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In vitro phamacology of MK-996, a new potent and selective angiotensin II (AT1) receptor antagonist

Drug development research, 1994-07, Vol.32 (3), p.161-171

1994

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Design and Synthesis of Novel α1 a Adrenoceptor-Selective Antagonists. 3. Approaches To Eliminate Opioid Agonist Metabolites by Using Substituted Phenylpiperazine Side Chains

Journal of medicinal chemistry, 1999-11, Vol.42 (23), p.4794-4803

1999

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Design and Synthesis of Novel α1 a Adrenoceptor-Selective Antagonists. 4. Structure−Activity Relationship in the Dihydropyrimidine Series

Journal of medicinal chemistry, 1999-11, Vol.42 (23), p.4804-4813

1999

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Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 1. Structure-activity relationship in dihydropyrimidinones

Journal of medicinal chemistry, 1999-11, Vol.42 (23), p.4764-4777

1999

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Design and Synthesis of Novel α1 a Adrenoceptor-Selective Antagonists. 1. Structure−Activity Relationship in Dihydropyrimidinones

Journal of medicinal chemistry, 1999-11, Vol.42 (23), p.4764-4777

1999

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Characterization of specific binding of [formula omitted]L-762,459, a selective α1A-adrenoceptor radioligand to rat and human tissues

European journal of pharmacology, 1998-05, Vol.348 (2), p.287-295

1998

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Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 3. Approaches to eliminate opioid agonist metabolites by using substituted phenylpiperazine side chains

Journal of medicinal chemistry, 1999-11, Vol.42 (23), p.4794-4803

1999

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Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 4. Structure-activity relationship in the dihydropyrimidine series

Journal of medicinal chemistry, 1999-11, Vol.42 (23), p.4804-4813

1999

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Design and synthesis of novel dihydropyridine alpha-1A antagonists

Bioorganic & medicinal chemistry letters, 1999-10, Vol.9 (19), p.2843-2848

1999

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Design and synthesis of N-alkylated saccharins as selective α-1a adrenergic receptor antagonists

Bioorganic & medicinal chemistry letters, 1998-09, Vol.8 (18), p.2467-2472

1998

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Design and Synthesis of Novel α 1 a Adrenoceptor-Selective Antagonists. 4. Structure−Activity Relationship in the Dihydropyrimidine Series

Journal of medicinal chemistry, 1999-11, Vol.42 (23), p.4804-4813

1999

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Design and Synthesis of Novel α 1 a Adrenoceptor-Selective Antagonists. 3. Approaches To Eliminate Opioid Agonist Metabolites by Using Substituted Phenylpiperazine Side Chains

Journal of medicinal chemistry, 1999-11, Vol.42 (23), p.4794-4803

1999

Volltextzugriff (PDF)

Design and Synthesis of Novel α 1 a Adrenoceptor-Selective Antagonists. 1. Structure−Activity Relationship in Dihydropyrimidinones

Journal of medicinal chemistry, 1999-11, Vol.42 (23), p.4764-4777

1999

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Characterization of the binding of [3H]L-158,809: a new potent and selective nonpeptide angiotensin II receptor (AT1) antagonist radioligand

Molecular pharmacology, 1992-12, Vol.42 (6), p.1077-1082

1992

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Two angiotensin II binding sites in rat brain revealed using [ 125I]Sar 1, Ile 8-angiotensin II and selective nonpeptide antagonists

Biochemical and biophysical research communications, 1990, Vol.171 (2), p.813-817

1990

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Characterization of [formula omitted] binding to solubilized cholecystokinin (CCK) receptors of rat pancreas

Biochemical pharmacology, 1987, Vol.36 (10), p.1709-1714

1987

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Characterization of [3H](±)L-364,718 binding to solubilized cholecystokinin (CCK) receptors of rat pancreas

Biochemical pharmacology, 1987-05, Vol.36 (10), p.1709-1714

1987

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Tifluadom, a κ-opiate agonist, acts as a peripheral cholecystokinin receptor antagonist

Neuroscience letters, 1986-12, Vol.72 (2), p.211-214

1986

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Two angiotensin II binding sites in rat brain revealed using [125I]Sar1, Ile8-angiotensin II and selective nonpeptide antagonists

Biochemical and biophysical research communications, 1990-09, Vol.171 (2), p.813-817

1990

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Cholecystokinin receptor mediated hydrolysis of inositol phospholipids in guinea pig gastric glands

