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kavain

chemical compound
Class type of: kavalactone Q3194310

Facts

10 properties
Instance of
type of chemical entity
Subclass of
kavalactone[4]
Canonical SMILES
COC1=CC(=O)OC(C1)C=CC2=CC=CC=C2[2]
Chemical formula
C₁₄H₁₄O₃[3]
Found in taxon
Piper methysticum, Acremonium neocaledoniae, Alnus sieboldiana, Piper majusculum[8][9][10]
Has part(s)
carbon, oxygen, hydrogen[5][6][7]
Isomeric SMILES
COC1=CC(=O)O[C@H](C1)/C=C/C2=CC=CC=C2
Mass
+230.094294
Stereoisomer of
(-)-kawain, (2R)-4-methoxy-2-(2-phenylethenyl)-2,3-dihydropyran-6-one
Subject has role
anticonvulsant agent, anxiolytic
🏷️ Also known as
en kavain en kawain fa کاوائین fr Kavaïne ja カバイン
🔖 Identifiers · 22
CAS Registry Number
500-64-1
ChEBI ID
6117
ChEMBL ID
CHEMBL578607
ChemSpider ID
4444888
DSSTOX compound identifier
DTXCID3013595
DSSTox substance ID
DTXSID5033595
EC number
207-907-2
ECHA Substance Infocard ID
100.007.189
Freebase ID
/m/04n2szf
InChI
InChI=1S/C14H14O3/c1-16-13-9-12(17-14(15)10-13)8-7-11-5-3-2-4-6-11/h2-8,10,12H,9H2,1H3/b8-7+/t12-/m0/s1
InChIKey
XEAQIWGXBXCYFX-GUOLPTJISA-N
KEGG ID
D08096, C09947
Show all 22 identifiers +10
KNApSAcK ID
C00003000
MeSH descriptor ID
C011889
Microsoft Academic ID (discontinued)
2778761374
NSC number
112162
Probes And Drugs ID
PD045756
PubChem CID
5281565
SPLASH
splash10-01p9-0930000000-ed9f122059bc27ec7f1c, splash10-0089-0590000000-80157340c7a0b59a6510, splash10-0udi-0900000000-08572345234e700db2d7, splash10-0uxr-0910000000-9c7d45e3202b0b0af6bc, splash10-0udi-0900000000-fceaf6c86396281a20ad
SureChEMBL ID
515202
UNII
W1ES06373M
UniChem compound ID
322322

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🔗 Connections
Found in taxon 3
Piper methysticum, Alnus sieboldiana, Piper majusculum
Has part(s) 3
hydrogen, oxygen, carbon
Subject has role 2
anticonvulsant agent, anxiolytic
Subclass of 1
kavalactone
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Summary

kavain 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] ↑ . wikidata.org.
  7. [8] ↑ . Anxiolytic properties of Piper methysticum extract samples and fractions in the chick social-separation-stress procedure. wikidata.org.
  8. [9] ↑ . Cytotoxins, mycotoxins and drugs from a new deuteromycete, Acremonium neo-caledoniae, from the southwestern lagoon of New Caledonia. wikidata.org.
  9. [10] ↑ . Bioactivity guided isolation of anticancer constituents from leaves of Alnus sieboldiana (Betulaceae).. 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). kavain. Retrieved November 4, 2026, from https://4ort.xyz/entity/kavain
MLA “kavain.” 4ort.xyz Knowledge Graph, 4ort.xyz, 4 Nov. 2026, https://4ort.xyz/entity/kavain.
BibTeX @misc{4ortxyz_kavain_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{kavain}}, year = {2026}, url = {https://4ort.xyz/entity/kavain}, note = {Accessed: 2026-11-04}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): kavain — https://4ort.xyz/entity/kavain (retrieved 2026-11-04)

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