A. Reeve

发表

L‐694,247: a potent 5‐HT1D receptor agonist

D. Middlemiss, V. Matassa, R. Hargreaves, 1993, British journal of pharmacology.

Selective, Orally Active γ-Aminobutyric AcidA α5 Receptor Inverse Agonists as Cognition Enhancers

Desmond O'Connor, G. Dawson, J. Atack, 2004 .

Synthesis and biological evaluation of 3-heterocyclyl-7,8,9,10-tetrahydro-(7,10-ethano)-1,2,4-triazolo[3,4-a]phthalazines and analogues as subtype-selective inverse agonists for the GABA(A)alpha5 benzodiazepine binding site.

G. Dawson, R. Mckernan, A. Pike, 2004, Journal of medicinal chemistry.

Synthesis and muscarinic activity of quinuclidinyl- and (1-azanorbornyl)pyrazine derivatives.

T. Willson, S. Freedman, S. Patel, 1992, Journal of medicinal chemistry.

Synthesis and conformational dynamics of tricyclic pyridones containing a fused seven-membered ring.

R. Mortishire-Smith, A. Nadin, U. Gerhard, 2002, The Journal of organic chemistry.

6,7-Dihydro-2-benzothiophen-4(5H)-ones: a novel class of GABA-A alpha5 receptor inverse agonists.

G. Dawson, J. Atack, H. Broughton, 2002, Journal of medicinal chemistry.

Selective, orally active 5-HT1D receptor agonists as potential antimigraine agents.

V. Matassa, M. Beer, J. Stanton, 1997, Journal of medicinal chemistry.

Synthesis and serotonergic activity of 5-(oxadiazolyl)tryptamines: potent agonists for 5-HT1D receptors.

D. Middlemiss, V. Matassa, M. Beer, 1993, Journal of medicinal chemistry.

Synthesis and serotonergic activity of 3-[2-(pyrrolidin-1-yl)ethyl]indoles: potent agonists for the h5-HT1D receptor with high selectivity over the h5-HT1B receptor.

V. Matassa, M. Beer, J. Stanton, 1999, Journal of medicinal chemistry.

Synthesis and serotonergic activity of N,N-dimethyl-2-[5-(1,2,4-triazol-1-ylmethyl)-1H-indol-3-yl]ethylamine and analogues: potent agonists for 5-HT1D receptors.

M. Beer, A. Reeve, L. Street, 1995, Journal of medicinal chemistry.

Synthesis of azabicyclic pyrazine derivatives as muscarinic agonists and the preparation of a chloropyrazine analogue with functional selectivity at sub-types of the muscarinic receptor

A. Reeve, L. Street, J. Saunders, 1991 .

3-(Piperazinylpropyl)indoles: selective, orally bioavailable h5-HT1D receptor agonists as potential antimigraine agents.

V. Matassa, M. Beer, J. Stanton, 1999, Journal of medicinal chemistry.

Identification of C-2 hydroxyethyl imidazopyrrolopyridines as potent JAK1 inhibitors with favorable physicochemical properties and high selectivity over JAK2.

Jane R Kenny, Philippe Bergeron, Ignacio Aliagas, 2013, Journal of medicinal chemistry.