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          "smiles": "CCCCCCCCCCCCCCCCCC(=O)OC(C)C(=O)OC(C)C(=O)[O-]",
          "formula": "C24H43O6",
          "atropisomerism": "No",
          "charge": -1,
          "count": 1,
          "stereochemistry": "MIXED",
          "count_amount": {
            "type": "MOL RATIO",
            "average": 1,
            "units": "MOL RATIO",
            "uuid": "e6caa3b2-b0a8-49f5-bdb7-d3f5e4b4d1fd"
          },
          "defined_stereo": 0,
          "ez_centers": 0,
          "molecular_weight": "427.5955",
          "optical_activity": "UNSPECIFIED",
          "stereo_centers": 2
        },
        {
          "uuid": "66107a3c-8253-4007-bab1-90a9bb95ac4b",
          "id": "66107a3c-8253-4007-bab1-90a9bb95ac4b",
          "molfile": "\n  Marvin  01132105192D          \n\n  1  0  0  0  0  0            999 V2000\n    5.1130   -2.0345    0.0000 Na  0  3  0  0  0  0  0  0  0  0  0  0\nM  CHG  1   1   1\nM  END",
          "smiles": "[Na+]",
          "formula": "Na",
          "atropisomerism": "No",
          "charge": 1,
          "count": 1,
          "stereochemistry": "ACHIRAL",
          "count_amount": {
            "type": "MOL RATIO",
            "average": 1,
            "units": "MOL RATIO",
            "uuid": "e214974f-0f6f-4209-831e-fc904c98489b"
          },
          "defined_stereo": 0,
          "ez_centers": 0,
          "molecular_weight": "22.9898",
          "optical_activity": "NONE",
          "stereo_centers": 0
        }
      ],
      "definition_level": "COMPLETE",
      "uuid": "24a2c997-37b8-483f-a640-7df7360928e3",
      "version": "8",
      "structure": {
        "id": "ad60ce5d-4082-4441-80b3-21744bd43456",
        "molfile": "\n  Marvin  01132109002D          \n\n 31 29  0  0  0  0            999 V2000\n    0.4274   -5.1078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.1282   -5.4789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8657   -5.1078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5664   -5.5109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5664   -6.3171    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2717   -5.1078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9908   -5.5109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6961   -5.1170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.4153   -5.5246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1206   -5.1170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8214   -5.5567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5588   -5.1491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2596   -5.5567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9604   -5.1629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7023   -5.5567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4306   -5.1629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0948   -5.5705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8230   -5.1949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5604   -5.6162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2612   -5.1949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9666   -5.6162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.7040   -5.1949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0306   -6.4925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.4274   -4.1990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.3597   -5.5622    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1467   -5.1078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9338   -5.5622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7209   -5.1078    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0\n   -1.9338   -6.4711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1680   -3.9161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1130   -2.0345    0.0000 Na  0  3  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0  0  0  0\n  3  2  1  0  0  0  0\n  4  3  1  0  0  0  0\n  5  4  2  0  0  0  0\n  6  4  1  0  0  0  0\n  7  6  1  0  0  0  0\n  8  7  1  0  0  0  0\n  9  8  1  0  0  0  0\n 10  9  1  0  0  0  0\n 11 10  1  0  0  0  0\n 12 11  1  0  0  0  0\n 13 12  1  0  0  0  0\n 14 13  1  0  0  0  0\n 15 14  1  0  0  0  0\n 16 15  1  0  0  0  0\n 17 16  1  0  0  0  0\n 18 17  1  0  0  0  0\n 19 18  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  2 23  1  0  0  0  0\n  1 24  2  0  0  0  0\n  1 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 27 29  2  0  0  0  0\n 26 30  1  0  0  0  0\nM  CHG  2  28  -1  31   1\nM  END",
        "smiles": "CCCCCCCCCCCCCCCCCC(=O)OC(C)C(=O)OC(C)C(=O)[O-].[Na+]",
        "formula": "C24H43O6.Na",
        "atropisomerism": "No",
        "charge": 0,
        "count": 1,
        "stereochemistry": "MIXED",
        "defined_stereo": 0,
        "ez_centers": 0,
        "molecular_weight": "450.5853",
        "optical_activity": "UNSPECIFIED",
        "references": [
          "be0d6422-11c0-41c9-961a-af6d24ff243a",
          "4cfdb33c-d665-49d9-9274-79d1d341e77a"
        ],
        "stereo_centers": 2
      },
      "unii": "IN99IT31LN"
    }
  ]
}