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Oxazolidinone Antibiotics Target the P Site on Escherichia coli Ribosomes

Antimicrobial Agents and Chemotherapy, 2002-04, Vol.46 (4), p.1080-1085

2002

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Novel riboswitch-binding flavin analog that protects mice against Clostridium difficile infection without inhibiting cecal flora

Antimicrobial agents and chemotherapy, 2015-09, Vol.59 (9), p.5736-5746

2015

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Substituted 4-aminopiperidines having high in vitro affinity and selectivity for the cloned human dopamine D4 receptor

European journal of pharmacology, 1997-03, Vol.322 (2-3), p.283-286

1997

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Pyrimidine Thioethers: A Novel Class of HIV-1 Reverse Transcriptase Inhibitors with Activity Against BHAP-Resistant HIV

Journal of medicinal chemistry, 1998-09, Vol.41 (20), p.3793-3803

1998

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Synthesis and Bioactivity of Novel Bis(heteroaryl)piperazine (BHAP) Reverse Transcriptase Inhibitors: Structure−Activity Relationships and Increased Metabolic Stability of Novel Substituted Pyridine Analogs

Journal of medicinal chemistry, 1996-12, Vol.39 (26), p.5267-5275

1996

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Synthesis and Structure−Activity Relationships of the (Alkylamino)piperidine-Containing BHAP Class of Non-Nucleoside Reverse Transcriptase Inhibitors: Effect of 3-Alkylpyridine Ring Substitution

Journal of medicinal chemistry, 1999-10, Vol.42 (20), p.4140-4149

1999

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Oxazolidinone Antibiotics Target the P Site on Escherichiacoli Ribosomes

Antimicrobial agents and chemotherapy, 2002-04, Vol.46 (4), p.1080-1085

2002

Volltextzugriff (PDF)

Substituted 4-aminopiperidines having high in vitro affinity and selectivity for the cloned human dopamine D 4 receptor

European journal of pharmacology, 1997-03, Vol.322 (2), p.283-286

1997

Volltextzugriff (PDF)

(Alkylamino) piperidine bis(heteroaryl)piperizine analogs are potent, broad-spectrum nonnucleoside reverse transcriptase inhibitors of drug-resistant isolates of human immunodeficiency virus type 1 (HIV-1) and select for drug-resistant variants of HIV-1IIIB with reduced replication phenotypes

Journal of Virology, 1996-06, Vol.70 (6), p.3698-3705

1996

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Stereoselective reactions of ester enolates with epoxides

Journal of organic chemistry, 1993-12, Vol.58 (25), p.7304-7307

1993

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Synthesis and Microbiological Evaluation of Novel Tetracyclic Fluoroquinolones

ChemMedChem, 2017-10, Vol.12 (20), p.1687-1692

2017

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Cover Feature: Synthesis and Microbiological Evaluation of Novel Tetracyclic Fluoroquinolones (ChemMedChem 20/2017)

ChemMedChem, 2017-10, Vol.12 (20), p.1656-1656

2017

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Repetitive use of levosimendan in advanced heart failure: need for stronger evidence in a field in dire need of a useful therapy

International journal of cardiology, 2017-09, Vol.243, p.389-395

2017

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Design and synthesis of hepatoselective, pyrrole-based HMG-CoA reductase inhibitors

Bioorganic & medicinal chemistry letters, 2007-08, Vol.17 (16), p.4538-4544

2007

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Pyrazole inhibitors of HMG-CoA reductase: An attempt to dramatically reduce synthetic complexity through minimal analog re-design

Bioorganic & medicinal chemistry letters, 2007-10, Vol.17 (20), p.5567-5572

2007

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Targeting Delavirdine/Atevirdine Resistant HIV-1: Identification of (Alkylamino)piperidine-Containing Bis(heteroaryl)piperazines as Broad Spectrum HIV-1 Reverse Transcriptase Inhibitors

Journal of medicinal chemistry, 1996-09, Vol.39 (19), p.3769-3789

1996

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Stereodivergent synthesis of sulfoxide-containing oxazolidinone antibiotics

Tetrahedron letters, 2000-06, Vol.41 (22), p.4301-4305

2000

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Pyrazole inhibitors of ΗΜΓ-CoA reductase : An attempt to dramatically reduce synthetic complexity through minimal analog re-design

Bioorganic & medicinal chemistry letters, 2007, Vol.17 (20), p.5567-5572

2007

Volltextzugriff (PDF)

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Oxazolidinone Antibiotics Target the P Site on Escherichia coli Ribosomes

Novel riboswitch-binding flavin analog that protects mice against Clostridium difficile infection without inhibiting cecal flora

Substituted 4-aminopiperidines having high in vitro affinity and selectivity for the cloned human dopamine D4 receptor

Pyrimidine Thioethers: A Novel Class of HIV-1 Reverse Transcriptase Inhibitors with Activity Against BHAP-Resistant HIV

Synthesis and Bioactivity of Novel Bis(heteroaryl)piperazine (BHAP) Reverse Transcriptase Inhibitors: Structure−Activity Relationships and Increased Metabolic Stability of Novel Substituted Pyridine Analogs

Synthesis and Structure−Activity Relationships of the (Alkylamino)piperidine-Containing BHAP Class of Non-Nucleoside Reverse Transcriptase Inhibitors: Effect of 3-Alkylpyridine Ring Substitution

Oxazolidinone Antibiotics Target the P Site on Escherichiacoli Ribosomes

Substituted 4-aminopiperidines having high in vitro affinity and selectivity for the cloned human dopamine D 4 receptor

(Alkylamino) piperidine bis(heteroaryl)piperizine analogs are potent, broad-spectrum nonnucleoside reverse transcriptase inhibitors of drug-resistant isolates of human immunodeficiency virus type 1 (HIV-1) and select for drug-resistant variants of HIV-1IIIB with reduced replication phenotypes

Stereoselective reactions of ester enolates with epoxides

Synthesis and Microbiological Evaluation of Novel Tetracyclic Fluoroquinolones

Cover Feature: Synthesis and Microbiological Evaluation of Novel Tetracyclic Fluoroquinolones (ChemMedChem 20/2017)

Repetitive use of levosimendan in advanced heart failure: need for stronger evidence in a field in dire need of a useful therapy

Design and synthesis of hepatoselective, pyrrole-based HMG-CoA reductase inhibitors

Antibacterial Oxazolidinones Possessing a Novel C-5 Side Chain. (5R)-trans-3-[3-Fluoro-4- (1-oxotetrahydrothiopyran-4-yl)phenyl]-2- oxooxazolidine-5-carboxylic Acid Amide (PF-00422602), a New Lead Compound

Pyrazole inhibitors of HMG-CoA reductase: An attempt to dramatically reduce synthetic complexity through minimal analog re-design

Targeting Delavirdine/Atevirdine Resistant HIV-1: Identification of (Alkylamino)piperidine-Containing Bis(heteroaryl)piperazines as Broad Spectrum HIV-1 Reverse Transcriptase Inhibitors

Stereodivergent synthesis of sulfoxide-containing oxazolidinone antibiotics

Pyrazole inhibitors of ΗΜΓ-CoA reductase : An attempt to dramatically reduce synthetic complexity through minimal analog re-design

(−)-6-Chloro-2-[(1-furo[2,3-c]pyridin-5-ylethyl)thio]-4-pyrimidinamine, PNU-142721, a New Broad Spectrum HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitor

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