reference/12181404

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	8531
issn	1520-4804 0022-2623
issueIdentifier	18
pageRange	8511-8531
publicationName	Journal of Medicinal Chemistry
startingPage	8511
hasFundingAgency	http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_25b0b7c0e601d8993b3b2e205f7e9832 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_4ac43d440a4b6872485314b8ded1964a http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_6dc5ad35c2c940c3419970baeff0e197
bibliographicCitation	Falsini M, Catarzi D, Varano F, Ceni C, Dal Ben D, Marucci G, Buccioni M, Volpini R, Di Cesare Mannelli L, Lucarini E, Ghelardini C, Bartolucci G, Menicatti M, Colotta V. Antioxidant-Conjugated 1,2,4-Triazolo[4,3-a]pyrazin-3-one Derivatives: Highly Potent and Selective Human A_2A Adenosine Receptor Antagonists Possessing Protective Efficacy in Neuropathic Pain. J. Med. Chem. 2019 Aug 27;62(18):8511–31. doi: 10.1021/acs.jmedchem.9b00778.
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date	2019-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/31453698 https://doi.org/10.1021/acs.jmedchem.9b00778
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Antioxidant-Conjugated 1,2,4-Triazolo[4,3-a]pyrazin-3-one Derivatives: Highly Potent and Selective Human A2A Adenosine Receptor Antagonists Possessing Protective Efficacy in Neuropathic Pain
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