flavokavain A

chemical compound
ChemicalSubstance type_of_chemical_entity Q5458164
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flavokavain A

Summary

flavokavain An is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (7 views/month).[2]

Key Facts

  • flavokavain A's instance of is recorded as type of chemical entity[3].
  • flavokavain A's chemical structure is recorded as Flavokavain A.png[4].
  • flavokavain A's CAS Registry Number is recorded as 37951-13-6[5].
  • flavokavain A's canonical SMILES is recorded as COC1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2OC)OC)O[6].
  • flavokavain A's InChI is recorded as InChI=1S/C18H18O5/c1-21-13-7-4-12(5-8-13)6-9-15(19)18-16(20)10-14(22-2)11-17(18)23-3/h4-11,20H,1-3H3/b9-6+[7].
  • flavokavain A's InChIKey is recorded as CGIBCVBDFUTMPT-RMKNXTFCSA-N[8].
  • flavokavain A's chemical formula is recorded as C₁₈H₁₈O₅[9].
  • flavokavain A's subclass of is recorded as chalcone[10].
  • flavokavain A's subclass of is recorded as flavokavain[11].
  • flavokavain A's ChEMBL ID is recorded as CHEMBL243829[12].
  • flavokavain A's Freebase ID is recorded as /m/07kfs9l[13].
  • flavokavain A's UNII is recorded as 8OM2XZ2ZM3[14].
  • flavokavain A's ChemSpider ID is recorded as 4511445[15].
  • flavokavain A's PubChem CID is recorded as 5355469[16].
  • flavokavain A's ChEBI ID is recorded as 157725[17].
  • flavokavain A's found in taxon is recorded as Boesenbergia rotunda[18].
  • flavokavain A's found in taxon is recorded as Goniothalamus gardneri[19].
  • flavokavain A's found in taxon is recorded as Piper methysticum[20].
  • flavokavain A's found in taxon is recorded as Gamochaeta malvinensis[21].
  • flavokavain A's found in taxon is recorded as Dahlia tenuicaulis[22].
  • flavokavain A's found in taxon is recorded as Kaempferia Angustifolia[23].
  • flavokavain A's found in taxon is recorded as Vitex quinata[24].
  • flavokavain A's found in taxon is recorded as Pseudognaphalium affine[25].
  • flavokavain A's found in taxon is recorded as Piper majusculum[26].
  • flavokavain A's isomeric SMILES is recorded as COC1=CC=C(C=C1)/C=C/C(=O)C2=C(C=C(C=C2OC)OC)O[27].

Why It Matters

flavokavain A ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (7 views/month).[2]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . PubChem. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . ChEMBL. Retrieved . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . Q2311683. Retrieved . wikidata.org.
  14. [16] . PubChem. Retrieved . wikidata.org.
  15. [17] . ChEBI release 2021-03-01. wikidata.org.
  16. [18] . Anti-inflammatory cyclohexenyl chalcone derivatives in Boesenbergia pandurata. wikidata.org.
  17. [19] . (Rel)-1beta,2alpha-di-(2,4-dihydroxy-6-methoxybenzoyl)-3beta, 4alpha-di-(4-methoxyphenyl)-cyclobutane and other flavonoids from the aerial parts of Goniothalamus gardneri and Goniothalamus thwaitesii. wikidata.org.
  18. [20] . Kavalactones from Piper methysticum, and their 13C NMR spectroscopic analyses. wikidata.org.
  19. [21] . Insect antifeedant flavonoids from Gnaphalium affine D. Don.. wikidata.org.
  20. [22] . Flavonoids and polyacetylenes in Dahlia tenuicaulis. wikidata.org.
  21. [23] . Cyclohexane oxide derivatives from Kaempferia angustifolia and Kaempferia species. wikidata.org.
  22. [24] . Phytochemical and Bioactivity Studies on Constituents of the Leaves of Vitex Quinata. wikidata.org.
  23. [25] . Insect antifeedant flavonoids from Gnaphalium affine D. Don.. wikidata.org.
  24. [26] . Flavokawain A, a novel chalcone from kava extract, induces apoptosis in bladder cancer cells by involvement of Bax protein-dependent and mitochondria-dependent apoptotic pathway and suppresses tumor growth in mice. wikidata.org.
  25. [27] . PubChem. Retrieved . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.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). flavokavain A. Retrieved May 3, 2026, from https://4ort.xyz/entity/flavokavain-a
MLA “flavokavain A.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/flavokavain-a.
BibTeX @misc{4ortxyz_flavokavain-a_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{flavokavain A}}, year = {2026}, url = {https://4ort.xyz/entity/flavokavain-a}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): flavokavain A — https://4ort.xyz/entity/flavokavain-a (retrieved 2026-05-03)

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