Tetrahydroalstonine

CAS: 6474-90-4

Ref. 3D-FT74459

Product Information

• Name: Tetrahydroalstonine
• Synonyms: (3α)-3,4,5,6-Tetrahydroalstonine, 4H-Indolo[2,3-a]pyrano[3,4-g]quinolizine-1-carboxylic acid, 4a,5,7,8,13,13b,14,14a-octahydro-4-methyl-, methyl ester, (4S,4aS,13bS,14aS)-, Alstonine, 3,4,5,6-tetrahydro-, Alstonine, 3,4,5,6-tetrahydro- (8CI), Alstonine, 3,4,5,6-tetrahydro-, (3alpha)-, Alstonine, 3,4,5,6-tetrahydro-, (3α)-, Alstonine, tetrahydro-, Brn 0097270, Methyl (19Alpha,20Alpha)-19-Methyl-16,17-Didehydro-18-Oxayohimban-16-Carboxylate, Methyl (19alpha,20alpha)-16,17-didehydro-19-methyloxayohimban-16-carboxylate, Methyl (3Xi,19Alpha,20Alpha)-19-Methyl-16,17-Didehydro-18-Oxayohimban-16-Carboxylate, Nsc 72115, Oxayohimban-16-carboxylic acid, 16,17-didehydro-19-methyl-, methyl ester, (19-alpha,20-alpha)-, Oxayohimban-16-carboxylic acid, 16,17-didehydro-19-methyl-, methyl ester, (19α,20α)-

Description

Tetrahydroalstonine is a monoterpenoid indole alkaloid that has been shown to have an effect on blood disorders. Tetrahydroalstonine is found in the plant families of Ranunculaceae and Papaveraceae, which includes plants such as the poppy and the buttercup. This compound inhibits the activity of enzymes such as fatty acid synthase and enoyl reductase, which are involved in fatty acid synthesis. Tetrahydroalstonine also has a chemical diversity that allows it to inhibit a number of enzymes associated with human diseases. The chemical structure of tetrahydroalstonine also contains a hydrogen bond that can be used in drug design or to control analysis for symptoms and ph optimum.

• Brand: Biosynth

Chemical properties

• Purity: Min. 95%