{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "codes": [
        {
          "uuid": "e694888c-6b5c-402a-b4f8-7744b65650f4",
          "code": "7PC32L43UZ",
          "type": "PRIMARY",
          "code_system": "FDA UNII"
        },
        {
          "uuid": "6ea9cb31-683d-4e15-ae07-d770520ce60e",
          "code": "1206592-01-9",
          "type": "PRIMARY",
          "url": "https://commonchemistry.cas.org/detail?cas_rn=1206592-01-9",
          "code_system": "CAS",
          "references": [
            "1f7ee90e-45cf-4547-866f-bf06c73de923",
            "0561ca54-3092-4239-9947-09dd4f33ae91"
          ]
        },
        {
          "uuid": "7add38ec-7a84-23e3-8154-ff2dd2102161",
          "code": "117847167",
          "type": "PRIMARY",
          "url": "https://pubchem.ncbi.nlm.nih.gov/compound/117847167",
          "code_system": "PUBCHEM",
          "references": [
            "b703fbf1-ae45-f435-8b40-36a148273dad"
          ]
        }
      ],
      "substance_class": "chemical",
      "names": [
        {
          "uuid": "edda0ea6-a59d-4cde-ae44-e22580993c49",
          "name": "L-Histidine, N-(1-oxohexadecyl)-L-alanyl-",
          "stdName": "L-HISTIDINE, N-(1-OXOHEXADECYL)-L-ALANYL-",
          "type": "sys",
          "languages": [
            "en"
          ],
          "preferred": false,
          "references": [
            "1f7ee90e-45cf-4547-866f-bf06c73de923"
          ],
          "display_name": false
        },
        {
          "uuid": "f9609d4f-0f1b-4435-9e9b-f0b392ff5b20",
          "name": "N-(1-Oxohexadecyl)-L-alanyl-L-histidine",
          "stdName": "N-(1-OXOHEXADECYL)-L-ALANYL-L-HISTIDINE",
          "type": "sys",
          "languages": [
            "en"
          ],
          "preferred": false,
          "references": [
            "1f7ee90e-45cf-4547-866f-bf06c73de923"
          ],
          "display_name": false
        },
        {
          "uuid": "55f73105-7fa0-4dbf-bd29-50e09e8b6aec",
          "name": "Palmitoyl Dipeptide-10",
          "stdName": "PALMITOYL DIPEPTIDE-10",
          "type": "of",
          "languages": [
            "en"
          ],
          "preferred": false,
          "references": [
            "0561ca54-3092-4239-9947-09dd4f33ae91"
          ],
          "display_name": true,
          "domains": [
            "cosmetic"
          ],
          "name_orgs": [
            {
              "uuid": "9abbb4a5-541d-410f-9ac6-2da31d272aa5",
              "name_org": "INCI"
            }
          ]
        }
      ],
      "references": [
        {
          "uuid": "b703fbf1-ae45-f435-8b40-36a148273dad",
          "citation": "PUBCHEM",
          "doc_type": "PUBCHEM",
          "public_domain": true
        },
        {
          "uuid": "1f7ee90e-45cf-4547-866f-bf06c73de923",
          "citation": "STN",
          "doc_type": "STN (SCIFINDER)",
          "public_domain": true,
          "tags": [
            "PUBLIC_DOMAIN_RELEASE"
          ]
        },
        {
          "uuid": "0561ca54-3092-4239-9947-09dd4f33ae91",
          "citation": "PCPC",
          "doc_type": "PERSONAL CARE PRODUCTS COUNCIL",
          "public_domain": true,
          "tags": [
            "PUBLIC_DOMAIN_RELEASE"
          ]
        }
      ],
      "definition_type": "PRIMARY",
      "moieties": [
        {
          "uuid": "b2fd678a-1561-4961-b0d0-f127a7d30c06",
          "id": "b2fd678a-1561-4961-b0d0-f127a7d30c06",
          "molfile": "\n  Marvin  03272315482D          \n\n 33 33  0  0  1  0            999 V2000\n    0.6674    2.0944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3819    2.5070    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0\n    2.0964    2.0944    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3819    3.3319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.8108    2.5070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0964    3.7444    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.6674    3.7444    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5252    2.0944    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0\n    2.8108    3.3319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2397    2.5070    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5252    1.2695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9542    2.0944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6686    2.5070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9542    1.2695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3830    2.0944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0976    2.5070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8120    2.0944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5264    2.5070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2409    2.0944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9554    2.5070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6698    2.0944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3842    2.5070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0987    2.0944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8132    2.5070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5276    2.0944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2421    2.5070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.9565    2.0944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.6710    