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Doug W. Hobbs
Observed names:
Doug Hobbs,
Douglas W Hobbs
Institution:
Ligand Pharmaceuticals (United States)
Observed institutions:
Merck & Co., Inc., Rahway, NJ, USA (United States),
Washington University in St. Louis,
Ligand Pharmaceuticals (United States),
Columbia University
OpenAlex ID:
A5113669931
Structure-Based Drug Design and Optimization of Mannoside Bacterial FimH Antagonists
2010
·
Zhenfu Han
, Jerome S. Pinkner
, et al.
·
Journal of Medicinal Chemistry
·
239
Development of BACE1 Inhibitors for Alzheimers Disease
2006
·
Tao Guo
, Doug Hobbs
·
Current Medicinal Chemistry
·
101
Orally active, nonpeptide oxytocin antagonists
1992
·
Ben E. Evans
, James L. Leighton
, et al.
·
Journal of Medicinal Chemistry
·
79
Development of Orally Active Oxytocin Antagonists: Studies on 1-(1-{4-[1-(2-Methyl-1-oxidopyridin-3-ylmethyl)piperidin-4-yloxy]-2- methoxybenzoyl}piperidin-4-yl)-1,4-dihydrobenz[d][1,3]oxazin-2-one (L-372,662) and Related Pyridines
1998
·
Ian M. Bell
, Jill M. Erb
, et al.
·
Journal of Medicinal Chemistry
·
60
Synthesis and anti-herpes virus activity of acyclic 2'-deoxyguanosine analogs related to 9-[(1,3-dihydroxy-2-propoxy)methyl]guanine
1986
·
John C. Martin
, Danny P. C. McGee
, et al.
·
Journal of Medicinal Chemistry
·
58
Deriving Knowledge through Data Mining High-Throughput Screening Data
2004
·
David J. Diller
, Doug W. Hobbs
·
Journal of Medicinal Chemistry
·
48
Privileged Structure-Based Combinatorial Libraries Targeting G Protein-Coupled Receptors
2003
·
Tao Guo
, Doug W. Hobbs
·
Assay and Drug Development Technologies
·
45
Design, synthesis, and evaluation of tetrahydroquinoline and pyrrolidine sulfonamide carbamates as γ-secretase inhibitors
2007
·
Tao Guo
, Huizhong Gu
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
37
Synthesis of diphenyl thioether derivatives of peptides and aminoacids
1987
·
Doug W. Hobbs
, W.Clark Still
·
Tetrahedron Letters
·
35
Novel CXCR3 antagonists with a piperazinyl-piperidine core
2009
·
Brian F. McGuinness
, Carolyn DiIanni Carroll
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
25
II. SAR studies of pyridyl–piperazinyl-piperidine derivatives as CXCR3 chemokine antagonists
2010
·
Yuefei Shao
, Gopinadhan N. Anilkumar
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
22
Understanding hERG inhibition with QSAR models based on a one-dimensional molecular representation
2007
·
David J. Diller
, Doug W. Hobbs
·
Journal of Computer-Aided Molecular Design
·
19
IV. Discovery of CXCR3 antagonists substituted with heterocycles as amide surrogates: Improved PK, hERG and metabolic profiles
2014
·
Anilkumar G. Nair
, Michael K.C. Wong
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
18
Discovery and SAR of 4-amino-2-biarylbutylurea MCH 1 receptor antagonists through solid-phase parallel synthesis
2005
·
Tao Guo
, Rachael C. Hunter
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
18
III. Identification of novel CXCR3 chemokine receptor antagonists with a pyrazinyl–piperazinyl–piperidine scaffold
2011
·
Seong Heon Kim
, Gopinadhan N. Anilkumar
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
17
Biological Examination of Melanin Concentrating Hormone Receptor 1: Multi-tasking from the Hypothalamus
2006
·
Laura L Rokosz
, Douglas W Hobbs
·
Drug News & Perspectives
·
16
Discovery and SAR of biaryl piperidine MCH1 receptor antagonists through solid-phase encoded combinatorial synthesis
2005
·
Tao Guo
, Yuefei Shao
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
15
Computational ADME/Tox Modeling: Aiding Understanding and Enhancing Decision Making in Drug Design
2005
·
Robert Delisle
, Jeffery Lowrie
, et al.
·
Current Computer - Aided Drug Design
·
14
Synthesis of a Thioether Analog of the Macrocyclic Tripeptide K-13
1989
·
Doug W. Hobbs
, W. Clark Still
·
Tetrahedron Letters
·
13
Non-peptide oxytocin antagonists: identification and synthesis of a potent camphor aminosuccinimide
1995
·
Doug W. Hobbs
, Norman P. Gould
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
7
Library Design Concepts and Implementation Strategies*
2001
·
Doug W. Hobbs
, Tao Guo
·
Journal of Receptors and Signal Transduction
·
6
Discovery of tetralin ureas as potent melanin concentrating hormone 1 receptor antagonists
2006
·
Tao Guo
, Huizhong Gu
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
5
Preparation of Encoded Combinatorial Libraries for Drug Discovery
2003
·
Tao Guo
, Doug W. Hobbs
·
Humana Press eBooks
·
4
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Works count:
23
Citation count:
901
H-index:
16
I10-index:
19
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