"pteridinyl" meaning in All languages combined

{
  "etymology_templates": [
    {
      "args": {
        "1": "en",
        "2": "pteridine",
        "3": "yl"
      },
      "expansion": "pteridine + -yl",
      "name": "suf"
    }
  ],
  "etymology_text": "pteridine + -yl",
  "head_templates": [
    {
      "args": {
        "1": "-"
      },
      "expansion": "pteridinyl (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": "English terms suffixed with -yl",
          "parents": [],
          "source": "w"
        },
        {
          "kind": "topical",
          "langcode": "en",
          "name": "Organic chemistry",
          "orig": "en:Organic chemistry",
          "parents": [
            "Chemistry",
            "Sciences",
            "All topics",
            "Fundamental"
          ],
          "source": "w"
        }
      ],
      "examples": [
        {
          "ref": "1988, D. J. Brown, The Chemistry of Heterocyclic Compounds, Fused Pyrimidines, page 340",
          "text": "Few of the potential displacement or other reactions of pteridinyl sulfoxides and sulfones have been reported but enough are known to confirm the utility of such substituents […]",
          "type": "quotation"
        },
        {
          "ref": "2016, Russ Hille, Carola Schulzke, Martin L. Kirk, Molybdenum and Tungsten Enzymes: Bioinorganic Chemistry, page 35",
          "text": "Simultaneously, Stiefel and taylor were exploiting this methodology of cyclo-addition of quinoxalyl and pteridinyl acetylenes with a Mo-(S₄) reagent 22 to generate mono-dithiolene complexes of molybdenum(IV) (Scheme 2.22).",
          "type": "quotation"
        }
      ],
      "glosses": [
        "The functional group derived from pteridine."
      ],
      "id": "en-pteridinyl-en-noun-R5lWLPwf",
      "links": [
        [
          "organic chemistry",
          "organic chemistry"
        ],
        [
          "functional group",
          "functional group"
        ],
        [
          "pteridine",
          "pteridine"
        ]
      ],
      "raw_glosses": [
        "(organic chemistry) The functional group derived from pteridine."
      ],
      "synonyms": [
        {
          "word": "pteridyl"
        }
      ],
      "tags": [
        "uncountable"
      ],
      "topics": [
        "chemistry",
        "natural-sciences",
        "organic-chemistry",
        "physical-sciences"
      ]
    }
  ],
  "word": "pteridinyl"
}

{
  "etymology_templates": [
    {
      "args": {
        "1": "en",
        "2": "pteridine",
        "3": "yl"
      },
      "expansion": "pteridine + -yl",
      "name": "suf"
    }
  ],
  "etymology_text": "pteridine + -yl",
  "head_templates": [
    {
      "args": {
        "1": "-"
      },
      "expansion": "pteridinyl (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 suffixed with -yl",
        "English terms with quotations",
        "English uncountable nouns",
        "Quotation templates to be cleaned",
        "en:Organic chemistry"
      ],
      "examples": [
        {
          "ref": "1988, D. J. Brown, The Chemistry of Heterocyclic Compounds, Fused Pyrimidines, page 340",
          "text": "Few of the potential displacement or other reactions of pteridinyl sulfoxides and sulfones have been reported but enough are known to confirm the utility of such substituents […]",
          "type": "quotation"
        },
        {
          "ref": "2016, Russ Hille, Carola Schulzke, Martin L. Kirk, Molybdenum and Tungsten Enzymes: Bioinorganic Chemistry, page 35",
          "text": "Simultaneously, Stiefel and taylor were exploiting this methodology of cyclo-addition of quinoxalyl and pteridinyl acetylenes with a Mo-(S₄) reagent 22 to generate mono-dithiolene complexes of molybdenum(IV) (Scheme 2.22).",
          "type": "quotation"
        }
      ],
      "glosses": [
        "The functional group derived from pteridine."
      ],
      "links": [
        [
          "organic chemistry",
          "organic chemistry"
        ],
        [
          "functional group",
          "functional group"
        ],
        [
          "pteridine",
          "pteridine"
        ]
      ],
      "raw_glosses": [
        "(organic chemistry) The functional group derived from pteridine."
      ],
      "synonyms": [
        {
          "word": "pteridyl"
        }
      ],
      "tags": [
        "uncountable"
      ],
      "topics": [
        "chemistry",
        "natural-sciences",
        "organic-chemistry",
        "physical-sciences"
      ]
    }
  ],
  "word": "pteridinyl"
}