Picamilon, a γ‐aminobutyric acid (GABA) analogue and marketed nootropic, is inactive against 50 biological targets

Author:

Santillo Michael F.1ORCID,Sprando Robert L.1

Affiliation:

1. Division of Toxicology, Office of Applied Research and Safety Assessment Center for Food Safety and Applied Nutrition, U.S. Food and Drug Administration (FDA) Laurel Maryland USA

Abstract

AbstractPicamilon is an analogue of the neurotransmitter γ‐aminobutyric acid (GABA), which is marketed as a nootropic claiming to enhance cognition. There is a lack of in silico, in vitro and in vivo data on the safety of picamilon. Therefore, to ascertain potential physiological effects of picamilon, it was screened against 50 safety‐related biological targets (receptors, ion channels, enzymes and transporters) by in silico and in vitro methods. Using two in silico tools, picamilon was not predicted to bind to the targets. Similarly, picamilon exhibited weak or no binding to the targets when measured in vitro at 10 μM. Overall, this data shows that picamilon, although structurally similar to other GABA analogues, has a different biological target binding profile. Picamilon's lack of binding to the 50 targets fills important data gaps among GABA analogues, a group of structurally related substances found in drugs and other consumer products.

Funder

U.S. Food and Drug Administration

Publisher

Wiley

Subject

Pharmacology,Toxicology,General Medicine

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