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16 articles for A Wood


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
Structure-based design of orally bioavailable 1H-pyrrolo[3,2-c]pyridine inhibitors of mitotic kinase monopolar spindle 1 (MPS1).EBI
The Institute of Cancer Research
Interaction of morphine, fentanyl, sufentanil, alfentanil, and loperamide with the efflux drug transporter P-glycoprotein.EBI
Vanderbilt University
The discovery of tropane-derived CCR5 receptor antagonists.EBI
TBA
Inhalation by design: novel tertiary amine muscarinic M3 receptor antagonists with slow off-rate binding kinetics for inhaled once-daily treatment of chronic obstructive pulmonary disease.EBI
Pfizer
Gymnochromes E and F, cytotoxic phenanthroperylenequinones from a deep-water crinoid, Holopus rangii.EBI
Florida Atlantic University
Pyrazole NNRTIs 4: selection of UK-453,061 (lersivirine) as a development candidate.EBI
Pfizer
The design and discovery of novel amide CCR5 antagonists.EBI
Pfizer
Highly potent and selective chiral inhibitors of PDE5: an illustration of Pfeiffer's rule.EBI
Pfizer
Mitogen-activated protein kinase (MEK/ERK) inhibition sensitizes cancer cells to centromere-associated protein E inhibition.EBI
Children's Hospital of Philadelphia
Overcoming HERG affinity in the discovery of the CCR5 antagonist maraviroc.EBI
Pfizer
Recent results from non-basic glycosidase inhibitors: How structural diversity can inform general strategies for improving inhibition potency.EBI
University of Newcastle
Metabolism-directed design of oxetane-containing arylsulfonamide derivatives as γ-secretase inhibitors.EBI
Pfizer
Lersivirine, a nonnucleoside reverse transcriptase inhibitor with activity against drug-resistant human immunodeficiency virus type 1.EBI
Pfizer
N-hydroxy-3-phenyl-2-propenamides as novel inhibitors of human histone deacetylase with in vivo antitumor activity: discovery of (2E)-N-hydroxy-3-[4-[[(2-hydroxyethyl)[2-(1H-indol-3-yl)ethyl]amino]methyl]phenyl]-2-propenamide (NVP-LAQ824).EBI
Novartis Institute For Biomedical Research
Pyrimidine FGFR4 inhibitorsBDB
Eisai R&D Management
Imidazo[1,2-a]pyridines. Part 2: SAR and optimisation of a potent and selective class of cyclin-dependent kinase inhibitors.BDB
Astrazeneca