21 articles for S Williams
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Potential role of UGT1A4 promoter SNPs in anastrozole pharmacogenomics.

University of Arkansas For Medical Sciences
Quantitative structure-activity relationships (QSARs) of N-terminus fragments of NK1 tachykinin antagonists: a comparison of classical QSARs and three-dimensional QSARs from similarity matrices.

Cambridge University Forvie Site
PD 165929 the first high affinity non-peptide neuromedin-B (NMB) receptor selective antagonist

TBA
Multidentate small-molecule inhibitors of vaccinia H1-related (VHR) phosphatase decrease proliferation of cervix cancer cells.

Institute For Medical Research
Discovery of Novel Quinoline-Based Proteasome Inhibitors for Human African Trypanosomiasis (HAT).

Novartis Institutes For Biomedical Research
Novel inhibitors of plasminogen activator inhibitor-1: development of new templates from diketopiperazines.

Xenova
Design of N-Benzoxaborole Benzofuran GSK8175-Optimization of Human Pharmacokinetics Inspired by Metabolites of a Failed Clinical HCV Inhibitor.

Glaxosmithkline
Discovery of a potent boronic acid derived inhibitor of the HCV RNA-dependent RNA polymerase.

Glaxosmithkline
Microscale High-Throughput Experimentation as an Enabling Technology in Drug Discovery: Application in the Discovery of (Piperidinyl)pyridinyl-1H-benzimidazole Diacylglycerol Acyltransferase 1 Inhibitors.

Merck
ALPHA-2A ADRENERGIC RECEPTOR MODULATORS AND USES THEREOF

University Of California
Compounds and methods for treating oxalate-related diseases

Oxalurx
Cycloalkyl-containing apoptosis signal-regulating kinase 1 inhibitors and methods of use thereof

Enanta Pharmaceuticals
Carbazole-containing amides, carbamates, and ureas as cryptochrome modulators

Synchronicity Pharma
Somatostatin receptor subtype 4 (SSTR4) agonists

Centrexion Therapeutics
TYK2 inhibitors, uses, and methods for production thereof

Nimbus Lakshmi
2,4-diamino-6,7-dihydro-5H-pyrrolo[2,3]pyrimidine derivatives as FAK/Pyk2 inhibitors

Centaurus Biopharma
Spiro ring compound as hepatitis C virus (HCV) inhibitor and uses thereof

Sunshine Lake Pharma
Dihydropyrimidine based hydrazine dihydrochloride derivatives as potent urease inhibitors.

University of Karachi
Inhibition of guinea pig aldehyde oxidase activity by different flavonoid compounds: An in vitro study.

Kermanshah University of Medical Sciences
Pharmaceutical compositions comprising RET inhibitors and methods for the treatment of cancer

Queen'S University At Kingston
Synthesis and biological evaluation of some new N(4)-substituted isatin-3-thiosemicarbazones.

Bahauddin Zakariya University