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Enlarging the NSAIDs family: ether, ester and acid derivatives of the 1,5-diarylpyrrole scaffold as novel anti-inflammatory and analgesic agents

Current medicinal chemistry, 2011-04, Vol.18 (10), p.1540-1554

2011

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Bactericidal Activities of the Pyrrole Derivative BM212 against Multidrug-Resistant and Intramacrophagic Mycobacterium tuberculosis Strains

Antimicrobial Agents and Chemotherapy, 1998-11, Vol.42 (11), p.3035-3037

1998

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New derivatives of BM212: A class of antimycobacterial compounds based on the pyrrole ring as a scaffold

Mini reviews in medicinal chemistry, 2007-01, Vol.7 (1), p.65-78

2007

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1,5-Diarylpyrrole-3-acetic Acids and Esters as Novel Classes of Potent and Highly Selective Cyclooxygenase-2 Inhibitors

Journal of medicinal chemistry, 2005-05, Vol.48 (9), p.3428-3432

2005

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New Pyrroles with Potential Antimycobacterial, Antifungal and Selective COX-2 Inhibiting Activities. Synthetic Methodologies

Current organic chemistry, 2007-08, Vol.11 (12), p.1092-1112

2007

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Building a pharmacophore model for a novel class of antitubercular compounds

Farmaco (Società chimica italiana : 1989), 2000-06, Vol.55 (6), p.484-491

2000

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New trends in development of antimycobacterial compounds

Infectious disorders drug targets, 2006-06, Vol.6 (2), p.159-172

2006

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The Antifungal Agent 1-[2-(4-Chlorobenzylamino)benzyl]-1H-imidazole

Acta crystallographica. Section C, Crystal structure communications, 1997-06, Vol.53 (6), p.761-762

1997

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Antimycobacterial activity of new ortho-, meta- and para-toluidine derivatives

Farmaco (Società chimica italiana : 1989), 1999-11, Vol.54 (11), p.721-727

1999

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Synthesis and microbiological evaluations of (N-heteroaryl) arylmethanamines and their Schiff bases

Farmaco (Società chimica italiana : 1989), 1996-10, Vol.51 (10), p.643

1996

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Research on antibacterial and antifungal agents. XII--Synthesis and antimicrobial activity of some Mannich bases of diarylpyrroles

Farmaco (Società chimica italiana : 1989), 1995-09, Vol.50 (9), p.617

1995

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Study of the Mannich reaction: beta-amino-methylation of N-aryl and N-azaheteroaryl-substituted 2,5-dimethylpyrroles, compounds with potential biological activity

Farmaco (Società chimica italiana : 1989), 1995-06, Vol.50 (6), p.431

1995

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Antimicrobial activity of a new derivative: N-(4-chlorobenzyl)-2-(1H-imidazol-1-ylmethyl)benzenamine

Drugs under experimental and clinical research, 1990, Vol.16 (4), p.181

1990

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Antifungal agents. 7. Dichlorophenylpyrrylimidazolylmethane derivatives: synthesis and antifungal activities

Farmaco (Società chimica italiana : 1989), 1994-01, Vol.49 (1), p.51

1994

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Crystal structure of 2-[5-(4-carbethoxyphenoxy)pentanoyl]-5-chlorothiophene, C18H19O4CIS

Zeitschrift für Kristallographie. New crystal structures, 1998-04, Vol.213 (1), p.129-130

1998

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Crystal structure of 2-[5-(4-carbethoxyphenoxy)pentanoyl]-5-chlorothiophene, C18H19O4ClS

Zeitschrift für Kristallographie. New crystal structures, 1998, Vol.213 (1), p.129-130

1998

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Antifungal Agents, II: Synthesis and Antifungal Activities of Aryl-1H-pyrrol-2-yl-1H-imidazol-1-yl-methane Derivatives with Unsaturated Chains

Archiv der Pharmazie (Weinheim), 1993, Vol.326 (9), p.539-546

1993

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Research on compounds with antiblastic activity. 43. Synthesis of 9H-pyrrolo-(1,2-a)-indole derivatives

Il Farmaco; edizione scientifica, 1972-01, Vol.27 (1), p.60

1972

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β-Aminomethylation of N-aryl- and N-azaheteroaryl-substituted methyl 2,5-dimethylpyrrole-3-carboxylates. Kinetic effect of the N-pyrrole substituent

