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      <title>Homophymine A, an anti-HIV cyclodepsipeptide from the sponge Homophymia sp</title>
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    <abstract>A new anti-HIV cyclodepsipeptide, homophymine A, was isolated from a New Caledonian collection of the marine sponge Homophymia sp. The structure of homophymine A was determined by interpretation of spectroscopic data, acid hydrolysis, and LC-MS analysis. Homophymine A contains 11 amino acid residues and an amide-linked 3-hydroxy-2,4,6-trimethyloctanoic acid moiety. Along with four D-, two L-, and one N-methyl arnino acids, it also contains four unusual amino acid residues: (2S,3S,4R)-3,4diMe-Gln, (2R,3R,4S)-4-amino-2,3-dihydroxy-1,7-heptandioic acid, L-ThrOMe, and (2R,3R,4R)-2-amino3-hydroxy-4,5-dimethylhexanoic acid. In a cell-based XTT assay, homophymine A exhibited cytoprotective activity against HIV-1 infection with a IC50 of 75 nM.</abstract>
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      <geographic>NOUVELLE CALEDONIE</geographic>
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        <title>Journal of Organic Chemistry</title>
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          <number>73</number>
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          <number>14</number>
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          <list> 5319-5327</list>
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      <identifier type="issn">0022-3263</identifier>
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    <identifier type="uri">https://www.documentation.ird.fr/hor/fdi:010055302</identifier>
    <identifier type="doi">10.1021/jo800583b</identifier>
    <identifier type="issn">0022-3263</identifier>
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