galanolactone

chemical compound
ChemicalSubstance type_of_chemical_entity Q754392
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galanolactone

Summary

galanolactone is a type of chemical entity[1]. galanolactone ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (10 views/month).[2]

Key Facts

  • galanolactone's instance of is recorded as type of chemical entity[3].
  • galanolactone's CAS Registry Number is recorded as 115753-79-2[4].
  • galanolactone's canonical SMILES is recorded as CC1(CCCC2(C1CCC3(C2CC=C4CCOC4=O)CO3)C)C[5].
  • galanolactone's InChI is recorded as InChI=1S/C20H30O3/c1-18(2)9-4-10-19(3)15(18)7-11-20(13-23-20)16(19)6-5-14-8-12-22-17(14)21/h5,15-16H,4,6-13H2,1-3H3/b14-5+/t15-,16+,19-,20+/m0/s1[6].
  • galanolactone's InChIKey is recorded as MBPTXJNHCBXMBP-SDIIOJARSA-N[7].
  • galanolactone's chemical formula is recorded as C₂₀H₃₀O₃[8].
  • galanolactone's subclass of is recorded as (3E)-3-{2-[(1R,2S)-5,5,8a-trimethyl-hexahydro-1H-spiro[naphthalene-2,2'-oxiran]-1-yl]ethylidene}oxolan-2-one[9].
  • galanolactone's Freebase ID is recorded as /m/05p0vb1[10].
  • galanolactone's UNII is recorded as 4FX4852TYQ[11].
  • galanolactone's ChemSpider ID is recorded as 9316811[12].
  • galanolactone's PubChem CID is recorded as 11141699[13].
  • galanolactone's KEGG ID is recorded as C17498[14].
  • galanolactone's ChEBI ID is recorded as 81135[15].
  • galanolactone's found in taxon is recorded as ginger[16].
  • galanolactone's found in taxon is recorded as Aframomum alboviolaceum[17].
  • galanolactone's found in taxon is recorded as Alpinia galanga[18].
  • galanolactone's found in taxon is recorded as Alpinia katsumadai[19].
  • galanolactone's found in taxon is recorded as Aframomum zambesiacum[20].
  • galanolactone's found in taxon is recorded as Zingiber mekongense[21].
  • galanolactone's found in taxon is recorded as Alpinia hainanensis[22].
  • galanolactone's isomeric SMILES is recorded as C[C@]12CCCC([C@@H]1CC[C@]3([C@@H]2C/C=C/4\CCOC4=O)CO3)(C)C[23].
  • galanolactone's mass is recorded as {'unit': 'Q483261', 'amount': '+318.219'}[24].
  • galanolactone's SureChEMBL ID is recorded as 29706409[25].
  • galanolactone's stereoisomer of is recorded as (3E)-3-[2-[(1R,2S,4aS,8aR)-5,5,8a-trimethylspiro[3,4,4a,6,7,8-hexahydro-1H-naphthalene-2,2'-oxirane]-1-yl]ethylidene]oxolan-2-one[26].
  • galanolactone's Microsoft Academic ID is recorded as 2779723770[27].

Why It Matters

galanolactone ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (10 views/month).[2] galanolactone has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [5] . PubChem. Retrieved . wikidata.org.
  4. [6] . PubChem. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . Freebase Data Dumps. wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . Q2311683. Retrieved . wikidata.org.
  11. [13] . PubChem. Retrieved . wikidata.org.
  12. [14] . ChEBI. Retrieved . wikidata.org.
  13. [15] . ChEBI. Retrieved . wikidata.org.
  14. [16] . Anti-5-hydroxytryptamine3 effect of galanolactone, diterpenoid isolated from ginger. wikidata.org.
  15. [17] . Antiplasmodial activity of labdanes from Aframomum latifolium and Aframomum sceptrum. wikidata.org.
  16. [18] . Cytotoxic and Antifungal Diterpenes from the Seeds of Alpinia galanga. wikidata.org.
  17. [19] . Stilbenes, monoterpenes, diarylheptanoids, labdanes and chalcones from Alpinia katsumadai. wikidata.org.
  18. [20] . Five labdane diterpenoids from the seeds of Aframomum zambesiacum.. wikidata.org.
  19. [21] . A new diarylheptanoid from the rhizomes of Zingiber mekongense. wikidata.org.
  20. [22] . Stilbenes, monoterpenes, diarylheptanoids, labdanes and chalcones from Alpinia katsumadai. wikidata.org.
  21. [23] . PubChem. Retrieved . wikidata.org.
  22. [24] . PubChem. Retrieved . wikidata.org.
  23. [25] . wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . Wikidata sitelinks. 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). galanolactone. Retrieved May 3, 2026, from https://4ort.xyz/entity/galanolactone
MLA “galanolactone.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/galanolactone.
BibTeX @misc{4ortxyz_galanolactone_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{galanolactone}}, year = {2026}, url = {https://4ort.xyz/entity/galanolactone}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): galanolactone — https://4ort.xyz/entity/galanolactone (retrieved 2026-05-03)

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