Concepedia

Author

Cristina Zocchi

University of Ferrara

Also Known As

C Zocchi, C. ZOCCHI, C. Zocchi, Cristina Zocchi, ZOCCHI C.

32

Publications

1.1K

Citations

15

H-Index

30

Concepts

All Affiliations

University of FerraraSan Raffaele University of RomeIstituto Superiore di SanitàUniversity of Turin
CZ

About

Cristina Zocchi is an author at University of Ferrara specializing in medicine, pharmacology, and drug discovery.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

10

10

361

2

Biochemistry

6

6

195

3

Natural Sciences

4

4

148

4

Chemical Biology

2

2

24

5

Health Sciences

1

1

52

Cristina Zocchi

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19

Publications

1K

Citations

15

H-Index

YearCitations

The non-xanthine heterocyclic compound SCH 58261 is a new potent and selective A2a adenosine receptor antagonist.

Cristina Zocchi, E. Ongini, Andrea Conti,

Journal of Pharmacology and Experimental Therapeutics

1996

197

Diagnosis of Glucocorticoid-Remediable Aldosteronism in Primary Aldosteronism: Aldosterone Response to Dexamethasone and Long Polymerase Chain Reaction for Chimeric Gene

Paolo Mulatero, Franco Veglio, Catia Pilon,

The Journal of Clinical Endocrinology & Metabolism

1998

120

Pyrazolo[4,3-<i>e</i>]-1,2,4-triazolo[1,5-<i>c</i>]pyrimidine Derivatives:  Potent and Selective A<sub>2A</sub>Adenosine Antagonists

Pier Giovanni Baraldi, Barbara Cacciari, Giampiero Spalluto,

Journal of Medicinal Chemistry

1996

111

Binding of the radioligand [<sup>3</sup>H]‐SCH 58261, a new non‐xanthine A<sub>2A</sub> adenosine receptor antagonist, to rat striatal membranes

Cristina Zocchi, Ennio Ongini, S. D. Ferrara,

British Journal of Pharmacology

1996

84

Synthesis of new pyrazolo[4,3-e]1,2,4-triazolo[1,5-c] pyrimidine and 1,2,3-triazolo[4,5-e]1,2,4-triazolo[1,5-c] pyrimidine displaying potent and selective activity as A2a adenosine receptor antagonists.

Pier Giovanni Baraldi, Stefano Manfredini, Daniele Simoni,

Bioorganic & Medicinal Chemistry Letters

1994

83

Characterization of human A<sub>2A</sub> adenosine receptors with the antagonist radioligand [<sup>3</sup>H]‐SCH 58261

Silvio Dionisotti, Ennio Ongini, Cristina Zocchi,

British Journal of Pharmacology

1997

63

2-Alkynyl Derivatives of Adenosine-5'-N-ethyluronamide: Selective A2 Adenosine Receptor Agonists with Potent Inhibitory Activity on Platelet Aggregation

G. Cristalli, Rosaria Volpini, Sauro Vittori,

Journal of Medicinal Chemistry

1994

58

Effects of adenosine derivatives on human and rabbit platelet aggregation

Silvio Dionisotti, Cristina Zocchi, Katia Varani,

Naunyn-Schmiedeberg s Archives of Pharmacology

1992

52

Labeling of A2A adenosine receptors in human platelets by use of the new nonxanthine antagonist radioligand [3H]SCH 58261.

Silvio Dionisotti, S. D. Ferrara, C Molta,

Journal of Pharmacology and Experimental Therapeutics

1996

38

Effects of the new A<sub>2</sub> adenosine receptor antagonist 8FB‐PTP, an 8 substituted pyrazolo‐triazolo‐pyrimidine, on <i>in vitro</i> functional models

Silvio Dionisotti, Annamaria Conti, Daniele Sandoli,

British Journal of Pharmacology

1994

37

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