<?xml version="1.0" encoding="UTF-8"?>
<modsCollection xmlns="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-3.xsd">
  <mods>
    <titleInfo>
      <title>Synthesis and cytotoxic activity of a novel dihydroisoquinoline-derived hydroxamic acid</title>
    </titleInfo>
    <name type="personnal">
      <namePart type="family">Ben Salah</namePart>
      <namePart type="given">H.</namePart>
      <role>
        <roleTerm type="text">auteur</roleTerm>
        <roleTerm type="code" authority="marcrelator">aut</roleTerm>
      </role>
      <affiliation>IRD</affiliation>
    </name>
    <name type="personnal">
      <namePart type="family">Carraz</namePart>
      <namePart type="given">Maëlle</namePart>
      <role>
        <roleTerm type="text">auteur</roleTerm>
        <roleTerm type="code" authority="marcrelator">aut</roleTerm>
      </role>
      <affiliation>IRD</affiliation>
    </name>
    <name type="personnal">
      <namePart type="family">Kammoun</namePart>
      <namePart type="given">M.</namePart>
      <role>
        <roleTerm type="text">auteur</roleTerm>
        <roleTerm type="code" authority="marcrelator">aut</roleTerm>
      </role>
      <affiliation>IRD</affiliation>
    </name>
    <typeOfResource>text</typeOfResource>
    <genre authority="local">journalArticle</genre>
    <language>
      <languageTerm type="code" authority="iso639-2b">eng</languageTerm>
    </language>
    <abstract>Naturally occurring hydroxamic acid derivatives are biosynthesized by microorganisms (siderophores) and plants (benzoxazinoids). Recent developments in drug related research have highlighted the promising biological and pharmacological properties that the hydroxamic acid function may offer for the enhancement of therapeutic applications. This study reports on the full synthesis of a new dihydroisoquinoline hydroxamic acid (2-Hydroxy-3,3-dimethyl-7-nitro-3,4-dihydroisoquinolin-1(2H)-one). It also describes its cytotoxicity with regard to the human hepatocarcinoma cell line Hep3B.</abstract>
    <targetAudience authority="marctarget">specialized</targetAudience>
    <classification authority="local">020PHYCHI</classification>
    <relatedItem type="host">
      <titleInfo>
        <title>Journal of Advances in Chemistry</title>
      </titleInfo>
      <part>
        <detail type="volume">
          <number>10</number>
        </detail>
        <detail type="volume">
          <number>4</number>
        </detail>
        <extent unit="pages">
          <list>2648-2653</list>
        </extent>
      </part>
      <originInfo>
        <dateIssued>2014</dateIssued>
      </originInfo>
      <identifier type="issn">2321-807X</identifier>
    </relatedItem>
    <identifier type="uri">https://www.documentation.ird.fr/hor/fdi:010092393</identifier>
    <identifier type="doi">10.24297/jac.v10i4.5503</identifier>
    <identifier type="issn">2321-807X</identifier>
    <location>
      <shelfLocator>[F B010092393]</shelfLocator>
      <url usage="primary display" access="object in context">https://www.documentation.ird.fr/hor/fdi:010092393</url>
    </location>
    <recordInfo>
      <recordContentSource>IRD - Base Horizon / Pleins textes</recordContentSource>
      <recordCreationDate encoding="w3cdtf">2024-11-28</recordCreationDate>
      <recordChangeDate encoding="w3cdtf">2024-11-28</recordChangeDate>
      <recordIdentifier>fdi:010092393</recordIdentifier>
      <languageOfCataloging>
        <languageTerm authority="iso639-2b">fre</languageTerm>
      </languageOfCataloging>
    </recordInfo>
  </mods>
</modsCollection>
