OLGA MARÍA
CRUZ LÓPEZ
PROFESORA TITULAR DE UNIVERSIDAD
University of Ferrara
Ferrara, ItaliaPublications in collaboration with researchers from University of Ferrara (28)
2015
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Synthesis and biological evaluation of a new series of 2-amino-3-aroyl thiophene derivatives as agonist allosteric modulators of the A1 adenosine receptor. A position-dependent effect study
European Journal of Medicinal Chemistry, Vol. 101, pp. 185-204
2014
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Synthesis and biological evaluation of novel 2-amino-3-aroyl-4-neopentyl-5- substituted thiophene derivatives as allosteric enhancers of the A1 adenosine receptor
Bioorganic and Medicinal Chemistry, Vol. 22, Núm. 1, pp. 148-166
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Synthesis and biological evaluation of novel allosteric enhancers of the A1adenosine receptor based on 2-amino-3-(4′-chlorobenzoyl)-4-substituted-5-arylethynyl thiophene
Journal of Medicinal Chemistry, Vol. 57, Núm. 18, pp. 7673-7686
2012
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Design, synthesis and biological evaluation of hybrid molecules containing conjugated styryl ketone and α-bromoacryloyl moieties
Letters in Drug Design and Discovery, Vol. 9, Núm. 2, pp. 140-152
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Structure-activity relationships of 2-amino-3-aroyl-4-[(4-arylpiperazin-1- yl)methyl]thiophenes. Part 2: Probing the influence of diverse substituents at the phenyl of the arylpiperazine moiety on allosteric enhancer activity at the A 1 adenosine receptor
Bioorganic and Medicinal Chemistry, Vol. 20, Núm. 2, pp. 996-1007
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Synthesis and biological evaluation of 2-amino-3-(4-chlorobenzoyl)-4-[(4- arylpiperazin-1-yl)methyl]-5-substituted-thiophenes. Effect of the 5-modification on allosteric enhancer activity at the A1 adenosine receptor
Journal of Medicinal Chemistry, Vol. 55, Núm. 17, pp. 7719-7735
2011
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Synthesis and Antitumor Molecular Mechanism of Agents Based on Amino 2-(3',4',5'-Trimethoxybenzoyl)benzo[b]furan: Inhibition of Tubulin and Induction of Apoptosis
ChemMedChem, Vol. 6, Núm. 10, pp. 1841-1853
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Synthesis of novel antimitotic agents based on 2-amino-3-aroyl-5-(hetero) arylethynyl thiophene derivatives
Bioorganic and Medicinal Chemistry Letters
2010
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Substituted 2-(3′,4′,5′-trimethoxybenzoyl)-benzo[b] thiophene derivatives as potent tubulin polymerization inhibitors
Bioorganic and Medicinal Chemistry, Vol. 18, Núm. 14, pp. 5114-5122
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Symmetrical α-bromoacryloylamido diaryldienone derivatives as a novel series of antiproliferative agents. Design, synthesis and biological evaluation
Bioorganic and Medicinal Chemistry Letters, Vol. 20, Núm. 9, pp. 2733-2739
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Synthesis and antitumor activity of 1,5-disubstituted 1,2,4-triazoles as cis-restricted combretastatin analogues
Journal of Medicinal Chemistry, Vol. 53, Núm. 10, pp. 4248-4258
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Synthesis and cellular pharmacology studies of a series of 2-amino-3-aroyl-4-substituted thiophene derivatives
Medicinal Chemistry, Vol. 6, Núm. 6, pp. 329-343
2009
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2-Arylamino-4-amino-5-aroylthiazoles. "One-pot" synthesis and biological evaluation of a new class of inhibitors of tubulin polymerization
Journal of Medicinal Chemistry, Vol. 52, Núm. 17, pp. 5551-5555
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Design, synthesis and structure-activity relationship of 2-(3′,4′,5′-trimethoxybenzoyl)-benzo[b]furan derivatives as a novel class of inhibitors of tubulin polymerization
Bioorganic and Medicinal Chemistry, Vol. 17, Núm. 19, pp. 6862-6871
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Discovery of 8-methoxypyrazino[1,2-a]indole as a new potent antiproliferative agent against human leukemia K562 cells. A structure-activity relationship study
Letters in Drug Design and Discovery, Vol. 6, Núm. 4, pp. 298-303
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Hybrid α-bromoacryloylamido chalcones. Design, synthesis and biological evaluation
Bioorganic and Medicinal Chemistry Letters, Vol. 19, Núm. 7, pp. 2022-2028
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α-bromoacrylamido N-substituted isatin derivatives as potent inducers of apoptosis in human myeloid leukemia cells
ChemMedChem, Vol. 4, Núm. 10, pp. 1668-1676
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α-halogenoacrylic derivatives of antitumor agents
Mini-Reviews in Medicinal Chemistry, Vol. 9, Núm. 1, pp. 81-94
2008
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Design, synthesis, and biological evaluation of thiophene analogues of chalcones
Bioorganic and Medicinal Chemistry, Vol. 16, Núm. 10, pp. 5367-5376
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Synthesis and biological evaluation of 1-methyl-2-(3′,4′, 5′-trimethoxybenzoyl)-3-aminoindoles as a new class of antimitotic agents and tubulin inhibitors
Journal of Medicinal Chemistry, Vol. 51, Núm. 5, pp. 1464-1468