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1-[2-[(Heteroarylmethoxy)aryl]carbamoyl]indolines are selective and orally active 5-HT 2C receptor inverse agonists

Bioorganic & medicinal chemistry letters, 2000, Vol.10 (16), p.1867-1870

2000

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1-[2-[(Heteroarylmethoxy)aryl]carbamoyl]indolines are selective and orally active 5-HT2C receptor inverse agonists

Bioorganic & medicinal chemistry letters, 2000-08, Vol.10 (16), p.1867-1870

2000

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1-[2-[(Heteroaryloxy)heteroaryl]carbamoyl]indolines: novel and selective 5-HT 2C receptor inverse agonists with potential as antidepressant/Anxiolytic agents

Bioorganic & medicinal chemistry letters, 2000, Vol.10 (16), p.1863-1866

2000

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1-[2-[(Heteroaryloxy)heteroaryl]carbamoyl]indolines : Novel and selective 5-HT2C receptor inverse agonists with potential as antidepressant/anxiolytic agents

Bioorganic & medicinal chemistry letters, 2000-08, Vol.10 (16), p.1863-1866

2000

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3,4-Dihydro-2H-benzoxazinones are 5-HT1A receptor antagonists with potent 5-HT reuptake inhibitory activity

Bioorganic & medicinal chemistry letters, 2005-02, Vol.15 (3), p.737-741

2005

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[(3)H]-SB-269970--A selective antagonist radioligand for 5-HT(7) receptors

British journal of pharmacology, 2000-05, Vol.130 (2), p.409-417

2000

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[ 3H]Ditolylguanidine binding to human brain σ sites is diminished after haloperidol treatment

European journal of pharmacology, 1991-03, Vol.194 (2), p.235-236

1991

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[3H]‐SB‐269970 – A selective antagonist radioligand for 5‐HT7 receptors

British journal of pharmacology, 2000-05, Vol.130 (2), p.409-417

2000

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5-Carboxamidotryptamine-insensitive 5-HT sub(1)-like receptors are concentrated in guinea pig but not rat, claustrum

European journal of pharmacology, 1993-01, Vol.236 (1), p.167-169

1993

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5-Carboxamidotryptamine-insensitive 5-HT1-like receptors are concentrated in guinea pig but not rat, claustrum

European journal of pharmacology, 1993-05, Vol.236 (1), p.167-169

1993

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5-Chloro- N -(4-methoxy-3-piperazin-1-yl- phenyl)-3-methyl-2-benzothiophenesulfon- amide (SB-271046): A Potent, Selective, and Orally Bioavailable 5-HT 6 Receptor Antagonist

Journal of medicinal chemistry, 1999-01, Vol.42 (2), p.202-205

1999

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5-Chloro-N-(4-methoxy-3-piperazin-1-yl- phenyl)-3-methyl-2-benzothiophenesulfon- amide (SB-271046): A Potent, Selective, and Orally Bioavailable 5-HT6 Receptor Antagonist

Journal of medicinal chemistry, 1999-01, Vol.42 (2), p.202-205

1999

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5-chloro-N-(4-methoxy-3-piperazin-1-yl-phenyl)-3-methyl-2-benzothiophenesulfonamide (SB-271046) : A potent, selective, and orally bioavailable 5-HT6 receptor antagonist

Journal of medicinal chemistry, 1999-01, Vol.42 (2), p.202-205

1999

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5‐CT stimulation of adenylyl cyclase activity in guinea‐pig hippocampus: evidence for involvement of 5‐HT7 and 5‐HT1A receptors

British journal of pharmacology, 1999-09, Vol.128 (1), p.158-164

1999

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5‐HT 2C receptor antagonists: Potential in schizophrenia

Drug development research, 2001-10, Vol.54 (2), p.88-94

2001

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The 5-HT hypothesis of depression revisited

Molecular psychiatry, 1996-12, Vol.1 (6), p.437

1996

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5-HT sub(1)-like receptors: Six down and still counting

Trends in pharmacological sciences (Regular ed.), 1993-01, Vol.14 (6), p.228-231

1993

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The 5-HT sub(1B) receptors

Annals of the New York Academy of Sciences [ANN. N.Y. ACAD. SCI.]. 1990, 1990

1990

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5-HT1-like receptors : six down and still counting

