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forrestine

chemical compound
ChemicalSubstance group_of_stereoisomers Q27225557
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forrestine

Summary

forrestine is a group of stereoisomers[1].

Key Facts

  • forrestine's instance of is recorded as group of stereoisomers[2].
  • forrestine's CAS Registry Number is recorded as 146439-78-3[3].
  • forrestine's canonical SMILES is recorded as CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C6=CC=CC=C6)C[4].
  • forrestine's InChI is recorded as InChI=1S/C43H49NO18/c1-20-21(2)37(50)61-34-32(60-38(51)27-14-11-10-12-15-27)36(59-26(7)49)42(19-54-22(3)45)35(58-25(6)48)31(56-23(4)46)29-33(57-24(5)47)43(42,41(34,9)53)62-40(29,8)18-55-39(52)28-16-13-17-44-30(20)28/h10-17,20-21,29,31-36,53H,18-19H2,1-9H3/t20?,21?,29-,31-,32+,33-,34+,35-,36+,40+,41+,42-,43+/m1/s1[5].
  • forrestine's InChIKey is recorded as LBQLWUULERJYOL-PDVUZMAKSA-N[6].
  • forrestine's chemical formula is recorded as C₄₃H₄₉NO₁₈[7].
  • forrestine's subclass of is recorded as eudesmane sesquiterpenoid[8].
  • forrestine's subclass of is recorded as pyridine alkaloid[9].
  • forrestine's subclass of is recorded as macrolides[10].
  • forrestine's PubChem CID is recorded as 44583774[11].
  • forrestine's ChEBI ID is recorded as 132393[12].
  • forrestine's found in taxon is recorded as Tripterygium wilfordii[13].
  • forrestine's found in taxon is recorded as Tripterygium forrestii[14].
  • forrestine's found in taxon is recorded as Monteverdia chiapensis[15].
  • forrestine's found in taxon is recorded as Maytenus chiapensis[16].
  • forrestine's Reaxys registry number is recorded as 8105266[17].
  • forrestine's isomeric SMILES is recorded as CC1C(C(=O)O[C@H]2C@@HOC(=O)C6=CC=CC=C6)CC@@HOC(=O)C6=C">[18].
  • forrestine's KNApSAcK ID is recorded as C00043510[19].
  • forrestine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+867.295'}[20].
  • forrestine's UniChem compound ID is recorded as 96980436[21].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . ChEBI. Retrieved . wikidata.org.
  3. [4] ↑ . PubChem. Retrieved . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . PubChem. Retrieved . wikidata.org.
  6. [7] ↑ . PubChem. Retrieved . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . wikidata.org.
  10. [11] ↑ . PubChem. Retrieved . wikidata.org.
  11. [12] ↑ . ChEBI. Retrieved . wikidata.org.
  12. [13] ↑ . Forrestine, an alkaloid from Tripterygium forrestii. wikidata.org.
  13. [14] ↑ . Forrestine, an alkaloid from Tripterygium forrestii. wikidata.org.
  14. [15] ↑ . Insecticidal sesquiterpene pyridine alkaloids from Maytenus chiapensis.. wikidata.org.
  15. [16] ↑ . Insecticidal sesquiterpene pyridine alkaloids from Maytenus chiapensis.. wikidata.org.
  16. [17] ↑ . ChEBI. Retrieved . wikidata.org.
  17. [18] ↑ . PubChem. Retrieved . wikidata.org.
  18. [19] ↑ . ChEBI. Retrieved . wikidata.org.
  19. [20] ↑ . PubChem. Retrieved . wikidata.org.
  20. [21] ↑ . 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). forrestine. Retrieved May 3, 2026, from https://4ort.xyz/entity/forrestine
MLA “forrestine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/forrestine.
BibTeX @misc{4ortxyz_forrestine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{forrestine}}, year = {2026}, url = {https://4ort.xyz/entity/forrestine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): forrestine — https://4ort.xyz/entity/forrestine (retrieved 2026-05-03)

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