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methysticin

chemical compound
Class type of: chemical compound Q3333720

Facts

9 properties
Instance of
type of chemical entity
Subclass of
chemical compound
Canonical SMILES
COC1=CC(=O)OC(C1)C=CC2=CC3=C(C=C2)OCO3
Chemical formula
C₁₅H₁₄O₅
Found in taxon
Piper methysticum, Piper majusculum
Isomeric SMILES
COC1=CC(=O)O[C@H](C1)/C=C/C2=CC3=C(C=C2)OCO3
Mass
+274.084124
Melting point
+138.5
Stereoisomer of
(2S)-2-[(E)-2-(1,3-benzodioxol-5-yl)ethenyl]-4-methoxy-2,3-dihydropyran-6-one
🏷️ Also known as
en methysticin fa متیستیسین fr méthysticine ja メチルスチシン zh 麻醉椒苦素
🔖 Identifiers · 18
CAS Registry Number
495-85-2
ChEBI ID
6895
ChEMBL ID
CHEMBL579224
ChemSpider ID
4444889
DSSTOX compound identifier
DTXCID3013674
DSSTox substance ID
DTXSID5033674
Freebase ID
/m/07k7y36
InChI
InChI=1S/C15H14O5/c1-17-12-7-11(20-15(16)8-12)4-2-10-3-5-13-14(6-10)19-9-18-13/h2-6,8,11H,7,9H2,1H3/b4-2+/t11-/m0/s1
InChIKey
GTEXBOVBADJOQH-FWEMWIAWSA-N
KEGG ID
C09952
KNApSAcK ID
C00003005
Microsoft Academic ID (discontinued)
2780072256
Show all 18 identifiers +6
NSC number
112158
Probes And Drugs ID
PD044448
PubChem CID
5281567
SureChEMBL ID
1393508
UNII
M832AIJ6HX
UniChem compound ID
613174

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🔗 Connections
Found in taxon 2
Piper methysticum, Piper majusculum
Subclass of 1
chemical compound
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Summary

methysticin is a type of chemical entity[1].

Key Facts

  • Canonical SMILES: COC1=CC(=O)OC(C1)C=CC2=CC3=C(C=C2)OCO3[2]
  • Chemical formula: C₁₅H₁₄O₅[3]
  • Subclass of: chemical compound[4]
  • Found in taxon: Piper methysticum[5], Piper majusculum[6]
  • Isomeric SMILES: COC1=CC(=O)OC@H/C=C/C2=CC3=C(C=C2)OCO3C@H/C=C/C2=CC3=C(C=C2)OCO3">[7]
  • Mass: 274.084124 dalton[8]
  • Melting point: 138.5 °C[9]
  • Stereoisomer of: (2S)-2-[(E)-2-(1,3-benzodioxol-5-yl)ethenyl]-4-methoxy-2,3-dihydropyran-6-one[10]

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] ↑ . Piper methysticum: enantiomeric separation of kavapyrones by high performance liquid chromatography. wikidata.org.
  5. [6] ↑ . Supercritical extraction of herbs I: Saw Palmetto, St John's Wort, Kava Root, and Echinacea. wikidata.org.
  6. [7] ↑ . PubChem. Retrieved . wikidata.org.
  7. [8] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . The Chemical Constituents of Piper Methysticum; The Chemical Constituents of the Active Principle of the Ava Root. wikidata.org.
  9. [10] ↑ . 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). methysticin. Retrieved November 4, 2026, from https://4ort.xyz/entity/methysticin
MLA “methysticin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 4 Nov. 2026, https://4ort.xyz/entity/methysticin.
BibTeX @misc{4ortxyz_methysticin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{methysticin}}, year = {2026}, url = {https://4ort.xyz/entity/methysticin}, note = {Accessed: 2026-11-04}}
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