6H-Benzofuro[3,2-c][1]benzopyran-3,9-diol, 6a,11a-dihydro-2,10-bis(3-methyl-2-buten-1-yl)-, (6aR,11aR)- - Names and Identifiers
Name | Erythrabyssin II
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Synonyms | Erythrabyssin II (6aR,11aR)-6a,11a-Dihydro-2,10-bis(3-methyl-2-buten-1-yl)-6H-benzofuro[3,2-c][1]benzopyran-3,9-diol 6H-Benzofuro[3,2-c][1]benzopyran-3,9-diol, 6a,11a-dihydro-2,10-bis(3-methyl-2-buten-1-yl)-, (6aR,11aR)-
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CAS | 77263-06-0
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6H-Benzofuro[3,2-c][1]benzopyran-3,9-diol, 6a,11a-dihydro-2,10-bis(3-methyl-2-buten-1-yl)-, (6aR,11aR)- - Physico-chemical Properties
Molecular Formula | C25H28O4
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Molar Mass | 392.49 |
Solubility | Methanol; Ether |
Storage Condition | 2-8℃ |
6H-Benzofuro[3,2-c][1]benzopyran-3,9-diol, 6a,11a-dihydro-2,10-bis(3-methyl-2-buten-1-yl)-, (6aR,11aR)- - Introduction
Erythrabyssin II is a natural product that belongs to the class of flavonoids. It is obtained from safflower chamomile (Erythrina abyssinica).
Regarding properties, Erythrabyssin II is a colorless to light yellow crystalline powder. It is slightly soluble in solvents, but less soluble in water. In addition, it has a certain degree of stability, relatively stable at room temperature, and also stable under acidic conditions.
Erythrabyssin II has potential application value in medicine, with anti-inflammatory, antioxidant and anti-tumor activities. It is used as one of the candidates for anti-tumor drugs because it has shown in experiments the potential to have cytotoxic effects on a variety of tumor cells.
The method of preparing Erythrabyssin II is relatively complicated, and usually requires multiple steps of synthesis or extraction from natural materials. Specific preparation methods may involve chemical synthesis, separation or purification techniques, etc.
As for safety information, studies on the toxicity and side effects of Erythrabyssin II are limited, so its safety has not been fully established. In the process of use, it is necessary to follow the safety operation procedures of the laboratory. A thorough toxicity assessment and safety testing is recommended prior to any health-related studies. During use, care should be taken to avoid contact with skin and eyes, as well as to avoid inhalation or ingestion. In case of any accident, seek medical assistance immediately.
Last Update:2024-04-09 22:09:11