Concepedia

Author

Peter R. Manninen

W.E. Upjohn Institute for Employment Research

Also Known As

P. R. MANNINEN, P. R. Manninen, PETER R. MANNINEN, Peter R. Manninen

14

Publications

972

Citations

10

H-Index

27

Concepts

All Affiliations

W.E. Upjohn Institute for Employment ResearchEli Lilly (United States)
PR

About

Peter R. Manninen is an author at W.E. Upjohn Institute for Employment Research specializing in pharmacology, drug discovery, and medicinal chemistry.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

7

7

722

2

Natural Sciences

7

7

187

3

Biochemistry

5

5

142

4

Chemical Biology

2

2

46

5

Chemistry

1

1

10

Peter R. Manninen

×

9

Publications

770

Citations

9

H-Index

YearCitations

Synthesis and Antibacterial Activity of U-100592 and U-100766, Two Oxazolidinone Antibacterial Agents for the Potential Treatment of Multidrug-Resistant Gram-Positive Bacterial Infections

Steven J. Brickner, Douglas K. Hutchinson, Michael R. Barbachyn,

Journal of Medicinal Chemistry

1996

570

Discovery of 6-(4-{[5-Cyclopropyl-3-(2,6-dichlorophenyl)isoxazol-4-yl]methoxy}piperidin-1-yl)-1-methyl-1<i>H</i>-indole-3-carboxylic Acid: A Novel FXR Agonist for the Treatment of Dyslipidemia

Michaël Génin, Ana B. Bueno, Javier Agejas Francisco,

Journal of Medicinal Chemistry

2015

57

Synthesis and antibacterial activity of [6,5,5] and [6,6,5] tricyclic fused oxazolidinones

D. M. GLEAVE, Steven J. Brickner, Peter R. Manninen,

Bioorganic & Medicinal Chemistry Letters

1998

35

Discovery and characterization of [(cyclopentyl)ethyl]benzoic acid inhibitors of microsomal prostaglandin E synthase-1

Katherine M. Partridge, Stephen Antonysamy, Shobha Bhattachar,

Bioorganic & Medicinal Chemistry Letters

2016

27

Characterization of 3,3-dimethyl substituted N-aryl piperidines as potent microsomal prostaglandin E synthase-1 inhibitors

Steven L. Kuklish, Stephen Antonysamy, Shobha Bhattachar,

Bioorganic & Medicinal Chemistry Letters

2016

26

Asymmetric Synthesis of the C3α Fragment of 5,6-Dihydro-α-pyrone Nonpeptidic HIV-1 Protease Inhibitors

Donna L. Romero, Peter R. Manninen, Fusen Han,

The Journal of Organic Chemistry

1999

19

7-Oxo-4,7-dihydrothieno[3,2-b]pyridine-6-carboxamides: Synthesis and biological activity of a new class of highly potent inhibitors of human cytomegalovirus DNA polymerase

Scott D. Larsen, Zhi‐Jun Zhang, Brian A. DiPaolo,

Bioorganic & Medicinal Chemistry Letters

2007

13

N-Acyl 3-alkylidenyl- and 3-alkyl azetidin-2-ones: A new class of monocyclic .BETA.-lactam antibacterial agents. 1. Structure-activity relationships of 3-isopropylidene and 3-isopropyl analogs.

Steven J. Brickner, Jeffrey J. Gaikema, Gary E. Zurenko,

The Journal of Antibiotics

1992

13

N-acyl-3-alkylidenyl- and 3-alkyl azeitidin-2-ones: a new class of monocyclic β-lactam antibacterial agents 2. Synthesis and structure-activity relationships of heteroatom substituted 3-isopropylidene and 3-isopropyl analogs

Steven J. Brickner, Jeffrey J. Gaikema, Laura J. Greenfield,

Bioorganic & Medicinal Chemistry Letters

1993

10

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