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Imre Bata

Observed names: Bata, Imre, I. BATA
ORCID: 0000-0002-8609-4663
Observed ORCID: 0000-0002-8609-4663
OpenAlex ID: A5003319104
A new potent calmodulin antagonist with arylalkylamine structure: crystallographic, spectroscopic and functional studies
2000 · Veronika Harmat, Zsolt Böcskei, et al. · Journal of Molecular Biology · 47
Synthesis and Characterization of New V1A Antagonist Compounds: The Separation of Four Atropisomeric Stereoisomers
2021 · Zsolt Szeleczky, Zoltán Szakács, et al. · Journal of Medicinal Chemistry · 18
Synthesis of 4‐Aminopyrimidines from 1,2,4‐Oxadiazoles, II A General Method for the Preparation of 4‐Substituted 6,7‐Dihydro‐9,10‐dialkoxy‐2H‐pyrimido[6,1‐a]isoquinolin‐2‐imine Hydrochlorides
1987 · Dezső Korbonits, PÁL Kiss, et al. · Chemische Berichte · 13
Synthesis of 4‐Aminopyrimidines from 1,2,4‐Oxadiazoles, V[1]. Reductive Formation of 2‐(Benzoylamino)indole from 3‐(2‐Aminobenzyl)‐5‐phenyl‐1,2,4‐oxadiazole and Its Transformation to 6‐Phenyl‐8H‐pyrimido‐[1,6‐a: 4,5‐b']diindole, a New Heterocyclic Ring System
1993 · Imre Bata, Dezső Korbonits, et al. · Chemische Berichte · 11
Multiparameter Optimization of Naphthyridine Derivatives as Selective α5-GABAA Receptor Negative Allosteric Modulators
2022 · György Szabó, Olivér Éliás, et al. · Journal of Medicinal Chemistry · 10
Discovery of New Heterocyclic Ring Systems as Novel and Potent V1A Receptor Antagonists
2020 · Ferenc Baska, Gábor Szántó, et al. · ACS Chemical Neuroscience · 8
I. Discovery of a novel series of CXCR3 antagonists. Multiparametric optimization of N,N-disubstituted benzylamines
2016 · Imre Bata, Zsuzsanna Tömösközi, et al. · Bioorganic & Medicinal Chemistry Letters · 7
Ring transformation of 1-[(1,2,4-oxadiazol-3-yl)methyl]isoquinolines into 2-acylaminopyrazolo[5,1-a]isoquinolines
1986 · Imre Bata, Gergely Héja, et al. · Journal of the Chemical Society Perkin Transactions 1 · 7
Identification of Triazolopyridines as Selective α5-GABAA Receptor Negative Allosteric Modulators by a Hybridization Approach
2022 · György Szabó, Benedek Imre Károlyi, et al. · ACS Chemical Neuroscience · 6
New V1a receptor antagonist. Part 2. Identification and optimization of triazolobenzazepines
2020 · Éva Bozó, Ferenc Baska, et al. · Bioorganic & Medicinal Chemistry Letters · 6
New P2X3 receptor antagonists. Part 2: Identification and SAR of quinazolinones
2016 · Gábor Szántó, Attila Makó, et al. · Bioorganic & Medicinal Chemistry Letters · 5
New P2X3 receptor antagonists. Part 1: Discovery and optimization of tricyclic compounds
2016 · Gábor Szántó, Attila Makó, et al. · Bioorganic & Medicinal Chemistry Letters · 5
Discovery and Characterization of RGH-122, a Potent, Selective, and Orally Bioavailable V1a Receptor Antagonist
2024 · Ferenc Baska, Éva Bozó, et al. · Journal of Medicinal Chemistry · 4
Novel-Type GABAB PAMs: Structure–Activity Relationship in Light of the Protein Structure
2024 · Balázs Krámos, Zsuzsa Hadady, et al. · ACS Medicinal Chemistry Letters · 3
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Optimization of Novel α7 Nicotinic Acetylcholine Receptor Positive Allosteric Modulators and the Discovery of a Preclinical Development Candidate Molecule (RGH-560)
2023 · István Ledneczki, Zsolt Némethy, et al. · Journal of Medicinal Chemistry · 3
Novel imidazo[1,5-a]quinoxaline derivatives: SAR, selectivity and modeling challenges en route to the identification of an α5-GABAA receptor NAM
2022 · Benedek Imre Károlyi, Attila Potor, et al. · Bioorganic & Medicinal Chemistry Letters · 3
II. Discovery of a novel series of CXCR3 antagonists with a beta amino acid core
2016 · Imre Bata, Zsuzsanna Tömösközi, et al. · Bioorganic & Medicinal Chemistry Letters · 3
New V1a receptor antagonist. Part 1. Synthesis and SAR development of urea derivatives
2020 · Gábor Szántó, Attila Makó, et al. · Bioorganic & Medicinal Chemistry Letters · 2
Development of dual V1a/V2 antagonists containing triazolobenzazepine scaffold
2024 · Gábor Varró, Éva Bozó, et al. · European Journal of Medicinal Chemistry · 1
ChemInform Abstract: Synthesis of 4‐Aminopyrimidines from 1,2,4‐Oxadiazoles. Part 5. Reductive Formation of 2‐(Benzoylamino)indole from 3‐(2‐Aminobenzyl)‐5‐ phenyl‐1,2,4‐oxadiazole and Its Transformation to 6‐Phenyl‐8H‐pyrimido( 1,6‐a:4,5‐b′)diindole, a New Heterocyclic Ring System.
1994 · I. BATA, D. KORBONITS, et al. · ChemInform
ChemInform Abstract: Synthesis of 4‐Aminopyrimidines from 1,2,4‐Oxadiazoles. Part 2. A General Method for the Preparation of 4‐Substituted 6,7‐Dihydro‐9,10‐dialkoxy‐2H‐pyrimido(6,1‐a)isoquinolin‐2‐imine Hydrochlorides.
1987 · D. KORBONITS, P. KISS, et al. · ChemInform
ChemInform Abstract: Ring Transformation of 1‐[(1,2,4‐Oxadiazol‐3‐yl)methyl]isoquinolines Into 2‐Acylaminopyrazolo[5,1‐a]isoquinolines.
1986 · I. BATA, G. HEJA, et al. · ChemInform
Works count: 23
Citation count: 162
H-index: 7
I10-index: 5
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