Thamnosin

group of stereoisomers with the chemical formula C₃₀H₂₈O₆
ChemicalSubstance group_of_stereoisomers Q105262639
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Thamnosin

Summary

Thamnosin is a group of stereoisomers[1].

Key Facts

  • Thamnosin's instance of is recorded as group of stereoisomers[2].
  • Thamnosin's canonical SMILES is recorded as O=C1OC=2C=C(OC)C(C=CC3(C)CCC(=CC3C4=CC=5C=CC(=O)OC5C=C4OC)C)=CC2C=C1[3].
  • Thamnosin's InChI is recorded as InChI=1S/C30H28O6/c1-18-9-11-30(2,12-10-21-14-19-5-7-28(31)35-25(19)16-24(21)33-3)23(13-18)22-15-20-6-8-29(32)36-26(20)17-27(22)34-4/h5-8,10,12-17,23H,9,11H2,1-4H3/b12-10+[4].
  • Thamnosin's InChIKey is recorded as SWGAQLQAABDHGT-ZRDIBKRKSA-N[5].
  • Thamnosin's chemical formula is recorded as C₃₀H₂₈O₆[6].
  • Thamnosin's subclass of is recorded as 1-ethyl-1,4-dimethylcyclohexane monoterpenoids[7].
  • Thamnosin's subclass of is recorded as biogenic coumarin[8].
  • Thamnosin's PubChem CID is recorded as 5377043[9].
  • Thamnosin's ChEBI ID is recorded as 178188[10].
  • Thamnosin's found in taxon is recorded as Citrus grandis[11].
  • Thamnosin's found in taxon is recorded as pomelo[12].
  • Thamnosin's found in taxon is recorded as Thamnosma montana[13].
  • Thamnosin's isomeric SMILES is recorded as COc1cc2oc(=O)ccc2cc1/C=C/C1(C)CCC(C)=CC1c1cc2ccc(=O)oc2cc1OC[14].
  • Thamnosin's Human Metabolome Database ID is recorded as HMDB0030550[15].
  • Thamnosin's KNApSAcK ID is recorded as C00054397[16].
  • Thamnosin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+484.188588616'}[17].
  • Thamnosin's SureChEMBL ID is recorded as 29801586[18].
  • Thamnosin's UniChem compound ID is recorded as 31996834[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] . wikidata.org.
  8. [9] . PubChem. Retrieved . wikidata.org.
  9. [10] . ChEBI release 2022-06-13. wikidata.org.
  10. [11] . Coumarins, acridone alkaloids and a flavone from Citrus grandis. wikidata.org.
  11. [12] . Coumarins, acridone alkaloids and a flavone from Citrus grandis. wikidata.org.
  12. [13] . Novel epoxides from Thamnosma Montana Torr. and Frem.. 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.

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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). Thamnosin. Retrieved May 3, 2026, from https://4ort.xyz/entity/thamnosin
MLA “Thamnosin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/thamnosin.
BibTeX @misc{4ortxyz_thamnosin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Thamnosin}}, year = {2026}, url = {https://4ort.xyz/entity/thamnosin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Thamnosin — https://4ort.xyz/entity/thamnosin (retrieved 2026-05-03)

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