dihydrokavain

chemical compound
Class type of: kavalactone Q5276436

Facts

6 properties
Instance of
group of stereoisomers
Subclass of
kavalactone[4]
Canonical SMILES
COC1=CC(=O)OC(C1)CCC2=CC=CC=C2[2]
Chemical formula
C₁₄H₁₆O₃[3]
Mass
+232.109944[8]
🏷️ Also known as
en dihydrokavain fa دی‌هیدروکاواین fa دی هیدروکاواین ja ジヒドロカバイン
🔖 Identifiers · 13
CAS Registry Number
19451-52-6
ChEMBL ID
CHEMBL1338909
ChemSpider ID
88817
DSSTOX compound identifier
DTXCID6013433
DSSTox substance ID
DTXSID8033433, DTXSID101018162
Freebase ID
/m/07kfxyd
Human Metabolome Database ID
HMDB0029504
Microsoft Academic ID (discontinued)
2776349665
PubChem CID
98356
SureChEMBL ID
2743647
Show all 13 identifiers +1
UniChem compound ID
945338

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🔗 Connections
Found in taxon 3
Subclass of 1
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Summary

dihydrokavain is a group of stereoisomers[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] ↑ . Extracts and kavalactones of Piper methysticum G. Forst (kava-kava) inhibit P-glycoprotein in vitro. wikidata.org.
  5. [6] ↑ . Bioactivity guided isolation of anticancer constituents from leaves of Alnus sieboldiana (Betulaceae).. wikidata.org.
  6. [7] ↑ . Extracts and kavalactones of Piper methysticum G. Forst (kava-kava) inhibit P-glycoprotein in vitro. wikidata.org.
  7. [8] ↑ . PubChem. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). dihydrokavain. Retrieved November 4, 2026, from https://4ort.xyz/entity/dihydrokavain
MLA “dihydrokavain.” 4ort.xyz Knowledge Graph, 4ort.xyz, 4 Nov. 2026, https://4ort.xyz/entity/dihydrokavain.
BibTeX @misc{4ortxyz_dihydrokavain_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{dihydrokavain}}, year = {2026}, url = {https://4ort.xyz/entity/dihydrokavain}, note = {Accessed: 2026-11-04}}
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