Life sciences (1973), 1985-03, Vol.36 (10), p.965-971

1985

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Inactivation of cholecystokinin receptors in rat pancreatic membranes by sulfhydryl reagents: Protection by guanosine 5′-triphosphate (GTP) but not N2, O2-dibutyryl guanosine 3′, 5′-cyclic monophosphate (dibutyryl cGMP)

Biochemical pharmacology, 1984-07, Vol.33 (14), p.2334-2335

1984

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Increase in brain 125I-cholecystokinin (CCK) receptor binding following chronic haloperidol treatment, intracisternal 6-hydroxydopamine or ventral tegmental lesions

Life sciences (1973), 1983-02, Vol.32 (8), p.871-878

1983

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A novel selective positive allosteric modulator of metabotropic glutamate receptor subtype 5 has in vivo activity and antipsychotic-like effects in rat behavioral models

The Journal of pharmacology and experimental therapeutics, 2005-04, Vol.313 (1), p.199-206

2005

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Persistence of Mycobacterium tuberculosis in macrophages and mice requires the glyoxylate shunt enzyme isocitrate lyase

Nature (London), 2000-08, Vol.406 (6797), p.735-738

2000

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A Family of Highly Selective Allosteric Modulators of the Metabotropic Glutamate Receptor Subtype 5

Molecular pharmacology, 2003-09, Vol.64 (3), p.731-740

2003

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In vitro phamacology of MK-996, a new potent and selective angiotensin II (AT1) receptor antagonist

Design and Synthesis of Novel α1 a Adrenoceptor-Selective Antagonists. 3. Approaches To Eliminate Opioid Agonist Metabolites by Using Substituted Phenylpiperazine Side Chains

Design and Synthesis of Novel α1 a Adrenoceptor-Selective Antagonists. 4. Structure−Activity Relationship in the Dihydropyrimidine Series

Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 1. Structure-activity relationship in dihydropyrimidinones

Design and Synthesis of Novel α1 a Adrenoceptor-Selective Antagonists. 1. Structure−Activity Relationship in Dihydropyrimidinones

Characterization of specific binding of [formula omitted]L-762,459, a selective α1A-adrenoceptor radioligand to rat and human tissues

Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 3. Approaches to eliminate opioid agonist metabolites by using substituted phenylpiperazine side chains

Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 4. Structure-activity relationship in the dihydropyrimidine series

Design and synthesis of novel dihydropyridine alpha-1A antagonists

Design and synthesis of N-alkylated saccharins as selective α-1a adrenergic receptor antagonists

Design and Synthesis of Novel α 1 a Adrenoceptor-Selective Antagonists. 4. Structure−Activity Relationship in the Dihydropyrimidine Series

Design and Synthesis of Novel α 1 a Adrenoceptor-Selective Antagonists. 3. Approaches To Eliminate Opioid Agonist Metabolites by Using Substituted Phenylpiperazine Side Chains

Design and Synthesis of Novel α 1 a Adrenoceptor-Selective Antagonists. 1. Structure−Activity Relationship in Dihydropyrimidinones

Characterization of the binding of [3H]L-158,809: a new potent and selective nonpeptide angiotensin II receptor (AT1) antagonist radioligand

Two angiotensin II binding sites in rat brain revealed using [ 125I]Sar 1, Ile 8-angiotensin II and selective nonpeptide antagonists

Characterization of [formula omitted] binding to solubilized cholecystokinin (CCK) receptors of rat pancreas

Characterization of [3H](±)L-364,718 binding to solubilized cholecystokinin (CCK) receptors of rat pancreas

Tifluadom, a κ-opiate agonist, acts as a peripheral cholecystokinin receptor antagonist

Two angiotensin II binding sites in rat brain revealed using [125I]Sar1, Ile8-angiotensin II and selective nonpeptide antagonists

Cholecystokinin receptor mediated hydrolysis of inositol phospholipids in guinea pig gastric glands

Inactivation of cholecystokinin receptors in rat pancreatic membranes by sulfhydryl reagents: Protection by guanosine 5′-triphosphate (GTP) but not N2, O2-dibutyryl guanosine 3′, 5′-cyclic monophosphate (dibutyryl cGMP)

Increase in brain 125I-cholecystokinin (CCK) receptor binding following chronic haloperidol treatment, intracisternal 6-hydroxydopamine or ventral tegmental lesions

A novel selective positive allosteric modulator of metabotropic glutamate receptor subtype 5 has in vivo activity and antipsychotic-like effects in rat behavioral models

Persistence of Mycobacterium tuberculosis in macrophages and mice requires the glyoxylate shunt enzyme isocitrate lyase

A Family of Highly Selective Allosteric Modulators of the Metabotropic Glutamate Receptor Subtype 5

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