CAS 74560-05-7
:Isomedicarpin
Description:
Isomedicarpin, with the CAS number 74560-05-7, is a flavonoid compound that belongs to the class of natural products known as flavonoids, which are widely distributed in the plant kingdom. This compound is characterized by its polyphenolic structure, which typically includes multiple hydroxyl groups that contribute to its antioxidant properties. Isomedicarpin is often studied for its potential health benefits, including anti-inflammatory, antimicrobial, and anticancer activities. It is commonly found in various plant species, particularly in legumes and some medicinal herbs. The compound's solubility and stability can vary depending on the pH and the presence of other substances, which can influence its bioavailability and efficacy in biological systems. Research into isomedicarpin continues to explore its mechanisms of action and potential therapeutic applications, making it a subject of interest in both pharmacology and nutrition.
Formula:C16H14O4
InChI:InChI=1S/C16H14O4/c1-18-10-3-5-12-14(7-10)19-8-13-11-4-2-9(17)6-15(11)20-16(12)13/h2-7,13,16-17H,8H2,1H3/t13-,16-/m0/s1
InChI key:InChIKey=YHZDBBUEVZEOIY-BBRMVZONSA-N
SMILES:O(C)C=1C=C2C([C@]3([C@](C=4C(O3)=CC(O)=CC4)(CO2)[H])[H])=CC1
Synonyms:- (-)-8-Hydroxy-3-methoxypterocarpan
- (6aR,11aR)-6a,11a-Dihydro-3-methoxy-6H-benzofuro[3,2-c][1]benzopyran-9-ol
- 3-Methoxy-9-hydroxypterocarpan
- 6H-Benzofuro[3,2-c][1]benzopyran-9-ol,6a,11a-dihydro-3-methoxy-, (6aR-cis)-
- Isomedicarpin
- 6H-Benzofuro[3,2-c][1]benzopyran-9-ol, 6a,11a-dihydro-3-methoxy-, (6aR,11aR)-
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.
Isomedicarpin
CAS:<p>Isomedicarpin is a phytoalexin.</p>Formula:C16H14O4Purity:98%Color and Shape:SolidMolecular weight:270.28Isomedicarpin
CAS:<p>Isomedicarpin is a flavonoid compound, which is naturally derived from plant sources. It is isolated predominantly from certain species within the Leguminosae family, where these compounds often play a role in the plant's defense mechanisms. The mode of action of isomedicarpin involves disrupting microbial cell membranes and interfering with essential biochemical pathways, which contributes to its antimicrobial efficacy.</p>Formula:C16H14O4Purity:Min. 95%Molecular weight:270.28 g/mol



