{
  "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": "2025-09-19",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "codes": [
        {
          "uuid": "63049a33-a49e-4e6b-86d2-5f099692612e",
          "code": "1459206-66-6",
          "type": "PRIMARY",
          "url": "https://commonchemistry.cas.org/detail?cas_rn=1459206-66-6",
          "code_system": "CAS",
          "references": [
            "d465a564-edf6-482c-a211-7f1ce5ae6108"
          ]
        },
        {
          "uuid": "b96ddae8-c7c0-fab6-a940-fefeae166f1a",
          "code": "138756748",
          "type": "PRIMARY",
          "url": "https://pubchem.ncbi.nlm.nih.gov/compound/138756748",
          "code_system": "PUBCHEM",
          "references": [
            "7a3c86a9-e0df-a1f3-9b16-606eda446cab"
          ]
        },
        {
          "uuid": "c3647aab-bcf5-41be-8e6d-19c31478886b",
          "code": "RZX9PV23DY",
          "type": "PRIMARY",
          "code_system": "FDA UNII"
        },
        {
          "uuid": "8a0226b4-abde-8e3e-77df-e064c0505e17",
          "code": "RZX9PV23DY",
          "type": "PRIMARY",
          "url": "https://dailymed.nlm.nih.gov/dailymed/search.cfm?adv=1&query=RZX9PV23DY",
          "code_system": "DAILYMED",
          "references": [
            "99d4b4a2-1725-f07a-f6ec-b037d0cfca01"
          ]
        }
      ],
      "substance_class": "chemical",
      "names": [
        {
          "uuid": "bfd45f10-b3f7-1e54-0f8a-2f70ee74b1d4",
          "name": "AC-GLU-GLU-MET-GLN-ARG-ARG-ALA",
          "stdName": "AC-GLU-GLU-MET-GLN-ARG-ARG-ALA",
          "type": "sys",
          "languages": [
            "en"
          ],
          "preferred": false,
          "references": [
            "d465a564-edf6-482c-a211-7f1ce5ae6108"
          ],
          "display_name": false
        },
        {
          "uuid": "f70b099b-0fe6-4b59-a3fc-b81c18f8e6fa",
          "name": "ACETYL HEPTAPEPTIDE-4",
          "stdName": "ACETYL HEPTAPEPTIDE-4",
          "type": "of",
          "languages": [
            "en"
          ],
          "preferred": false,
          "references": [
            "d465a564-edf6-482c-a211-7f1ce5ae6108"
          ],
          "display_name": true,
          "domains": [
            "cosmetic"
          ],
          "name_orgs": [
            {
              "uuid": "8d7eaefc-cb0e-4d4c-9e18-771202a3444f",
              "name_org": "INCI"
            }
          ]
        },
        {
          "uuid": "7f04f5af-fbbb-dc9c-44fe-b1c4c1ae61fa",
          "name": "L-ALANINE, N-ACETYL-L-.ALPHA.-GLUTAMYL-L-.ALPHA.-GLUTAMYL-L-METHIONYL-L-GLUTAMINYL-L-ARGINYL-L-ARGINYL-",
          "stdName": "L-ALANINE, N-ACETYL-L-.ALPHA.-GLUTAMYL-L-.ALPHA.-GLUTAMYL-L-METHIONYL-L-GLUTAMINYL-L-ARGINYL-L-ARGINYL-",
          "type": "sys",
          "languages": [
            "en"
          ],
          "preferred": false,
          "references": [
            "d465a564-edf6-482c-a211-7f1ce5ae6108"
          ],
          "display_name": false
        }
      ],
      "references": [
        {
          "uuid": "d465a564-edf6-482c-a211-7f1ce5ae6108",
          "citation": "STN",
          "doc_type": "STN (SCIFINDER)",
          "public_domain": true,
          "tags": [
            "PUBLIC_DOMAIN_RELEASE",
            "NOMEN"
          ]
        },
        {
          "uuid": "67dbf74f-b59c-43a9-af14-dd89277d6d34",
          "citation": "Stage C, Jürgens G, Guski LS et al. The impact of CES1 genotypes on the pharmacokinetics of methylphenidate in healthy Danish subjects. Br J Clin Pharmacol. 2017 Jul;83(7):1506-1514.",
          "doc_type": "JA",
          "public_domain": true
        },
        {
          "uuid": "ba8bb2d2-ff99-4359-8394-5fa753b33210",
          "citation": "Nemoda Z, Angyal N, Tarnok Z et al. Carboxylesterase 1 gene polymorphism and methylphenidate response in ADHD. Neuropharmacology. 2009 Dec;57(7-8):731-3.",
          "doc_type": "JA",
          "public_domain": true
        },
        {
          "uuid": "4a156a7c-400d-478b-9748-c118d9c23f96",
          "citation": "Zhu HJ, Patrick KS, Yuan HJ et al. Two CES1 gene mutations lead to dysfunctional carboxylesterase 1 activity in man: clinical significance and molecular basis. Am J Hum Genet. 2008 Jun;82(6):1241-8.",
          "doc_type": "JA",
          "public_domain": true
        },
        {
          "uuid": "7a3c86a9-e0df-a1f3-9b16-606eda446cab",
          "citation": "PUBCHEM",
          "doc_type": "PUBCHEM",
          "public_domain": true
        },
        {
          "uuid": "99d4b4a2-1725-f07a-f6ec-b037d0cfca01",
          "citation": "DailyMed",
          "doc_type": "DAILYMED",
          "public_domain": true
        }
      ],
      "definition_type": "PRIMARY",
