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Steven V. O’Neil
Observed names:
O'Neil, S.V.,
S. V. O'NEIL,
S.V. O'Neil,
Steven O’Neil,
Steven V O'Neil,
Steven V. O'Neil
show all 6
Institution:
Pfizer (United States)
Observed institutions:
University of North Carolina at Chapel Hill,
Pfizer (United States),
Pfizer (United Kingdom),
Bristol-Myers Squibb (United States),
The Ohio State University,
Brandeis University,
Procter & Gamble (United States)
show all 7
ORCID:
0000-0002-0458-2322
Observed ORCID:
0000-0002-0458-2322
OpenAlex ID:
A5090701159
Discovery of Trifluoromethyl Glycol Carbamates as Potent and Selective Covalent Monoacylglycerol Lipase (MAGL) Inhibitors for Treatment of Neuroinflammation
2018
·
Laura A. McAllister
, Christopher R. Butler
, et al.
·
Journal of Medicinal Chemistry
·
88
Discovery of the Potent and Selective M1 PAM-AgonistN-[(3R,4S)-3-Hydroxytetrahydro-2H-pyran-4-yl]-5-methyl-4-[4-(1,3-thiazol-4-yl)benzyl]pyridine-2-carboxamide (PF-06767832): Evaluation of Efficacy and Cholinergic Side Effects
2016
·
Jennifer E. Davoren
, Che-Wah Lee
, et al.
·
Journal of Medicinal Chemistry
·
88
Negative allosteric modulation of metabotropic glutamate receptor 5 results in broad spectrum activity relevant to treatment resistant depression
2012
·
Z.A. Hughes
, S.J. Neal
, et al.
·
Neuropharmacology
·
87
Design and Synthesis of γ- and δ-Lactam M 1 Positive Allosteric Modulators (PAMs): Convulsion and Cholinergic Toxicity of an M 1 -Selective PAM with Weak Agonist Activity
2017
·
Jennifer E. Davoren
, Michelle Garnsey
, et al.
·
Journal of Medicinal Chemistry
·
62
Design and synthesis of novel N-sulfonyl-2-indole carboxamides as potent PPAR-γ binding agents with potential application to the treatment of osteoporosis
2006
·
Corey R. Hopkins
, Steven V. O’Neil
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
50
Design and optimization of selective azaindole amide M1 positive allosteric modulators
2015
·
Jennifer E. Davoren
, Steven V. O’Neil
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
44
Synthesis and biological activity of 5-aryl-4-(4-(5-methyl-1H-imidazol-4-yl)piperidin-1-yl)pyrimidine analogs as potent, highly selective, and orally bioavailable NHE-1 inhibitors
2006
·
Karnail S. Atwal
, Steven V. O’Neil
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
42
Discovery of Nirmatrelvir (PF-07321332): A Potent, Orally Active Inhibitor of the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS CoV-2) Main Protease
2025
·
Jamison B. Tuttle
, Christophe Allais
, et al.
·
Journal of Medicinal Chemistry
·
38
Identification and Development of an Irreversible Monoacylglycerol Lipase (MAGL) Positron Emission Tomography (PET) Radioligand with High Specificity
2019
·
Lei Zhang
, Christopher R. Butler
, et al.
·
Journal of Medicinal Chemistry
·
37
Synthesis of (±)-Allocyathin B2 and (+)-Erinacine A
1998
·
Barry B. Snider
, Nha Huu Vo
, et al.
·
The Journal of Organic Chemistry
·
37
Advances in the development of novel aggrecanase inhibitors
2010
·
Adam M Gilbert
, Jack A Bikker
, et al.
·
Expert Opinion on Therapeutic Patents
·
32
Synthesis of (±)-Gymnomitrol. Mn(OAc)3-Initiated Free-Radical Cyclization of Alkynyl Ketones
1997
·
Steven V. O'Neil
, Cheri A. Quickley
, et al.
·
The Journal of Organic Chemistry
·
32
Discovery of novel conformationally restricted diazocan peptidomimetics as inhibitors of interleukin-1β synthesis
2005
·
Kofi A. Oppong
, Christopher D. Ellis
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
24
Synthesis and evaluation of novel 8,6-fused bicyclic peptidomimetic compounds as interleukin-1β converting enzyme inhibitors
2005
·
Steven V. O’Neil
, Yili Wang
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
20
Synthesis and evaluation of unsaturated caprolactams as interleukin-1β converting enzyme (ICE) inhibitors
2006
·
Yili Wang
, Steven V. O’Neil
, et al.
·
Bioorganic & Medicinal Chemistry
·
19
Studies Toward an Asymmetric Synthesis of CP-263,114 and CP-225,917
2000
·
Jean-François Devaux
, Steven V. O'Neil
, et al.
·
Collection of Czechoslovak Chemical Communications
·
19
The Need for an Incisive Analysis of the Regioselectivity Associated with the Deprotonation of α-Alkoxy and α-Acyloxy Ketones
1999
·
Leo A. Paquette
, Steven V. O'Neil
, et al.
·
Synlett
·
18
Formal synthesis of (±)-upial. Oxidative free-radical cyclization of unsaturated 1,3-cyclohexanediones
1995
·
Barry B. Snider
, Steven V. O'Neil
·
Tetrahedron
·
18
Synthesis and evaluation of thiazepines as interleukin-1β converting enzyme (ICE) inhibitors
2006
·
Christopher D. Ellis
, Kofi A. Oppong
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
17
Application of Flow and Biocatalytic Transaminase Technology for the Synthesis of a 1-Oxa-8-azaspiro[4.5]decan-3-amine
2021
·
Jeffrey T. Kohrt
, Peter H. Dorff
, et al.
·
Organic Process Research & Development
·
16
Synthesis and evaluation of novel 8,5-fused bicyclic peptidomimetic compounds as interleukin-1β converting enzyme (ICE) inhibitors
2006
·
David L. Soper
, Justin X. Sheville
, et al.
·
Bioorganic & Medicinal Chemistry
·
15
Stereochemical Dependence of Base-Catalyzed Cleavage of Cyclic Peroxy Ketals
1994
·
Barry B. Snider
, Zhongping Shi
, et al.
·
The Journal of Organic Chemistry
·
14
Synthesis and evaluation of tricyclic pyrrolopyrimidinones as dipeptide mimetics: Inhibition of interleukin-1β-converting enzyme
2005
·
Michael C. Laufersweiler
, Yili Wang
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
13
Discovery and Characterization of (R)-6-Neopentyl-2-(pyridin-2-ylmethoxy)-6,7-dihydropyrimido[2,1-c][1,4]oxazin-4(9H)-one (PF-06462894), an Alkyne-Lacking Metabotropic Glutamate Receptor 5 Negative Allosteric Modulator Profiled in both Rat and Nonhuman Primates
2017
·
Antonia F. Stepan
, Michelle M. Claffey
, et al.
·
Journal of Medicinal Chemistry
·
9
Synthesis of (−)-Acetylsaturejol and (+)-Isoacetylsaturejol
1995
·
Barry B. Snider
, Steven V. O'Neil
·
Synthetic Communications
·
9
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Works count:
38
Citation count:
867
H-index:
18
I10-index:
23
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