Mario Grifantini - Concepedia

Author

Mario Grifantini

Università di Camerino

Also Known As

Carter, Rhonda L., HARDEN T. K., M GRIFANTINI, M Grifantini, M. GRIFANTINI, M. Grifantini, Mario Grifantini

212

Publications

2.7K

Citations

H-Index

Concepts

All Affiliations

Università di Camerino Indiana University – Purdue University Indianapolis University of Pisa University of Urbino Indiana University School of Medicine

About

Mario Grifantini is an author at Università di Camerino specializing in pharmacology, medicine, and biochemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	22	39	1.5K
2	Biochemistry	22	35	1.4K
3	Natural Sciences	18	32	1.1K
4	Health Sciences	2	2	84
5	Engineering	1	1	23

Mario Grifantini

Publications

2.3K

Citations

H-Index

Page 1

	Year	Citations
2-Chloro-N6-cyclopentyladenosine: a highly selective agonist at A1 adenosine receptors Martin J. Lohse, Karl‐Norbert Klotz, Ulrich Schwabe, Naunyn-Schmiedeberg s Archives of Pharmacology Molecular PharmacologyBiochemistryFunctional SelectivityMedicineMechanism Of Action	1988	160
2-Chloro-N6-[3H]cyclopentyladenosine ([3HCCPA) ?a high affinity agonist radioligand for A1 adenosine receptors Karl‐Norbert Klotz, Martin J. Lohse, Ulrich Schwabe, Naunyn-Schmiedeberg s Archives of Pharmacology HeterocyclicBiochemistryFunctional SelectivityMedicineG Protein-coupled Receptor	1989	128
Furanfurin and Thiophenfurin: Two Novel Tiazofurin Analogs. Synthesis, Structure, Antitumor Activity, and Interactions with Inosine Monophosphate Dehydrogenase Palmarisa Franchetti, Loredana Cappellacci, Mario Grifantini, Journal of Medicinal Chemistry	1995	120
Nucleoside and Non-nucleoside IMP Dehydrogenase- Inhibitors as Antitumor and Antiviral Agents Palmarisa Franchetti, Mario Grifantini Current Medicinal Chemistry Aldo-keto ReductasePharmacotherapyAntiviral DrugImp DehydrogenaseTumor Biology	1999	113
Photoaffinity labeling of A1-adenosine receptors. Karl‐Norbert Klotz, G. Cristalli, Mario Grifantini, Journal of Biological Chemistry Molecular PharmacologySignal TransductionA1-adenosine ReceptorsBiochemistryG Protein-coupled Receptor	1985	96
Decomposition Pathways and <i>in Vitro</i> HIV Inhibitory Effects of IsoddA Pronucleotides: Toward a Rational Approach for Intracellular Delivery of Nucleoside 5‘-Monophosphates Gilles Valette, Alain Pompon, Jean‐Luc Girardet, Journal of Medicinal Chemistry Isodda PronucleotidesRational ApproachMolecular BiologyAntiviral DrugChemical Biology	1996	95
Synthesis, Structure, and Antiproliferative Activity of Selenophenfurin, an Inosine 5‘-Monophosphate Dehydrogenase Inhibitor Analogue of Selenazofurin Palmarisa Franchetti, Loredana Cappellacci, Ghassan Abu Sheikha, Journal of Medicinal Chemistry Medicinal ChemistryBioorganic ChemistryChemoprevention StrategyBiochemistryAntiproliferative Activity	1997	75
Synthesis and potency of novel uracil nucleotides and derivatives as P2Y2 and P2Y6 receptor agonists Hyojin Ko, Rhonda L. Carter, Liesbet Cosyn, Bioorganic & Medicinal Chemistry Molecular PharmacologyMedicinal ChemistryPharmaceutical ScienceBiochemistryNovel Uracil Nucleotides	2008	67
2‘-<i>C</i>-Methyl Analogues of Selective Adenosine Receptor Agonists: Synthesis and Binding Studies Palmarisa Franchetti, Loredana Cappellacci, Stefano Marchetti, Journal of Medicinal Chemistry Molecular PharmacologyMedicinal ChemistryBiochemistryRibose MoietyMedicine	1998	62
Elucidation of the structure of the antineoplastic agents, 2-formylpyridine and 1-formylisoquinoline thiosemicarbazones Ippolito Antonini, Francesco Claudi, Palmarisa Franchetti, Journal of Medicinal Chemistry Medicinal ChemistryE ConfigurationHeterocyclicPharmaceutical ChemistryDerivative (Chemistry)	1977	56

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