Hericenone F

group of stereoisomers with the chemical formula C₃₅H₅₄O₆
ChemicalSubstance group_of_stereoisomers Q105091213
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Hericenone F

Summary

Hericenone F is a group of stereoisomers[1].

Key Facts

  • Hericenone F's instance of is recorded as group of stereoisomers[2].
  • Hericenone F's CAS Registry Number is recorded as 141996-36-3[3].
  • Hericenone F's canonical SMILES is recorded as O=CC1=C2OC(C)(CC(=O)C=C(C)C)CCC2=C(OC)C=C1COC(=O)CCCCCCCCCCCCCCC[4].
  • Hericenone F's InChI is recorded as InChI=1S/C35H54O6/c1-6-7-8-9-10-11-12-13-14-15-16-17-18-19-33(38)40-26-28-23-32(39-5)30-20-21-35(4,24-29(37)22-27(2)3)41-34(30)31(28)25-36/h22-23,25H,6-21,24,26H2,1-5H3[5].
  • Hericenone F's InChIKey is recorded as ACYSSVIUKOTZQD-UHFFFAOYSA-N[6].
  • Hericenone F's chemical formula is recorded as C₃₅H₅₄O₆[7].
  • Hericenone F's subclass of is recorded as 2,6-dimethyloctane monoterpenoid[8].
  • Hericenone F's subclass of is recorded as chromane[9].
  • Hericenone F's PubChem CID is recorded as 11757751[10].
  • Hericenone F's ChEBI ID is recorded as 176109[11].
  • Hericenone F's found in taxon is recorded as Hericium erinaceus[12].
  • Hericenone F's Human Metabolome Database ID is recorded as HMDB0039593[13].
  • Hericenone F's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+570.392039448'}[14].
  • Hericenone F's SureChEMBL ID is recorded as 29543282[15].
  • Hericenone F's SureChEMBL ID is recorded as 9617870[16].
  • Hericenone F's DSSTox substance ID is recorded as DTXSID101106626[17].
  • Hericenone F's Natural Product Atlas ID is recorded as NPA017208[18].
  • Hericenone F's UniChem compound ID is recorded as 32023052[19].

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] . wikidata.org.
  9. [10] . PubChem. Retrieved . wikidata.org.
  10. [11] . ChEBI release 2022-06-13. wikidata.org.
  11. [12] . Benzyl alcohol derivatives from the mushroomHericium erinaceumattenuate LPS-stimulated inflammatory response through the regulation of NF-κB and AP-1 activity. wikidata.org.
  12. [13] . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . wikidata.org.
  17. [18] . wikidata.org.
  18. [19] . UniChem. 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). Hericenone F. Retrieved May 3, 2026, from https://4ort.xyz/entity/hericenone-f
MLA “Hericenone F.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hericenone-f.
BibTeX @misc{4ortxyz_hericenone-f_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Hericenone F}}, year = {2026}, url = {https://4ort.xyz/entity/hericenone-f}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Hericenone F — https://4ort.xyz/entity/hericenone-f (retrieved 2026-05-03)

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