David J. Madar
AbbVie (United States)(US)
Publications by Year
Research Areas
Diabetes Treatment and Management, Peptidase Inhibition and Analysis, Neuropeptides and Animal Physiology, Chemical Synthesis and Analysis, Synthetic Organic Chemistry Methods
Most-Cited Works
- → A Convergent Synthetic Route to (+)-Dynemicin A and Analogs of Wide Structural Variability(1997)208 cited
- → Structure-Guided Design of a Series of MCL-1 Inhibitors with High Affinity and Selectivity(2015)150 cited
- → 3,5-Bis(trifluoromethyl)pyrazoles: A Novel Class of NFAT Transcription Factor Regulator(2000)120 cited
- → Potential Drug Targets and Progress Towards Pharmacologic Inhibition of Hepatic Glucose Production(2003)87 cited
- → Synthesis of (+)-dynemicin A and analogs of wide structural variability: establishment of the absolute configuration of natural dynemicin A(1995)83 cited
- → Discovery, Structure−Activity Relationship, and Pharmacological Evaluation of (5-Substituted-pyrrolidinyl-2-carbonyl)-2-cyanopyrrolidines as Potent Dipeptidyl Peptidase IV Inhibitors(2006)61 cited
- → Discovery of ((4R,5S)-5-Amino-4-(2,4,5- trifluorophenyl)cyclohex-1-enyl)-(3- (trifluoromethyl)-5,6-dihydro- [1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone (ABT-341), a Highly Potent, Selective, Orally Efficacious, and Safe Dipeptidyl Peptidase IV Inhibitor for the Treatment of Type 2 Diabetes(2006)52 cited
- → Prospects for Pharmacologic Inhibition of Hepatic Glucose Production(2003)51 cited
- → Total Synthesis of (+)-Damavaricin D(1997)50 cited
- → Synthesis of N-arylated oxazolidinones via a palladium catalyzed cross coupling reaction. Application to the synthesis of the antibacterial agent Dup-721(2001)48 cited