Información del producto
- Corynoxan-16-carboxylic acid, 16,17-didehydro-17-methoxy-2-oxo-, methyl ester, (16E)-
- Methyl (16E)-16-(methoxymethylene)-2-oxocorynoxan-17-oate
- Spiro[3H-indole-3,1′(5′H)-indolizine]-7′-acetic acid, 6′-ethyl-1,2,2′,3′,6′,7′,8′,8′a-octahydro-α-(methoxymethylene)-2-oxo-, methyl ester, (αE,1′S,6′S,7′S,8′aS)-
- Spiro[3H-indole-3,1′(5′H)-indolizine]-7′-acetic acid, 6′-ethyl-1,2,2′,3′,6′,7′,8′,8′a-octahydro-α-(methoxymethylene)-2-oxo-, methyl ester, [1′S-[1′α,6′β,7′β(E),8′aα]]-
- spiro[3H-indole-3,1'(5'H)-indolizine]-7'-acetic acid, 6'-ethyl-1,2,2',3',6',7',8',8'a-octahydro-alpha-(methoxymethylene)-2-oxo-, methyl ester, (alphaE,3S,6'S,7'S,8'aS)-
Corynoxine is a pentacyclic triterpenoid that was isolated from the roots of Pueraria lobata. It has shown to have a variety of biological activities, such as receptor activity and autophagy induction. Corynoxine is a potent agonist for the human toll-like receptor 2 (TLR2) with an EC50 value of 1.0 µM and inhibits locomotor activity in mice at doses of 20 mg/kg. Corynoxine also has been shown to induce autophagy in rat liver cells by preventing the formation of protein aggregates, which are thought to be involved in Parkinson's disease. The chemical structure includes nitrogen atoms and five carbon rings, which form two hydrogen bonds.
Propiedades químicas
Consulta técnica sobre: 3D-FC74140 Corynoxine
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