<?xml version="1.0" encoding="UTF-8"?>
<?xml-stylesheet type="text/xsl" href="https://www.peertechzpublications.org/assets/xsl/oaitohtml.xsl"?>
<OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:mml="http://www.w3.org/1998/Math/MathML" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd">
										<responseDate>2026-04-30T02:24:56Z</responseDate>
										<request verb="GetRecord" metadataPrefix="oai_dc" identifier="oai:www.peertechzpublications.org:10.17352/2455-5363.000038">https://www.peertechzpublications.org/oai-pmh</request><GetRecord><record>
								<header>
									<identifier>oai:www.peertechzpublications.org:10.17352/2455-5363.000038</identifier>
									<datestamp>2020-12-22</datestamp>
									<setSpec>PTZ.GJIDCR:VOL6</setSpec>
								</header>
								<metadata>
									<oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:mml="http://www.w3.org/1998/Math/MathML" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
										<dc:title>
										A strategy for finding new medicines against the novel coronavirus disease (COVID-19) derived from base pairing with DNA damages
										</dc:title><dc:creator>Katsuhito Kino</dc:creator><dc:creator> Takayuki Ohshima</dc:creator><dc:creator> Taishu Kawada</dc:creator><dc:creator> Takanobu Kobayashi</dc:creator><dc:creator>Hiroshi Miyazawa</dc:creator><dc:description>&lt;p&gt;The spread of the novel coronavirus disease (COVID-19) has caused a global pandemic. Exiting agents that act on proteins including 3-chymotrypsin-like protease (3CLpro), papain-like protease (PLpro), helicase, RNA-dependent RNA polymerase (RdRp), spike glycoprotein (S protein), and others in similar viruses [1,2] are likely used as antiviral drugs against the novel coronavirus (SARS-CoV-2). Data on Chemical Abstract Service show that the potential drug candidates against 3CLpro and RdRp are more than those against other targets [2].&lt;/p&gt;&lt;p&gt;&lt;br&gt;&lt;/p&gt;</dc:description>
										<dc:publisher>Global Journal of Infectious Diseases and Clinical Research - Peertechz Publications</dc:publisher>
										<dc:date>2020-12-22</dc:date>
										<dc:type>Opinion</dc:type>
										<dc:identifier>https://doi.org/10.17352/2455-5363.000038</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Katsuhito Kino et al.</dc:rights>
									</oai_dc:dc>
								</metadata>
							</record></GetRecord>
						</OAI-PMH>
