Péter Mátyus - Concepedia

Author

Péter Mátyus

Semmelweis University ORCID

Also Known As

MASON PETER, Matyus, P., Mezei, Péter, Màtyus, Peter, P MATYUS, P Matyus, P Mátyus, P. MATYUS, P. Matyus, P. M·atyus

284

Publications

3.7K

Citations

H-Index

105

Concepts

All Affiliations

Semmelweis University University of Antwerp HUN-REN Research Centre for Natural Sciences University of Szeged Hungarian Academy of Sciences

About

Péter Mátyus is an author at Semmelweis University specializing in chemistry, pharmacology, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	36	1.2K
2	Natural Sciences	16	25	805
3	Engineering	14	22	690
4	Social Sciences	3	3	238
5	Health Sciences	2	2	42

Péter Mátyus

Publications

2.6K

Citations

H-Index

Page 1

	Year	Citations
Use of TTC staining for the evaluation of tissue injury in the early phases of reperfusion after focal cerebral ischemia in rats Angéla Benedek, Krisztina Móricz, Zsolt Jurányi, Brain Research Cerebral Vascular RegulationIschemic StrokeNeurophysiologyMedicineBrain Injury	2006	196
Ring-Closure Reactions of <i>ortho-</i>Vinyl<i>-tert-</i>anilines and (Di)Aza-Heterocyclic Analogues via the <i>tert</i>-Amino Effect: Recent Developments Péter Mátyus, Olivér Éliás, Pál Tapolcsányi, Synthesis Aza-heterocyclic AnaloguesEngineeringHeterocyclicTert-amino EffectNatural Sciences	2006	158
Isoneocryptolepine, a Synthetic Indoloquinoline Alkaloid, as an Antiplasmodial Lead Compound Sabine Van Miert, Steven Hostyn, Bert U. W. Maes, Journal of Natural Products Antiparasitic AgentPharmacotherapyPharmaceutical ChemistryDrug ResistanceMedicinal Chemistry	2005	112
Synthesis of the benzo-β-carboline isoneocryptolepine: the missing indoloquinoline isomer in the alkaloid series cryptolepine, neocryptolepine and isocryptolepine Steven Hostyn, Bert U. W. Maes, Luc Pieters, Tetrahedron MedicineBenzo-β-carboline IsoneocryptolepineAlkaloid Series CryptolepinePharmacologyIndoloquinoline Isomer	2004	81
Structure–activity relationship of antiparasitic and cytotoxic indoloquinoline alkaloids, and their tricyclic and bicyclic analogues Gitte Van Baelen, Steven Hostyn, Liene Dhooghe, Bioorganic & Medicinal Chemistry Structure–activity RelationshipBiochemistryAntiparasitic AgentMedicineCytotoxic Indoloquinoline Alkaloids	2009	80
Novel (Hetero)arylalkenyl propargylamine compounds are protective in toxin-induced models of Parkinson’s disease Mária Baranyi, Pier Francesca Porceddu, Flóra Gölöncsér, Molecular Neurodegeneration	2016	74
3-Acetyl-2,5-diaryl-2,3-dihydro-1,3,4-oxadiazoles: A New Scaffold for the Selective Inhibition of Monoamine Oxidase B Elias Maccioni, Stefano Alcaro, Roberto Cirilli, Journal of Medicinal Chemistry Combinatorial ChemistryPharmacotherapyChemistryPharmaceutical ChemistryHuman Monoamine Oxidase	2011	60
Water-soluble isoindolo[2,1-a]quinoxalin-6-imines: In vitro antiproliferative activity and molecular mechanism(s) of action Barbara Parrino, Anna Carbone, Cristina Ciancimino, European Journal of Medicinal Chemistry Medicinal ChemistryAntiparasitic AgentMedicineMolecular MechanismPharmacology	2015	59
An efficient microwave-assisted solvent-free synthesis of pyrido-fused ring systems applying the tert-amino effect Nadya Kaval, Beata Halasz‐Dajka, Giang Vo‐Thanh, Tetrahedron EngineeringTert-amino EffectOrganic ChemistryChemistrySynthesis Method	2005	58
A 5-HT7 Heteroreceptor-Mediated Inhibition of [3H]Serotonin Release in Raphe Nuclei Slices of the Rat: Evidence for a Serotonergic–Glutamatergic Interaction László G. Hársing, Ibolya Prauda, József Barkóczy, Neurochemical Research	2004	56

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