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An approach to solve contradiction problems for the safety integration in innovative design process

Computers in industry, 2011-05, Vol.62 (4), p.398-406

2011

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Maintainability and safety indicators at design stage for mechanical products

Computers in industry, 2008-05, Vol.59 (5), p.438-449

2008

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Information system based on a working situation model for a new design approach in concurrent engineering

Journal of engineering design, 2006-01, Vol.17 (1), p.35-54

2006

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Solid-phase synthesis and pharmacological evaluation of a library of peptidomimetics as potential farnesyltransferase inhibitors: an approach to new lead compounds

European journal of medicinal chemistry, 2006-06, Vol.41 (6), p.745-755

2006

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An approach to solve contradiction problems for the safety integration in innovative design process: Computer-Supported Innovation Pipelines: Current Research and Trends

Computers in industry, 2011, Vol.62 (4), p.398-406

2011

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DNA Interaction of the Tyrosine Protein Kinase Inhibitor PD153035 and Its N-Methyl Analogue

Biochemistry (Easton), 2001-04, Vol.40 (15), p.4663-4671

2001

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New COX-2/5-LOX Inhibitors: Apoptosis-Inducing Agents Potentially Useful in Prostate Cancer Chemotherapy

Journal of medicinal chemistry, 2004-12, Vol.47 (25), p.6195-6206

2004

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Synthesis of condensed quinolines and quinazolines as DNA ligands

Bioorganic & medicinal chemistry, 2004-02, Vol.12 (3), p.641-647

2004

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A synthesis of new pyrrolo[3,2-c]quinolines

Journal of heterocyclic chemistry, 2001-05, Vol.38 (3), p.755-758

2001

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A flexible approach to the design of new potent substance P receptor ligands

Journal of pharmacy and pharmacology, 2001-07, Vol.53 (7), p.929-934

2001

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An overview on olive oil waste valorization scenarios: Life Cycle Approach

IFAC-PapersOnLine, 2022, Vol.55 (10), p.1477-1482

2022

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Synthesis and Activity of a New Methoxytetrahydropyran Derivative as Dual Cyclooxygenase-2/5-Lipoxygenase Inhibitor

Bioorganic & medicinal chemistry letters, 2002-03, Vol.12 (5), p.779-782

2002

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DNA Binding To Guide the Development of Tetrahydroindeno[1,2-b]pyrido[4,3,2-d e]quinoline Derivatives as Cytotoxic Agents

Journal of medicinal chemistry, 2004-07, Vol.47 (14), p.3665-3673

2004

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New benzo[5,6]pyrrolizino[1,2-b]quinolines as cytotoxic agents

Bioorganic & medicinal chemistry letters, 2004-05, Vol.14 (9), p.2363-2365

2004

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Potent and Selective Farnesyl Transferase Inhibitors

Journal of medicinal chemistry, 2004-12, Vol.47 (27), p.6812-6820

2004

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Synthesis and Pharmacological Evaluation of New Pyrazolidine-3,5-diones as AT1 Angiotensin II Receptor Antagonists

Journal of medicinal chemistry, 2000-07, Vol.43 (14), p.2685-2697

2000

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Comparative subcellular distribution of the copper complexes of bleomycin-A2 and deglycobleomycin-A2

Anti-cancer drugs, 1994-04, Vol.5 (2), p.199-201

1994

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Novel N-(4-Piperidinyl)benzamide Antimalarials with Mammalian Protein Farnesyltransferase Inhibitory Activity

Chemical and Pharmaceutical Bulletin, 2005, Vol.53(10), pp.1324-1326

2005

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DNA-binding properties of a distamycin-ellipticine hybrid molecule

Molecular pharmacology, 1992-05, Vol.41 (5), p.845-855

1992

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Synthesis of an azabicycloalkane amino acid scaffold as potential rigid dipeptide mimetic

Tetrahedron letters, 2002-07, Vol.43 (29), p.5087-5088

2002

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Synthesis and pharmacological evaluation of new pyrazolidine-3, 5-diones as AT(1) angiotensin II receptor antagonists

Journal of medicinal chemistry, 2000-07, Vol.43 (14), p.2685-2697

2000

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An Efficient Synthesis of the New Benzo[c]pyrido[2,3,4-kl]acridine Skeleton

Journal of organic chemistry, 2002-05, Vol.67 (10), p.3502-3505

2002

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Novel potent substance P and neurokinin A receptor antagonists. Conception, synthesis and biological evaluation of indolizine derivatives

Bioorganic & medicinal chemistry, 2002-09, Vol.10 (9), p.2905-2912

2002

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Design, Synthesis, and Pharmacological Evaluation of New Farnesyl Protein Transferase Inhibitors

Journal of medicinal chemistry, 2002-01, Vol.45 (2), p.533-536

2002

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Formaldehyde-Induced DNA Cross-Link of Indolizino[1,2-b]quinolines Derived from the A−D Rings of Camptothecin

Journal of medicinal chemistry, 2002-12, Vol.45 (26), p.5809-5812

2002

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An approach to solve contradiction problems for the safety integration in innovative design process

Maintainability and safety indicators at design stage for mechanical products

Information system based on a working situation model for a new design approach in concurrent engineering

Solid-phase synthesis and pharmacological evaluation of a library of peptidomimetics as potential farnesyltransferase inhibitors: an approach to new lead compounds

An approach to solve contradiction problems for the safety integration in innovative design process: Computer-Supported Innovation Pipelines: Current Research and Trends

DNA Interaction of the Tyrosine Protein Kinase Inhibitor PD153035 and Its N-Methyl Analogue

New COX-2/5-LOX Inhibitors: Apoptosis-Inducing Agents Potentially Useful in Prostate Cancer Chemotherapy

Synthesis of condensed quinolines and quinazolines as DNA ligands

A synthesis of new pyrrolo[3,2-c]quinolines

A flexible approach to the design of new potent substance P receptor ligands

An overview on olive oil waste valorization scenarios: Life Cycle Approach

Synthesis and Activity of a New Methoxytetrahydropyran Derivative as Dual Cyclooxygenase-2/5-Lipoxygenase Inhibitor

DNA Binding To Guide the Development of Tetrahydroindeno[1,2-b]pyrido[4,3,2-d e]quinoline Derivatives as Cytotoxic Agents

New benzo[5,6]pyrrolizino[1,2-b]quinolines as cytotoxic agents

Potent and Selective Farnesyl Transferase Inhibitors

Synthesis and Pharmacological Evaluation of New Pyrazolidine-3,5-diones as AT1 Angiotensin II Receptor Antagonists

Comparative subcellular distribution of the copper complexes of bleomycin-A2 and deglycobleomycin-A2

Novel N-(4-Piperidinyl)benzamide Antimalarials with Mammalian Protein Farnesyltransferase Inhibitory Activity

DNA-binding properties of a distamycin-ellipticine hybrid molecule

Synthesis of an azabicycloalkane amino acid scaffold as potential rigid dipeptide mimetic

Synthesis and pharmacological evaluation of new pyrazolidine-3, 5-diones as AT(1) angiotensin II receptor antagonists

An Efficient Synthesis of the New Benzo[c]pyrido[2,3,4-kl]acridine Skeleton

Novel potent substance P and neurokinin A receptor antagonists. Conception, synthesis and biological evaluation of indolizine derivatives

Design, Synthesis, and Pharmacological Evaluation of New Farnesyl Protein Transferase Inhibitors

Formaldehyde-Induced DNA Cross-Link of Indolizino[1,2-b]quinolines Derived from the A−D Rings of Camptothecin

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