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  <titleInfo>
    <title>Synthesis and biological evaluation of C-13, C-14 modified taxane analogues from 1-deoxybaccatin VI</title>
  </titleInfo>
  <name type="personal">
    <namePart>Tang, P.</namePart>
  </name>
  <name type="personal">
    <namePart>Lin, H. X.</namePart>
  </name>
  <name type="personal">
    <namePart>Yuan, T. H.</namePart>
  </name>
  <name type="personal">
    <namePart>Cui, Y. M.</namePart>
  </name>
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  <abstract>our C-13, C-14 side chain modified 9(R)-hydroxy-1-deoxy-taxane analogues 15, 16, 19 and 22 were semi-synthesized from 1-deoxybaccatin VI. The in vitro antitumor activity of these compounds was evaluated against A549 and A2780 cell lines. The preliminary SAR analysis showed that introduction of oxygen-containing group on C-14 could improve the cytotoxic activities.</abstract>
  <subject>
    <topic>1-DEOXYBACCATIN VI</topic>
  </subject>
  <subject>
    <topic>TAXANE</topic>
  </subject>
  <subject>
    <topic>CYTOTOXICITY</topic>
  </subject>
  <subject>
    <topic>OXIDATION</topic>
  </subject>
  <subject>
    <topic>SYNTHESIS</topic>
  </subject>
  <relatedItem type="series">
    <titleInfo>
      <title>Natural Product Research, 33(24), p.3478-3484, 2019</title>
    </titleInfo>
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  <identifier type="uri">https://drive.google.com/file/d/13_-dOfCiQFwRqElhG1uxktUxkLUAN_6H/view?usp=drivesdk</identifier>
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