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Convergent, parallel synthesis of a series of β-substituted 1,2,4-oxadiazole butanoic acids as potent and selective αvβ3 receptor antagonists

Bioorganic & medicinal chemistry letters, 2006-02, Vol.16 (4), p.839-844

2006

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Synthesis of imidazopyridines and purines as potent inhibitors of leukotriene A4 hydrolase

Bioorganic & medicinal chemistry letters, 2003-03, Vol.13 (6), p.1137-1139

2003

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Synthesis of cinnamic acids and related isosteres as potent and selective αvβ3 receptor antagonists

Bioorganic & medicinal chemistry letters, 2004-03, Vol.14 (6), p.1471-1476

2004

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Pyrrolidine and piperidine analogues of SC-57461A as potent, orally active inhibitors of leukotriene A4 hydrolase

Bioorganic & medicinal chemistry letters, 2002-12, Vol.12 (23), p.3383-3386

2002

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Synthesis and structure-activity relationships of a new series of antiarrhythmic agents: monobasic derivatives of disobutamide

Journal of medicinal chemistry, 1988-11, Vol.31 (11), p.2158-2164

1988

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Synthesis of cinnamic acids and related isosteres as potent and selective alpha v beta 3 receptor antagonists

Bioorganic & medicinal chemistry letters, 2004-03, Vol.14 (6), p.1471-1476

2004

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Synthesis of 4-phenyl-5H-pyrido[3,4-b][1,4]benzothiazin-3(2H)-ones (4-phenylazaphenothiazines) via activated dimethylformamide reagents

Journal of organic chemistry, 1987-04, Vol.52 (7), p.1366-1369

1987

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Pyrrolidine and piperidine analogues of SC-57461A as potent, orally active inhibitors of leukotriene A(4) hydrolase

Bioorganic & medicinal chemistry letters, 2002-12, Vol.12 (23), p.3383

2002

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Synthesis, benzodiazepine receptor binding, and anticonvulsant activity of 2,3-dihydro-3-oxo-5H-pyrido[3,4-b][1,4]benzothiazine-4-carbonitriles

Journal of medicinal chemistry, 1983-06, Vol.26 (6), p.845-850

1983

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Structure-activity relationship study of spirolactones. Contribution of the cyclopropane ring to antimineralocorticoid activity

Journal of medicinal chemistry, 1981-09, Vol.24 (9), p.1103-1107

1981

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Steroidal ethers. Analogs of 7-ketocholesterol

Journal of organic chemistry, 1979-05, Vol.44 (10), p.1590-1596

1979

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Facile synthesis of 3.beta.-hydroxy-5.alpha.-cholest-8(14)-en-15-one 3-acetate

Journal of organic chemistry, 1979-10, Vol.44 (22), p.3974-3976

1979

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22-Hydroxycholesterol derivatives as HMG CoA reductase suppressors and serum cholesterol lowering agents

Journal of medicinal chemistry, 1985-02, Vol.28 (2), p.194-200

1985

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Synthesis of Imidazopyridines and Purines as Potent Inhibitors of Leukotriene A 4 Hydrolase

Bioorganic & medicinal chemistry letters, 2003, Vol.13 (6), p.1137-1139

2003

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Synthesis of 15-keto-6.beta.,7.beta.-methyleneprogesterone. Effect of the 6.beta.,7.beta.-methylene group on mineralocorticoid activity

Journal of medicinal chemistry, 1975-03, Vol.18 (3), p.268-271

1975

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Possible anchimeric assistance in the hydration-decarboxylation of a propiolic acid. Synthesis of methyl 3-(17.beta.-acetoxy-3-oxoandrosta-4,6-dien-17.alpha.-yl)propionate

Journal of organic chemistry, 1975-05, Vol.40 (9), p.1328-1331

1975

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Pyrrolidine and piperidine analogues of SC-57461A as potent, orally active inhibitors of leukotriene A 4 hydrolase

Bioorganic & medicinal chemistry letters, 2002, Vol.12 (23), p.3383-3386

2002

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Synthesis of 3,9‐dihydro‐3,9‐dioxo‐2 H ‐indeno[2,1‐ c ] pyridine‐4‐carbonitriles

