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Fatty acid amide hydrolase inhibitors--progress and potential

CNS & neurological disorders drug targets, 2011-08, Vol.10 (5), p.545

2011

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Buprenorphine - an attractive opioid with underutilized potential in treatment of chronic pain

Journal of Pain Research, 2015-01, Vol.8 (Issue 1), p.859-870

2015

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1,2-Diarylimidazoles as Potent, Cyclooxygenase-2 Selective, and Orally Active Antiinflammatory Agents

Journal of medicinal chemistry, 1997-05, Vol.40 (11), p.1634-1647

1997

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1,2-Diarylpyrroles as Potent and Selective Inhibitors of Cyclooxygenase-2

Journal of medicinal chemistry, 1997-05, Vol.40 (11), p.1619-1633

1997

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Discovery of + (2 -{4 -[2 -(5,6,7,8 -tetrahydro -1,8 -naphthyridin -2-yl )ethoxy ]phenyl} -cyclopropyl )acetic acid as potent and selective αvβ3 inhibitor : Design, synthesis, and optimization

Bioorganic & medicinal chemistry, 2007-05, Vol.15 (10), p.3390-3412

2007

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Facile, Regioselective Syntheses of N-Alkylated 2,3-Diaminopyridines and Imidazo[4,5-b]pyridines

Journal of organic chemistry, 1995-02, Vol.60 (4), p.960-965

1995

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Selective Cyclooxygenase-2 Inhibitors: Heteroaryl Modified 1,2-Diarylimidazoles Are Potent, Orally Active Antiinflammatory Agents

Journal of medicinal chemistry, 2000-08, Vol.43 (16), p.3168-3185

2000

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Regiospecific addition of Grignard reagents to the 4-position of activated imidazo[4,5-c]pyridine. A convenient method for the synthesis of 4-alkyl(ary

Tetrahedron letters, 1993-03, Vol.34 (12), p.1885-1888

1993

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The synthesis of 1,5-dideoxy-1,5-(alkyl)imino-2-C-methyl- d-glucitols

Tetrahedron letters, 1996-02, Vol.37 (9), p.1355-1358

1996

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The mild and selective N-debenzylation of tertiary alkylamines using β-trimethylsilylethyl chloroformate

Tetrahedron letters, 1987, Vol.28 (21), p.2331-2334

1987

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Nucleophilic Opening of N-Carboalkoxy-2,3-anhydro-1-deoxymannojirimycin. A Useful Method for the Syntheses of 2-, 3- and 2,3-Disubstituted 1-Deoxynojirimycin Analogs

Journal of carbohydrate chemistry, 1995-08, Vol.14 (6), p.843-878

1995

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Total synthesis of 4-Demethoxy-8-nordaunomycinone

Tetrahedron letters, 1985, Vol.26 (6), p.691-694

1985

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Antimicrobial agents from higher plants: Activity and structural revision of flemiflavanone-D from Flemingia stricta

Phytochemistry (Oxford), 1985-01, Vol.24 (12), p.2885-2887

1985

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Design and optimization of quinazoline derivatives as melanin concentrating hormone receptor 1 (MCHR1) antagonists

Bioorganic & medicinal chemistry letters, 2012-05, Vol.22 (9), p.3157-3162

2012

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Design and optimization of quinazoline derivatives as melanin concentrating hormone receptor 1 (MCHR1) antagonists: Part 2

Bioorganic & medicinal chemistry letters, 2012-05, Vol.22 (9), p.3163-3167

2012

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Optimisation of in silico derived 2-aminobenzimidazole hits as unprecedented selective kappa opioid receptor agonists

Bioorganic & medicinal chemistry letters, 2015-02, Vol.25 (4), p.887-892

2015

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Central nervous system fungal infections: Observations from a large tertiary hospital in northern India

Clinical neurology and neurosurgery, 2012-11, Vol.114 (9), p.1232-1237

2012

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Discovery of novel, orally available benzimidazoles as melanin concentrating hormone receptor 1 (MCHR1) antagonists

Bioorganic & medicinal chemistry letters, 2010-09, Vol.20 (18), p.5443-5448

2010

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Synthesis and SAR studies of benzimidazole derivatives as melanin concentrating hormone receptor 1 (MCHR1) antagonists: Focus to detune hERG inhibition

MedChemComm, 2011-05, Vol.2 (5), p.385

2011

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BIOSYNTHESIS OF CETOCYCLINE

The Journal of Antibiotics, 1983, Vol.36(10), pp.1405-1407

1983

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Fatty acid amide hydrolase inhibitors--progress and potential

Buprenorphine - an attractive opioid with underutilized potential in treatment of chronic pain

1,2-Diarylimidazoles as Potent, Cyclooxygenase-2 Selective, and Orally Active Antiinflammatory Agents

1,2-Diarylpyrroles as Potent and Selective Inhibitors of Cyclooxygenase-2

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

Discovery of + (2 -{4 -[2 -(5,6,7,8 -tetrahydro -1,8 -naphthyridin -2-yl )ethoxy ]phenyl} -cyclopropyl )acetic acid as potent and selective αvβ3 inhibitor : Design, synthesis, and optimization

Facile, Regioselective Syntheses of N-Alkylated 2,3-Diaminopyridines and Imidazo[4,5-b]pyridines

Selective Cyclooxygenase-2 Inhibitors: Heteroaryl Modified 1,2-Diarylimidazoles Are Potent, Orally Active Antiinflammatory Agents

Discovery of +(2-{4-[2-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)ethoxy]phenyl}-cyclopropyl)acetic acid as potent and selective α vβ 3 inhibitor: Design, synthesis, and optimization

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

Regiospecific addition of Grignard reagents to the 4-position of activated imidazo[4,5-c]pyridine. A convenient method for the synthesis of 4-alkyl(ary

The synthesis of 1,5-dideoxy-1,5-(alkyl)imino-2-C-methyl- d-glucitols

The mild and selective N-debenzylation of tertiary alkylamines using β-trimethylsilylethyl chloroformate

Nucleophilic Opening of N-Carboalkoxy-2,3-anhydro-1-deoxymannojirimycin. A Useful Method for the Syntheses of 2-, 3- and 2,3-Disubstituted 1-Deoxynojirimycin Analogs

Total synthesis of 4-Demethoxy-8-nordaunomycinone

Antimicrobial agents from higher plants: Activity and structural revision of flemiflavanone-D from Flemingia stricta

Design and optimization of quinazoline derivatives as melanin concentrating hormone receptor 1 (MCHR1) antagonists

Design and optimization of quinazoline derivatives as melanin concentrating hormone receptor 1 (MCHR1) antagonists: Part 2

Optimisation of in silico derived 2-aminobenzimidazole hits as unprecedented selective kappa opioid receptor agonists

Central nervous system fungal infections: Observations from a large tertiary hospital in northern India

Discovery of novel, orally available benzimidazoles as melanin concentrating hormone receptor 1 (MCHR1) antagonists

Synthesis and SAR studies of benzimidazole derivatives as melanin concentrating hormone receptor 1 (MCHR1) antagonists: Focus to detune hERG inhibition

BIOSYNTHESIS OF CETOCYCLINE

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