Wilma Quaglia - Concepedia

Author

Wilma Quaglia

Also Known As

Alessia Piergentili, LIBERATI, SONIA, Quaglia W, Quaglia, W., Quaglia, Wilma, W Quaglia, W. QUAGLIA, W. Quaglia, Wilma QUAGLIA, Wilma Quaglia

181

Publications

2.3K

Citations

H-Index

Concepts

All Affiliations

Università di Camerino University of Florence University of Milan National Institute on Drug Abuse Recordati (Italy)

About

Wilma Quaglia is an author at Università di Camerino specializing in medicine, pharmacology, and drug discovery.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	30	695
2	Natural Sciences	10	11	280
3	Health Sciences	5	5	127
4	Social Sciences	1	1	11
5	Anesthesia	1	1	32

Wilma Quaglia

Publications

1.8K

Citations

H-Index

Page 1

	Year	Citations
Differential blockade of muscarinic receptor subtypes by polymethylene tetraamines. Novel class of selective antagonists of cardiac M-2 muscarinic receptors Carlo Melchiorre, Anna Cassinelli, Wilma Quaglia Journal of Medicinal Chemistry	1987	137
Structure−Activity Relationships in 1,4-Benzodioxan-Related Compounds. 7. Selectivity of 4-Phenylchroman Analogues for α<sub>1</sub>−Adrenoreceptor Subtypes Wilma Quaglia, Maria Pigini, Alessandro Piergentili, Journal of Medicinal Chemistry	2002	82
Coupling of I1 Imidazoline Receptors to the cAMP Pathway: Studies with a Highly Selective Ligand, Benazoline H. Greney, Philippe Rondé, C Magnier, Molecular Pharmacology	2000	61
Imidazoline receptors: Qualitative structure-activity relationships and discovery of tracizoline and benazoline. Two ligands with high affinity and unprecedented selectivity Maria Pigini, Pascal Bousquet, Angelo Carotti, Bioorganic & Medicinal Chemistry Medicinal ChemistryDrug TargetBiochemistryMedicineNatural Sciences	1997	60
Cross-talk between alpha1D-adrenoceptors and transient receptor potential vanilloid type 1 triggers prostate cancer cell proliferation Maria Beatrice Morelli, Consuelo Amantini, Massimo Nabissi, BMC Cancer	2014	44
Favourable involvement of α2A-adrenoreceptor antagonism in the I2-imidazoline binding sites-mediated morphine analgesia enhancement Valerio Mammoli, Alessandro Bonifazi, Fabio Del Bello, Bioorganic & Medicinal Chemistry Molecular Pharmacologyα2A-adrenoreceptor AntagonismHealth SciencesBiochemistryPain Medicine	2012	44
Dioxane and oxathiane nuclei: Suitable substructures for muscarinic agonists Alessandro Piergentili, Wilma Quaglia, Mario Giannella, Bioorganic & Medicinal Chemistry MedicineOxathiane NucleiMechanism Of ActionExperimental PharmacologyPharmacotherapy	2006	41
Structure−Activity Relationships in 1,4-Benzodioxan-Related Compounds. 9. From 1,4-Benzodioxane to 1,4-Dioxane Ring as a Promising Template of Novel α<sub>1D</sub>-Adrenoreceptor Antagonists, 5-HT<sub>1A</sub>Full Agonists, and Cytotoxic Agents Wilma Quaglia, Alessandro Piergentili, Fabio Del Bello, Journal of Medicinal Chemistry	2008	39
Synthesis, Absolute Configuration, and Biological Profile of the Enantiomers of<i>trans</i>-[2-(2,6-Dimethoxyphenoxy)ethyl][(3-<i>p</i>-tolyl-2,3-dihydro-1,4- benzodioxin-2-yl)methyl]amine (Mephendioxan), a Potent Competitive α<sub>1A</sub>-Adrenoreceptor Antagonist Wilma Quaglia, Maria Pigini, Seyed Khosrow Tayebati, Journal of Medicinal Chemistry	1996	38
Structure-activity relationships in 1,4-benzodioxan related compounds. 3. 3-Phenyl analogs of 2-[[[2-(2,6-dimethoxyphenoxy)ethyl]amino]methyl]-1,4-benzodioxan (WB 4101) as highly selective .alpha.1-adrenoreceptor antagonists Wilma Quaglia, Maria Pigini, Mario Giannella, Journal of Medicinal Chemistry 3-Phenyl AnalogsMolecular PharmacologyDerivative (Chemistry)Pharmaceutical ChemistryBiochemistry	1990	38

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