About: (Thiazol-2-yl)hydrazone derivatives from acetylpyridines as dual inhibitors of MAO and AChE: synthesis, biological evaluation and molecular modeling studies

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About: (Thiazol-2-yl)hydrazone derivatives from acetylpyridines as dual inhibitors of MAO and AChE: synthesis, biological evaluation and molecular modeling studies Goto Sponge NotDistinct Permalink

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scientific article published on 25 September 2015

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у вересні 2015 (uk) scientific article published on 25 September 2015 (en) artículu científicu espublizáu en setiembre de 2015 (ast)
publication date	wds:Q61657232-A20E8FC9-5E8E-4B2A-8BF0-4CD7C619F844
publication date	2015-09-25 00:00:00Z (xsd:dateTime)
author name string	wds:Q61657232-24837925-4E9D-4BEB-8EF4-6E00B33EBAE0 wds:Q61657232-255C43C2-5C3B-4699-B15C-228A67BEBF68 wds:Q61657232-39DF8589-78F3-4D8E-9853-26D5DCB50608 wds:Q61657232-3F174E4D-12C5-48AA-AD0A-C497C2DB4847 wds:Q61657232-58FE5A8F-4673-4963-A9D1-20B012E19A99 wds:Q61657232-7C093CDC-27BE-4E4E-A593-BF21B7375599 wds:Q61657232-A83BD347-CE55-4915-982F-6F400B442ED0 wds:Q61657232-A8FA156A-52B4-477B-A855-86D6E0DE0A95
author name string	Arianna Granese Celeste De Monte Stefano Alcaro Matilde Yáñez Daniela De Vita Melissa D'Ascenzio Paola Chimenti Maria Concetta Gidaro
rdfs:label	(Thiazol-2-yl)hydrazone derivatives from acetylpyridines as dual inhibitors of MAO and AChE: synthesis, biological evaluation and molecular modeling studies (en) (Thiazol-2-yl)hydrazone derivatives from acetylpyridines as dual inhibitors of MAO and AChE: synthesis, biological evaluation and molecular modeling studies (nl)
skos:prefLabel	(Thiazol-2-yl)hydrazone derivatives from acetylpyridines as dual inhibitors of MAO and AChE: synthesis, biological evaluation and molecular modeling studies (en) (Thiazol-2-yl)hydrazone derivatives from acetylpyridines as dual inhibitors of MAO and AChE: synthesis, biological evaluation and molecular modeling studies (nl)
name	(Thiazol-2-yl)hydrazone derivatives from acetylpyridines as dual inhibitors of MAO and AChE: synthesis, biological evaluation and molecular modeling studies (en) (Thiazol-2-yl)hydrazone derivatives from acetylpyridines as dual inhibitors of MAO and AChE: synthesis, biological evaluation and molecular modeling studies (nl)
author	wds:Q61657232-05C2DD4C-1AB4-400B-B34D-ACE13583B67E wds:Q61657232-2AE65C84-B7AE-4AA6-9BD9-8DFB043AF09B wds:Q61657232-4D60714A-239E-48F5-AA74-D259EE7CE632 wds:Q61657232-6B956D6B-733E-4EFA-8C5C-8A6C08502919
author	Simone Carradori Roberto Di Santo Luigi Scipione Giosuè Costa
title	wds:Q61657232-F9901584-DF34-4CC2-B979-137FCD20F732
title	(Thiazol-2-yl)hydrazone derivatives from acetylpyridines as dual inhibitors of MAO and AChE: synthesis, biological evaluation and molecular modeling studies (en)
page(s)	wds:Q61657232-DC1629C0-CF96-4418-B230-53637ACA1146
page(s)	908-919
instance of	wds:Q61657232-2284B5DB-99FC-49FB-A8FF-E5B9B391F165
instance of	scholarly article
PubMed ID	wds:Q61657232-C41EE6E0-B0A4-4077-BDA2-4F3A8973DF2D
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/25807300
PubMed ID	25807300
published in	wds:Q61657232-B128B078-8397-444F-BC2D-EB2A1AAEA1E1
published in	Journal of Enzyme Inhibition and Medicinal Chemistry
issue	wds:Q61657232-B82D5E05-A400-444F-9C41-A954C5B525EA
volume	wds:Q61657232-A433F0E8-DF36-4EB2-B69B-CE3F3ABFF30B
issue	6
volume	30
DOI	wds:Q61657232-04159D24-8723-4EE3-92B8-4A3D863026B9
DOI	http://dx.doi.org/10.3109/14756366.2014.987138
DOI	10.3109/14756366.2014.987138
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q61657232
is cites work of	Design, Synthesis, and Evaluation of 2-Amino-6-nitrobenzothiazole-Derived Hydrazones as MAO Inhibitors: Role of the Methylene Spacer Group A Target-Based Whole Cell Screen Approach To Identify Potential Inhibitors of Mycobacterium tuberculosis Signal Peptidase 4-(3-Nitrophenyl)thiazol-2-ylhydrazone derivatives as antioxidants and selective hMAO-B inhibitors: synthesis, biological activity and computational analysis Design, synthesis, and pharmacological evaluation of 2-amino-5-nitrothiazole derived semicarbazones as dual inhibitors of monoamine oxidase and cholinesterase: effect of the size of aryl binding site. Synthesis and Evaluation of a New Series of Thiazolyl-pyrazoline Derivatives as Cholinesterase Inhibitors
is cites work of	wds:Q39664171-42111404-0018-4A7A-8392-EB102BF20EDB wds:Q61798857-456A3B10-F66B-4183-B78E-04DE9B068A52 wds:Q95852902-5969ED4F-371B-42AE-A58E-990C478F5CD3 wds:Q28817990-3C933046-BAB8-4189-A949-4A6F47885EE2 wds:Q47178186-6D6CA335-7EB8-48C8-A575-A78414BB8876

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