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daphnetoxin

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q905363
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daphnetoxin

Summary

daphnetoxin is a group of stereoisomers[1].

Key Facts

  • daphnetoxin's instance of is recorded as group of stereoisomers[2].
  • daphnetoxin's canonical SMILES is recorded as CC1CC2(C3C4C1(C5C=C(C(=O)C5(C(C6(C4O6)CO)O)O)C)OC(O3)(O2)C7=CC=CC=C7)C(=C)C[3].
  • daphnetoxin's InChI is recorded as InChI=1S/C27H30O8/c1-13(2)23-11-15(4)26-17-10-14(3)19(29)25(17,31)22(30)24(12-28)21(32-24)18(26)20(23)33-27(34-23,35-26)16-8-6-5-7-9-16/h5-10,15,17-18,20-22,28,30-31H,1,11-12H2,2-4H3/t15-,17-,18-,20-,21+,22-,23-,24+,25-,26+,27?/m1/s1[4].
  • daphnetoxin's InChIKey is recorded as LGEROVMQYFTBDI-CDBNQIKXSA-N[5].
  • daphnetoxin's chemical formula is recorded as C₂₇H₃₀O₈[6].
  • daphnetoxin's subclass of is recorded as daphnane diterpenoid[7].
  • daphnetoxin's ChemSpider ID is recorded as 390576[8].
  • daphnetoxin's PubChem CID is recorded as 442018[9].
  • daphnetoxin's found in taxon is recorded as Daphne mezereum[10].
  • daphnetoxin's isomeric SMILES is recorded as C[C@@H]1C[C@]2([C@H]3[C@H]4[C@]1([C@@H]5C=C(C(=O)[C@]5(C@@HO)O)C)OC(O3)(O2)C7=CC=CC=C7)C(=C)CC@@HO)O)C)OC(O3)(O2)C7=CC=CC=C7)C(=C)C">[11].
  • daphnetoxin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+482.194068'}[12].
  • daphnetoxin's Nikkaji ID is recorded as J17.134D[13].
  • daphnetoxin's Google Knowledge Graph ID is recorded as /g/121fwhpz[14].
  • daphnetoxin's SureChEMBL ID is recorded as 29366163[15].
  • daphnetoxin's DSSTox substance ID is recorded as DTXSID70950907[16].
  • daphnetoxin's Römpp online ID is recorded as RD-04-00104[17].
  • daphnetoxin's DSSTOX compound identifier is recorded as DTXCID301379045[18].
  • daphnetoxin's UniChem compound ID is recorded as 1068326[19].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . PubChem. Retrieved . wikidata.org.
  3. [4] ↑ . PubChem. Retrieved . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . PubChem. Retrieved . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . Q2311683. Retrieved . wikidata.org.
  8. [9] ↑ . PubChem. Retrieved . wikidata.org.
  9. [10] ↑ . Mitochondrial toxicity of the phyotochemicals daphnetoxin and daphnoretin--relevance for possible anti-cancer application.. wikidata.org.
  10. [11] ↑ . PubChem. Retrieved . wikidata.org.
  11. [12] ↑ . PubChem. Retrieved . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . wikidata.org.
  18. [19] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

📑 Cite this page

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). daphnetoxin. Retrieved May 3, 2026, from https://4ort.xyz/entity/daphnetoxin
MLA “daphnetoxin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/daphnetoxin.
BibTeX @misc{4ortxyz_daphnetoxin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{daphnetoxin}}, year = {2026}, url = {https://4ort.xyz/entity/daphnetoxin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): daphnetoxin — https://4ort.xyz/entity/daphnetoxin (retrieved 2026-05-03)

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