Vallesamine

CAS: 3368-87-4

Ref. 3D-DAA36887

Produktinformation

• Name: Vallesamine
• Synonyme: (+)-Vallesamine, (E)-Vallesamine, 19,20-(E)-Vallesamine, 19E-Vallesamine, 2,5-Ethano-2H-azocino[4,3-b]indole-6-carboxylic acid, 4-ethylidene-1,3,4,5,6,7-hexahydro-6-(hydroxymethyl)-, methyl ester, (2R,4E,5S,6S)-, 2,5-Ethano-2H-azocino[4,3-b]indole-6-carboxylic acid, 4-ethylidene-1,3,4,5,6,7-hexahydro-6-(hydroxymethyl)-, methyl ester, (4E,5S,6R)-, 2,5-Ethano-2H-azocino[4,3-b]indole-6-carboxylic acid,4-ethylidene-1,3,4,5,6,7-hexahydro-6-(hydroxymethyl)-, methyl ester, [5S-(4E,5a,6b)]-, 2,5-Ethano-2H-azocino[4,3-b]indole-6-carboxylicacid, 4-ethylidene-1,3,4,5,6,7-hexahydro-6-(hydroxymethyl)-, methyl ester,(4E,5S,6R)- (9CI), Vallesamine (7CI)

Beschreibung

Vallesamine is a natural product that belongs to the class of indole alkaloids. It was originally isolated from the Apocynaceae plant, Vallesia corymbosa. This drug has shown anti-inflammatory and anti-cancer effects in clinical studies and has been found to have synergistic effects when combined with other drugs. Vallesamine is synthesized from tryptophan by a series of reactions that include oxidation, reduction, and methylation. The final step in the synthesis involves condensation of two molecules of tryptophan to produce vallesamine. The preparation of this drug can be achieved through high-performance liquid chromatography (HPLC) or preparative hplc. The process is complicated due to the number of steps involved, but can be simplified through a cycle analysis approach or an asymmetric synthesis method.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 340.4 g/mol
• Formel: C₂₀H₂₄N₂O₃
• Reinheit: Min. 95%