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Substituent Effects on the Antibacterial Activity of Nitrogen−Carbon-Linked (Azolylphenyl)oxazolidinones with Expanded Activity Against the Fastidious Gram-Negative Organisms Haemophilus influenzae and Moraxella catarrhalis

Journal of medicinal chemistry, 2000-03, Vol.43 (5), p.953-970

2000

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Progress toward the Development of a Safe and Effective Agent for Treating Reentrant Cardiac Arrhythmias: Synthesis and Evaluation of Ibutilide Analogues with Enhanced Metabolic Stability and Diminished Proarrhythmic Potential

Journal of medicinal chemistry, 2001-03, Vol.44 (7), p.1099-1115

2001

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N-[(.omega.-Amino-1-hydroxyalkyl)phenyl]methanesulfonamide derivatives with class III antiarrhythmic activity

Journal of medicinal chemistry, 1991-01, Vol.34 (1), p.308-315

1991

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4-Amino-4-arylcyclohexanones and their derivatives, a novel class of analgesics. 1. Modification of the aryl ring

Journal of medicinal chemistry, 1980-04, Vol.23 (4), p.424-430

1980

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4-Aryl-4-aminocyclohexanones and their derivatives, a novel class of analgesics. 3. m-Hydroxyphenyl derivatives

Journal of medicinal chemistry, 1981-03, Vol.24 (3), p.341-346

1981

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Partly reduced biphenyls as central nervous system agents. 1. 4-Arylcyclohex-3-enylamines

Journal of medicinal chemistry, 1972-12, Vol.15 (12), p.1235-1238

1972

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Partly reduced biphenyls as central nervous system agents. 2. Cis- and trans-4-arylcyclohexylamines

Journal of medicinal chemistry, 1972-12, Vol.15 (12), p.1239-1243

1972

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Substituent Effects on the Antibacterial Activity of Nitrogen−Carbon-Linked (Azolylphenyl)oxazolidinones with Expanded Activity Against the Fastidious Gram-Negative Organisms Haemophilus i nfluenzae and Moraxella c atarrhalis

Journal of medicinal chemistry, 2000-03, Vol.43 (5), p.953-970

2000

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Partly reduced biphenyls as central nervous system agents. 3. cis- and trans-4-Aryl-4-methoxycyclohexylamines

Journal of medicinal chemistry, 1973-11, Vol.16 (11), p.1251-1256

1973

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N([ω-amino-1-hydroxyalkyl)phenyl]methanesulfonamide derivatives with class III antiarrhythmic activity

Journal of medicinal chemistry, 1991, Vol.34 (1), p.308-315

1991

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4-aryl-4-aminocyclohexanones and their derivatives, a novel class of analgesics. 3. m-Hydroxyphenyl derivates

Journal of medicinal chemistry, 1981-03, Vol.24 (3), p.341-346

1981

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Partly reduced biphenyls as cetral nervous system agents. 3. Cis- and trans-4-aryl-4-methoxycyclohexylamines

Journal of medicinal chemistry, 1973-11, Vol.16 (11), p.1251

1973

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Substituent Effects on the Antibacterial Activity of Nitrogen−Carbon-Linked (Azolylphenyl)oxazolidinones with Expanded Activity Against the Fastidious Gram-Negative Organisms Haemophilus influenzae and Moraxella catarrhalis

Progress toward the Development of a Safe and Effective Agent for Treating Reentrant Cardiac Arrhythmias: Synthesis and Evaluation of Ibutilide Analogues with Enhanced Metabolic Stability and Diminished Proarrhythmic Potential

N-[(.omega.-Amino-1-hydroxyalkyl)phenyl]methanesulfonamide derivatives with class III antiarrhythmic activity

4-Amino-4-arylcyclohexanones and their derivatives, a novel class of analgesics. 1. Modification of the aryl ring

4-Aryl-4-aminocyclohexanones and their derivatives, a novel class of analgesics. 3. m-Hydroxyphenyl derivatives

Partly reduced biphenyls as central nervous system agents. 1. 4-Arylcyclohex-3-enylamines

Partly reduced biphenyls as central nervous system agents. 2. Cis- and trans-4-arylcyclohexylamines

Substituent Effects on the Antibacterial Activity of Nitrogen−Carbon-Linked (Azolylphenyl)oxazolidinones with Expanded Activity Against the Fastidious Gram-Negative Organisms Haemophilus i nfluenzae and Moraxella c atarrhalis

Partly reduced biphenyls as central nervous system agents. 3. cis- and trans-4-Aryl-4-methoxycyclohexylamines

N([ω-amino-1-hydroxyalkyl)phenyl]methanesulfonamide derivatives with class III antiarrhythmic activity

4-aryl-4-aminocyclohexanones and their derivatives, a novel class of analgesics. 3. m-Hydroxyphenyl derivates

Partly reduced biphenyls as cetral nervous system agents. 3. Cis- and trans-4-aryl-4-methoxycyclohexylamines

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