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Timosaponin A-I

chemical compound
ChemicalSubstance group_of_stereoisomers Q27151408
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Timosaponin A-I

Summary

Timosaponin A-I is a group of stereoisomers[1].

Key Facts

  • Timosaponin A-I's instance of is recorded as group of stereoisomers[2].
  • Timosaponin A-I's canonical SMILES is recorded as CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)OC1[3].
  • Timosaponin A-I's InChI is recorded as InChI=1S/C33H54O8/c1-17-7-12-33(38-16-17)18(2)26-24(41-33)14-23-21-6-5-19-13-20(8-10-31(19,3)22(21)9-11-32(23,26)4)39-30-29(37)28(36)27(35)25(15-34)40-30/h17-30,34-37H,5-16H2,1-4H3/t17?,18-,19+,20-,21+,22-,23-,24-,25+,26-,27-,28-,29+,30+,31-,32-,33+/m0/s1[4].
  • Timosaponin A-I's InChIKey is recorded as ZNEIIZNXGCIAAL-GEUMLUQESA-N[5].
  • Timosaponin A-I's chemical formula is recorded as C₃₃H₅₄O₈[6].
  • Timosaponin A-I's subclass of is recorded as chemical compound[7].
  • Timosaponin A-I's ChemSpider ID is recorded as 30791712[8].
  • Timosaponin A-I's PubChem CID is recorded as 46173862[9].
  • Timosaponin A-I's KEGG ID is recorded as C17074[10].
  • Timosaponin A-I's ChEBI ID is recorded as 80909[11].
  • Timosaponin A-I's found in taxon is recorded as Anemarrhena asphodeloides[12].
  • Timosaponin A-I's isomeric SMILES is recorded as C[C@H]1[C@H]2C@HO[C@]17CCC(CO7)CC@HO[C@]17CCC(CO7)C">[13].
  • Timosaponin A-I's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+578.381869'}[14].
  • Timosaponin A-I's SureChEMBL ID is recorded as 29405632[15].
  • Timosaponin A-I's UniChem compound ID is recorded as 1067679[16].

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] ↑ . ChEBI. Retrieved . wikidata.org.
  10. [11] ↑ . ChEBI. Retrieved . wikidata.org.
  11. [12] ↑ . Plasma pharmacochemistry combined with microdialysis to screen potential bioactive components and their metabolites in Anemarrhena asphodeloides saponin extract using ultrahigh-performance liquid chromatography/quadrupole-time-of-flight mass spectro. wikidata.org.
  12. [13] ↑ . PubChem. Retrieved . wikidata.org.
  13. [14] ↑ . PubChem. Retrieved . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . 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). Timosaponin A-I. Retrieved May 3, 2026, from https://4ort.xyz/entity/timosaponin-a-i
MLA “Timosaponin A-I.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/timosaponin-a-i.
BibTeX @misc{4ortxyz_timosaponin-a-i_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Timosaponin A-I}}, year = {2026}, url = {https://4ort.xyz/entity/timosaponin-a-i}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Timosaponin A-I — https://4ort.xyz/entity/timosaponin-a-i (retrieved 2026-05-03)

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