Clusin

group of stereoisomers with the chemical formula C₂₂H₂₆O₇
ChemicalSubstance group_of_stereoisomers Q105256845
Press Enter · cited answer in seconds

Clusin

Summary

Clusin is a group of stereoisomers[1].

Key Facts

  • Clusin's instance of is recorded as group of stereoisomers[2].
  • Clusin's CAS Registry Number is recorded as 86992-94-1[3].
  • Clusin's canonical SMILES is recorded as OC1OCC(CC2=CC=C3OCOC3=C2)C1CC4=CC(OC)=C(OC)C(OC)=C4[4].
  • Clusin's InChI is recorded as InChI=1S/C22H26O7/c1-24-19-9-14(10-20(25-2)21(19)26-3)7-16-15(11-27-22(16)23)6-13-4-5-17-18(8-13)29-12-28-17/h4-5,8-10,15-16,22-23H,6-7,11-12H2,1-3H3[5].
  • Clusin's InChIKey is recorded as SOCNBZCAGNYAED-UHFFFAOYSA-N[6].
  • Clusin's chemical formula is recorded as C₂₂H₂₆O₇[7].
  • Clusin's subclass of is recorded as chemical compound[8].
  • Clusin's PubChem CID is recorded as 44575537[9].
  • Clusin's ChEBI ID is recorded as 168832[10].
  • Clusin's found in taxon is recorded as Hernandia nymphaeifolia[11].
  • Clusin's found in taxon is recorded as Piper cubeba[12].
  • Clusin's Human Metabolome Database ID is recorded as HMDB0029542[13].
  • Clusin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+402.167853172'}[14].
  • Clusin's SureChEMBL ID is recorded as 29583644[15].
  • Clusin's SureChEMBL ID is recorded as 15783195[16].
  • Clusin's DSSTox substance ID is recorded as DTXSID301127446[17].
  • Clusin's UniChem compound ID is recorded as 478306[18].

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] . ChEBI release 2022-06-13. wikidata.org.
  10. [11] . Antineoplastic Agents 522. Hernandia peltata (Malaysia) and Hernandia nymphaeifolia (Republic of Maldives). wikidata.org.
  11. [12] . Metabolite-cytochrome P450 complex formation by methylenedioxyphenyl lignans of Piper cubeba: mechanism-based inhibition. wikidata.org.
  12. [13] . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . wikidata.org.
  17. [18] . UniChem. 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). Clusin. Retrieved May 3, 2026, from https://4ort.xyz/entity/clusin
MLA “Clusin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/clusin.
BibTeX @misc{4ortxyz_clusin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Clusin}}, year = {2026}, url = {https://4ort.xyz/entity/clusin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Clusin — https://4ort.xyz/entity/clusin (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/clusin · Last refreshed: