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Saponin D

group of stereoisomers with the chemical formula C₄₈H₇₈O₁₇
ChemicalSubstance group_of_stereoisomers Q104996015
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Saponin D

Summary

Saponin D is a group of stereoisomers[1].

Key Facts

  • Saponin D's instance of is recorded as group of stereoisomers[2].
  • Saponin D's CAS Registry Number is recorded as 79190-14-0[3].
  • Saponin D's canonical SMILES is recorded as OCC1OC(OC2CCC3(C)C(CCC4(C)C3CCC5C6C7(OCC54C7)OC(C=C(C)C)CC6(OC8OC(C)C(O)C(O)C8O)C)C2(C)C)C(OC9OC(C)C(O)C(O)C9O)C(O)C1O[4].
  • Saponin D's InChI is recorded as InChI=1S/C48H78O17/c1-21(2)16-24-17-46(9,65-41-37(57)34(54)31(51)23(4)60-41)39-25-10-11-28-44(7)14-13-29(43(5,6)27(44)12-15-45(28,8)47(25)19-48(39,64-24)58-20-47)62-42-38(35(55)32(52)26(18-49)61-42)63-40-36(56)33(53)30(50)22(3)59-40/h16,22-42,49-57H,10-15,17-20H2,1-9H3[5].
  • Saponin D's InChIKey is recorded as FJESIUXDUUJRCG-UHFFFAOYSA-N[6].
  • Saponin D's chemical formula is recorded as C₄₈H₇₈O₁₇[7].
  • Saponin D's subclass of is recorded as protostane/dammarane triterpenoid[8].
  • Saponin D's PubChem CID is recorded as 131752825[9].
  • Saponin D's ChEBI ID is recorded as 172857[10].
  • Saponin D's found in taxon is recorded as Tetrapleura tetraptera[11].
  • Saponin D's Human Metabolome Database ID is recorded as HMDB0040468[12].
  • Saponin D's KNApSAcK ID is recorded as C00057560[13].
  • Saponin D's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+926.523901036'}[14].
  • Saponin D's DSSTox substance ID is recorded as DTXSID201101029[15].
  • Saponin D's UniChem compound ID is recorded as 32018970[16].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . Chemical Abstracts Service. Retrieved . 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] ↑ . Use of liquid chromatography—thermospray mass spectrometry in phytochemical analysis of crude plant extracts. wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . 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). Saponin D. Retrieved May 3, 2026, from https://4ort.xyz/entity/saponin-d
MLA “Saponin D.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/saponin-d.
BibTeX @misc{4ortxyz_saponin-d_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Saponin D}}, year = {2026}, url = {https://4ort.xyz/entity/saponin-d}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Saponin D — https://4ort.xyz/entity/saponin-d (retrieved 2026-05-03)

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