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- 3-Hydroxy-16-methoxy-2,3-dihydrotabersonine is a terpene indole alkaloid produced by Catharanthus roseus. The metabolite is a substrate for 3-hydroxy-16-methoxy-2,3-dihydrotabersonine N-methyltransferase (NMT) which transfers a methyl group to the nitrogen of the indole ring forming desacetoxyvindoline. The enzyme catalyzing the formation of 3-hydroxy-16-methoxy-2,3-dihydrotabersonine from 16-methoxytabersonine is currently unknown, but is a result of hydration of the double bond connecting the 6 and 13 position carbons. (en)
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| dbo:iupacName
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- Methyl (2β,3β,5α,12β,19α)-3-hydroxy-16-methoxy-6,7-didehydroaspidospermidine-3-carboxylate (en)
- Methyl (3aR,3a1S,5R,5aR,10bS)-3a-ethyl-5-hydroxy-8-methoxy-3a,3a1,4,5,5a,6,11,12-octahydro-1H-indolizino[8,1-cd]carbazole-5-carboxylate (en)
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- 2658 (xsd:nonNegativeInteger)
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- File:3-Hydroxy-16-methoxy-2,3-dihydrotabersonine.svg (en)
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- Methyl -3-hydroxy-16-methoxy-6,7-didehydroaspidospermidine-3-carboxylate (en)
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- Methyl -3a-ethyl-5-hydroxy-8-methoxy-3a,3a1,4,5,5a,6,11,12-octahydro-1H-indolizino[8,1-cd]carbazole-5-carboxylate (en)
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| rdfs:comment
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- 3-Hydroxy-16-methoxy-2,3-dihydrotabersonine is a terpene indole alkaloid produced by Catharanthus roseus. The metabolite is a substrate for 3-hydroxy-16-methoxy-2,3-dihydrotabersonine N-methyltransferase (NMT) which transfers a methyl group to the nitrogen of the indole ring forming desacetoxyvindoline. The enzyme catalyzing the formation of 3-hydroxy-16-methoxy-2,3-dihydrotabersonine from 16-methoxytabersonine is currently unknown, but is a result of hydration of the double bond connecting the 6 and 13 position carbons. (en)
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- 3-Hydroxy-16-methoxy-2,3-dihydrotabersonine (en)
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