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Flavokavain C

chemical compound
Class type of: chalcone, 2-phenylchromane flavonoid, flavokavain Q5458168

Facts

7 properties
Instance of
type of chemical entity
Subclass of
chalcone, 2-phenylchromane flavonoid, flavokavain[4][5][6]
Canonical SMILES
COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=C(C=C2)O)O[2]
Chemical formula
C₁₇H₁₆O₅[3]
Found in taxon
Humulus lupulus, Boesenbergia rotunda, Argyrochosma dealbata, Piper dilatatum, Piper methysticum, Gamochaeta malvinensis, Piper murrayanum, Pseudognaphalium affine, Piper majusculum[7][8][9][10][11][12][13][14][15]
Isomeric SMILES
COC1=CC(=C(C(=C1)OC)C(=O)/C=C/C2=CC=C(C=C2)O)O
Mass
+300.099774
🏷️ Also known as
en Flavokavain C fa فلاووکاوائین ثی fa فلاووکاوائین سی zh 黄醉椒素C
🔖 Identifiers · 18
CAS Registry Number
37308-75-1
ChEBI ID
157718
ChEMBL ID
CHEMBL251958
ChemSpider ID
4874893
DSSTOX compound identifier
DTXCID801386342
DSSTox substance ID
DTXSID60958437
Freebase ID
/m/07k8h0c
Human Metabolome Database ID
HMDB0030875
InChI
InChI=1S/C17H16O5/c1-21-13-9-15(20)17(16(10-13)22-2)14(19)8-5-11-3-6-12(18)7-4-11/h3-10,18,20H,1-2H3/b8-5+
InChIKey
UXUFMIJZNYXWDX-VMPITWQZSA-N
KNApSAcK ID
C00006957
LIPID MAPS ID
LMPK12120320
Show all 18 identifiers +6
Microsoft Academic ID (discontinued)
2779548713
Probes And Drugs ID
PD148831
PubChem CID
6293081
SureChEMBL ID
144230
UNII
5LE8KTR6G2
UniChem compound ID
556347

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🔗 Connections
Found in taxon 7
Humulus lupulus, Piper methysticum, Boesenbergia rotunda, Pseudognaphalium affine, Argyrochosma dealbata, Piper dilatatum, Piper majusculum
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Summary

Flavokavain C 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] ↑ . wikidata.org.
  6. [7] ↑ . Synthesis, cytotoxicity, and antioxidative activity of minor prenylated chalcones from Humulus lupulus. wikidata.org.
  7. [8] ↑ . Bioactive secondary metabolites from Boesenbergia pandurata of Myanmar and their preferential cytotoxicity against human pancreatic cancer PANC-1 cell line in nutrient-deprived medium.. wikidata.org.
  8. [9] ↑ . New Frond Exudate Flavonoids From Cheilanthoid Ferns. wikidata.org.
  9. [10] ↑ . ChemInform Abstract: Antifungal Benzoic Acid Derivatives from Piper Dilatatum.. wikidata.org.
  10. [11] ↑ . Kavalactones from Piper methysticum, and their 13C NMR spectroscopic analyses. wikidata.org.
  11. [12] ↑ . Insect antifeedant flavonoids from Gnaphalium affine D. Don.. wikidata.org.
  12. [13] ↑ . Prenylated hydroxybenzoic acid derivatives from Piper murrayanum. wikidata.org.
  13. [14] ↑ . Insect antifeedant flavonoids from Gnaphalium affine D. Don.. wikidata.org.
  14. [15] ↑ . Electrospray high performance liquid chromatography-mass spectrometry in phytochemical analysis of kava (Piper methysticum) extract. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. 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). Flavokavain C. Retrieved November 9, 2026, from https://4ort.xyz/entity/flavokavain-c
MLA “Flavokavain C.” 4ort.xyz Knowledge Graph, 4ort.xyz, 9 Nov. 2026, https://4ort.xyz/entity/flavokavain-c.
BibTeX @misc{4ortxyz_flavokavain-c_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Flavokavain C}}, year = {2026}, url = {https://4ort.xyz/entity/flavokavain-c}, note = {Accessed: 2026-11-09}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Flavokavain C — https://4ort.xyz/entity/flavokavain-c (retrieved 2026-11-09)

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