"brenzcatechin" meaning in All languages combined

{
  "head_templates": [
    {
      "args": {
        "1": "-"
      },
      "expansion": "brenzcatechin (uncountable)",
      "name": "en-noun"
    }
  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "senses": [
    {
      "categories": [
        {
          "kind": "other",
          "name": "English entries with incorrect language header",
          "parents": [
            "Entries with incorrect language header",
            "Entry maintenance"
          ],
          "source": "w"
        },
        {
          "kind": "other",
          "name": "Pages with 1 entry",
          "parents": [],
          "source": "w"
        },
        {
          "kind": "other",
          "name": "Pages with entries",
          "parents": [],
          "source": "w"
        },
        {
          "kind": "topical",
          "langcode": "en",
          "name": "Organic compounds",
          "orig": "en:Organic compounds",
          "parents": [
            "Matter",
            "Chemistry",
            "Nature",
            "Sciences",
            "All topics",
            "Fundamental"
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          "source": "w"
        }
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      "examples": [
        {
          "ref": "2015 November 11, “Cinnamic Acid Bornyl Ester Derivatives from Valeriana wallichii Exhibit Antileishmanial In Vivo Activity in Leishmania major -Infected BALB/c Mice”, in PLOS ONE, →DOI:",
          "text": "In general, compounds having a brenzcatechin moiety were found to be active, but also cytotoxic against host cells due to oxidation and formation of a highly reactive Michael system, whereas analogue compounds without the 3,4-dihydroxy substitution at the phenyl ring (e.g. compound 1 ) were still active but less toxic.",
          "type": "quote"
        }
      ],
      "glosses": [
        "catechol"
      ],
      "id": "en-brenzcatechin-en-noun-xS2A1d4i",
      "links": [
        [
          "organic chemistry",
          "organic chemistry"
        ],
        [
          "catechol",
          "catechol"
        ]
      ],
      "raw_glosses": [
        "(organic chemistry) catechol"
      ],
      "tags": [
        "uncountable"
      ],
      "topics": [
        "chemistry",
        "natural-sciences",
        "organic-chemistry",
        "physical-sciences"
      ]
    }
  ],
  "word": "brenzcatechin"
}

{
  "head_templates": [
    {
      "args": {
        "1": "-"
      },
      "expansion": "brenzcatechin (uncountable)",
      "name": "en-noun"
    }
  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "senses": [
    {
      "categories": [
        "English entries with incorrect language header",
        "English lemmas",
        "English nouns",
        "English terms with quotations",
        "English uncountable nouns",
        "Pages with 1 entry",
        "Pages with entries",
        "en:Organic compounds"
      ],
      "examples": [
        {
          "ref": "2015 November 11, “Cinnamic Acid Bornyl Ester Derivatives from Valeriana wallichii Exhibit Antileishmanial In Vivo Activity in Leishmania major -Infected BALB/c Mice”, in PLOS ONE, →DOI:",
          "text": "In general, compounds having a brenzcatechin moiety were found to be active, but also cytotoxic against host cells due to oxidation and formation of a highly reactive Michael system, whereas analogue compounds without the 3,4-dihydroxy substitution at the phenyl ring (e.g. compound 1 ) were still active but less toxic.",
          "type": "quote"
        }
      ],
      "glosses": [
        "catechol"
      ],
      "links": [
        [
          "organic chemistry",
          "organic chemistry"
        ],
        [
          "catechol",
          "catechol"
        ]
      ],
      "raw_glosses": [
        "(organic chemistry) catechol"
      ],
      "tags": [
        "uncountable"
      ],
      "topics": [
        "chemistry",
        "natural-sciences",
        "organic-chemistry",
        "physical-sciences"
      ]
    }
  ],
  "word": "brenzcatechin"
}