About: Ondrej Holas

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher ORCID ID = 0000-0002-8335-0123

Attributes	Values
rdf:type	Item
field of work	wds:Q59661895-02F90E99-B02E-45C2-BAE3-990F82B598F8 wds:Q59661895-639C0B7F-966B-489A-9CA9-A4C86CFBFABF
field of work	pharmaceutics pharmacy
description	farmaceut (cs) wetenschapper (nl) дослідник (uk) researcher ORCID ID = 0000-0002-8335-0123 (en)
rdfs:label	Ondrej Holas (en) Ondrej Holas (es) Ondrej Holas (nl) Ondrej Holas (sq) Ondrej Holas (ast) Ondřej Holas (cs)
skos:prefLabel	Ondrej Holas (en) Ondrej Holas (es) Ondrej Holas (nl) Ondrej Holas (sq) Ondrej Holas (ast) Ondřej Holas (cs)
name	Ondrej Holas (en) Ondrej Holas (es) Ondrej Holas (nl) Ondrej Holas (sq) Ondrej Holas (ast) Ondřej Holas (cs)
Scopus author ID	wds:Q59661895-26A49B8A-44AF-47ED-8159-462723088B91
Scopus author ID	14622671800
described by source	wds:Q59661895-B1EB0063-2EDD-468D-B971-165424214151
instance of	wds:Q59661895-82191D2E-3E39-4B67-8E33-30B399E7A8E8
NL CR AUT ID	wds:Q59661895-b144fe25-4fb6-8520-b4d8-3ae42958316c
described by source	Medvik
instance of	Homo sapiens
NL CR AUT ID	xx0128555
occupation	wds:Q59661895-0989d0bf-5d97-4e8b-9c46-b63bea6ebc0e wds:Q59661895-71BEF4A9-CAA3-453A-8358-8751469B2C20
employer	wds:Q59661895-D38B0EE6-9480-4E9F-A234-2B3C18F72C62
languages spoken, written or signed	wds:Q59661895-0000D745-6AC7-4A5C-8886-FDB0AAD32E33 wds:Q59661895-BD463646-F53F-450E-AD38-DB52ABDBAD4B
sex or gender	wds:Q59661895-1419D214-7A6F-437F-B961-A32944122770
VIAF ID	wds:Q59661895-E9D96BF0-B230-4D42-ACB6-B09115477A76
date of birth	wds:Q59661895-06A82772-C39A-409B-9FE9-96A121603236
WorldCat Identities ID (superseded)	wds:Q59661895-B3995C50-47D6-44B8-A9AE-241A599A739B
VIAF ID	http://viaf.org/viaf/160164865
occupation	university teacher pharmacist
employer	Charles University
languages spoken, written or signed	English Czech
sex or gender	male
VIAF ID	160164865
date of birth	1983-12-10 00:00:00Z (xsd:dateTime)
WorldCat Identities ID (superseded)	viaf-160164865
ORCID iD	wds:Q59661895-07EE92CF-6687-4626-9415-405D1167E7E0
ORCID iD	https://orcid.org/0000-0002-8335-0123
ORCID iD	0000-0002-8335-0123
ResearcherID	wds:Q59661895-D142E6A3-965C-4CF9-996B-0A200C14DF8E
ResearcherID	S-5526-2017
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q59661895
is author of	Synthesis and in vitro evaluation of N-alkyl-7-methoxytacrine hydrochlorides as potential cholinesterase inhibitors in Alzheimer disease. Synthesis of Novel Pyrazinamide Derivatives Based on 3-Chloropyrazine-2-carboxamide and Their Antimicrobial Evaluation Preparation and in vitro screening of symmetrical bis-isoquinolinium cholinesterase inhibitors bearing various connecting linkage – Implications for early Myasthenia gravis treatment The preparation,in vitroscreening and molecular docking of symmetrical bisquaternary cholinesterase inhibitors containing a but-(2E)-en-1,4-diyl connecting linkage Preparation, in vitro screening and molecular modelling of symmetrical bis-quinolinium cholinesterase inhibitors--implications for early myasthenia gravis treatment The progress in the cholinesterase quantification methods. Monooxime reactivators of acetylcholinesterase with (E)-but-2-ene linker: preparation and reactivation of tabun- and paraoxon-inhibited acetylcholinesterase. Synthesis of a novel series of non-symmetrical bispyridinium compounds bearing a xylene linker and evaluation of their reactivation activity against tabun and paraoxon-inhibited acetylcholinesterase. Colorimetric dipstick for assay of organophosphate pesticides and nerve agents represented by