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Isolicopyranocoumarin

group of stereoisomers with the chemical formula C₂₁H₂₀O₇
ChemicalSubstance group_of_stereoisomers Q105127949
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Isolicopyranocoumarin

Summary

Isolicopyranocoumarin is a group of stereoisomers[1].

Key Facts

  • Isolicopyranocoumarin's instance of is recorded as group of stereoisomers[2].
  • Isolicopyranocoumarin's CAS Registry Number is recorded as 197303-94-9[3].
  • Isolicopyranocoumarin's canonical SMILES is recorded as O=C1OC=2C=C3OC(C)(C)C(O)CC3=C(OC)C2C=C1C=4C=CC(O)=CC4O[4].
  • Isolicopyranocoumarin's InChI is recorded as InChI=1S/C21H20O7/c1-21(2)18(24)8-14-17(28-21)9-16-13(19(14)26-3)7-12(20(25)27-16)11-5-4-10(22)6-15(11)23/h4-7,9,18,22-24H,8H2,1-3H3[5].
  • Isolicopyranocoumarin's InChIKey is recorded as JHGBGRLHQJNGPN-UHFFFAOYSA-N[6].
  • Isolicopyranocoumarin's chemical formula is recorded as C₂₁H₂₀O₇[7].
  • Isolicopyranocoumarin's subclass of is recorded as 6C-prenylarylcoumarin[8].
  • Isolicopyranocoumarin's PubChem CID is recorded as 10810040[9].
  • Isolicopyranocoumarin's ChEBI ID is recorded as 175894[10].
  • Isolicopyranocoumarin's found in taxon is recorded as Glycyrrhiza uralensis[11].
  • Isolicopyranocoumarin's Human Metabolome Database ID is recorded as HMDB0035479[12].
  • Isolicopyranocoumarin's KNApSAcK ID is recorded as C00060647[13].
  • Isolicopyranocoumarin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+384.12090298'}[14].
  • Isolicopyranocoumarin's DSSTox substance ID is recorded as DTXSID801108835[15].
  • Isolicopyranocoumarin's UniChem compound ID is recorded as 32003359[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] ↑ . ChEBI release 2022-06-13. wikidata.org.
  10. [11] ↑ . Phenolic Constituents of Liquorice. VII. A New Chalcone with a Potent Radical Scavenging Activity and Accompanying Phenolics from Liquorice.. wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . 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). Isolicopyranocoumarin. Retrieved May 3, 2026, from https://4ort.xyz/entity/isolicopyranocoumarin
MLA “Isolicopyranocoumarin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/isolicopyranocoumarin.
BibTeX @misc{4ortxyz_isolicopyranocoumarin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Isolicopyranocoumarin}}, year = {2026}, url = {https://4ort.xyz/entity/isolicopyranocoumarin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Isolicopyranocoumarin — https://4ort.xyz/entity/isolicopyranocoumarin (retrieved 2026-05-03)

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