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Majoroside F1

group of stereoisomers with the chemical formula C₄₈H₈₂O₁₉
ChemicalSubstance group_of_stereoisomers Q104992299
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Majoroside F1

Summary

Majoroside F1 is a group of stereoisomers[1].

Key Facts

  • Majoroside F1's instance of is recorded as group of stereoisomers[2].
  • Majoroside F1's CAS Registry Number is recorded as 114128-16-4[3].
  • Majoroside F1's canonical SMILES is recorded as OCC1OC(OC2C(O)C(O)C(OC2OC3CCC4(C)C(CCC5(C)C4CC(O)C6C(CCC65C)C(OC7OC(CO)C(O)C(O)C7O)(C)CCC(O)C(=C)C)C3(C)C)CO)C(O)C(O)C1O[4].
  • Majoroside F1's InChI is recorded as InChI=1S/C48H82O19/c1-21(2)23(52)10-16-48(8,67-42-39(61)36(58)33(55)26(19-50)63-42)22-9-14-47(7)31(22)24(53)17-29-45(5)13-12-30(44(3,4)28(45)11-15-46(29,47)6)65-43-40(37(59)34(56)27(20-51)64-43)66-41-38(60)35(57)32(54)25(18-49)62-41/h22-43,49-61H,1,9-20H2,2-8H3[5].
  • Majoroside F1's InChIKey is recorded as FAJNTKKJVSRNEJ-UHFFFAOYSA-N[6].
  • Majoroside F1's chemical formula is recorded as C₄₈H₈₂O₁₉[7].
  • Majoroside F1's subclass of is recorded as protostane/dammarane triterpenoid[8].
  • Majoroside F1's PubChem CID is recorded as 13992211[9].
  • Majoroside F1's ChEBI ID is recorded as 172863[10].
  • Majoroside F1's found in taxon is recorded as American ginseng[11].
  • Majoroside F1's Human Metabolome Database ID is recorded as HMDB0030511[12].
  • Majoroside F1's KNApSAcK ID is recorded as C00056499[13].
  • Majoroside F1's KNApSAcK ID is recorded as C00057925[14].
  • Majoroside F1's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+962.545030404'}[15].
  • Majoroside F1's DSSTox substance ID is recorded as DTXSID201106750[16].
  • Majoroside F1's UniChem compound ID is recorded as 32005721[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 saponins from Panax quinquefolium and their inhibition activity on human breast cancer MCF-7 cells. wikidata.org.
  11. [12] ↑ . 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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APA 4ort.xyz Knowledge Graph. (2026). Majoroside F1. Retrieved May 3, 2026, from https://4ort.xyz/entity/majoroside-f1
MLA “Majoroside F1.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/majoroside-f1.
BibTeX @misc{4ortxyz_majoroside-f1_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Majoroside F1}}, year = {2026}, url = {https://4ort.xyz/entity/majoroside-f1}, note = {Accessed: 2026-05-03}}
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