Trends in pharmacological sciences (Regular ed.), 1993-06, Vol.14 (6), p.228-231

1993

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5-HT1A receptor activation increases hippocampal acetylcholine efflux and motor activity in the guinea pig: agonist efficacy influences functional activity in vivo

The Journal of pharmacology and experimental therapeutics, 1994-08, Vol.270 (2), p.656

1994

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The 5-HT1B Receptors

Annals of the New York Academy of Sciences, 1990-01, Vol.600 (1), p.132-147

1990

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5-HT1D receptors

Pharmacochemistry Library, 1997, Vol.27, p.101-138

1997

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5-HT2C receptor antagonists: Potential in schizophrenia

Drug development research, 2001-10, Vol.54 (2), p.88-94

2001

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5-Hydroxytryptamine1A but not 5-hydroxytryptamine2 receptors are enriched on neocortical pyramidal neurones destroyed by intrastriatal volkensin

The Journal of pharmacology and experimental therapeutics, 1992-06, Vol.261 (3), p.1273

1992

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L-694,247: A potent 5-HT sub(1D) receptor agonist

British journal of pharmacology, 1993-01, Vol.110 (3), p.1196-1200

1993

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1-[2-[(Heteroarylmethoxy)aryl]carbamoyl]indolines are selective and orally active 5-HT 2C receptor inverse agonists

1-[2-[(Heteroarylmethoxy)aryl]carbamoyl]indolines are selective and orally active 5-HT2C receptor inverse agonists

1-[2-[(Heteroaryloxy)heteroaryl]carbamoyl]indolines: novel and selective 5-HT 2C receptor inverse agonists with potential as antidepressant/Anxiolytic agents

1-[2-[(Heteroaryloxy)heteroaryl]carbamoyl]indolines : Novel and selective 5-HT2C receptor inverse agonists with potential as antidepressant/anxiolytic agents

3,4-Dihydro-2H-benzoxazinones are 5-HT1A receptor antagonists with potent 5-HT reuptake inhibitory activity

[(3)H]-SB-269970--A selective antagonist radioligand for 5-HT(7) receptors

[ 3H]Ditolylguanidine binding to human brain σ sites is diminished after haloperidol treatment

[3H]‐SB‐269970 – A selective antagonist radioligand for 5‐HT7 receptors

5-Carboxamidotryptamine-insensitive 5-HT sub(1)-like receptors are concentrated in guinea pig but not rat, claustrum

5-Carboxamidotryptamine-insensitive 5-HT1-like receptors are concentrated in guinea pig but not rat, claustrum

5-Chloro- N -(4-methoxy-3-piperazin-1-yl- phenyl)-3-methyl-2-benzothiophenesulfon- amide (SB-271046): A Potent, Selective, and Orally Bioavailable 5-HT 6 Receptor Antagonist

5-Chloro-N-(4-methoxy-3-piperazin-1-yl- phenyl)-3-methyl-2-benzothiophenesulfon- amide (SB-271046): A Potent, Selective, and Orally Bioavailable 5-HT6 Receptor Antagonist

5-chloro-N-(4-methoxy-3-piperazin-1-yl-phenyl)-3-methyl-2-benzothiophenesulfonamide (SB-271046) : A potent, selective, and orally bioavailable 5-HT6 receptor antagonist

5‐CT stimulation of adenylyl cyclase activity in guinea‐pig hippocampus: evidence for involvement of 5‐HT7 and 5‐HT1A receptors

5‐HT 2C receptor antagonists: Potential in schizophrenia

The 5-HT hypothesis of depression revisited

5-HT sub(1)-like receptors: Six down and still counting

The 5-HT sub(1B) receptors

5-HT1-like receptors : six down and still counting

5-HT1A receptor activation increases hippocampal acetylcholine efflux and motor activity in the guinea pig: agonist efficacy influences functional activity in vivo

The 5-HT1B Receptors

5-HT1D receptors

5-HT2C receptor antagonists: Potential in schizophrenia

5-Hydroxytryptamine1A but not 5-hydroxytryptamine2 receptors are enriched on neocortical pyramidal neurones destroyed by intrastriatal volkensin

L-694,247: A potent 5-HT sub(1D) receptor agonist

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