{"@context":{"@vocab":"https://cir.nii.ac.jp/schema/1.0/","rdfs":"http://www.w3.org/2000/01/rdf-schema#","dc":"http://purl.org/dc/elements/1.1/","dcterms":"http://purl.org/dc/terms/","foaf":"http://xmlns.com/foaf/0.1/","prism":"http://prismstandard.org/namespaces/basic/2.0/","cinii":"http://ci.nii.ac.jp/ns/1.0/","datacite":"https://schema.datacite.org/meta/kernel-4/","ndl":"http://ndl.go.jp/dcndl/terms/","jpcoar":"https://github.com/JPCOAR/schema/blob/master/2.0/"},"@id":"https://cir.nii.ac.jp/crid/1362825894581806976.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1002/jhet.457"}},{"identifier":{"@type":"URI","@value":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fjhet.457"}},{"identifier":{"@type":"URI","@value":"https://onlinelibrary.wiley.com/doi/pdf/10.1002/jhet.457"}}],"dc:title":[{"@value":"Synthesis and antiviral activities of some heteroaryl‐substituted triarylmethanes"}],"description":[{"type":"abstract","notation":[{"@value":"<jats:title>Abstract</jats:title><jats:p><jats:boxed-text content-type=\"graphic\" position=\"anchor\"><jats:graphic xmlns:xlink=\"http://www.w3.org/1999/xlink\" mimetype=\"image/gif\" position=\"anchor\" specific-use=\"enlarged-web-image\" xlink:href=\"graphic/mgra001.gif\"><jats:alt-text>magnified image</jats:alt-text></jats:graphic></jats:boxed-text>Some molecular modifications were attempted to find antiviral active compounds in the class of triarylmethanes against herpes simplex virus type 1 (HSV‐1). All the synthesized compounds were evaluated for antiviral activity with HSV‐1 by a plaque reduction assay. Some of the compounds showed significant antiviral activities. J. Heterocyclic Chem., (2010).</jats:p>"}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1382825894581806977","@type":"Researcher","foaf:name":[{"@value":"Nobuko Mibu"}]},{"@id":"https://cir.nii.ac.jp/crid/1420282801201402368","@type":"Researcher","personIdentifier":[{"@type":"KAKEN_RESEARCHERS","@value":"80240919"},{"@type":"NRID","@value":"1000080240919"},{"@type":"NRID","@value":"9000004368225"},{"@type":"NRID","@value":"9000020717596"},{"@type":"NRID","@value":"9000019948585"},{"@type":"NRID","@value":"9000020770252"},{"@type":"NRID","@value":"9000014647341"},{"@type":"NRID","@value":"9000240034775"},{"@type":"NRID","@value":"9000014197374"},{"@type":"NRID","@value":"9000259830818"},{"@type":"NRID","@value":"9000019947572"},{"@type":"NRID","@value":"9000300212749"},{"@type":"NRID","@value":"9000020171423"},{"@type":"RESEARCHMAP","@value":"https://researchmap.jp/read-yokomi"}],"foaf:name":[{"@value":"Kazumi Yokomizo"}]},{"@id":"https://cir.nii.ac.jp/crid/1382825894581806978","@type":"Researcher","foaf:name":[{"@value":"Takeshi Miyata"}]},{"@id":"https://cir.nii.ac.jp/crid/1382825894581806979","@type":"Researcher","foaf:name":[{"@value":"Kunihiro Sumoto"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"0022152X"},{"@type":"EISSN","@value":"19435193"}],"prism:publicationName":[{"@value":"Journal of Heterocyclic Chemistry"}],"dc:publisher":[{"@value":"Wiley"}],"prism:publicationDate":"2010-08-24","prism:volume":"47","prism:number":"6","prism:startingPage":"1434","prism:endingPage":"1438"},"reviewed":"false","dc:rights":["http://onlinelibrary.wiley.com/termsAndConditions#vor"],"url":[{"@id":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fjhet.457"},{"@id":"https://onlinelibrary.wiley.com/doi/pdf/10.1002/jhet.457"}],"createdAt":"2010-08-29","modifiedAt":"2025-02-25","relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1390282679154902784","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Molecular Symmetry and Biological Activities of New Symmetrical Tris(2-aminoethyl)amine Derivatives"}]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1002/jhet.457"},{"@type":"OPENAIRE","@value":"doi_dedup___::5ee36cdb64979bc5cfca4710a1f377ff"},{"@type":"CROSSREF","@value":"10.1248/cpb.60.408_references_DOI_E43glCQIR7hmnraV3rAlQCeJM6q"}]}