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Vinaginsenoside R6

group of stereoisomers with the chemical formula C₄₇H₈₀O₁₉
ChemicalSubstance group_of_stereoisomers Q105163535
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Vinaginsenoside R6

Summary

Vinaginsenoside R6 is a group of stereoisomers[1].

Key Facts

  • Vinaginsenoside R6's instance of is recorded as group of stereoisomers[2].
  • Vinaginsenoside R6's CAS Registry Number is recorded as 156009-82-4[3].
  • Vinaginsenoside R6's canonical SMILES is recorded as OCC1OC(OCC2OC(OC3CC4(C)C(CC(O)C5C(CCC54C)C6(OC(CC6)C(O)(C)C)C)C7(C)CCC(O)C(C)(C)C37)C(OC8OCC(O)C(O)C8O)C(O)C2O)C(O)C(O)C1O[4].
  • Vinaginsenoside R6's InChI is recorded as InChI=1S/C47H80O19/c1-42(2)27(51)10-12-44(5)26-15-21(49)29-20(47(8)14-11-28(66-47)43(3,4)59)9-13-45(29,6)46(26,7)16-23(38(42)44)62-41-37(65-40-35(57)30(52)22(50)18-60-40)34(56)32(54)25(64-41)19-61-39-36(58)33(55)31(53)24(17-48)63-39/h20-41,48-59H,9-19H2,1-8H3[5].
  • Vinaginsenoside R6's InChIKey is recorded as MGROSLQKCJXSBT-UHFFFAOYSA-N[6].
  • Vinaginsenoside R6's chemical formula is recorded as C₄₇H₈₀O₁₉[7].
  • Vinaginsenoside R6's subclass of is recorded as protostane/dammarane triterpenoid[8].
  • Vinaginsenoside R6's PubChem CID is recorded as 75054976[9].
  • Vinaginsenoside R6's ChEBI ID is recorded as 191508[10].
  • Vinaginsenoside R6's found in taxon is recorded as Panax vietnamensis[11].
  • Vinaginsenoside R6's found in taxon is recorded as Panax japonicus[12].
  • Vinaginsenoside R6's Human Metabolome Database ID is recorded as HMDB0040420[13].
  • Vinaginsenoside R6's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+948.52938034'}[14].
  • Vinaginsenoside R6's SureChEMBL ID is recorded as 29934832[15].
  • Vinaginsenoside R6's DSSTox substance ID is recorded as DTXSID401101601[16].
  • Vinaginsenoside R6's UniChem compound ID is recorded as 32018110[17].

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] ↑ . Dammarane-type triterpene saponins from Panax japonicus. wikidata.org.
  11. [12] ↑ . Dammarane saponins of leaves of Panax pseudo-ginseng subsp. himalaicus. wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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BibTeX @misc{4ortxyz_vinaginsenoside-r6_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Vinaginsenoside R6}}, year = {2026}, url = {https://4ort.xyz/entity/vinaginsenoside-r6}, note = {Accessed: 2026-05-03}}
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