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8'-Hydroxyrotenone

group of stereoisomers with the chemical formula C₂₃H₂₂O₇
ChemicalSubstance group_of_stereoisomers Q105377977
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8'-Hydroxyrotenone

Summary

8'-Hydroxyrotenone is a group of stereoisomers[1].

Key Facts

  • 8'-Hydroxyrotenone's instance of is recorded as group of stereoisomers[2].
  • 8'-Hydroxyrotenone's CAS Registry Number is recorded as 10475-72-6[3].
  • 8'-Hydroxyrotenone's canonical SMILES is recorded as O=C1C2=CC=C3OC(C(=C)CO)CC3=C2OC4COC5=CC(OC)=C(OC)C=C5C14[4].
  • 8'-Hydroxyrotenone's InChI is recorded as InChI=1S/C23H22O7/c1-11(9-24)16-7-14-15(29-16)5-4-12-22(25)21-13-6-18(26-2)19(27-3)8-17(13)28-10-20(21)30-23(12)14/h4-6,8,16,20-21,24H,1,7,9-10H2,2-3H3[5].
  • 8'-Hydroxyrotenone's InChIKey is recorded as ZJMLELXRQUXRIU-UHFFFAOYSA-N[6].
  • 8'-Hydroxyrotenone's chemical formula is recorded as C₂₃H₂₂O₇[7].
  • 8'-Hydroxyrotenone's subclass of is recorded as rotenoid[8].
  • 8'-Hydroxyrotenone's PubChem CID is recorded as 4342730[9].
  • 8'-Hydroxyrotenone's found in taxon is recorded as Amorpha fruticosa[10].
  • 8'-Hydroxyrotenone's LIPID MAPS ID is recorded as LMPK12060012[11].
  • 8'-Hydroxyrotenone's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+410.136553044'}[12].
  • 8'-Hydroxyrotenone's SureChEMBL ID is recorded as 74860[13].
  • 8'-Hydroxyrotenone's DSSTox substance ID is recorded as DTXSID501105094[14].
  • 8'-Hydroxyrotenone's MassBank accession ID is recorded as MSBNK-RIKEN_NPDepo-CB000314[15].
  • 8'-Hydroxyrotenone's UniChem compound ID is recorded as 831789[16].

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] ↑ . Formation and dehydration of a prochiral 2-hydroxyisopropyl centre during biosynthesis: the rot-2′-enonic acid–rotenone transformation in Amorpha fruticosa. wikidata.org.
  10. [11] ↑ . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  15. [16] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). 8'-Hydroxyrotenone. Retrieved May 3, 2026, from https://4ort.xyz/entity/8-hydroxyrotenone
MLA “8'-Hydroxyrotenone.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/8-hydroxyrotenone.
BibTeX @misc{4ortxyz_8-hydroxyrotenone_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{8'-Hydroxyrotenone}}, year = {2026}, url = {https://4ort.xyz/entity/8-hydroxyrotenone}, note = {Accessed: 2026-05-03}}
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