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Peter J. Webb
Observed names:
P. Webb,
Peter Webb
Institution:
Amplyx Pharmaceuticals (United States)
Observed institutions:
Merck & Co., Inc., Rahway, NJ, USA (United States),
Williams College,
Amplyx Pharmaceuticals (United States),
Arena Pharmaceuticals (United States)
OpenAlex ID:
A5015658574
In Vitro and In Vivo Evaluation of APX001A/APX001 and Other Gwt1 Inhibitors against Cryptococcus
2018
·
Karen Joy Shaw
, Wiley A. Schell
, et al.
·
Antimicrobial Agents and Chemotherapy
·
127
3-(1 H -Tetrazol-5-yl)-1,4,5,6-tetrahydro-cyclopentapyrazole (MK-0354): A Partial Agonist of the Nicotinic Acid Receptor, G-Protein Coupled Receptor 109a, with Antilipolytic but No Vasodilatory Activity in Mice
2008
·
Graeme Semple
, Philip J. Skinner
, et al.
·
Journal of Medicinal Chemistry
·
104
1-Alkyl-benzotriazole-5-carboxylic Acids Are Highly Selective Agonists of the Human Orphan G-Protein-Coupled Receptor GPR109b
2006
·
Graeme Semple
, Philip J. Skinner
, et al.
·
Journal of Medicinal Chemistry
·
80
(1aR,5aR)1a,3,5,5a-Tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene-4-carboxylic Acid (MK-1903): A Potent GPR109a Agonist that Lowers Free Fatty Acids in Humans
2012
·
P. Douglas Boatman
, Brett Lauring
, et al.
·
Journal of Medicinal Chemistry
·
54
Fluorinated pyrazole acids are agonists of the high affinity niacin receptor GPR109a
2007
·
Philip J. Skinner
, Martin C. Cherrier
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
37
Potent tricyclic pyrazole tetrazole agonists of the nicotinic acid receptor (GPR109a)
2010
·
P. Douglas Boatman
, Thomas O. Schrader
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
34
Agonist lead identification for the high affinity niacin receptor GPR109a
2007
·
Tawfik Gharbaoui
, Philip J. Skinner
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
31
3-Nitro-4-amino benzoic acids and 6-amino nicotinic acids are highly selective agonists of GPR109b
2007
·
Philip J. Skinner
, Martin C. Cherrier
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
30
A calcineurin antifungal strategy with analogs of FK506
2017
·
Mitchell Nambu
, Jonathan A. Covel
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
28
Synthesis of analogs of the Gwt1 inhibitor manogepix (APX001A) and in vitro evaluation against Cryptococcus spp
2019
·
Michael Trzoss
, Jonathan A. Covel
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
27
PDF
5-N,N-Disubstituted 5-aminopyrazole-3-carboxylic acids are highly potent agonists of GPR109b
2009
·
Philip J. Skinner
, Peter J. Webb
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
25
A versatile route to benzocanthinones
2005
·
J. Hodge Markgraf
, Adrian A. Dowst
, et al.
·
Tetrahedron
·
25
Solid-Phase Organic Synthesis and Combinatorial Chemistry: A Laboratory Preparation of Oligopeptides
2002
·
George A. Truran
, Karelle S. Aiken
, et al.
·
Journal of Chemical Education
·
15
The Discovery of Manogepix/Fosmanogepix and Other Gwt1 Inhibitors for the Treatment of Invasive Fungal Infections
2019
·
Jonathan A. Covel
, Quinlyn A. Soltow
, et al.
·
Medicinal chemistry reviews
·
7
A Versatile Route to Benzocanthinones.
2005
·
J. Hodge Markgraf
, Adrian A. Dowst
, et al.
·
ChemInform
·
1
A Versatile Synthesis of Benzacanthinones by Intramolecular Radical Coupling
2005
·
J. Markgraf
, A. Dowst
, et al.
·
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Works count:
16
Citation count:
624
H-index:
13
I10-index:
13
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