1,11B-DIHYDRO-11B-HYDROXYMEDICAR - Names and Identifiers
Name | 1,11b-Dihydro-11b-hydroxymedicarpin
|
Synonyms | 1,11B-DIHYDRO-11B-HYDROXYMEDICAR 1,11b-Dihydro-11b-hydroxyMedicarpin 1,11b-Dihydro-11b-hydroxymedicarpin (6aR,11aR,11bS)-1,2,6,6a,11a,11b-Hexahydro-11b-hydroxy-9-methoxy-3H-benzofuro[3,2-c][1]benzopyran-3-one 3H-Benzofuro[3,2-c][1]benzopyran-3-one, 1,2,6,6a,11a,11b-hexahydro-11b-hydroxy-9-methoxy-, (6aR,11aR,11bS)-
|
CAS | 210537-04-5
|
1,11B-DIHYDRO-11B-HYDROXYMEDICAR - Physico-chemical Properties
Molecular Formula | C16H16O5
|
Molar Mass | 288.3 |
Density | 1.40±0.1 g/cm3(Predicted) |
Boling Point | 490.0±45.0 °C(Predicted) |
pKa | 13.53±0.20(Predicted) |
Storage Condition | 2-8℃ |
1,11B-DIHYDRO-11B-HYDROXYMEDICAR - Introduction
1,11b-dihydro-11b-hydroxycarbapine (1,11b-dihydro-11b-hydroxycarbapine) is a compound which is an isoflavone-like natural product isolated from the legume Medicago spp.
The nature of this compound is a solid with a molecular formula of C16H14O4 and a molecular weight of 270.28g/mol. Its appearance is usually white crystalline. 1. It is an optically active compound with optical rotation, and its optical rotation degree can be between positive and negative optical rotation.
In Terms of Use, 1, it has a certain potential application value in pharmaceutical research. It has been found to have anti-cancer activity, in particular a significant inhibitory effect on breast cancer cells. In addition, it also shows certain anti-inflammatory and antioxidant properties, and has the potential to treat diseases related to inflammation and oxidative stress.
Regarding the preparation method of 1, a common method is to extract and isolate from Medicago spp. Plants. This typically involves grinding the plant material into a powder and extracting it using a solvent such as ethanol or ether. Next, purification and separation are carried out using a chromatographic technique and a crystallization method, and the target compound is finally obtained.
Regarding safety information, the safety evaluation of 1, 2 is not complete at present. Because it is a natural product, it is generally considered to be relatively safe. However, more toxicological and safety studies are still needed in the course of use and research, especially for long-term and high-dose use. In addition, for individuals who have allergic reactions, allergic reactions may result. Before using the compound, safety evaluation and corresponding laboratory operation should be carried out.
Last Update:2024-04-09 21:54:55