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hyponine F

chemical compound
ChemicalSubstance group_of_stereoisomers Q27225554
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hyponine F

Summary

hyponine F is a group of stereoisomers[1].

Key Facts

  • hyponine F's instance of is recorded as group of stereoisomers[2].
  • hyponine F's CAS Registry Number is recorded as 259823-33-1[3].
  • hyponine F'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=CO6)C[4].
  • hyponine F's InChI is recorded as InChI=1S/C41H47NO19/c1-18-19(2)35(48)60-32-30(59-37(50)26-13-11-15-52-26)34(58-24(7)47)40(17-53-20(3)43)33(57-23(6)46)29(55-21(4)44)27-31(56-22(5)45)41(40,39(32,9)51)61-38(27,8)16-54-36(49)25-12-10-14-42-28(18)25/h10-15,18-19,27,29-34,51H,16-17H2,1-9H3/t18?,19?,27-,29-,30+,31-,32+,33-,34+,38+,39+,40-,41+/m1/s1[5].
  • hyponine F's InChIKey is recorded as ALJJHPQWUBVQNM-KSTPHJKESA-N[6].
  • hyponine F's chemical formula is recorded as C₄₁H₄₇NO₁₉[7].
  • hyponine F's subclass of is recorded as eudesmane sesquiterpenoid[8].
  • hyponine F's subclass of is recorded as pyridine alkaloid[9].
  • hyponine F's subclass of is recorded as macrolides[10].
  • hyponine F's ChEMBL ID is recorded as CHEMBL525633[11].
  • hyponine F's ChemSpider ID is recorded as 24720950[12].
  • hyponine F's PubChem CID is recorded as 44583773[13].
  • hyponine F's ChEBI ID is recorded as 132390[14].
  • hyponine F's found in taxon is recorded as Tripterygium wilfordii[15].
  • hyponine F's Reaxys registry number is recorded as 8105536[16].
  • hyponine F's isomeric SMILES is recorded as CC1C(C(=O)O[C@H]2C@@HOC(=O)C6=CC=CO6)CC@@HOC(=O)C6=C">[17].
  • hyponine F's KNApSAcK ID is recorded as C00039397[18].
  • hyponine F's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+857.274'}[19].
  • hyponine F's UniChem compound ID is recorded as 193654[20].

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] ↑ . ChEMBL. Retrieved . wikidata.org.
  11. [12] ↑ . Q2311683. Retrieved . wikidata.org.
  12. [13] ↑ . PubChem. Retrieved . wikidata.org.
  13. [14] ↑ . ChEBI. Retrieved . wikidata.org.
  14. [15] ↑ . Tripfordines A-C, sesquiterpene pyridine alkaloids from Tripterygium wilfordii, and structure anti-HIV activity relationships of Tripterygium alkaloids. wikidata.org.
  15. [16] ↑ . ChEBI. Retrieved . wikidata.org.
  16. [17] ↑ . PubChem. Retrieved . wikidata.org.
  17. [18] ↑ . ChEBI. Retrieved . wikidata.org.
  18. [19] ↑ . PubChem. Retrieved . wikidata.org.
  19. [20] ↑ . 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). hyponine F. Retrieved May 3, 2026, from https://4ort.xyz/entity/hyponine-f
MLA “hyponine F.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hyponine-f.
BibTeX @misc{4ortxyz_hyponine-f_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hyponine F}}, year = {2026}, url = {https://4ort.xyz/entity/hyponine-f}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hyponine F — https://4ort.xyz/entity/hyponine-f (retrieved 2026-05-03)

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