{
  "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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          "smiles": "CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)CCCNC(=O)/C=C/c1ccc(cc1)OC",
          "formula": "C37H67N2O2",
          "atropisomerism": "No",
          "charge": 1,
          "count": 1,
          "stereochemistry": "RACEMIC",
          "count_amount": {
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            "units": "MOL RATIO",
            "uuid": "151744eb-0fd1-4776-bf14-b58b4ce902a3"
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          "defined_stereo": 0,
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          "molecular_weight": "571.9415",
          "optical_activity": "NONE",
          "stereo_centers": 0
        }
      ],
      "definition_level": "COMPLETE",
      "uuid": "f6f3536d-89a7-4234-aedc-c61968acf9c7",
      "version": "5",
      "structure": {
        "id": "b895ec2d-eb74-4ad6-9c91-10d2c6a31366",
        "molfile": "\n  Marvin  01132109332D          \n\n 42 41  0  0  0  0            999 V2000\n   15.4553  -10.9782    0.0000 Cl  0  5  0  0  0  0  0  0  0  0  0  0\n    9.5468   -7.8330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8323   -8.2456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8323   -9.0704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1179   -9.4830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4034   -9.0704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6890   -9.4830    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9747   -9.0704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4034   -8.2456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1179   -7.8330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2612   -8.2456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9757   -7.8330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9757   -7.0081    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6901   -8.2456    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4046   -7.8330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1190   -8.2456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8335   -7.8330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5478   -8.2456    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0\n   14.9604   -8.9600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1354   -8.9600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.2623   -7.8330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.9767   -8.2456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.6912   -7.8330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.4056   -8.2456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.1200   -7.8330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.8345   -8.2456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   19.5489   -7.8330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   20.2635   -8.2454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   20.9779   -7.8330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   21.6924   -8.2454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   22.4067   -7.8330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.1212   -8.2454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.8356   -7.8330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   24.5501   -8.2454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   25.2645   -7.8330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   25.9790   -8.2454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   26.6934   -7.8330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   27.4078   -8.2454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   28.1223   -7.8330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   28.8367   -8.2454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   29.5511   -7.8330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   30.2655   -8.2454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  2  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  9  6  2  0  0  0  0\n 10  9  1  0  0  0  0\n  3 10  2  0  0  0  0\n  2 11  2  0  0  0  0\n 11 12  1  0  0  0  0\n 12 13  2  0  0  0  0\n 12 14  1  0  0  0  0\n 14 15  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 18 20  1  0  0  0  0\n 18 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 31 32  1  0  0  0  0\n 32 33  1  0  0  0  0\n 33 34  1  0  0  0  0\n 34 35  1  0  0  0  0\n 35 36  1  0  0  0  0\n 36 37  1  0  0  0  0\n 37 38  1  0  0  0  0\n 38 39  1  0  0  0  0\n 39 40  1  0  0  0  0\n 40 41  1  0  0  0  0\n 41 42  1  0  0  0  0\nM  CHG  2   1  -1  18   1\nM  END",
        "smiles": "CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)CCCNC(=O)/C=C/c1ccc(cc1)OC.[Cl-]",
        "formula": "C37H67N2O2.Cl",
        "atropisomerism": "No",
        "charge": 0,
        "count": 1,
        "stereochemistry": "ACHIRAL",
        "defined_stereo": 0,
        "ez_centers": 1,
        "molecular_weight": "607.3944",
        "optical_activity": "NONE",
        "references": [
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        "stereo_centers": 0
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      "unii": "IM2H0V13N9"
    }
  ]
}