Journal of heterocyclic chemistry, 1980-09, Vol.17 (6), p.1313-1315

1980

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Synthesis of 3,9-dihydro-3,9-dioxo-2H-indeno[2,1-c] pyridine-4-carbonitriles

Journal of heterocyclic chemistry, 1980-09, Vol.17 (6), p.1313-1315

1980

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Effect of 23-methyl-21-norcholest-5-ene-3β,23,25-triol on hepatic cholesterol 7α-hydroxylase activity in the rat

Journal of steroid biochemistry, 1979-06, Vol.10 (6), p.709-710

1979

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Convergent, parallel synthesis of a series of β-substituted 1,2,4-oxadiazole butanoic acids as potent and selective αvβ3 receptor antagonists

Synthesis of imidazopyridines and purines as potent inhibitors of leukotriene A4 hydrolase

Structure−Activity Relationship Studies on 1-[2-(4-Phenylphenoxy)ethyl]pyrrolidine (SC-22716), a Potent Inhibitor of Leukotriene A4 (LTA4) Hydrolase

Synthesis of cinnamic acids and related isosteres as potent and selective αvβ3 receptor antagonists

Pyrrolidine and piperidine analogues of SC-57461A as potent, orally active inhibitors of leukotriene A4 hydrolase

Synthesis and structure-activity relationships of a new series of antiarrhythmic agents: monobasic derivatives of disobutamide

Synthesis of cinnamic acids and related isosteres as potent and selective alpha v beta 3 receptor antagonists

Synthesis of 4-phenyl-5H-pyrido[3,4-b][1,4]benzothiazin-3(2H)-ones (4-phenylazaphenothiazines) via activated dimethylformamide reagents

Convergent, parallel synthesis of a series of beta-substituted 1,2,4-oxadiazole butanoic acids as potent and selective alpha(v)beta3 receptor antagonists

Convergent, parallel synthesis of a series of beta -substituted 1,2,4- oxadiazole butanoic acids as potent and selective alpha sub(v) beta sub(3) receptor antagonists

Convergent, parallel synthesis of a series of β-substituted 1,2,4-oxadiazole butanoic acids as potent and selective α vβ 3 receptor antagonists

Pyrrolidine and piperidine analogues of SC-57461A as potent, orally active inhibitors of leukotriene A(4) hydrolase

Synthesis, benzodiazepine receptor binding, and anticonvulsant activity of 2,3-dihydro-3-oxo-5H-pyrido[3,4-b][1,4]benzothiazine-4-carbonitriles

Structure-activity relationship study of spirolactones. Contribution of the cyclopropane ring to antimineralocorticoid activity

Steroidal ethers. Analogs of 7-ketocholesterol

Facile synthesis of 3.beta.-hydroxy-5.alpha.-cholest-8(14)-en-15-one 3-acetate

22-Hydroxycholesterol derivatives as HMG CoA reductase suppressors and serum cholesterol lowering agents

Synthesis of Imidazopyridines and Purines as Potent Inhibitors of Leukotriene A 4 Hydrolase

Synthesis of 15-keto-6.beta.,7.beta.-methyleneprogesterone. Effect of the 6.beta.,7.beta.-methylene group on mineralocorticoid activity

Possible anchimeric assistance in the hydration-decarboxylation of a propiolic acid. Synthesis of methyl 3-(17.beta.-acetoxy-3-oxoandrosta-4,6-dien-17.alpha.-yl)propionate

Pyrrolidine and piperidine analogues of SC-57461A as potent, orally active inhibitors of leukotriene A 4 hydrolase

Structure−Activity Relationship Studies on 1-[2-(4-Phenylphenoxy)ethyl]pyrrolidine (SC-22716), a Potent Inhibitor of Leukotriene A 4 (LTA 4 ) Hydrolase

Synthesis of 3,9‐dihydro‐3,9‐dioxo‐2 H ‐indeno[2,1‐ c ] pyridine‐4‐carbonitriles

Synthesis of 3,9-dihydro-3,9-dioxo-2H-indeno[2,1-c] pyridine-4-carbonitriles

Effect of 23-methyl-21-norcholest-5-ene-3β,23,25-triol on hepatic cholesterol 7α-hydroxylase activity in the rat

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