Controlled substance analgesic amides and amines

DescriptionAmine dendrons can be covalently attached through conjugation to carboxyl groups, primary amines, or sulfhydryl groups. Amines can also attach to oxidized carbohydrate groups (usually aldehydes) by reductive amination.

DescriptionAmine dendrons can be covalently attached through conjugation to carboxyl groups, primary amines, or sulfhydryl groups. Amines can also attach to oxidized carbohydrate groups (usually aldehydes) by reductive amination.

Descriptioncalculated mol. wt. 950Amine dendrons can be covalently attached through conjugation to carboxyl groups, primary amines, or sulfhydryl groups. Amines can also attach to oxidized carbohydrate groups (usually aldehydes) by reductive

The ethanolamine-amide analog of PGE1.

The ethanolamine-amide analog of PGE1.

The ethanolamine-amide analog of PGE1.

Prostaglandin E|1|ethanolamide (PGE|1|-EA) is the ethanolamine-amide analog of PGE|1|. The conversion of the ethanolamide of arachidonic acid (AEA) to PGE|2|-EA has been determined in vitro.

Prostaglandin E|1|ethanolamide (PGE|1|-EA) is the ethanolamine-amide analog of PGE|1|. The conversion of the ethanolamide of arachidonic acid (AEA) to PGE|2|-EA has been determined in vitro.

PYRIDINE-2-CARBOXYLIC ACID (2-BENZOYL-5-METHYL-PHENYL)-AMIDE-

Pyrrolidine-1-carboxylic acid amide.

Application Organocatalyst for the first enatioselective organocatalytic reductive amination reaction.

A CB analog with a methyl group in the (R) configuration at C-2 of the ethanolamine group is not a FAAH inhibitor and is nearly as susceptible to amide hydrolysis as AEA itself.