carbostyril

chemical compound
ChemicalSubstance type_of_chemical_entity Q27095480
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carbostyril

Summary

carbostyril is a type of chemical entity[1]. carbostyril ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (8 views/month).[2]

Key Facts

  • carbostyril's instance of is recorded as type of chemical entity[3].
  • carbostyril's canonical SMILES is recorded as C1=CC=C2C(=C1)C=CC(=O)N2[4].
  • carbostyril's chemical formula is recorded as C₉H₇NO[5].
  • carbostyril is a type of quinoline alkaloid[6].
  • carbostyril is part of 2-hydroxyquinoline 5,6-dioxygenase activity[7].
  • carbostyril is part of 2-hydroxyquinoline 8-monooxygenase activity[8].
  • carbostyril's Commons category is recorded as 2-Quinolone[9].
  • carbostyril's found in taxon is recorded as Aconitum ferox[10].
  • carbostyril's found in taxon is recorded as Glycosmis pentaphylla[11].
  • carbostyril's found in taxon is recorded as Houttuynia cordata[12].
  • carbostyril's mass is recorded as {'unit': 'Q483261', 'amount': '+145.053'}[13].
  • carbostyril's melting point is recorded as {'unit': 'Q25267', 'amount': '+198.0'}[14].
  • carbostyril's tautomer of is recorded as quinolin-2(1H)-one[15].

Why It Matters

carbostyril ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (8 views/month).[2] carbostyril is known by 7 alternative names across languages and contexts.[16]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . PubChem. Retrieved . wikidata.org.
  3. [5] . PubChem. Retrieved . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . Gene Ontology release 2020-05-02. wikidata.org.
  6. [8] . Gene Ontology release 2020-05-02. wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . Isolation of Quinolinones from Ayurvedic Processed Root Tubers ofAconitum ferox1. wikidata.org.
  9. [11] . Chemical constituents of Glycosmis arborea: three new carbazole alkaloids and their biological activity. wikidata.org.
  10. [12] . The constituents and their bioactivities of Houttuynia cordata. wikidata.org.
  11. [13] . PubChem. Retrieved . wikidata.org.
  12. [14] . Jean-Claude Bradley Open Melting Point Dataset. wikidata.org.
  13. [15] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [16] . Wikidata aliases. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). carbostyril. Retrieved May 3, 2026, from https://4ort.xyz/entity/carbostyril
MLA “carbostyril.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/carbostyril.
BibTeX @misc{4ortxyz_carbostyril_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{carbostyril}}, year = {2026}, url = {https://4ort.xyz/entity/carbostyril}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): carbostyril — https://4ort.xyz/entity/carbostyril (retrieved 2026-05-03)

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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 24d ago · Shuaib-bot bot · 2026-05-07 view diff on Wikidata ↗
    Melting point {'unit': 'Q25267', 'amount': '+198.0'}
    Tautomer of quinolin-2(1H)-one
    Mass {'unit': 'Q483261', 'amount': '+145.053'}
    Instance of
    + 7 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.