paraoxon, sarin and VX. Steviol, an aglycone of steviol glycoside sweeteners, interacts with the pregnane X (PXR) and aryl hydrocarbon (AHR) receptors in detoxification regulation. Mycobacterium tuberculosis enoyl-acyl carrier protein reductase inhibitors as potential antituberculotics: development in the past decade. Enantiospecific effects of chiral drugs on cytochrome P450 inhibition in vitro Mono-oxime bisquaternary acetylcholinesterase reactivators with prop-1,3-diyl linkage-Preparation, in vitro screening and molecular docking. Monooxime-monocarbamoyl Bispyridinium Xylene-Linked Reactivators of Acetylcholinesterase-Synthesis, In vitro and Toxicity Evaluation, and Docking Studies. Novel series of bispyridinium compounds bearing a (Z)-but-2-ene linker--synthesis and evaluation of their reactivation activity against tabun and paraoxon-inhibited acetylcholinesterase. Synthesis and in vitro evaluation of N-(Bromobut-3-en-2-yl)-7-methoxy-1,2,3,4-tetrahydroacridin-9-amine as a cholinesterase inhibitor with regard to Alzheimer's disease treatment. Synthesis of monooxime-monocarbamoyl bispyridinium compounds bearing (E)-but-2-ene linker and evaluation of their reactivation activity against tabun- and paraoxon-inhibited acetylcholinesterase Synthesis of asymmetrical bispyridinium compounds bearing cyano-moiety and evaluation of their reactivation activity against tabun and paraoxon-inhibited acetylcholinesterase. Evaluation of 2,6-dichlorophenolindophenol acetate as a substrate for acetylcholinesterase activity assay Preparation, in vitro screening and molecular modelling of symmetrical 4-tert-butylpyridinium cholinesterase inhibitors--analogues of SAD-128. Novel tacrine/acridine anticholinesterase inhibitors with piperazine and thiourea linkers. Synthesis and in vitro evaluation of 7-methoxy-N-(pent-4-enyl)-1,2,3,4-tetrahydroacridin-9-amine—new tacrine derivate with cholinergic properties Nanomaterials for direct and indirect immunomodulation: A review of applications Preparation and in vitro screening of symmetrical bispyridinium cholinesterase inhibitors bearing different connecting linkage-initial study for Myasthenia gravis implications. Monooxime Bispyridinium Reactivators Bearing Xylene Linker Synthesis and In Vitro Evaluation on Model of Organophosphate-Inhibited Acetylcholinesterase Stilbene compound trans-3,4,5,4´-tetramethoxystilbene, a potential anticancer drug, regulates constitutive androstane receptor (Car) target genes, but does not possess proliferative activity in mouse liver Oligonucleotide Delivery across the Caco-2 Monolayer: The Design and Evaluation of Self-Emulsifying Drug Delivery Systems (SEDDS) Influence of Amlodipine Enantiomers on Human Microsomal Cytochromes P450: Stereoselective Time-Dependent Inhibition of CYP3A Enzyme Activity. Teriflunomide Is an Indirect Human Constitutive Androstane Receptor (CAR) Activator Interacting With Epidermal Growth Factor (EGF) Signaling PLGA Based Nanospheres as a Potent Macrophage-Specific Drug Delivery System
is author of	wds:Q38718136-00E241A6-2852-4CB1-B028-C080DF623E10 wds:Q47957586-3CC47F5F-0570-4DC2-83DA-EC8E67574A17 wds:Q62073273-FA853307-B87E-4049-85C4-9E2FBEB12D8E wds:Q60949581-C9BA683E-1856-4923-82DE-447EA0EC4827 wds:Q91195444-2336BF96-EEE2-4D29-9800-5DA8E0519724 wds:Q53312514-B995018F-00D6-48FF-B73F-E6DB0CF8B4A6 wds:Q62073277-140CBE13-123D-46C3-84A9-4AD3CA1E9B9E wds:Q86068488-E265FEF0-9F78-4243-AAB3-CC3CA0AB5A58 wds:Q43199541-8714D57A-831A-45BE-A50C-53795134EE20 wds:Q43170420-63751C66-E07D-4B45-8184-3E924A755871

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