23 articles for R Jones
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Identification of potent, selective, CNS-targeted inverse agonists of the ghrelin receptor.

Pfizer
Synthesis and Cardiac Imaging of (18)F-Ligands Selective for ß1-Adrenoreceptors.

TBA
The discovery of long acting beta2-adrenoreceptor agonists.

Pfizer
Mapping the melatonin receptor. 6. Melatonin agonists and antagonists derived from 6H-isoindolo[2,1-a]indoles, 5,6-dihydroindolo[2,1-a]isoquinolines, and 6,7-dihydro-5H-benzo[c]azepino[2,1-a]indoles.

King'S College London
An in situ oxidation strategy towards overcoming hERG affinity.

Pfizer
Discovery of quinazoline HPK1 inhibitors with high cellular potency.

Emd Serono Research & Development Institute
Discovery of PF-06873600, a CDK2/4/6 Inhibitor for the Treatment of Cancer.

Pfizer
Identification of Clinical Candidate M2698, a Dual p70S6K and Akt Inhibitor, for Treatment of PAM Pathway-Altered Cancers.

Emd Serono Research & Development Institute
Discovery of potent and selective reversible Bruton's tyrosine kinase inhibitors.

Emd Serono Research & Development Institute
The Discovery of a Potent, Selective, and Peripherally Restricted Pan-Trk Inhibitor (PF-06273340) for the Treatment of Pain.

Pfizer
Discovery of Lanraplenib (GS-9876): A Once-Daily Spleen Tyrosine Kinase Inhibitor for Autoimmune Diseases.

Gilead Sciences
Mapping the melatonin receptor. 3. Design and synthesis of melatonin agonists and antagonists derived from 2-phenyltryptamines.

University College London
Discovery of a novel series of pyridine and pyrimidine carboxamides as potent and selective covalent inhibitors of Btk.

Emd Serono Research & Development Institute
Optimization of the efflux ratio and permeability of covalent irreversible BTK inhibitors.

Emd Serono Research & Development Institute
Discovery of potent, highly selective covalent irreversible BTK inhibitors from a fragment hit.

Emd Serono Research & Development Institute
Discovery of Potent and Orally Bioavailable Macrocyclic Peptide-Peptoid Hybrid CXCR7 Modulators.

Pfizer
NUCLEOTIDE AND NUCLEOSIDE THERAPEUTIC COMPOSITIONS, COMBINATIONS AND USES RELATED THERETO

Emory University
Macrocyclic immunomodulators

Chemocentryx
Compounds as inhibitors of DNA methyltransferases

FundaciÓN Para La InvestigaciÓN MÉDica Aplicada
Heterocyclic compounds and their use as dopamine D1 ligands

Pfizer
Kinase inhibitors

Allergan
Pyrimidooxazocine derivatives as mTOR-inhibitors

Sanofi