<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>3(1)</volume><submitter>Mallick T</submitter><pubmed_abstract>The visible fluorescent chromophoric moiety present in the water-soluble photoactive yellow protein (PYP) of &lt;i>Ectothiorhodospira halophila&lt;/i> is &lt;i>p&lt;/i>-hydroxycinnamic acid linked to the cysteine residue (Cys-69) by a thioester bond and it controls the key photoinduced biological processes of the host organism. In the present work, we have synthesized and characterized three structurally different thiophenyl esters [viz., &lt;i>p-&lt;/i>hydroxycinnamic-thiophenyl ester (&lt;b>1&lt;/b>), &lt;i>p&lt;/i>-&lt;i>N&lt;/i>,&lt;i>N&lt;/i>-dimethylaminocinnamic-thiophenyl ester (&lt;b>2&lt;/b>), and &lt;i>S&lt;/i>-phenyl-3-(4-chlorophenyl)-3-(phenylthio)propanethioate (&lt;b>3&lt;/b>)] in addition to a novel (to the best of our knowledge) stilbene-type olefinic compound, &lt;i>N&lt;/i>&lt;sup>1&lt;/sup>,&lt;i>N&lt;/i>&lt;sup>1&lt;/sup>,&lt;i>N&lt;/i>&lt;sup>2&lt;/sup>,&lt;i>N&lt;/i</pubmed_abstract><journal>ACS omega</journal><pagination>334-348</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6044905</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Fluorescent Small Molecules Are BIG Enough To Sense Biomacromolecule: Synthesis of Aromatic Thioesters and Understanding Their Interactions with ctDNA.</pubmed_title><pmcid>PMC6044905</pmcid><pubmed_authors>Ahamed G</pubmed_authors><pubmed_authors>Batuta S</pubmed_authors><pubmed_authors>Alam MN</pubmed_authors><pubmed_authors>Mandal D</pubmed_authors><pubmed_authors>Das S</pubmed_authors><pubmed_authors>Mukherjee M</pubmed_authors><pubmed_authors>Das N</pubmed_authors><pubmed_authors>Karmakar A</pubmed_authors><pubmed_authors>Mallick T</pubmed_authors><pubmed_authors>Begum NA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Fluorescent Small Molecules Are BIG Enough To Sense Biomacromolecule: Synthesis of Aromatic Thioesters and Understanding Their Interactions with ctDNA.</name><description>The visible fluorescent chromophoric moiety present in the water-soluble photoactive yellow protein (PYP) of &lt;i>Ectothiorhodospira halophila&lt;/i> is &lt;i>p&lt;/i>-hydroxycinnamic acid linked to the cysteine residue (Cys-69) by a thioester bond and it controls the key photoinduced biological processes of the host organism. In the present work, we have synthesized and characterized three structurally different thiophenyl esters [viz., &lt;i>p-&lt;/i>hydroxycinnamic-thiophenyl ester (&lt;b>1&lt;/b>), &lt;i>p&lt;/i>-&lt;i>N&lt;/i>,&lt;i>N&lt;/i>-dimethylaminocinnamic-thiophenyl ester (&lt;b>2&lt;/b>), and &lt;i>S&lt;/i>-phenyl-3-(4-chlorophenyl)-3-(phenylthio)propanethioate (&lt;b>3&lt;/b>)] in addition to a novel (to the best of our knowledge) stilbene-type olefinic compound, &lt;i>N&lt;/i>&lt;sup>1&lt;/sup>,&lt;i>N&lt;/i>&lt;sup>1&lt;/sup>,&lt;i>N&lt;/i>&lt;sup>2&lt;/sup>,&lt;i>N&lt;/i</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jan</publication><modification>2026-04-29T22:59:58.467Z</modification><creation>2019-03-26T23:47:15Z</creation></dates><accession>S-EPMC6044905</accession><cross_references><pubmed>30023778</pubmed><doi>10.1021/acsomega.7b01933</doi></cross_references></HashMap>