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<Article>
<Journal>
<PublisherName>aaspjournal</PublisherName>
<JournalTitle>Journal of Asian Association of Schools of Pharmacy</JournalTitle>
<PISSN>I</PISSN>
<EISSN>S</EISSN>
<Volume-Issue>Volume 1 No.4</Volume-Issue>
<PartNumber/>
<IssueTopic>Multidisciplinary</IssueTopic>
<IssueLanguage>English</IssueLanguage>
<Season>October - December, 2012</Season>
<SpecialIssue>N</SpecialIssue>
<SupplementaryIssue>N</SupplementaryIssue>
<IssueOA>Y</IssueOA>
<PubDate>
<Year>-0001</Year>
<Month>11</Month>
<Day>30</Day>
</PubDate>
<ArticleType>Pharmacy</ArticleType>
<ArticleTitle>Isoindole-1,3-dione-based __ampersandsignalpha;,__ampersandsigngamma;-diketo acid bioisosteres as hepatitis C virus NS5B polymerase inhibitors</ArticleTitle>
<SubTitle/>
<ArticleLanguage>English</ArticleLanguage>
<ArticleOA>Y</ArticleOA>
<FirstPage>210</FirstPage>
<LastPage>225</LastPage>
<AuthorList>
<Author>
<FirstName>Ravindra Ramesh</FirstName>
<LastName>Deore</LastName>
<AuthorLanguage>English</AuthorLanguage>
<Affiliation/>
<CorrespondingAuthor>N</CorrespondingAuthor>
<ORCID/>
<FirstName>Ajit Dhananjay</FirstName>
<LastName>Jagtap</LastName>
<AuthorLanguage>English</AuthorLanguage>
<Affiliation/>
<CorrespondingAuthor>Y</CorrespondingAuthor>
<ORCID/>
<FirstName>Pei-Teh</FirstName>
<LastName>Chang</LastName>
<AuthorLanguage>English</AuthorLanguage>
<Affiliation/>
<CorrespondingAuthor>Y</CorrespondingAuthor>
<ORCID/>
<FirstName>WirunyaTrimethasil</FirstName>
<AuthorLanguage>English</AuthorLanguage>
<Affiliation/>
<CorrespondingAuthor>Y</CorrespondingAuthor>
<ORCID/>
<FirstName>Ji-Wang</FirstName>
<LastName>Chern</LastName>
<AuthorLanguage>English</AuthorLanguage>
<Affiliation/>
<CorrespondingAuthor>Y</CorrespondingAuthor>
<ORCID/>
</Author>
</AuthorList>
<DOI/>
<Abstract>Integration of 2-N-hydroxyl- and 2-N-benzoyl-1,3- diketo acid moieties into isoindole-1,3-dione led to the development of two series of hepatitis C virus NS5B polymerase inhibitors. Structural optimization to translate enzyme inhibitory activity to cellular cytotoxicity yielded compound 16c, a moderate enzyme inhibitor (IC50 = 27.3 µM) with selective toxicity to hepatitis C virus 1b replicon-containing Ava5 cells (EC50 = 18.0 µM). Binding experiments indicated that 16c (Kd = 1.25 µM) not only competed with fluorescein-labeled GTP for NS5B binding, but also displaced bound GTP from the polymerase active site.</Abstract>
<AbstractLanguage>English</AbstractLanguage>
<Keywords>Hepatitis C virus NS5B polymerase ?,?-diketo acid bioisostere isoindole-1,3-dione</Keywords>
<URLs>
<Abstract>https://aaspjournal.org/ubijournal-v1copy/journals/abstract.php?article_id=5945&title=Isoindole-1,3-dione-based __ampersandsignalpha;,__ampersandsigngamma;-diketo acid bioisosteres as hepatitis C virus NS5B polymerase inhibitors</Abstract>
</URLs>
<References>
<ReferencesarticleTitle>References</ReferencesarticleTitle>
<ReferencesfirstPage>16</ReferencesfirstPage>
<ReferenceslastPage>19</ReferenceslastPage>
<References/>
</References>
</Journal>
</Article>
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