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flavokavain A

chemical compound
Class type of: chalcone, flavokavain Q5458164

Facts

7 properties
Instance of
type of chemical entity
Subclass of
chalcone, flavokavain[4][5]
Canonical SMILES
COC1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2OC)OC)O[2]
Chemical formula
C₁₈H₁₈O₅[3]
Found in taxon
Boesenbergia rotunda, Goniothalamus gardneri, Piper methysticum, Gamochaeta malvinensis, Dahlia tenuicaulis, Kaempferia Angustifolia, Vitex quinata, Pseudognaphalium affine, Piper majusculum[6][7][8][9][10][11][12][13][14]
Isomeric SMILES
COC1=CC=C(C=C1)/C=C/C(=O)C2=C(C=C(C=C2OC)OC)O[15]
Mass
+314.115424
🏷️ Also known as
en flavokavain A en flavokawain A fa فلاووکاوائین ای zh 黄醉椒素A
🔖 Identifiers · 15
CAS Registry Number
37951-13-6
ChEBI ID
157725
ChEMBL ID
CHEMBL243829
ChemSpider ID
4511445
DSSTox substance ID
DTXSID601317535
Freebase ID
/m/07kfs9l
Human Metabolome Database ID
HMDB0033586
InChI
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+
InChIKey
CGIBCVBDFUTMPT-RMKNXTFCSA-N
KNApSAcK ID
C00006958, C00037157
Probes And Drugs ID
PD087997
PubChem CID
5355469
Show all 15 identifiers +3
SureChEMBL ID
29349587, 2289181
UNII
8OM2XZ2ZM3
UniChem compound ID
238629

Report an error or request removal Lineage (PROV-JSON)

🔗 Connections
Found in taxon 8
Piper methysticum, Boesenbergia rotunda, Pseudognaphalium affine, Goniothalamus gardneri, Vitex quinata, Dahlia tenuicaulis, Kaempferia Angustifolia, Piper majusculum
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Summary

flavokavain An is a type of chemical entity[1].

References

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

Direct Wikidata claims

  1. [2] ↑ . PubChem. Retrieved . wikidata.org.
  2. [3] ↑ . PubChem. Retrieved . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . Anti-inflammatory cyclohexenyl chalcone derivatives in Boesenbergia pandurata. wikidata.org.
  6. [7] ↑ . (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.
  7. [8] ↑ . Kavalactones from Piper methysticum, and their 13C NMR spectroscopic analyses. wikidata.org.
  8. [9] ↑ . Insect antifeedant flavonoids from Gnaphalium affine D. Don.. wikidata.org.
  9. [10] ↑ . Flavonoids and polyacetylenes in Dahlia tenuicaulis. wikidata.org.
  10. [11] ↑ . Cyclohexane oxide derivatives from Kaempferia angustifolia and Kaempferia species. wikidata.org.
  11. [12] ↑ . Phytochemical and Bioactivity Studies on Constituents of the Leaves of Vitex Quinata. wikidata.org.
  12. [13] ↑ . Insect antifeedant flavonoids from Gnaphalium affine D. Don.. wikidata.org.
  13. [14] ↑ . 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.
  14. [15] ↑ . PubChem. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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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 November 8, 2026, from https://4ort.xyz/entity/flavokavain-a
MLA “flavokavain A.” 4ort.xyz Knowledge Graph, 4ort.xyz, 8 Nov. 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: 2026-11-08}}
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 2026-11-08)

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