2.5070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.6674    1.2695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3349    0.7846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.7846    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0799    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2549    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1  0  0  0\n  1 29  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  4  6  1  0  0  0  0\n  4  7  2  0  0  0  0\n  5  8  1  0  0  0  0\n  5  9  2  0  0  0  0\n  8 10  1  0  0  0  0\n  8 11  1  1  0  0  0\n 10 12  1  0  0  0  0\n 12 13  1  0  0  0  0\n 12 14  2  0  0  0  0\n 13 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 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 29 30  2  0  0  0  0\n 29 31  1  0  0  0  0\n 30 32  1  0  0  0  0\n 31 33  1  0  0  0  0\n 32 33  2  0  0  0  0\nM  END",
          "smiles": "CCCCCCCCCCCCCCCC(=O)N[C@@H](C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)O",
          "formula": "C25H44N4O4",
          "atropisomerism": "No",
          "charge": 0,
          "count": 1,
          "stereochemistry": "ABSOLUTE",
          "count_amount": {
            "type": "MOL RATIO",
            "average": 1,
            "units": "MOL RATIO",
            "uuid": "b28b2616-6a63-422e-8b74-2a4ce2069ce9"
          },
          "defined_stereo": 2,
          "ez_centers": 0,
          "molecular_weight": "464.6422",
          "optical_activity": "UNSPECIFIED",
          "stereo_centers": 2
        }
      ],
      "definition_level": "COMPLETE",
      "uuid": "1fb8d0d0-6b78-4166-a22f-292982bbc595",
      "version": "3",
      "structure": {
        "id": "54aac067-6d45-4cce-b2bf-daca1108f824",
        "molfile": "N-(1-Oxohexadecyl)-L-alanyl-L-histidine\n   JSDraw203272315482D\n\n 33 33  0  0  1  0              0 V2000\n   11.6141   -7.2758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9651   -6.4957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3161   -7.2758    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9651   -4.9358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.6669   -6.4957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3161   -4.1559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6141   -4.1559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   17.0178   -7.2758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.6669   -4.9358    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   18.3688   -6.4957    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   17.0178   -8.8357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   19.7198   -7.2758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   21.0707   -6.4957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   19.7198   -8.8357    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   22.4215   -7.2758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.7727   -6.4957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   25.1235   -7.2758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   26.4744   -6.4957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   27.8253   -7.2758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   29.1764   -6.4957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   30.5273   -7.2758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   31.8781   -6.4957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   33.2291   -7.2758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   34.5801   -6.4957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   35.9310   -7.2758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   37.2819   -6.4957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   38.6328   -7.2758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   39.9839   -6.4957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6141   -8.8357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8762   -9.7526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3521   -9.7526    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3940  -11.2361    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8341  -11.2361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1  0  0  0\n  1 29  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  4  6  1  0  0  0  0\n  4  7  2  0  0  0  0\n  5  8  1  0  0  0  0\n  5  9  2  0  0  0  0\n  8 10  1  0  0  0  0\n  8 11  1  1  0  0  0\n 10 12  1  0  0  0  0\n 12 13  1  0  0  0  0\n 12 14  2  0  0  0  0\n 13 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 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 29 30  2  0  0  0  0\n 29 31  1  0  0  0  0\n 30 32  1  0  0  0  0\n 31 33  1  0  0  0  0\n 32 33  2  0  0  0  0\nM  END",
        "smiles": "CCCCCCCCCCCCCCCC(=O)N[C@@H](C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)O",
        "formula": "C25H44N4O4",
        "atropisomerism": "No",
        "charge": 0,
        "count": 1,
        "stereochemistry": "ABSOLUTE",
        "defined_stereo": 2,
        "ez_centers": 0,
        "molecular_weight": "464.6422",
        "optical_activity": "UNSPECIFIED",
        "references": [
          "0561ca54-3092-4239-9947-09dd4f33ae91"
        ],
        "stereo_centers": 2
      },
      "modifications": {
        "uuid": "01d5a2c3-32b0-4846-b60c-1a13fd244701"
      },
      "unii": "7PC32L43UZ"
    }
  ]
}