Novel 5-Hydroxytryptamine (5-HT3) Receptor Antagonists. I. Synthesis and Structure-Activity Relationships of Conformationally Restricted Fused Imidazole Derivatives.

Mitsuaki OHTA; Takeshi SUZUKI; Tokuo KOIDE; Akira MATSUHISA; Toshio FURUYA; Keiji MIYATA; Isao YANAGISAWA

doi:10.1248/cpb.44.991

Novel 5-Hydroxytryptamine (5-HT3) Receptor Antagonists. I. Synthesis and Structure-Activity Relationships of Conformationally Restricted Fused Imidazole Derivatives.

Chemical and Pharmaceutical Bulletin ◽

10.1248/cpb.44.991 ◽

1996 ◽

Vol 44 (5) ◽

pp. 991-999 ◽

Cited By ~ 14

Author(s):

Mitsuaki OHTA ◽

Takeshi SUZUKI ◽

Tokuo KOIDE ◽

Akira MATSUHISA ◽

Toshio FURUYA ◽

...

Keyword(s):

Receptor Antagonists ◽

Structure Activity Relationships ◽

Imidazole Derivatives ◽

Conformationally Restricted ◽

Structure Activity

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ChemInform Abstract: Novel 5-Hydroxytryptamine (5-HT3) Receptor Antagonists. Part 1. Synthesis and Structure-Activity Relationships of Conformationally Restricted Fused Imidazole Derivatives.

ChemInform ◽

10.1002/chin.199647064 ◽

2010 ◽

Vol 27 (47) ◽

pp. no-no

Author(s):

M. OHTA ◽

T. SUZUKI ◽

T. KOIDE ◽

A. MATSUHISA ◽

T. FURUYA ◽

...

Keyword(s):

Receptor Antagonists ◽

Structure Activity Relationships ◽

Imidazole Derivatives ◽

Conformationally Restricted ◽

Structure Activity

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Nonpeptide angiotensin II receptor antagonists. 2. Design, synthesis, and structure-activity relationships of 2-alkyl-4-(1H-pyrrol-l-yl)-1H-imidazole derivatives: profile of 2-propyl-1-[[2'-(1H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl]-methyl]-4-[2-(trifluoroacetyl)-1H-pyrrol-1-yl]-1H-imidazole-5-carboxylic acid (CI-996)

Journal of Medicinal Chemistry ◽

10.1021/jm00068a002 ◽

1993 ◽

Vol 36 (16) ◽

pp. 2253-2265 ◽

Cited By ~ 9

Author(s):

Ila Sircar ◽

John C. Hodges ◽

John Quin ◽

Amy M. Bunker ◽

R. Thomas Winters ◽

...

Keyword(s):

Angiotensin Ii ◽

Carboxylic Acid ◽

Angiotensin Ii Receptor ◽

Angiotensin Ii Receptor Antagonists ◽

Receptor Antagonists ◽

Design Synthesis ◽

Structure Activity Relationships ◽

Imidazole Derivatives ◽

Structure Activity

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ChemInform Abstract: Nonpeptide Angiotensin II Receptor Antagonists. Part 2. Design, Synthesis, and Structure-Activity Relationships of 2-Alkyl-4-(1H-pyrrol-1-yl)-1H-imidazole Derivatives: Profile of 2-Propyl-1-((2′-(1H-tetrazol-5-yl)-(1,1′-biphenyl)-4-yl

ChemInform ◽

10.1002/chin.199352180 ◽

2010 ◽

Vol 24 (52) ◽

pp. no-no

Author(s):

I. SIRCAR ◽

J. C. HODGES ◽

J. III QUIN ◽

A. M. BUNKER ◽

R. T. WINTERS ◽

...

Keyword(s):

Angiotensin Ii ◽

Angiotensin Ii Receptor ◽

Angiotensin Ii Receptor Antagonists ◽

Receptor Antagonists ◽

Design Synthesis ◽

Structure Activity Relationships ◽

Imidazole Derivatives ◽

Structure Activity

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Nonpeptide angiotensin II receptor antagonists. 1. Synthesis and in vitro structure-activity relationships of 4-[[[(1H-pyrrol-1-ylacetyl)amino]phenyl]methyl]imidazole derivatives as angiotensin II receptor antagonists

Journal of Medicinal Chemistry ◽

10.1021/jm00064a007 ◽

1993 ◽

Vol 36 (12) ◽

pp. 1735-1745 ◽

Cited By ~ 12

Author(s):

Ila Sircar ◽

R. Thomas Winters ◽

John Quin ◽

Gina H. Lu ◽

Terry C. Major ◽

...

