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Austin J. Reeve
Observed names:
A. J. REEVE,
A.J. Reeve,
Austin Reeve
Observed institutions:
Merck & Co., Inc., Rahway, NJ, USA (United States),
MSD (UK) Limited (United Kingdom)
OpenAlex ID:
A5110056834
Identification of a Novel, Selective GABAAα5 Receptor Inverse Agonist Which Enhances Cognition
2003
·
Mark S. Chambers
, John R. Atack
, et al.
·
Journal of Medicinal Chemistry
·
141
Selective, Orally Active γ-Aminobutyric Acid A α5 Receptor Inverse Agonists as Cognition Enhancers
2004
·
Francine Sternfeld
, Robert W. Carling
, et al.
·
Journal of Medicinal Chemistry
·
106
Synthesis and Serotonergic Activity of N,N-Dimethyl-2-[5-(1,2,4-triazol-1-ylmethyl)-1H-indol-3-yl]ethylamine and Analogs: Potent Agonists for 5-HT1D Receptors
1995
·
Leslie J. Street
, Raymond Baker
, et al.
·
Journal of Medicinal Chemistry
·
77
Synthesis and serotonergic activity of 5-(oxadiazolyl)tryptamines: potent agonists for 5-HT1D receptors
1993
·
Leslie J. Street
, Raymond Baker
, et al.
·
Journal of Medicinal Chemistry
·
75
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 GABAAα5 Benzodiazepine Binding Site
2004
·
Leslie J. Street
, Francine Sternfeld
, et al.
·
Journal of Medicinal Chemistry
·
74
Identification of C-2 Hydroxyethyl Imidazopyrrolopyridines as Potent JAK1 Inhibitors with Favorable Physicochemical Properties and High Selectivity over JAK2
2013
·
Mark Zak
, Christopher A. Hurley
, et al.
·
Journal of Medicinal Chemistry
·
67
L‐694,247: a potent 5‐HT1Dreceptor agonist
1993
·
M.S. Beer
, J.A. Stanton
, et al.
·
British Journal of Pharmacology
·
51
PDF
Synthesis and muscarinic activity of quinuclidinyl- and (1-azanorbornyl)pyrazine derivatives
1992
·
Leslie J. Street
, Raymond Baker
, et al.
·
Journal of Medicinal Chemistry
·
44
Synthesis and Conformational Dynamics of Tricyclic Pyridones Containing a Fused Seven-Membered Ring
2002
·
Karl R. Gibson
, Laure Hitzel
, et al.
·
The Journal of Organic Chemistry
·
38
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
1999
·
Francine Sternfeld
, Alexander R. Guiblin
, et al.
·
Journal of Medicinal Chemistry
·
29
Selective, Orally Active 5-HT1D Receptor Agonists as Potential Antimigraine Agents
1997
·
Angus M. MacLeod
, Leslie J. Street
, et al.
·
Journal of Medicinal Chemistry
·
29
6,7-Dihydro-2-benzothiophen-4(5H)-ones: A Novel Class of GABA-A α5 Receptor Inverse Agonists
2002
·
Mark S. Chambers
, John R. Atack
, et al.
·
Journal of Medicinal Chemistry
·
28
3-(Piperazinylpropyl)indoles: Selective, Orally Bioavailable h5-HT1DReceptor Agonists as Potential Antimigraine Agents
1999
·
Mark S. Chambers
, Leslie J. Street
, et al.
·
Journal of Medicinal Chemistry
·
28
The chemical evolution of N,N-dimethyl-2-[5-(1,2,4-triazol-4-yl)-1H-indol-3-yl]ethylamine (L-741,604) and analogues: Potent and selective agonists for 5-HT1D receptors
1996
·
Francine Sternfeld
, Raymond Baker
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
18
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
1991
·
Raymond Baker
, Leslie J. Street
, et al.
·
Journal of the Chemical Society Chemical Communications
·
18
Stereoselective Synthesis of a Potent Human NK1Receptor Antagonist via Acyl-Claisen Rearrangement
2006
·
Piotr Raubo
, Claudio Giuliano
, et al.
·
Synlett
·
6
ChemInform Abstract: Synthesis and Serotonergic Activity of 5‐(Oxadiazolyl)tryptamines: Potent Agonists for 5‐HT1D Receptors.
1993
·
L. J. STREET
, R. BAKER
, et al.
·
ChemInform
·
2
ChemInform Abstract: The Chemical Evolution of N,N‐Dimethyl‐2‐(5‐(1,2,4‐triazol‐4‐yl)‐1H‐ indol‐3‐yl)ethylamine (L‐741,604) and Analogues: Potent and Selective Agonists for 5‐HT1D Receptors.
1996
·
F. STERNFELD
, R. BAKER
, et al.
·
ChemInform
ChemInform Abstract: 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.
1992
·
R. BAKER
, L. J. STREET
, et al.
·
ChemInform
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Works count:
19
Citation count:
830
H-index:
15
I10-index:
15
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