CAS 1165-40-8
:Andrographin
Description:
Andrographin, with the CAS number 1165-40-8, is a bioactive compound primarily derived from the plant Andrographis paniculata, commonly known as the "king of bitters." This compound is a diterpenoid lactone and is known for its various pharmacological properties, including anti-inflammatory, antioxidant, and antimicrobial activities. Andrographin is often studied for its potential therapeutic effects in treating conditions such as respiratory infections, liver disorders, and certain types of cancer. The substance exhibits a bitter taste, which is characteristic of many compounds derived from medicinal plants. Its mechanism of action is believed to involve modulation of immune responses and inhibition of pro-inflammatory cytokines. Additionally, andrographin has been explored for its role in enhancing the bioavailability of other therapeutic agents. Due to its diverse biological activities, it has garnered interest in both traditional medicine and modern pharmacology, although further research is necessary to fully elucidate its mechanisms and potential clinical applications.
Formula:C18H16O6
InChI:InChI=1S/C18H16O6/c1-21-13-7-5-4-6-10(13)14-8-11(19)16-12(20)9-15(22-2)17(23-3)18(16)24-14/h4-9,20H,1-3H3
InChI key:InChIKey=AJMNTEFGXPRZHG-UHFFFAOYSA-N
SMILES:O(C)C1=C2C(C(=O)C=C(O2)C3=C(OC)C=CC=C3)=C(O)C=C1OC
Synonyms:- 2'-O-Methylskullcapflavone I
- 5-Hydroxy-2',7,8-trimethoxyflavone
- 5-Hydroxy-2′,7,8-trimethoxyflavone
- 5-Hydroxy-7,8-dimethoxy-2-(2-methoxyphenyl)-4H-1-benzopyran-4-one
- Andrographin
- Flavone, 5-hydroxy-2′,7,8-trimethoxy-
- Flavone,5-hydroxy-2',7,8-trimethoxy- (7CI,8CI)
- Skullcapflavone I 2'-methylether
- Skullcapflavone I 2′-methyl ether
- 4H-1-Benzopyran-4-one, 5-hydroxy-7,8-dimethoxy-2-(2-methoxyphenyl)-
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Found 1 products.
5-Hydroxy-7,8,2'-trimethoxyflavone
CAS:<p>5-Hydroxy-7,8,2'-trimethoxyflavone is a flavonoid compound, which is a type of polyphenolic molecule. Flavonoids are primarily derived from plants, where they function in various biological roles, including pigmentation, UV filtration, and symbiotic nitrogen fixation. The source of 5-Hydroxy-7,8,2'-trimethoxyflavone is often plants, particularly those known for their medicinal properties.</p>Formula:C18H16O6Purity:Min. 95%Color and Shape:PowderMolecular weight:328.32 g/mol
