Vindoline

CAS: 2182-14-1

Ref. 3D-FV10830

Produktinformation

• Name: Vindoline
• Synonyme: (2β,3β,4β,5α,12β,19α)-4-(Acetyloxy)-6,7-didehydro-3-hydroxy-16-methoxy-1 -methyl-aspidospermidine-3-carboxylic acid methyl esterNSC91994(-)-Vindoline, (2beta,3beta,4beta,5alpha,12beta,19alpha)-4-(Acetyloxy)-6,7-didehydro-3-hydroxy-16-methoxy-1-methyl-aspidospermidine-3-carboxylic acid methyl ester, 1H-Indolizino[8,1-cd]carbazole, aspidospermidine-3-carboxylic acid deriv., Aspidospermidine-3-Carboxylicacid,4-(Acetyloxy)-6,7-Didehydro-3-Hydroxy-16-Me, Aspidospermidine-3-carboxylic acid, 4-(acetyloxy)-6,7-didehydro-3-hydroxy-16-methoxy-1-methyl-, methyl ester, (2beta,3beta,4beta,5alpha,12beta,19alpha)-, Aspidospermidine-3-carboxylic acid, 4-(acetyloxy)-6,7-didehydro-3-hydroxy-16-methoxy-1-methyl-, methyl ester, (2β,3β,4β,5α,12R,19α)-, Aspidospermidine-3-carboxylic acid, 4-(acetyloxy)-6,7-didehydro-3-hydroxy-16-methoxy-1-methyl-, methyl ester, (2β,3β,4β,5α,12β,19α)-, Bufexamacum, Methyl (2Beta,3Beta,4Beta,5Alpha,12Beta,19Alpha)-4-(Acetyloxy)-3-Hydroxy-16-Methoxy-1-Methyl-6,7-Didehydroaspidospermidine-3-Carboxylate, Methyl (2Beta,3Beta,4Beta,5Alpha,19Alpha)-4-(Acetyloxy)-3-Hydroxy-16-Methoxy-1-Methyl-6,7-Didehydroaspidospermidine-3-Carboxylate, Methyl (2Beta,3Beta,4Beta,5Xi,12Beta,19Alpha)-4-(Acetyloxy)-3-Hydroxy-16-Methoxy-1-Methyl-6,7-Didehydroaspidospermidine-3-Carboxylate, Methyl (2Beta,4Beta,5Alpha,12Beta,19Alpha)-4-(Acetyloxy)-3-Hydroxy-16-Methoxy-1-Methyl-6,7-Didehydroaspidospermidine-3-Carboxylate, NSC 91994, Thoxy-1-Methyl-,Methylester,(2-Beta,3-Beta,4-Beta,5-Alpha,12-Beta,19-Alpha), Vindolin, Vindoline Tartrate, Vindoline free base

Beschreibung

Vindoline is a monoterpenoid indole alkaloid that is found in plants of the genus Vinca. It has been used to prepare samples for thin-layer chromatography, and can be detected by sephadex g-100. The reaction mechanism of vindoline is thought to be similar to other indole alkaloids, such as tryptamine, where two molecules are combined through a covalent bond between the amine group and the carbonyl group. Vindoline has been shown to inhibit polymerase chain reactions and also has a number of biological properties that could be useful in tissue culture. This natural product structure has been shown to have steric interactions with enzymes, including tyrosinase, which is involved in plant metabolism. Vindoline may also be able to inhibit plant physiology by altering photosynthesis or respiration.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 456.53 g/mol
• Formel: C₂₅H₃₂N₂O₆
• Reinheit: Min. 98 Area-%
• Farbe/Form: White Powder