About: Benzofuroxane Derivatives as Multi-Effective Agents for the Treatment of Cardiovascular Diabetic Complications. Synthesis, Functional Evaluation, and Molecular Modeling Studies

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scientific article published on 20 November 2012

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в листопаді 2012 (uk) im November 2012 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 20 November 2012 (en) artículu científicu espublizáu en payares de 2012 (ast)
publication date	wds:Q58855699-6708742B-C1A6-4AC7-91B3-81DC61671D5C
publication date	2012-11-20 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q58855699-9A031486-F968-4D13-B7E6-ACEA9FB67680
language of work or name	English
rdfs:label	Benzofuroxane Derivatives as Multi-Effective Agents for the Treatment of Cardiovascular Diabetic Complications. Synthesis, Functional Evaluation, and Molecular Modeling Studies (en) Benzofuroxane Derivatives as Multi-Effective Agents for the Treatment of Cardiovascular Diabetic Complications. Synthesis, Functional Evaluation, and Molecular Modeling Studies (nl)
skos:prefLabel	Benzofuroxane Derivatives as Multi-Effective Agents for the Treatment of Cardiovascular Diabetic Complications. Synthesis, Functional Evaluation, and Molecular Modeling Studies (en) Benzofuroxane Derivatives as Multi-Effective Agents for the Treatment of Cardiovascular Diabetic Complications. Synthesis, Functional Evaluation, and Molecular Modeling Studies (nl)
name	Benzofuroxane Derivatives as Multi-Effective Agents for the Treatment of Cardiovascular Diabetic Complications. Synthesis, Functional Evaluation, and Molecular Modeling Studies (en) Benzofuroxane Derivatives as Multi-Effective Agents for the Treatment of Cardiovascular Diabetic Complications. Synthesis, Functional Evaluation, and Molecular Modeling Studies (nl)
author	wds:Q58855699-0B59A8A0-B33A-42B9-A1D6-E086FBE332CA wds:Q58855699-3CC24F42-B544-456B-AD5B-7824A12F4556 wds:Q58855699-47AF1ED1-F630-4CDF-A733-7AB87B56E6D5 wds:Q58855699-511C1B00-49AC-4AAC-AE95-7742DA36DB5A wds:Q58855699-6933BAF2-592F-4468-B1E6-BE1823283860 wds:Q58855699-76F2578E-C68B-42DA-8DDD-F03F087D2F2E wds:Q58855699-7F15A1CE-C45E-47DC-8880-F67B4A5E798A wds:Q58855699-8A8F44ED-BBD8-4FAC-95BD-0D34D5D0FF1B wds:Q58855699-ACA61108-C9EB-49EE-9856-C061DD1E4C13 wds:Q58855699-CDBBDB4C-D38A-40ED-96D5-79A3A40D2F55 wds:Q58855699-E7FFF8FA-A0A7-4A74-B897-9CF47309C129 wds:Q58855699-F60C340E-DD22-4D1F-A5E0-EDDEC0264A2B
author	Luciana Marinelli Sandro Cosconati Ettore Novellino Anna Maria Marini Concettina La Motta Sabrina Taliani Federico Da Settimo Passetti Francesca Simorini Salvatore Di Maro Elisabetta Barresi Stefania Sartini Silvia Salerno
title	wds:Q58855699-DB6477BB-A0EF-4DA3-9B87-11EC8100ED8C
title	Benzofuroxane derivatives as multi-effective agents for the treatment of cardiovascular diabetic complications. Synthesis, functional evaluation, and molecular modeling studies (en)
page(s)	wds:Q58855699-BE955A9E-0A3B-4028-B6C3-4E04D166D577
page(s)	10523-10531
instance of	wds:Q58855699-200D6378-0207-4723-8C52-5F2AAF87B682
instance of	scholarly article
PubMed ID	wds:Q58855699-B2FE6E48-BF76-4BA4-B94A-01E4A7D7BAF4
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/23134227
PubMed ID	23134227
published in	wds:Q58855699-E623E63C-C5BE-499E-8AF0-9E7B482281C8
published in	Journal of Medicinal Chemistry
issue	wds:Q58855699-F2958FBC-6627-4D0F-830F-46B03D581A7B
volume	wds:Q58855699-43078C7E-FC1F-416E-A02B-B61DB49DDF8D
issue	23
volume	55
DOI	wds:Q58855699-C04C92A0-A9EE-42F7-951F-301D84F279D0
DOI	http://dx.doi.org/10.1021/JM301124S
DOI	10.1021/JM301124S
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58855699
is cites work of	Identification, synthesis and evaluation of substituted benzofurazans as inhibitors of CREB-mediated gene transcription Synthesis and Functional Evaluation of Novel Aldose Reductase Inhibitors Bearing a Spirobenzopyran Scaffold Inhibition of ocular aldose reductase by a new benzofuroxane derivative ameliorates rat endotoxic uveitis Addition of the Aldose Reductase Inhibitor Benzofuroxane Derivative BF-5m to Prolonged and Moderate Exercise Training Enhanced Protection of the Rat Heart From Type-1 Diabetes Paeonol Inhibits Proliferation of Vascular Smooth Muscle Cells Stimulated by High Glucose via Ras-Raf-ERK1/2 Signaling Pathway in Coculture Model Inhibition of aldose-reductase-2 by a benzofuroxane derivative bf-5m increases the expression of kcne1, kcnq1 in high glucose cultured H9c2 cardiac cells and sudden cardiac death. Effects of the New Aldose Reductase Inhibitor Benzofuroxane Derivative BF-5m on High Glucose Induced Prolongation of Cardiac QT Interval and Increase of Coronary Perfusion Pressure. Novel quinazolinone-based 2,4-thiazolidinedione-3-acetic acid derivatives as potent aldose reductase inhibitors. Novel 2-phenoxypyrido[3,2-b]pyrazin-3(4H)-one derivatives as potent and selective aldose reductase inhibitors with antioxidant activity
is cites work of	wds:Q42104428-4C9103FB-4B80-49C5-A899-BF8D9324E2B3 wds:Q64108671-6841A563-19A5-4258-B8D1-4276D459D229 wds:Q34569761-EBBBE6E3-5807-4139-9DF7-5159B89CE16E wds:Q37198882-DD87A118-0EFB-48E3-8470-85DFF30149CF wds:Q33796768-E14CBB9E-7A8C-4531-A34C-EBD6E7EE288E wds:Q52715790-4C88A532-49BC-4AC7-A6D5-2FD225DD95A1 wds:Q43093239-35F311E6-10BC-433D-B905-CA23920D3FA7 wds:Q47446145-4209F5E7-18E1-4E77-BFE8-9DC935AFA542 wds:Q92199427-C6EC894E-319C-4A2F-BA8B-111BD04701CE

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