artonin L

group of stereoisomers with the chemical formula C₂₂H₂₀O₇
ChemicalSubstance group_of_stereoisomers Q105150330
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artonin L

Summary

artonin L is a group of stereoisomers[1].

Key Facts

  • artonin L's instance of is recorded as group of stereoisomers[2].
  • artonin L's CAS Registry Number is recorded as 148719-52-2[3].
  • artonin L's canonical SMILES is recorded as O=C1C2=C(O)C=C(OC)C=C2OC=3C=4C(OC)=CC(O)=C5OC(C)(C)C(C54)CC13[4].
  • artonin L's InChI is recorded as InChI=1S/C22H20O7/c1-22(2)11-7-10-19(25)17-12(23)5-9(26-3)6-15(17)28-20(10)18-14(27-4)8-13(24)21(29-22)16(11)18/h5-6,8,11,23-24H,7H2,1-4H3[5].
  • artonin L's InChIKey is recorded as LDQNIBPJKBVZEF-UHFFFAOYSA-N[6].
  • artonin L's chemical formula is recorded as C₂₂H₂₀O₇[7].
  • artonin L's subclass of is recorded as 5,6-dihydrobenzo[c]xanthen-7-one flavonoid[8].
  • artonin L's PubChem CID is recorded as 44258662[9].
  • artonin L's ChEBI ID is recorded as 175165[10].
  • artonin L's found in taxon is recorded as Artocarpus chama[11].
  • artonin L's found in taxon is recorded as Artocarpus chaplasha[12].
  • artonin L's found in taxon is recorded as Artocarpus integer[13].
  • artonin L's Human Metabolome Database ID is recorded as HMDB0040674[14].
  • artonin L's LIPID MAPS ID is recorded as LMPK12111520[15].
  • artonin L's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+396.12090298'}[16].
  • artonin L's DSSTox substance ID is recorded as DTXSID101119007[17].
  • artonin L's UniChem compound ID is recorded as 32002685[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] . New isoprenylated flavones, artochamins A--E, and cytotoxic principles from Artocarpus chama. wikidata.org.
  11. [12] . New isoprenylated flavones, artochamins A--E, and cytotoxic principles from Artocarpus chama. wikidata.org.
  12. [13] . Artonins J, K, and L, Three New Isoprenylated Flavones from the Root Bark of Artocarpus heterophyllus Lamk.. wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . wikidata.org.
  17. [18] . 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). artonin L. Retrieved May 3, 2026, from https://4ort.xyz/entity/artonin-l
MLA “artonin L.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/artonin-l.
BibTeX @misc{4ortxyz_artonin-l_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{artonin L}}, year = {2026}, url = {https://4ort.xyz/entity/artonin-l}, note = {Accessed: 2026-05-03}}
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