313652-75-4Relevant academic research and scientific papers
Structure-activity relationships of pregabalin and analogues that target the α2-δ protein
Belliotti, Thomas R.,Capiris, Thomas,Ekhato, I. Victor,Kinsora, Jack J.,Field, Mark J.,Heffner, Thomas G.,Meltzer, Leonard T.,Schwarz, Jacob B.,Taylor, Charles P.,Thorpe, Andrew J.,Vartanian, Mark G.,Wise, Lawrence D.,Zhi-Su, Ti,Weber, Mark L.,Wustrow, David J.
, p. 2294 - 2307 (2007/10/03)
Pregabalin exhibits robust activity in preclinical assays indicative of potential antiepileptic, anxiolytic, and antihyperalgesic clinical efficacy. It binds with high affinity to the α2-δ subunit of voltage-gated calcium channels and is a substrate of the system L neutral amino acid transporter. A series of pregabalin analogues were prepared and evaluated for their α2-δ binding affinity as demonstrated by their ability to inhibit binding of [3H]gabapentin to pig brain membranes and for their potency to inhibit the uptake of [3H]leucine into CHO cells, a measure of their ability to compete with the endogenous substrate at the system L transporter. Compounds were also assessed in vivo for their ability to promote anxiolytic, analgesic, and anticonvulsant actions. These studies suggest that distinct structure activity relationships exist for α2-δ binding and system L transport inhibition. However, both interactions appear to play an important role in the in vivo profile of these compounds.
