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cymarin

group of stereoisomers with the chemical formula C₃₀H₄₄O₉
ChemicalSubstance group_of_stereoisomers Q105339552
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cymarin

Summary

cymarin is a group of stereoisomers[1].

Key Facts

  • cymarin's instance of is recorded as group of stereoisomers[2].
  • cymarin's canonical SMILES is recorded as O=CC12CCC(OC3OC(C)C(O)C(OC)C3)CC2(O)CCC4C1CCC5(C)C(C6=CC(=O)OC6)CCC45O[3].
  • cymarin's InChI is recorded as InChI=1S/C30H44O9/c1-17-26(33)23(36-3)13-25(38-17)39-19-4-9-28(16-31)21-5-8-27(2)20(18-12-24(32)37-15-18)7-11-30(27,35)22(21)6-10-29(28,34)14-19/h12,16-17,19-23,25-26,33-35H,4-11,13-15H2,1-3H3[4].
  • cymarin's InChIKey is recorded as XQCGNURMLWFQJR-UHFFFAOYSA-N[5].
  • cymarin's chemical formula is recorded as C₃₀H₄₄O₉[6].
  • cymarin's subclass of is recorded as cardanolides[7].
  • cymarin's PubChem CID is recorded as 539061[8].
  • cymarin's found in taxon is recorded as Castilla elastica[9].
  • cymarin's found in taxon is recorded as Apocynum cannabinum[10].
  • cymarin's found in taxon is recorded as Strophanthus hispidus[11].
  • cymarin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+548.298532988'}[12].
  • cymarin's SureChEMBL ID is recorded as 20592360[13].
  • cymarin's MassBank accession ID is recorded as MSBNK-Univ_Connecticut-CO000111[14].
  • cymarin's MassBank accession ID is recorded as MSBNK-Univ_Connecticut-CO000112[15].
  • cymarin's MassBank accession ID is recorded as MSBNK-Univ_Connecticut-CO000113[16].
  • cymarin's MassBank accession ID is recorded as MSBNK-Univ_Connecticut-CO000114[17].
  • cymarin's MassBank accession ID is recorded as MSBNK-Univ_Connecticut-CO000115[18].
  • cymarin's UniChem compound ID is recorded as 65983[19].
  • cymarin's Probes And Drugs ID is recorded as PD075122[20].

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] ↑ . Die Cardenolide vonCastilla elastica CERV. Glykoside und Aglykone, 222. Mitteilung. wikidata.org.
  9. [10] ↑ . Die Glykoside der Rhizome von Apocynum cannabinum L. 3. Mitteilung. Glykoside und Aglykone, 208. Mitteilung. wikidata.org.
  10. [11] ↑ . Die Glykoside der Samen von Strophanthus hispidusP. DC. 1. Mitteilung. Glykoside und Aglykone, 62. Mitteilung. wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . 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] ↑ . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  18. [19] ↑ . UniChem. wikidata.org.
  19. [20] ↑ . 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). cymarin. Retrieved May 3, 2026, from https://4ort.xyz/entity/cymarin-q105339552
MLA “cymarin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/cymarin-q105339552.
BibTeX @misc{4ortxyz_cymarin-q105339552_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{cymarin}}, year = {2026}, url = {https://4ort.xyz/entity/cymarin-q105339552}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): cymarin — https://4ort.xyz/entity/cymarin-q105339552 (retrieved 2026-05-03)

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