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Synthesis and antibacterial activity of HMR 3647 a new ketolide highly potent against erythromycin-resistant and susceptible pathogens

Bioorganic & medicinal chemistry letters, 1999-11, Vol.9 (21), p.3075-3080

1999

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Synthesis and Antibacterial Activity of Ketolides (6-O-Methyl-3-oxoerythromycin Derivatives): A New Class of Antibacterials Highly Potent Against Macrolide-Resistant and -Susceptible Respiratory Pathogens

Journal of medicinal chemistry, 1998-10, Vol.41 (21), p.4080-4100

1998

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A New Ketolide, HMR 3004, Active against Streptococci Inducibly Resistant to Erythromycin

Antimicrobial Agents and Chemotherapy, 1998-06, Vol.42 (6), p.1392-1396

1998

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Antibacterial activity of RU 64004 (HMR 3004), a novel ketolide derivative active against respiratory pathogens

Antimicrobial Agents and Chemotherapy, 1997-10, Vol.41 (10), p.2149-2158

1997

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Classification and structure-activity relationships of fluoroquinolones

Drugs (Basel), 1995, Vol.49 (Supplement 2), p.16-28

1995

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Ketolides lack inducibility properties of MLS(B) resistance phenotype

Journal of antimicrobial chemotherapy, 1997-07, Vol.40 (1), p.85-90

1997

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Ketolides lack inducibility properties of MLSB resistance phenotype

Journal of antimicrobial chemotherapy, 1997-07, Vol.40 (1), p.85-90

1997

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New ether oxime derivatives of erythromycin A a structure-activity relationship study

Journal of antibiotics, 1991, Vol.44 (3), p.313-330

1991

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In-vitro activity of ketolides against mycoplasmas

Journal of antimicrobial chemotherapy, 1997-05, Vol.39 (5), p.669-670

1997

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ANTIBACTERIAL ACTIVITY OF ROXITHROMYCIN: A LABORATORY EVALUATION

The Journal of Antibiotics, 1986, Vol.39(5), pp.660-668

1986

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Antibacterial activity of ofloxacin and other 4-quinolone derivatives: in-vitro and in-vivo comparison

Journal of antimicrobial chemotherapy, 1985-10, Vol.16 (4), p.475-484

1985

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Perspectives thérapeutiques des nouvelles fluoroquinolones

La Presse médicale (1983), 1985, Vol.14 (45), p.2291-2294

1985

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Antibacterial activity of RU44790, a new N-tetrazolyl monocyclic beta-lactam

Antimicrobial Agents and Chemotherapy, 1992-08, Vol.36 (8), p.1756-1763

1992

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Four-Stranded Nucleic Acid Structures 25 Years Later: From Guanosine Gels to Telomer DNA

Journal of biomolecular structure & dynamics, 1990-12, Vol.8 (3), p.491-511

1990

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Physicochemical properties of nucleosides 3. Gel formation by 8-bromoguanosine

FEBS letters, 1969-08, Vol.4 (3), p.173-176

1969

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RU 51807 (cefpodoxime proxétil) : évaluation de l'activité antibactérienne in vitro et in vivo d'une nouvelle céphalaosporine active par voie orale

Pathologie biologie (Paris), 1991, Vol.39 (1), p.17-27

1991

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A new method for measuring binding of labeled ligands to membrane receptors

Analytical biochemistry, 1978, Vol.84 (1), p.256-262

1978

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Synthesis of 3-(alkyl and aryl)thio-2-isocephems

Heterocycles, 1989, Vol.28 (2), p.1061-1076

1989

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New trends in oral cephalosporin research

Journal of chemotherapy (Florence), 1989-07, Vol.1 (4 Suppl), p.108-109

1989

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Structure cristalline et moléculaire d'une forme N(7)-protonée de la guanosine: le bromhydrate de guanosine hémihydraté

Acta crystallographica. Section B, Structural crystallography and crystal chemistry, 1974-01, Vol.30 (1), p.214-220

1974

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Ketolides lack inducibility properties of MLS sub(B) resistance phenotype

Journal of antimicrobial chemotherapy, 1997-07, Vol.40 (1), p.85-90

1997

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RU 51807 (cefpodoxime proxetil). In vitro and in vivo antibacterial activity of a new orally administered active cephalosporin

Pathologie biologie (Paris), 1991-01, Vol.39 (1), p.17

1991

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Classification and structure-activity relationships of fluoroquinolones

Drugs. Vol. 49, no. 2 Suppl. 1995, 1995, Vol.49, p.no. 2 Sul.-no. 2 Sul.

1995

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New medical targets for macrolides

Expert opinion on investigational drugs, 1994-04, Vol.3 (4), p.405-410

1994

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New trends in macrolide research

Chemioterapia : international journal of the Mediterranean Society of Chemotherapy, 1987-06, Vol.6 (2 Suppl), p.343

1987

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Synthesis and antibacterial activity of HMR 3647 a new ketolide highly potent against erythromycin-resistant and susceptible pathogens

Synthesis and Antibacterial Activity of Ketolides (6-O-Methyl-3-oxoerythromycin Derivatives): A New Class of Antibacterials Highly Potent Against Macrolide-Resistant and -Susceptible Respiratory Pathogens

A New Ketolide, HMR 3004, Active against Streptococci Inducibly Resistant to Erythromycin

Antibacterial activity of RU 64004 (HMR 3004), a novel ketolide derivative active against respiratory pathogens

Classification and structure-activity relationships of fluoroquinolones

Ketolides lack inducibility properties of MLS(B) resistance phenotype

Ketolides lack inducibility properties of MLSB resistance phenotype

New ether oxime derivatives of erythromycin A a structure-activity relationship study

In-vitro activity of ketolides against mycoplasmas

ANTIBACTERIAL ACTIVITY OF ROXITHROMYCIN: A LABORATORY EVALUATION

Antibacterial activity of ofloxacin and other 4-quinolone derivatives: in-vitro and in-vivo comparison

Perspectives thérapeutiques des nouvelles fluoroquinolones

Antibacterial activity of RU44790, a new N-tetrazolyl monocyclic beta-lactam

Four-Stranded Nucleic Acid Structures 25 Years Later: From Guanosine Gels to Telomer DNA

Physicochemical properties of nucleosides 3. Gel formation by 8-bromoguanosine

RU 51807 (cefpodoxime proxétil) : évaluation de l'activité antibactérienne in vitro et in vivo d'une nouvelle céphalaosporine active par voie orale

A new method for measuring binding of labeled ligands to membrane receptors

Synthesis of 3-(alkyl and aryl)thio-2-isocephems

New trends in oral cephalosporin research

Structure cristalline et moléculaire d'une forme N(7)-protonée de la guanosine: le bromhydrate de guanosine hémihydraté

Ketolides lack inducibility properties of MLS sub(B) resistance phenotype

RU 51807 (cefpodoxime proxetil). In vitro and in vivo antibacterial activity of a new orally administered active cephalosporin

Classification and structure-activity relationships of fluoroquinolones

New medical targets for macrolides

New trends in macrolide research

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