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lanoxin

group of stereoisomers with the chemical formula C₄₁H₆₄O₁₄
ChemicalSubstance group_of_stereoisomers Q105157023
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lanoxin

Summary

lanoxin is a group of stereoisomers[1].

Key Facts

  • lanoxin's instance of is recorded as group of stereoisomers[2].
  • lanoxin's canonical SMILES is recorded as O=C1OCC(=C1)C2CCC3(O)C4CCC5CC(OC6OC(C)C(OC7OC(C)C(OC8OC(C)C(O)C(O)C8)C(O)C7)C(O)C6)CCC5(C)C4CC(O)C23C[3].
  • lanoxin's InChI is recorded as InChI=1S/C41H64O14/c1-19-36(47)28(42)15-34(50-19)54-38-21(3)52-35(17-30(38)44)55-37-20(2)51-33(16-29(37)43)53-24-8-10-39(4)23(13-24)6-7-26-27(39)14-31(45)40(5)25(9-11-41(26,40)48)22-12-32(46)49-18-22/h12,19-21,23-31,33-38,42-45,47-48H,6-11,13-18H2,1-5H3[4].
  • lanoxin's InChIKey is recorded as LTMHDMANZUZIPE-UHFFFAOYSA-N[5].
  • lanoxin's chemical formula is recorded as C₄₁H₆₄O₁₄[6].
  • lanoxin's subclass of is recorded as cardanolides[7].
  • lanoxin's PubChem CID is recorded as 3062[8].
  • lanoxin's found in taxon is recorded as Streptomyces purpurascens[9].
  • lanoxin's found in taxon is recorded as Streptomyces violaceus[10].
  • lanoxin's Human Metabolome Database ID is recorded as HMDB0250399[11].
  • lanoxin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+780.429606728'}[12].
  • lanoxin's SureChEMBL ID is recorded as 126382[13].
  • lanoxin's DSSTox substance ID is recorded as DTXSID10860258[14].
  • lanoxin's MassBank accession ID is recorded as MSBNK-Washington_State_Univ-BML81100[15].
  • lanoxin's MassBank accession ID is recorded as MSBNK-Washington_State_Univ-BML81103[16].
  • lanoxin's MassBank accession ID is recorded as MSBNK-Washington_State_Univ-BML81101[17].
  • lanoxin's UniChem compound ID is recorded as 23147823[18].
  • lanoxin's Probes And Drugs ID is recorded as PD055699[19].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . Transformation of 12-deoxycardenolids with Streptomyces purpurascens. wikidata.org.
  9. [10] ↑ . Transformation of 12-deoxycardenolids with Streptomyces purpurascens. wikidata.org.
  10. [11] ↑ . 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] ↑ . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  16. [17] ↑ . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  17. [18] ↑ . UniChem. wikidata.org.
  18. [19] ↑ . 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). lanoxin. Retrieved May 3, 2026, from https://4ort.xyz/entity/lanoxin
MLA “lanoxin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/lanoxin.
BibTeX @misc{4ortxyz_lanoxin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{lanoxin}}, year = {2026}, url = {https://4ort.xyz/entity/lanoxin}, note = {Accessed: 2026-05-03}}
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