      "moieties": [
        {
          "uuid": "dfae7df1-f703-d76f-ca01-5d3f09aded63",
          "id": "dfae7df1-f703-d76f-ca01-5d3f09aded63",
          "molfile": "\n  Marvin  01132111352D          \n\n 66 65  0  0  1  0            999 V2000\n   23.9168   -2.0624    0.0000 C   0  0  2  0  0  0  0  0  0  2  0  0\n   24.6313   -1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.9168   -2.8874    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   23.2024   -3.2999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   22.4879   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   23.2024   -4.1249    0.0000 C   0  0  2  0  0  0  0  0  0  2  0  0\n   23.9168   -4.5374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   24.6313   -4.1249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   25.3457   -4.5374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   26.0601   -4.1249    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   26.7746   -4.5374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   27.4891   -4.1249    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   26.7746   -5.3624    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   22.4879   -4.5374    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   21.7735   -4.1249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   21.7735   -3.2999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   21.0590   -4.5374    0.0000 C   0  0  2  0  0  0  0  0  0  2  0  0\n   20.3445   -4.1249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   19.6301   -4.5374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.9157   -4.1249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.2012   -4.5374    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   17.4868   -4.1249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.7723   -4.5374    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   17.4868   -3.2999    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   21.0590   -5.3624    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   21.7735   -5.7748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   22.4879   -5.3624    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   21.7735   -6.5998    0.0000 C   0  0  2  0  0  0  0  0  0  2  0  0\n   21.0590   -7.0123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   20.3445   -6.5998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   19.6301   -7.0123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.9157   -6.5998    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   19.6301   -7.8373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   22.4879   -7.0123    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   23.2024   -6.5998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.2024   -5.7748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   23.9168   -7.0123    0.0000 C   0  0  2  0  0  0  0  0  0  2  0  0\n   24.6313   -6.5998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   25.3457   -7.0123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   26.0601   -6.5998    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n   26.7746   -7.0123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.9168   -7.8373    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   24.6313   -8.2497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   25.3457   -7.8373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   24.6313   -9.0747    0.0000 C   0  0  2  0  0  0  0  0  0  2  0  0\n   23.9168   -9.4872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.2024   -9.0747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   22.4879   -9.4872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   22.4879  -10.3122    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   21.7735   -9.0747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   25.3457   -9.4872    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   26.0602   -9.0747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   26.0602   -8.2497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   26.7746   -9.4872    0.0000 C   0  0  2  0  0  0  0  0  0  2  0  0\n   27.4891   -9.0747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   28.2036   -9.4872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   28.9180   -9.0747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   28.9180   -8.2497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   29.6324   -9.4872    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   26.7746  -10.3122    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   27.4891  -10.7247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   28.2036  -10.3122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   27.4891  -11.5496    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   23.2024   -1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.2024   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   22.4879   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  6  0  0  0\n  1  3  1  0  0  0  0\n  1 64  1  0  0  0  0\n  4  3  1  0  0  0  0\n  4  5  2  0  0  0  0\n  6  4  1  0  0  0  0\n  6  7  1  0  0  0  0\n  6 14  1  6  0  0  0\n  7  8  1  0  0  0  0\n  8  9  1  0  0  0  0\n  9 10  1  0  0  0  0\n 10 11  2  3  0  0  0\n 11 12  1  0  0  0  0\n 11 13  1  0  0  0  0\n 15 14  1  0  0  0  0\n 15 16  2  0  0  0  0\n 17 15  1  0  0  0  0\n 17 18  1  0  0  0  0\n 17 25  1  1  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  2  3  0  0  0\n 22 23  1  0  0  0  0\n 22 24  1  0  0  0  0\n 25 26  1  0  0  0  0\n 26 27  2  0  0  0  0\n 28 26  1  0  0  0  0\n 28 29  1  0  0  0  0\n 28 34  1  1  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 31 33  2  0  0  0  0\n 34 35  1  0  0  0  0\n 35 36  2  0  0  0  0\n 37 35  1  0  0  0  0\n 37 38  1  0  0  0  0\n 37 42  1  6  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 42 43  1  0  0  0  0\n 43 44  2  0  0  0  0\n 45 43  1  0  0  0  0\n 45 46  1  0  0  0  0\n 45 51  1  1  0  0  0\n 46 47  1  0  0  0  0\n 47 48  1  0  0  0  0\n 48 49  1  0  0  0  0\n 48 50  2  0  0  0  0\n 51 52  1  0  0  0  0\n 52 53  2  0  0  0  0\n 54 52  1  0  0  0  0\n 54 55  1  0  0  0  0\n 54 60  1  6  0  0  0\n 55 56  1  0  0  0  0\n 56 57  1  0  0  0  0\n 57 58  1  0  0  0  0\n 57 59  2  0  0  0  0\n 60 61  2  3  0  0  0\n 61 62  1  0  0  0  0\n 61 63  1  0  0  0  0\n 64 65  1  0  0  0  0\n 64 66  2  0  0  0  0\nM  END",
          "smiles": "C[C@@H](C(=O)O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(=O)O)N=C(C)O",
          "formula": "C37H64N14O14S",
          "atropisomerism": "No",
          "charge": 0,
          "count": 1,
          "stereochemistry": "ABSOLUTE",
          "count_amount": {
            "type": "MOL RATIO",
            "average": 1,
            "units": "MOL RATIO",
            "uuid": "7a7127cf-915a-4820-869f-607398dc9d04"
          },
          "defined_stereo": 7,
          "ez_centers": 0,
          "molecular_weight": "961.057",
          "optical_activity": "UNSPECIFIED",
          "stereo_centers": 7
        }
      ],
      "definition_level": "COMPLETE",
      "uuid": "42579277-a5cb-4aa8-93a6-b82821c17675",
      "version": "14",
      "structure": {
        "id": "994979b5-d907-4246-af5a-ebfb59a1f4d6",
        "molfile": "L-Alanine, N-acetyl-L-.alpha.-glutamyl-L-.alpha.-glutamyl-L-methionyl-L-gluta...\n  Marvin  01132107582D          \n\n 66 65  0  0  1  0            999 V2000\n   21.0590   -4.5374    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0\n   20.3445   -4.1249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   19.6301   -4.5374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.9157   -4.1249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.2012   -4.5374    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   17.4868   -4.1249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.7723   -4.5374    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   17.4868   -3.2999    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   21.7735   -4.1249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   21.7735   -3.2999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   22.4879   -4.5374    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   23.2024   -4.1249    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0\n   23.9168   -4.5374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   24.6313   -4.1249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   25.3457   -4.5374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   26.0601   -4.1249    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   26.7746   -4.5374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   27.4891   -4.1249    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   26.7746   -5.3624    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   23.2024   -3.2999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   22.4879   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   23.9168   -2.8874    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   23.9168   -2.0624    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0\n   24.6313   -1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.2024   -1.6499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.2024   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   22.4879   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   