has a number of biological activities, including antioxidant and anti-inflammatory properties. It has shown inhibitory effects on bacteria, fungi and tumor cells, which makes it potentially useful in the field of medicine.
The preparation of Eichlerianic acid usually involves extraction from plants, and then the use of chemical separation and purification techniques. The purified Eichlerianic acid can be used in research and drug development.
Regarding safety, there is currently limited safety data on Eichlerianic acid. Therefore, proper laboratory practices and precautions are required when using or handling Eichlerianic acid. Before use or research, it is recommended to consult with relevant institutions or literature, and operate in accordance with the corresponding safety operation procedures.
Last Update:2024-04-09 21:54:55