16 articles for H Nar
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Structure-Based Design of an in Vivo Active Selective BRD9 Inhibitor.

Boehringer Ingelheim Rcv
Potent cholesteryl ester transfer protein inhibitors of reduced lipophilicity: 1,1'-spiro-substituted hexahydrofuroquinoline derivatives.

Boehringer Ingelheim Pharma
3,5-Dihydro-imidazo[4,5-d]pyridazin-4-ones: a class of potent DPP-4 inhibitors.

Boehringer Ingelheim Pharma
Discovery and optimization of adamantyl carbamate inhibitors of 11ß-HSD1.

Vitae Pharmaceuticals
8-(3-(R)-aminopiperidin-1-yl)-7-but-2-ynyl-3-methyl-1-(4-methyl-quinazolin-2-ylmethyl)-3,7-dihydropurine-2,6-dione (BI 1356), a highly potent, selective, long-acting, and orally bioavailable DPP-4 inhibitor for the treatment of type 2 diabetes.

Boehringer Ingelheim Pharma
Discovery of BI 7446: A Potent Cyclic Dinucleotide STING Agonist with Broad-Spectrum Variant Activity for the Treatment of Cancer.

Boehringer Ingelheim Pharma
Discovery and Structure-Based Optimization of Fragments Binding the Mixed Lineage Kinase Domain-like Protein Executioner Domain.

Boehringer Ingelheim Pharma
Heterocyclic thrombin inhibitors. Part 2: quinoxalinone derivatives as novel, potent antithrombotic agents.

Boehringer Ingelheim Pharma
Heterocyclic thrombin inhibitors. Part 1: design and synthesis of amidino-phenoxy quinoline derivatives.

Boehringer Ingelheim Pharma
Structure-based design of novel potent nonpeptide thrombin inhibitors.

Boehringer Ingelheim Pharma
Hybrid Screening Approach for Very Small Fragments: X-ray and Computational Screening on FKBP51.

Boehringer Ingelheim Pharma
Comparative Analysis of Binding Kinetics and Thermodynamics of Dipeptidyl Peptidase-4 Inhibitors and Their Relationship to Structure.

Boehringer Ingelheim Pharma
Synthesis and structure-activity relationships of 6,7-benzomorphan derivatives as use-dependent sodium channel blockers for the treatment of stroke.

Boehringer Ingelheim Pharma
Orvinol and thevinol derivatives useful in the treatment of depression

The University of Bath
Inhibitors of src tyrosine kinase: the preparation and structure-activity relationship of 4-anilino-3-cyanoquinolines and 4-anilinoquinazolines.

Wyeth-Ayerst Research