Irene Giorgi - Concepedia

Author

Irene Giorgi

University of Pisa

Also Known As

Giorgi I, I Giorgi, I. GIORGI, I. Giorgi, Irene Giorgi

164

Publications

1.3K

Citations

H-Index

Concepts

All Affiliations

University of Pisa Istituto di Farmacologia Traslazionale

About

Irene Giorgi is an author at University of Pisa specializing in pharmacology, medicine, and organic chemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	22	584
2	Natural Sciences	11	14	213
3	Biochemistry	10	11	198
4	Engineering	1	1	20
5	Biomolecular Engineering	1	1	20

Irene Giorgi

Publications

980

Citations

H-Index

Page 1

	Year	Citations
New 1,2,3-triazolo[1,5-a]quinoxalines: synthesis and binding to benzodiazepine and adenosine receptors. II Giuliana Biagi, Irene Giorgi, Oreste Livi, European Journal of Medicinal Chemistry Molecular PharmacologyHeterocyclicMedicineMechanism Of ActionOrganic Chemistry	2002	72
Benzoyl and/or benzyl substituted 1,2,3-triazoles as potassium channel activators. VIII Vincenzo Calderone, Irene Giorgi, Oreste Livi, European Journal of Medicinal Chemistry MedicineIon ChannelsOrganic ChemistryPharmacologyBenzoyl And/or Benzyl	2005	51
1,2,3-Triazolo[1,5-a]quinoxalines: synthesis and binding to benzodiazepine and adenosine receptors Lucia Bertelli, Giuliana Biagi, Irene Giorgi, European Journal of Medicinal Chemistry Molecular PharmacologyHeterocyclicMedicinePharmacotherapyHeterocycle Chemistry	1998	48
5-(4′-Substituted-2′-nitroanilino)-1,2,3-triazoles as new potential potassium channel activators. I Giuliana Biagi, Vincenzo Calderone, Irene Giorgi, European Journal of Medicinal Chemistry PharmacologyMedicineHeterocycle ChemistryIon Channels	2000	46
Synthesis and biological activity of novel substituted benzanilides as potassium channel activators. V Giuliana Biagi, Irene Giorgi, Oreste Livi, European Journal of Medicinal Chemistry Biological ActivityOrganic ChemistryPharmacologyPotassium Channel Activators	2004	45
1,5-Diarylsubstituted 1,2,3-triazoles as potassium channel activators. VI Giuliana Biagi, Vincenzo Calderone, Irene Giorgi, Il Farmaco Ion ChannelsOrganic Chemistry1,5-Diarylsubstituted 1,2,3-TriazolesHeterocycle ChemistryChemistry	2004	44
Synthesis and Biological Evaluation of New Imidazole, Pyrimidine, and Purine Derivatives and Analogs as Inhibitors of Xanthine Oxidase Giuliana Biagi, Alberto Costantini, Luca Costantino, Journal of Medicinal Chemistry	1996	40
1,2,3-Triazolo[1,5-a][1,4]- and 1,2,3-triazolo[1,5-a][1,5]benzodiazepine derivatives: synthesis and benzodiazepine receptor binding Lucia Bertelli, Giuliana Biagi, Irene Giorgi, Il Farmaco Derivative (Chemistry)MedicinePharmacotherapyHeterocycle ChemistryPharmacology	1998	31
Some structural changes on triazolyl-benzotriazoles and triazolyl-benzimidazolones as potential potassium channel activators. III Giuliana Biagi, Vincenzo Calderone, Irene Giorgi, Il Farmaco Medicinal ChemistryBiochemistryNatural SciencesMedicineStructural Changes	2001	31
Triazolyl–benzimidazolones and triazolyl–benzotriazoles: new potential potassium channel activators. II Barbara Baragatti, Giuliana Biagi, Vincenzo Calderone, European Journal of Medicinal Chemistry MedicineMechanism Of ActionIon ChannelsOrganic ChemistryHeterocycle Chemistry	2000	29

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