Informations sur le produit
- Ginkgolide A, 3-deoxy-1,7-dihydroxy-, (1α,7β)-
- 5H-Dicyclopenta[b,c]furan-3,5a(6H)-diacetic acid, 6-tert-butyl-3a-carboxyhexahydro-α5a,1,2,5,7,8-hexahydroxy-α3-methyl-, tri-γ-lactone
- 9H-1,7a-(Epoxymethano)-1H,6aH-cyclopenta[c]furo[2,3-b]furo[3′,2′:3,4]cyclopenta[1,2-d]furan-5,9,12(4H)-trione, 3-tert-butylhexahydro-2,4,11-trihydroxy-8-methyl-
- 9H-1,7a-(Epoxymethano)-1H,6aH-cyclopenta[c]furo[2,3-b]furo[3′,2′:3,4]cyclopenta[1,2-d]furan-5,9,12(4H)-trione, 3-(1,1-dimethylethyl)hexahydro-2,4,11-trihydroxy-8-methyl-, (1S,2R,3S,3aS,4R,6aR,7aR,7bR,8S,10aS,11R,11aS)-
- (1S,2R,3S,3aS,4R,6aR,7aR,7bR,8S,10aS,11R,11aS)-3-(1,1-Dimethylethyl)hexahydro-2,4,11-trihydroxy-8-methyl-9H-1,7a-(epoxymethano)-1H,6aH-cyclopenta[c]furo[2,3-b]furo[3′,2′:3,4]cyclopenta[1,2-d]furan-5,9,12(4H)-trione
Ginkgolide M is a terpene that has been shown to have drug transporter activity. It inhibits the efflux of drugs from cells by competing with them for the protein-mediated transport, leading to an increase in intracellular concentrations of drugs. Ginkgolide M also protects against mitochondrial membrane potential loss and intracellular calcium overload. The synergistic effect of Ginkgolide M with other agents is due to its inhibition of ATPase, p-glycoprotein substrates, ryanodine receptor and urea nitrogen. Ginkgolide M has been shown to exhibit biological activity in natural compounds, hydrogen bond formation and acetylcholine release studies.
Propriétés chimiques
Question d’ordre technique sur : 3D-FG44844 Ginkgolide M
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