Keyword(s):

Angiotensin Ii ◽

Angiotensin Ii Receptor ◽

Angiotensin Ii Receptor Antagonists ◽

Receptor Antagonists ◽

Structure Activity Relationships ◽

Imidazole Derivatives ◽

Structure Activity ◽

Methyl Imidazole

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Synthesis, Molecular Pharmacology, and Structure–Activity Relationships of 3-(Indanoyl)indoles as Selective Cannabinoid Type 2 Receptor Antagonists

Journal of Medicinal Chemistry ◽

10.1021/acs.jmedchem.1c00442 ◽

2021 ◽

Author(s):

Harvey F. Fulo ◽

Amal Shoeib ◽

Christian V. Cabanlong ◽

Alexander H. Williams ◽

Chang-Guo Zhan ◽

...

Keyword(s):

Molecular Pharmacology ◽

Receptor Antagonists ◽

Structure Activity Relationships ◽

Structure Activity

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Synthesis and Structure−Activity Relationships of 2-Substitutedd-Tryptophan-Containing Peptidic Endothelin Receptor Antagonists: Importance of the C-2 Substituent of thed-Tryptophan Residue for Endothelin A and B Receptor Subtype Selectivity

Journal of Medicinal Chemistry ◽

10.1021/jm9600914 ◽

1996 ◽

Vol 39 (12) ◽

pp. 2313-2330 ◽

Cited By ~ 14

Author(s):

Takehiro Fukami ◽

Takeru Yamakawa ◽

Kenji Niiyama ◽

Hisaki Kojima ◽

Yuuka Amano ◽

...

Keyword(s):

Tryptophan Residue ◽

Receptor Subtype ◽

Endothelin Receptor Antagonists ◽

Endothelin Receptor ◽

Receptor Antagonists ◽

Structure Activity Relationships ◽

Subtype Selectivity ◽

Structure Activity ◽

Endothelin A

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Selective endothelin A receptor antagonists. 2. Discovery and structure-activity relationships of 5-ketopentanoic acid derivatives

European Journal of Medicinal Chemistry ◽

10.1016/s0223-5234(97)84014-7 ◽

1997 ◽

Vol 32 (6) ◽

pp. 515-522 ◽

Cited By ~ 8

Author(s):

P.C. Astles ◽

T.J. Brown ◽

N.V. Harris ◽

M.F. Harper ◽

C McCarthy ◽

...

Keyword(s):

Receptor Antagonists ◽

Structure Activity Relationships ◽

Structure Activity ◽

Endothelin A Receptor ◽

Endothelin A

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Synthesis and structure–activity relationships of ( R )-1-alkyl-3-[2-(2-amino)phenethyl]-5-(2-fluorophenyl)-6-methyluracils as human GnRH receptor antagonists

Bioorganic & Medicinal Chemistry Letters ◽

10.1016/j.bmcl.2004.02.004 ◽

2004 ◽

Vol 14 (9) ◽

pp. 2269-2274 ◽

Cited By ~ 14

Author(s):

Martin W Rowbottom ◽

Fabio C Tucci ◽

Yun-Fei Zhu ◽

Zhiqiang Guo ◽

Timothy D Gross ◽

...

Keyword(s):

Gnrh Receptor ◽

Receptor Antagonists ◽

Structure Activity Relationships ◽

Structure Activity

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Design of 2,5-Dimethyl-3-(6-dimethyl-4-methylpyridin-3-yl)-7-dipropylaminopyrazolo[1,5-a]pyrimidine (NBI 30775/R121919) and Structure−Activity Relationships of a Series of Potent and Orally Active Corticotropin-Releasing Factor Receptor Antagonists

Journal of Medicinal Chemistry ◽

10.1021/jm040058e ◽

2004 ◽

Vol 47 (19) ◽

pp. 4787-4798 ◽

Cited By ~ 91

Author(s):

Chen ◽

Keith M. Wilcoxen ◽

Charles Q. Huang ◽

Yun-Feng Xie ◽

James R. McCarthy ◽

...

Keyword(s):

Corticotropin Releasing Factor ◽

Receptor Antagonists ◽

Structure Activity Relationships ◽

Structure Activity ◽

Orally Active

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Structure–activity relationships of a novel series of melanin-concentrating hormone (MCH) receptor antagonists

Bioorganic & Medicinal Chemistry Letters ◽

10.1016/j.bmcl.2004.05.051 ◽

2004 ◽

Vol 14 (15) ◽

pp. 4099-4102 ◽

Cited By ~ 31

Author(s):

Rosa Arienzo ◽

David E Clark ◽

Sue Cramp ◽

Stephen Daly ◽

Hazel J Dyke ◽

...

Keyword(s):

Receptor Antagonists ◽

Structure Activity Relationships ◽

Structure Activity ◽

Melanin Concentrating Hormone

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