ARKIVOC, 2004-04, Vol.2004 (5), p.325-333

2004

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The Antifungal Agent 1-[2-(4-Chlorobenzylamino)benzyl]-1 H -imidazole

Acta crystallographica. Section C, Crystal structure communications, 1997-06, Vol.53 (6), p.761-762

1997

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Antifungal Agents, Part 11: Biphenyl Analogues of Naftifine: Synthesis and Antifungal Activities

Archiv der Pharmazie (Weinheim), 1995, Vol.328 (9), p.667-672

1995

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Electron impact mass spectra of para-substituted N-heteroaryl benzylamines

Heterocycles, 1994, Vol.37 (1), p.367-377

1994

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ChemInform Abstract: New Pyrroles with Potential Antimycobacterial, Antifungal, and Selective COX-2 Inhibiting Activities. Synthetic Methodologies

ChemInform, 2008-04, Vol.39 (14), p.no-no

2008

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Antifungal agents. XI: Biphenyl analogues of naftifine : synthesis and antifungal activities

Archiv der Pharmazie (Weinheim), 1995, Vol.328 (9), p.667-672

1995

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Synthesis of 5H-pyrrolo[2,1-c][1,4]benzodiazepine and some of its derivatives related to anthramycin

Journal of the Chemical Society D: Chemical Communications, 1969 (12), p.671

1969

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Enlarging the NSAIDs family: ether, ester and acid derivatives of the 1,5-diarylpyrrole scaffold as novel anti-inflammatory and analgesic agents

Bactericidal Activities of the Pyrrole Derivative BM212 against Multidrug-Resistant and Intramacrophagic Mycobacterium tuberculosis Strains

New derivatives of BM212: A class of antimycobacterial compounds based on the pyrrole ring as a scaffold

1,5-Diarylpyrrole-3-acetic Acids and Esters as Novel Classes of Potent and Highly Selective Cyclooxygenase-2 Inhibitors

New Pyrroles with Potential Antimycobacterial, Antifungal and Selective COX-2 Inhibiting Activities. Synthetic Methodologies

Building a pharmacophore model for a novel class of antitubercular compounds

New trends in development of antimycobacterial compounds

The Antifungal Agent 1-[2-(4-Chlorobenzylamino)benzyl]-1H-imidazole

Antimycobacterial activity of new ortho-, meta- and para-toluidine derivatives

Synthesis and microbiological evaluations of (N-heteroaryl) arylmethanamines and their Schiff bases

Research on antibacterial and antifungal agents. XII--Synthesis and antimicrobial activity of some Mannich bases of diarylpyrroles

Study of the Mannich reaction: beta-amino-methylation of N-aryl and N-azaheteroaryl-substituted 2,5-dimethylpyrroles, compounds with potential biological activity

Antimicrobial activity of a new derivative: N-(4-chlorobenzyl)-2-(1H-imidazol-1-ylmethyl)benzenamine

Antifungal agents. 7. Dichlorophenylpyrrylimidazolylmethane derivatives: synthesis and antifungal activities

Crystal structure of 2-[5-(4-carbethoxyphenoxy)pentanoyl]-5-chlorothiophene, C18H19O4CIS

Crystal structure of 2-[5-(4-carbethoxyphenoxy)pentanoyl]-5-chlorothiophene, C18H19O4ClS

Antifungal Agents, II: Synthesis and Antifungal Activities of Aryl-1H-pyrrol-2-yl-1H-imidazol-1-yl-methane Derivatives with Unsaturated Chains

Research on compounds with antiblastic activity. 43. Synthesis of 9H-pyrrolo-(1,2-a)-indole derivatives

β-Aminomethylation of N-aryl- and N-azaheteroaryl-substituted methyl 2,5-dimethylpyrrole-3-carboxylates. Kinetic effect of the N-pyrrole substituent

The Antifungal Agent 1-[2-(4-Chlorobenzylamino)benzyl]-1 H -imidazole

Antifungal Agents, Part 11: Biphenyl Analogues of Naftifine: Synthesis and Antifungal Activities

Electron impact mass spectra of para-substituted N-heteroaryl benzylamines

ChemInform Abstract: New Pyrroles with Potential Antimycobacterial, Antifungal, and Selective COX-2 Inhibiting Activities. Synthetic Methodologies

Antifungal agents. XI: Biphenyl analogues of naftifine : synthesis and antifungal activities

Synthesis of 5H-pyrrolo[2,1-c][1,4]benzodiazepine and some of its derivatives related to anthramycin

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