Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Novel imidazole frameworks have been identified as potent partial agonists of the alpha(1A) adrenergic receptor, with good selectivity over the alpha(1B), alpha(1D) and alpha(2A) receptor sub-types. Nitrile 28 possessed attractive CNS drug-like properties with good membrane permeability and no P-pg mediated efflux. 28 also possessed excellent solubility, metabolic stability and wide ligand selectivity.

Original publication

DOI

10.1016/j.bmcl.2009.03.162

Type

Journal article

Journal

Bioorg Med Chem Lett

Publication Date

01/06/2009

Volume

19

Pages

3118 - 3121

Keywords

ATP Binding Cassette Transporter, Subfamily B, Member 1, Adrenergic alpha-1 Receptor Agonists, Adrenergic alpha-2 Receptor Agonists, Animals, Cell Line, Dogs, Humans, Imidazoles, Receptors, Adrenergic, alpha-1, Receptors, Adrenergic, alpha-2