sesamin

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q102015395
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sesamin

Summary

sesamin is a group of stereoisomers[1].

Key Facts

  • sesamin's instance of is recorded as group of stereoisomers[2].
  • sesamin's CAS Registry Number is recorded as 7076-24-6[3].
  • sesamin's canonical SMILES is recorded as c1cc2c(cc1C1OCC3C(c4ccc5c(c4)OCO5)OCC13)OCO2[4].
  • sesamin's InChI is recorded as InChI=1S/C20H18O6/c1-3-15-17(25-9-23-15)5-11(1)19-13-7-22-20(14(13)8-21-19)12-2-4-16-18(6-12)26-10-24-16/h1-6,13-14,19-20H,7-10H2[5].
  • sesamin's InChIKey is recorded as PEYUIKBAABKQKQ-UHFFFAOYSA-N[6].
  • sesamin's chemical formula is recorded as C₂₀H₁₈O₆[7].
  • sesamin's subclass of is recorded as chemical compound[8].
  • sesamin's PubChem CID is recorded as 5204[9].
  • sesamin's found in taxon is recorded as Cuscuta chinensis[10].
  • sesamin's found in taxon is recorded as Magnolia praecocissima[11].
  • sesamin's found in taxon is recorded as Ruta montana[12].
  • sesamin's found in taxon is recorded as Piper acutifolium[13].
  • sesamin's found in taxon is recorded as Piper arboreum[14].
  • sesamin's found in taxon is recorded as Ruta microcarpa[15].
  • sesamin's found in taxon is recorded as Firmiana simplex[16].
  • sesamin's found in taxon is recorded as Stemona japonica[17].
  • sesamin's found in taxon is recorded as Machilus thunbergii[18].
  • sesamin's found in taxon is recorded as Eleutherococcus senticosus[19].
  • sesamin's found in taxon is recorded as Garcinia oligantha[20].
  • sesamin's found in taxon is recorded as Garcinia hombroniana[21].
  • sesamin's found in taxon is recorded as Sideritis canariensis[22].
  • sesamin's found in taxon is recorded as Eucalyptus[23].
  • sesamin's found in taxon is recorded as Bridelia[24].
  • sesamin's found in taxon is recorded as Cinnamomum camphora[25].
  • sesamin's found in taxon is recorded as Phyllanthus oligospermus[26].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . Chemical Abstracts Service. Retrieved . wikidata.org.
  3. [4] . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . PubChem. Retrieved . wikidata.org.
  9. [10] . wikidata.org.
  10. [11] . Lignans and sesquiterpenes from Magnolia praecocissima. wikidata.org.
  11. [12] . Allelochemicals from Stauranthus perforatus, a Rutaceous tree of the Yucatan Peninsula, Mexico. wikidata.org.
  12. [13] . Short and stereoselective total synthesis of furano lignans (+/-)-dihydrosesamin, (+/-)-lariciresinol dimethyl ether, (+/-)-acuminatin methyl ether, (+/-)-sanshodiol methyl ether, (+/-)-lariciresinol, (+/-)-acuminatin, and (+/-)-lariciresinol monome. wikidata.org.
  13. [14] . Short and stereoselective total synthesis of furano lignans (+/-)-dihydrosesamin, (+/-)-lariciresinol dimethyl ether, (+/-)-acuminatin methyl ether, (+/-)-sanshodiol methyl ether, (+/-)-lariciresinol, (+/-)-acuminatin, and (+/-)-lariciresinol monome. wikidata.org.
  14. [15] . Allelochemicals from Stauranthus perforatus, a Rutaceous tree of the Yucatan Peninsula, Mexico. wikidata.org.
  15. [16] . Isoprenylated naphthoquinone dimers firmianones A, B, and C from Firmiana platanifolia. wikidata.org.
  16. [17] . Nonalkaloid Constituents fromStemona japonica. wikidata.org.
  17. [18] . Neuroprotective lignans from the bark of Machilus thunbergii. wikidata.org.
  18. [19] . A new 3,4-seco-lupane-type triterpenoid from the pulp of Acanthopanax senticosus (Rupr. et Maxim) Harms. wikidata.org.
  19. [20] . Benzophenone derivatives from the fruits of Garcinia multiflora and their anti-inflammatory activity. wikidata.org.
  20. [21] . Benzophenone derivatives from the fruits of Garcinia multiflora and their anti-inflammatory activity. wikidata.org.
  21. [22] . A chemotaxonomic study of nine Canarian Sideritis species. wikidata.org.
  22. [23] . Natural antioxidants isolated from Eucalyptus leaf waxes. wikidata.org.
  23. [24] . Antifungal constituents of the stem bark of Bridelia retusa. wikidata.org.
  24. [25] . Cytotoxic compounds from the stems of Cinnamomum tenuifolium.. wikidata.org.
  25. [26] . Cytotoxic arylnaphthalene lignans from Phyllanthus oligospermus. wikidata.org.

Class ancestry

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

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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). sesamin. Retrieved May 3, 2026, from https://4ort.xyz/entity/sesamin-q102015395
MLA “sesamin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/sesamin-q102015395.
BibTeX @misc{4ortxyz_sesamin-q102015395_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{sesamin}}, year = {2026}, url = {https://4ort.xyz/entity/sesamin-q102015395}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): sesamin — https://4ort.xyz/entity/sesamin-q102015395 (retrieved 2026-05-03)

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