<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Perrone MG</submitter><funding>University of Bergen</funding><funding>Italian Association for Cancer Research</funding><funding>Italian Ministero dello Sviluppo Economic (MISE, Ministry of Economic Development)</funding><funding>The Research Council of Norway</funding><funding>Ministry of Economic Development</funding><funding>Fondazione G.A.I.A and Fondazione Onlus MiaNeri</funding><funding>H2020 program MSCA-ITN</funding><funding>First AIRC Grant-MFAG2015</funding><funding>Helse Vest RHF and Helse Bergen HF</funding><funding>The Norwegian Cancer Society</funding><pagination>668</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9230671</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(6)</volume><pubmed_abstract>The identification and removal of all gross and microscopic tumor to render the patient disease free represents a huge challenge in ovarian cancer treatment. The presence of residual disease is an independent negative prognostic factor. Herein, we describe the synthesis and the "in vitro" evaluation of compounds as cyclooxygenase (COX)-1 inhibitors, the COX-1 isoform being an ovarian cancer biomarker, each bearing fluorochromes with different fluorescence features. Two of these compounds &lt;i>N&lt;/i>-[4-(9-dimethylimino-9H-benzo[a]phenoxazin-5-ylamino) butyl]-2-(3,4-bis(4-methoxyphenyl)isoxazol-5-yl)acetamide chloride (RR11) and 3-(6-(4-(2-(3,4-bis(4-methoxyphenyl)isoxazole-5-yl)acetamido)butyl)amino-6-oxohexyl)-2-[7-(1,3-dihydro-1,1-dimethyl-3-ethyl 2&lt;i>H&lt;/i>-benz[e]indolin-2-yl-idene)-1,3,5-</pubmed_abstract><journal>Pharmaceuticals (Basel, Switzerland)</journal><pubmed_title>Fluorochrome Selection for Imaging Intraoperative Ovarian Cancer Probes.</pubmed_title><pmcid>PMC9230671</pmcid><funding_grant_id>240222</funding_grant_id><funding_grant_id>17566</funding_grant_id><funding_grant_id>182735</funding_grant_id><funding_grant_id>911809</funding_grant_id><funding_grant_id>675743</funding_grant_id><funding_grant_id>815900</funding_grant_id><funding_grant_id>092</funding_grant_id><funding_grant_id>223250</funding_grant_id><funding_grant_id>226244</funding_grant_id><funding_grant_id>911852</funding_grant_id><funding_grant_id>HV1269</funding_grant_id><funding_grant_id>F-12183/4800003665</funding_grant_id><funding_grant_id>912171</funding_grant_id><pubmed_authors>Kleinmanns K</pubmed_authors><pubmed_authors>Bonaccorso C</pubmed_authors><pubmed_authors>Vitale P</pubmed_authors><pubmed_authors>Bjorge L</pubmed_authors><pubmed_authors>Scilimati A</pubmed_authors><pubmed_authors>Perrone MG</pubmed_authors><pubmed_authors>Solidoro R</pubmed_authors><pubmed_authors>Fortuna CG</pubmed_authors><pubmed_authors>Centonze A</pubmed_authors><pubmed_authors>Munzone C</pubmed_authors><pubmed_authors>Miciaccia M</pubmed_authors><pubmed_authors>Ferorelli S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Fluorochrome Selection for Imaging Intraoperative Ovarian Cancer Probes.</name><description>The identification and removal of all gross and microscopic tumor to render the patient disease free represents a huge challenge in ovarian cancer treatment. The presence of residual disease is an independent negative prognostic factor. Herein, we describe the synthesis and the "in vitro" evaluation of compounds as cyclooxygenase (COX)-1 inhibitors, the COX-1 isoform being an ovarian cancer biomarker, each bearing fluorochromes with different fluorescence features. Two of these compounds &lt;i>N&lt;/i>-[4-(9-dimethylimino-9H-benzo[a]phenoxazin-5-ylamino) butyl]-2-(3,4-bis(4-methoxyphenyl)isoxazol-5-yl)acetamide chloride (RR11) and 3-(6-(4-(2-(3,4-bis(4-methoxyphenyl)isoxazole-5-yl)acetamido)butyl)amino-6-oxohexyl)-2-[7-(1,3-dihydro-1,1-dimethyl-3-ethyl 2&lt;i>H&lt;/i>-benz[e]indolin-2-yl-idene)-1,3,5-</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2026-04-08T10:12:34.563Z</modification><creation>2025-04-07T00:33:17.081Z</creation></dates><accession>S-EPMC9230671</accession><cross_references><pubmed>35745587</pubmed><doi>10.3390/ph15060668</doi></cross_references></HashMap>