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Anita J. Kempf-Grote
Observed names:
A.J. Kempf-Grote,
Anita J Kempf-Grote,
Anita Kempf-Grote
Institution:
AbbVie (United States)
Observed institutions:
Australian National University,
AbbVie (United States),
Abbott (United Kingdom),
Abbott (United States),
Abbott (Germany)
OpenAlex ID:
A5086306992
Discovery and Structure−Activity Relationships of Piperidinone- and Piperidine-Constrained Phenethylamines as Novel, Potent, and Selective Dipeptidyl Peptidase IV Inhibitors
2007
·
Zhonghua Pei
, Xiaofeng Li
, et al.
·
Journal of Medicinal Chemistry
·
93
Discovery, Structure−Activity Relationship, and Pharmacological Evaluation of (5-Substituted-pyrrolidinyl-2-carbonyl)-2-cyanopyrrolidines as Potent Dipeptidyl Peptidase IV Inhibitors
2006
·
Zhonghua Pei
, Xiaofeng Li
, et al.
·
Journal of Medicinal Chemistry
·
61
Structure-Based Characterization and Optimization of Novel Hydrophobic Binding Interactions in a Series of Pyrrolidine Influenza Neuraminidase Inhibitors
2005
·
Clarence J. Maring
, Vincent S. Stoll
, et al.
·
Journal of Medicinal Chemistry
·
59
Selective Inhibition of ICAM-1 and E-Selectin Expression in Human Endothelial Cells. 2. Aryl Modifications of 4-(Aryloxy)thieno[2,3-c]pyridines with Fine-Tuning at C-2 Carbamides
2001
·
Gui-Dong Zhu
, David L. Arendsen
, et al.
·
Journal of Medicinal Chemistry
·
57
Discovery of a Potent Chloroacetamide GPX4 Inhibitor with Bioavailability to Enable Target Engagement in Mice, a Potential Tool Compound for Inducing Ferroptosis In Vivo
2023
·
John T. Randolph
, Matthew J. O’Connor
, et al.
·
Journal of Medicinal Chemistry
·
54
Discovery of ((4 R ,5 S )-5-Amino-4-(2,4,5- trifluorophenyl)cyclohex-1-enyl)-(3- (trifluoromethyl)-5,6-dihydro- [1,2,4]triazolo[4,3-a]pyrazin-7(8 H )-yl)methanone (ABT-341), a Highly Potent, Selective, Orally Efficacious, and Safe Dipeptidyl Peptidase IV Inhibitor for the Treatment of Type 2 Diabetes
2006
·
Zhonghua Pei
, Xiaofeng Li
, et al.
·
Journal of Medicinal Chemistry
·
54
Discovery of Inhibitors of Cell Adhesion Molecule Expression in Human Endothelial Cells. 1. Selective Inhibition of ICAM-1 and E-Selectin Expression
2001
·
Andrew O. Stewart
, Pramila A. Bhatia
, et al.
·
Journal of Medicinal Chemistry
·
52
A-366833: A novel nicotinonitrile-substituted 3,6-diazabicyclo[3.2.0]-heptane α4β2 nicotinic acetylcholine receptor selective agonist: Synthesis, analgesic efficacy and tolerability profile in animal models
2007
·
Jianguo Ji
, William H. Bunnelle
, et al.
·
Biochemical Pharmacology
·
41
Pyrrolidine-constrained phenethylamines: The design of potent, selective, and pharmacologically efficacious dipeptidyl peptidase IV (DPP4) inhibitors from a lead-like screening hit
2007
·
Bradley J. Backes
, Kenton Longenecker
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
39
Discovery of 2-[4-{{2-(2S,5R)-2-Cyano-5-ethynyl-1-pyrrolidinyl]-2-oxoethyl]amino]- 4-methyl-1-piperidinyl]-4-pyridinecarboxylic Acid (ABT-279): A Very Potent, Selective, Effective, and Well-Tolerated Inhibitor of Dipeptidyl Peptidase-IV, Useful for the Treatment of Diabetes
2006
·
David J. Madar
, Hana Kopecka
, et al.
·
Journal of Medicinal Chemistry
·
37
Cardiovascular Effects of Torcetrapib in Conscious and Pentobarbital-anesthetized Dogs
2009
·
James S Polakowski
, Andrew J King
, et al.
·
Journal of Cardiovascular Pharmacology
·
15
Use of drug efflux transporter knockout mice to differentiate peripheral from centrally-mediated cardiovascular effects
2011
·
Patricia N. Banfor
, Scott Mittelstadt
, et al.
·
Journal of Pharmacological and Toxicological Methods
·
3
Discovery, Structure−Activity Relationship, and Pharmacological Evaluation of (5-Substituted-pyrrolidinyl-2-carbonyl)-2-cyanopyrrolidines as Potent Dipeptidyl Peptidase IV Inhibitors.
2006
·
Zhonghua Pei
, Xiaofeng Li
, et al.
·
Journal of Medicinal Chemistry
·
2
PDF
Cardiovascular effects of torcetrapib in conscious and pentobarbital anesthetized dogs
2009
·
S.W. Mittelstadt
, R.A. Nelson
, et al.
·
Journal of Pharmacological and Toxicological Methods
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Works count:
14
Citation count:
567
H-index:
11
I10-index:
11
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