Saponarin
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Saponarin
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CAS No:
20310-89-8
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Formula:
C27H30O15
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Chemical Name:
Saponarin
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Synonyms:
4H-1-Benzopyran-4-one,6-β-D-glucopyranosyl-7-(β-D-glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-;Saponarin;6-β-D-Glucopyranosyl-7-(β-D-glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one;Isovitexin 7-β-D-glucopyranoside;Petrocomoside;6-C-Glucosyl-7-O-glucosylapigenin;Isovitexin 7-glucoside;7-O-Glucosylisovitexin;Isovitexin 7-β-D-glucoside;Apigenin 6-C-glucosyl-7-O-glucoside;Apigenin-6-C-glucoside-7-O-glucoside;98601-05-9;1329-51-7;11018-95-4;21753-79-7;61383-36-6;66982-79-4
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CAS No:
Description
Saponarin is a natural flavonoid isolated from Gypsophila trichotoma, with antioxidant, anti-inflammatory and hepatoprotective activities. Saponarin activates AMPK in a calcium-dependent manner, thus regulating gluconeogenesis and glucose uptake[1][2][3].
7-O-(beta-D-glucosyl)isovitexin is a C-glycosyl compound that is isovitexin in which the hydroxyl hydrogen at position 7 is replaced by a beta-D-glucosyl residue. It has a role as a metabolite. It is a C-glycosyl compound, a dihydroxyflavone, a glycosyloxyflavone and a monosaccharide derivative. It derives from an isovitexin.
Computed Properties
Molecular Weight:594.5
XLogP3:-1.6
Hydrogen Bond Donor Count:10
Hydrogen Bond Acceptor Count:15
Rotatable Bond Count:6
Exact Mass:594.15847025
Monoisotopic Mass:594.15847025
Topological Polar Surface Area:256
Heavy Atom Count:42
Complexity:971
Defined Atom Stereocenter Count:10
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Drug Function and Efficacy
Antioxidant, anti-inflammatory, liver protective effects; activates AMPK in a calcium-dependent manner to regulate gluconeogenesis and glucose uptake
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