Search Results - "Rampa, A"
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Design of multifunctional compounds for cardiovascular disease: from natural scaffolds to "classical" multitarget approach
Published in Current medicinal chemistry (01-04-2013)“…Cardiovascular disease represents the main cause of death worldwide. Novel therapies to reduce elevated blood pressure and treat resistant hypertension, to…”
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A New Class of Nonsteroidal Aromatase Inhibitors: Design and Synthesis of Chromone and Xanthone Derivatives and Inhibition of the P450 Enzymes Aromatase and 17α-Hydroxylase/C17,20-Lyase
Published in Journal of medicinal chemistry (01-03-2001)“…Aromatase (P450arom) is a target of pharmacological interest for the treatment of breast cancer. In this paper, we report the design, synthesis, and in vitro…”
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La cerámica de Pichanal 4. Un puesto pastoril Tardío de la Sierra del Cajón (Provincia de Catamarca)
Published in Temas (Editorial Universitaria de Buenos Aires). (01-02-2016)Get full text
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Coumarin 1,4-Dihydropyridine Derivatives
Published in Bioorganic & medicinal chemistry (01-06-1998)“…A series of 1,4-dihydropyridines bearing a coumarin moiety in 4-position was synthesized. The compounds were evaluated for inotropic, chronotropic and calcium…”
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Cardiovascular Profile of Xanthone-Based 1,4 Dihydropyridines Bearing a Lidoflazine Pharmacophore Fragment
Published in Molecules (Basel, Switzerland) (27-11-2018)“…As a follow-up to our previous studies on differently substituted 1,4-dihydropyridines endowed with a peculiar cardiac selectivity, in this paper, a small…”
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3-(4-{[Benzyl(methyl)amino]methyl}phenyl)-6,7-dimethoxy-2H-2-chromenone (AP2238) Inhibits Both Acetylcholinesterase and Acetylcholinesterase-Induced β-Amyloid Aggregation: A Dual Function Lead for Alzheimer's Disease Therapy
Published in Journal of medicinal chemistry (05-06-2003)“…In recent years, the investigation of acetylcholinesterase (AChE) inhibitors has gained further interest, because the involvement of the peripheral site of the…”
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1,4-Dihydropyridines bearing a pharmacophoric fragment of lidoflazine
Published in Bioorganic & medicinal chemistry (01-10-1996)“…A series of 1,4-dihydropyridines bearing a pharmacophoric fragment of lidoflazine was synthesized. The compounds were evaluated for inotropic, chronotropic,…”
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Cholinesterase Inhibitors: Xanthostigmine Derivatives Blocking the Acetylcholinesterase-Induced β-Amyloid Aggregation
Published in Journal of medicinal chemistry (30-06-2005)“…In continuing research that led us to identify a new class of carbamate derivatives acting as potent (Rampa et al. J. Med. Chem. 1998, 41, 3976) and…”
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Synthesis of a series of Homopterocarpane derivatives with potential antitumor and anti-AIDS activity
Published in Farmaco (Società chimica italiana : 1989) (01-01-1997)“…The synthesis of a series of derivatives related to (+/-) cis 6a, 12a-dihydro-6H,7H-[1]-benzopyrano-[4,3-b]-[1]-benzopyran (Homopterocarpane) is described. The…”
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Enantioselective Nonsteroidal Aromatase Inhibitors Identified through a Multidisciplinary Medicinal Chemistry Approach
Published in Journal of medicinal chemistry (17-11-2005)“…To identify enantioselective nonsteroidal aromatase inhibitors, a multidisciplinary medicinal chemistry approach was pursued. First, our earlier CoMFA model…”
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Benzo-gamma-pyrone analogues of geiparvarin: synthesis and biological evaluation against B16 melanoma cells
Published in Anti-cancer drug design (01-10-1993)“…Chromone, flavone and xanthone analogues of geiparvarin (1) are described. Compounds 2a and 2b are more active in inhibiting the proliferation of F10…”
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SAR of 9-Amino-1,2,3,4-tetrahydroacridine-Based Acetylcholinesterase Inhibitors: Synthesis, Enzyme Inhibitory Activity, QSAR, and Structure-Based CoMFA of Tacrine Analogues
Published in Journal of medicinal chemistry (18-05-2000)“…In this study, we attempted to derive a comprehensive SAR picture for the class of acetylcholinesterase (AChE) inhibitors related to tacrine, a drug currently…”
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1,4-Dihydropyridine derivatives as calcium channel modulators: the role of 3-methoxy-flavone moiety
Published in Bioorganic & medicinal chemistry (16-05-2005)“…The synthesis and negative chronotropic activity of 1,4-dihydropyridine derivative 3b (EC 30 = 9.7 nM) is reported. It was earlier recognized that calcium…”
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SAR studies in the field of Ca-antagonists: 2-substituted 1,4-dihydropyridines with a xanthone backbone
Published in Farmaco (Società chimica italiana : 1989) (01-11-1993)“…A series of 2-substituted 1,4-dihydropyridines with a xanthone backbone was prepared. The compounds were evaluated for inotropic, chronotropic and calcium…”
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Synthesis and Biological Evaluation of 3-Alkoxy Analogues of Flavone-8-acetic Acid
Published in Journal of medicinal chemistry (14-08-2003)“…New analogues of flavone-8-acetic acid were synthesized, bearing an alkoxy group in position 3 and different substituents on the benzene ring in position 2 of…”
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Acetylcholinesterase inhibitors for potential use in Alzheimer's disease : Molecular modeling, synthesis and kinetic evaluation of 11H-indeno-[1,2-b]-quinolin-10-ylamine derivatives
Published in Bioorganic & medicinal chemistry (01-03-2000)“…Continuing our work on tetracyclic tacrine analogues, we synthesized a series of acetylcholinesterase (AChE) inhibitors of…”
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Acetylcholinesterase Inhibitors: SAR and Kinetic Studies on ω-[N-Methyl-N-(3-alkylcarbamoyloxyphenyl)methyl]aminoalkoxyaryl Derivatives
Published in Journal of medicinal chemistry (08-11-2001)“…In this work, we further investigated a class of carbamic cholinesterase inhibitors introduced in a previous paper (Rampa et al. J. Med. Chem. 1998, 41, 3976)…”
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Synthesis and biological activity of some rigid analogues of flavone-8-acetic acid
Published in Bioorganic & medicinal chemistry (2000)“…Some rigid analogues of flavone-8-acetic acid are described. Direct in vitro toxicity of the synthesised compounds was evaluated towards four tumoral cell…”
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Cytotoxicity of simple geiparvarin analogues
Published in Archives of Toxicology [ARCH. TOXICOL.]. 1988 (01-01-1988)Get full text
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Some new prazosin-like derivatives
Published in Bollettino chimico farmaceutico (01-04-1989)“…The preparation of a number of prazosin-like derivatives is reported. The new derivatives differ from the parent compound for the 2-side-chain which is…”
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