29 articles for Q Zeng
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Discovery of silyl proline containing HCV NS5A inhibitors with pan-genotype activity: SAR development.

Merck Research Laboratories
Discovery and Evaluation of Clinical Candidate AZD3759, a Potent, Oral Active, Central Nervous System-Penetrant, Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor.

Astrazeneca
IV. Discovery of CXCR3 antagonists substituted with heterocycles as amide surrogates: improved PK, hERG and metabolic profiles.

Merck Research Laboratories
Discovery of an irreversible HCV NS5B polymerase inhibitor.

Merck Research Laboratories
Synthesis and SAR studies of benzimidazolone derivatives as histamine H3-receptor antagonists.

Merck Research Laboratories
Structure-activity relationship (SAR) development and discovery of potent indole-based inhibitors of the hepatitis C virus (HCV) NS5B polymerase.

Merck Research Laboratories
Discovery of a 5H-benzo[4,5]cyclohepta[1,2-b]pyridin-5-one (MK-2461) inhibitor of c-Met kinase for the treatment of cancer.

Merck Research Laboratories
III. Identification of novel CXCR3 chemokine receptor antagonists with a pyrazinyl-piperazinyl-piperidine scaffold.

Merck Research Laboratories
II. SAR studies of pyridyl-piperazinyl-piperidine derivatives as CXCR3 chemokine antagonists.

Ligand Pharmaceuticals
The discovery of an orally efficacious positive allosteric modulator of the calcium sensing receptor containing a dibenzylamine core.

Amgen
Azole-based inhibitors of AKT/PKB for the treatment of cancer.

Amgen
2-Aminothiadiazole inhibitors of AKT1 as potential cancer therapeutics.

Amgen
Structure-Activity Relationships of Cyano-substituted Indole Derivatives as Ligands for α-Synuclein Aggregates.

Beijing Normal University
Dual-Targeting Antiproliferation Hybrids Derived from 1-Deoxynojirimycin and Kaempferol Induce MCF-7 Cell Apoptosis through the Mitochondria-Mediated Pathway.

Jiangsu University of Science and Technology
Berberine Directly Targets the NEK7 Protein to Block the NEK7-NLRP3 Interaction and Exert Anti-inflammatory Activity.

Peking Union Medical College
Design of new topoisomerase II inhibitors based upon a quinobenzoxazine self-assembly model.

The University of Texas At Austin
MK-8325: A silyl proline-containing NS5A inhibitor with pan-genotype activity for treatment of HCV.

Merck
Substituted condensed thiophenes as modulators of sting

Ctxt Pty
Combination therapies using caspase-1 dependent anticancer agents and PGE2 antagonists

Tufts College
Cyclopropyl fused thiazine derivatives as beta-secretase inhibitors and methods of use

Amgen
1,2-dithiolane compounds useful in neuroprotection, autoimmune and cancer diseases and conditions

Sabila Biosciences
3-((hetero-)aryl)-8-amino-2-oxo-1,3-diaza-spiro-[4.5]-decane derivatives

GrüNenthal
Therapeutically active compounds and their methods of use

Agios Pharmaceuticals
Substituted pyrazolo[1,5-a]pyrimidines as bruton's tyrosine kinase modulators

Beigene
Sorafenib derivatives as sEH inhibitors

University of California
Unsaturated nitrogen heterocyclic compounds useful as PDE10 inhibitors

Amgen
Identification and characterization of human apurinic/apyrimidinic endonuclease-1 inhibitors.

University of Pittsburgh
Affinity and selectivity of PD156707, a novel nonpeptide endothelin antagonist, for human ET(A) and ET(B) receptors.

University of Cambridge