<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lv W</submitter><funding>NIGMS NIH HHS</funding><pagination>4611-8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4043309</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>56(11)</volume><pubmed_abstract>The first synthesis of the tamoxifen metabolite norendoxifen is reported. This included syntheses of (E)-norendoxifen, (Z)-norendoxifen, and (E,Z)-norendoxifen isomers. (Z)-Norendoxifen displayed affinity for aromatase (Ki 442 nM), estrogen receptor-α (EC50 17 nM), and estrogen receptor-β (EC50 27.5 nM), while the corresponding values for (E)-norendoxifen were aromatase (Ki 48 nM), estrogen receptor-α (EC50 58.7 nM), and estrogen receptor-β (EC50 78.5 nM). Docking and energy minimization studies were performed with (E)-norendoxifen on aromatase, and the results provide a foundation for structure-based drug design. The oral pharmacokinetic parameters for (E,Z)-norendoxifen were determined in mice, and (Z)-norendoxifen was found to result in significantly higher plasma concentrations and exp</pubmed_abstract><journal>Journal of medicinal chemistry</journal><pubmed_title>Synthesis of mixed (E,Z)-, (E)-, and (Z)-norendoxifen with dual aromatase inhibitory and estrogen receptor modulatory activities.</pubmed_title><pmcid>PMC4043309</pmcid><funding_grant_id>T32 GM008425</funding_grant_id><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Flockhart DA</pubmed_authors><pubmed_authors>Cushman M</pubmed_authors><pubmed_authors>Lv W</pubmed_authors><pubmed_authors>Lu D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis of mixed (E,Z)-, (E)-, and (Z)-norendoxifen with dual aromatase inhibitory and estrogen receptor modulatory activities.</name><description>The first synthesis of the tamoxifen metabolite norendoxifen is reported. This included syntheses of (E)-norendoxifen, (Z)-norendoxifen, and (E,Z)-norendoxifen isomers. (Z)-Norendoxifen displayed affinity for aromatase (Ki 442 nM), estrogen receptor-α (EC50 17 nM), and estrogen receptor-β (EC50 27.5 nM), while the corresponding values for (E)-norendoxifen were aromatase (Ki 48 nM), estrogen receptor-α (EC50 58.7 nM), and estrogen receptor-β (EC50 78.5 nM). Docking and energy minimization studies were performed with (E)-norendoxifen on aromatase, and the results provide a foundation for structure-based drug design. The oral pharmacokinetic parameters for (E,Z)-norendoxifen were determined in mice, and (Z)-norendoxifen was found to result in significantly higher plasma concentrations and exp</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Jun</publication><modification>2025-04-19T15:57:25.492Z</modification><creation>2019-03-27T01:29:22Z</creation></dates><accession>S-EPMC4043309</accession><cross_references><pubmed>23731360</pubmed><doi>10.1021/jm400364h</doi></cross_references></HashMap>