21.0590   -5.3624    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   21.7735   -5.7748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   21.7735   -6.5998    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0\n   21.0590   -7.0123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   20.3445   -6.5998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   19.6301   -7.0123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   19.6301   -7.8373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   18.9157   -6.5998    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   22.4879   -7.0123    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   23.2024   -6.5998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.2024   -5.7748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   23.9168   -7.0123    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0\n   24.6313   -6.5998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   25.3457   -7.0123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   26.0601   -6.5998    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n   26.7746   -7.0123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.9168   -7.8373    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   24.6313   -8.2497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   24.6313   -9.0747    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0\n   23.9168   -9.4872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.2024   -9.0747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   22.4879   -9.4872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   22.4879  -10.3122    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   21.7735   -9.0747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   25.3457   -9.4872    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   26.0602   -9.0747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   26.0602   -8.2497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   26.7746   -9.4872    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0\n   26.7746  -10.3122    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   27.4891  -10.7247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   27.4891  -11.5496    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   28.2036  -10.3122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   27.4891   -9.0747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   28.2036   -9.4872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   28.9180   -9.0747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   28.9180   -8.2497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   29.6324   -9.4872    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   25.3457   -7.8373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   22.4879   -5.3624    0.0000 O   0  0  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  6  7  1  0  0  0  0\n  6  8  2  0  0  0  0\n  1  9  1  0  0  0  0\n  9 10  2  0  0  0  0\n  9 11  1  0  0  0  0\n 11 12  1  0  0  0  0\n 12 13  1  0  0  0  0\n 13 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 17 19  2  0  0  0  0\n 12 20  1  6  0  0  0\n 20 21  2  0  0  0  0\n 20 22  1  0  0  0  0\n 23 22  1  6  0  0  0\n 23 24  1  0  0  0  0\n 23 25  1  0  0  0  0\n 25 26  2  0  0  0  0\n 25 27  1  0  0  0  0\n  1 28  1  1  0  0  0\n 28 29  1  0  0  0  0\n 30 29  1  1  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  2  0  0  0  0\n 33 35  1  0  0  0  0\n 30 36  1  0  0  0  0\n 36 37  1  0  0  0  0\n 37 38  2  0  0  0  0\n 37 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\n 42 43  1  0  0  0  0\n 39 44  1  6  0  0  0\n 44 45  1  0  0  0  0\n 46 45  1  1  0  0  0\n 46 47  1  0  0  0  0\n 47 48  1  0  0  0  0\n 48 49  1  0  0  0  0\n 49 50  2  0  0  0  0\n 49 51  1  0  0  0  0\n 46 52  1  0  0  0  0\n 52 53  1  0  0  0  0\n 53 54  2  0  0  0  0\n 53 55  1  0  0  0  0\n 55 56  1  6  0  0  0\n 56 57  1  0  0  0  0\n 57 58  2  0  0  0  0\n 57 59  1  0  0  0  0\n 55 60  1  0  0  0  0\n 60 61  1  0  0  0  0\n 61 62  1  0  0  0  0\n 62 63  2  0  0  0  0\n 62 64  1  0  0  0  0\n 45 65  2  0  0  0  0\n 29 66  2  0  0  0  0\nM  END",
        "smiles": "C[C@@H](C(=O)O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)C",
        "formula": "C37H64N14O14S",
        "atropisomerism": "No",
        "charge": 0,
        "count": 1,
        "stereochemistry": "ABSOLUTE",
        "defined_stereo": 7,
        "ez_centers": 0,
        "molecular_weight": "961.057",
        "optical_activity": "UNSPECIFIED",
        "references": [
          "d465a564-edf6-482c-a211-7f1ce5ae6108"
        ],
        "stereo_centers": 7
      },
      "unii": "RZX9PV23DY"
    }
  ]
}