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1P-ETH-LAD: Difference between revisions
>Dextromethorphan |
>Dextromethorphan |
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1P-ETH-LAD's structure contains a bicyclic hexahydroindole fused to a bicyclic quinoline group (nor-lysergic acid). 1P-ETH-LAD does not contain a methyl group substituted at R<sub>6</sub> of its nor-lysgeric acid skeleton, this is represented by the nor- prefix. Instead, 1P-ETH-LAD is substituted at R<sub>6</sub> with an ethyl group and at R<sub>1</sub> with a propionyl group. At carbon 8 of the quinoline a N,N-diethyl carboxamide is bound. | 1P-ETH-LAD's structure contains a bicyclic hexahydroindole fused to a bicyclic quinoline group (nor-lysergic acid). 1P-ETH-LAD does not contain a methyl group substituted at R<sub>6</sub> of its nor-lysgeric acid skeleton, this is represented by the nor- prefix. Instead, 1P-ETH-LAD is substituted at R<sub>6</sub> with an ethyl group and at R<sub>1</sub> with a propionyl group. At carbon 8 of the quinoline a N,N-diethyl carboxamide is bound. | ||
1P-ETH-LAD is a chiral compound with two stereocenters at R<sub>5</sub> and R<sub>8</sub>. | 1P-ETH-LAD is a chiral compound with two stereocenters at R<sub>5</sub> and R<sub>8</sub>. 1P-ETH-LAD, also called (+)-D-1P-ETH-LAD, has an absolute configuration of (5''R'', 8''R''). The three other stereoisomers of 1P-ETH-LAD do not have psychoactive properties.{{citation needed}} | ||
==Pharmacology== | ==Pharmacology== | ||