{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-09-09",
    "results": {
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          "code": "5EN0DE4P7X",
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          "url": "http://www.brenda-enzymes.org/Mol/Mol.php4?n=257037&compound=stearyl&s_type=5&back=1&limit_start=10",
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          "citation": "SRS import [5EN0DE4P7X]",
          "url": "http://fdasis.nlm.nih.gov/srs/srsdirect.jsp?regno=5EN0DE4P7X",
          "doc_type": "SRS",
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          "smiles": "[Na+]",
          "formula": "Na",
          "atropisomerism": "No",
          "charge": 1,
          "count": 2,
          "stereochemistry": "ACHIRAL",
          "count_amount": {
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            "units": "MOL RATIO",
            "uuid": "fe6c2867-aa7c-4ece-a987-2979300b32f8"
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          "molfile": "\n  Marvin  01132106312D          \n\n 34 34  0  0  1  0            999 V2000\n   14.9082   -5.1322    0.0000 C   0  0  1  0  0  0  0  0  0  2  0  0\n   15.7053   -5.3796    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0\n   14.3036   -5.6819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5064   -5.4345    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0\n   14.7433   -4.3076    0.0000 C   0  0  1  0  0  0  0  0  0  1  0  0\n   15.2930   -3.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.8808   -2.9883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.2106   -2.2462    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0836   -3.1533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4515   -2.6035    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7382   -2.3458    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0\n   13.0607   -1.5985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4157   -3.0932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2275   -1.6857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2320   -1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5174   -2.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8028   -1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0882   -2.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3736   -1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6589   -2.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9443   -1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2297   -2.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5151   -1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8005   -2.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0859   -1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3712   -2.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6566   -1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9420   -2.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2273   -1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5457   -2.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.1689   -1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5457   -2.9471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0012   -3.9778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2866   -4.3901    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  1  0  0  0\n  1  3  1  0  0  0  0\n  5  1  1  0  0  0  0\n  3  4  1  0  0  0  0\n  5  6  1  6  0  0  0\n  5 33  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  7  9  2  3  0  0  0\n  9 10  1  0  0  0  0\n 33  9  1  0  0  0  0\n 11 10  1  0  0  0  0\n 11 12  1  0  0  0  0\n 11 13  2  0  0  0  0\n 11 14  1  0  0  0  0\n 15 14  1  0  0  0  0\n 15 16  1  0  0  0  0\n 16 17  1  0  0  0  0\n 17 18  1  0  0  0  0\n 18 19  1  0  0  0  0\n 19 20  1  0  0  0  0\n 20 21  1  0  0  0  0\n 21 22  1  0  0  0  0\n 22 23  1  0  0  0  0\n 23 24  1  0  0  0  0\n 24 25  1  0  0  0  0\n 25 26  1  0  0  0  0\n 26 27  1  0  0  0  0\n 27 28  1  0  0  0  0\n 28 29  1  0  0  0  0\n 29 30  1  0  0  0  0\n 30 31  1  0  0  0  0\n 30 32  1  0  0  0  0\n 34 33  2  0  0  0  0\nM  CHG  2   2  -1   4  -1\nM  END",
          "smiles": "CC(C)CCCCCCCCCCCCCCCOP(=O)(O)OC1=C(O)O[C@H]([C@H](C[O-])[O-])C1=O",
          "formula": "C24H43O9P",
          "atropisomerism": "No",
          "charge": -2,
          "count": 1,
          "stereochemistry": "ABSOLUTE",
          "count_amount": {
            "type": "MOL RATIO",
            "average": 1,
            "units": "MOL RATIO",
            "uuid": "e36c9c91-4dcd-4fa5-ba49-6d0387e09e77"
          },
          "defined_stereo": 2,
          "ez_centers": 0,
          "molecular_weight": "506.5675",
          "optical_activity": "UNSPECIFIED",
          "stereo_centers": 2
        }
      ],
      "definition_level": "REPRESENTATIVE",
      "uuid": "cb40e1a2-212c-44c2-b5d4-1f90736c4371",
      "version": "4",
      "structure": {
        "id": "ae86647e-4484-4709-b260-06ad9c112176",
        "molfile": "\n  Marvin  01132109032D          \n\n 36 34  0  0  1  0            999 V2000\n   13.2866   -4.3901    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0\n   14.0012   -3.9778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.7433   -4.3076    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0\n   14.9082   -5.1322    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0\n   14.3036   -5.6819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5064   -5.4345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.2930   -3.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.8808   -2.9883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.2106   -2.2462    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0836   -3.1533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4515   -2.6035    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.7053   -5.3796    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4157   -3.0932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2275   -1.6857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.0607   -1.5985    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0\n   12.7382   -2.3458    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.1689   -1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5457   -2.9471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5457   -2.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2273   -1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9420   -2.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6566   -1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3712   -2.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0859   -1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8005   -2.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5151   -1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2297   -2.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9443   -1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6589   -2.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3736   -1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0882   -2.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8028   -1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5174   -2.1226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2320   -1.7103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3285   -0.9572    0.0000 Na  0  3  0  0  0  0  0  0  0  0  0  0\n   12.4131   -4.1770    0.0000 Na  0  3  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  3  7  1  6  0  0  0\n  7  8  1  0  0  0  0\n  8  9  2  0  0  0  0\n  8 10  1  0  0  0  0\n  2 10  2  0  0  0  0\n 10 11  1  0  0  0  0\n  4 12  1  1  0  0  0\n 16 13  2  0  0  0  0\n 16 14  1  0  0  0  0\n 16 15  1  0  0  0  0\n 16 11  1  0  0  0  0\n 19 18  1  0  0  0  0\n 19 17  1  0  0  0  0\n 20 19  1  0  0  0  0\n 21 20  1  0  0  0  0\n 22 21  1  0  0  0  0\n 23 22  1  0  0  0  0\n 24 23  1  0  0  0  0\n 25 24  1  0  0  0  0\n 26 25  1  0  0  0  0\n 27 26  1  0  0  0  0\n 28 27  1  0  0  0  0\n 29 28  1  0  0  0  0\n 30 29  1  0  0  0  0\n 31 30  1  0  0  0  0\n 32 31  1  0  0  0  0\n 33 32  1  0  0  0  0\n 34 33  1  0  0  0  0\n 34 14  1  0  0  0  0\nM  CHG  4   1  -1  15  -1  35   1  36   1\nM  END",
        "smiles": "CC(C)CCCCCCCCCCCCCCCOP(=O)([O-])OC1=C([C@@H]([C@H](CO)O)OC1=O)[O-].[Na+].[Na+]",
        "formula": "C24H43O9P.2Na",
        "atropisomerism": "No",
        "charge": 0,
        "count": 1,
        "stereochemistry": "ABSOLUTE",
        "defined_stereo": 2,
        "ez_centers": 0,
        "molecular_weight": "552.5471",
        "optical_activity": "UNSPECIFIED",
        "references": [
          "e66473c9-bca9-4f99-93d3-e0d8e0992d89",
          "e4b90a0d-48a0-4c7a-88aa-4ad49032d24a"
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        "stereo_centers": 2
      },
      "unii": "5EN0DE4P7X"
    }
  ]
}