lupeol

ChemicalSubstance group_of_stereoisomers Q105170364
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lupeol

Summary

lupeol is a group of stereoisomers[1].

Key Facts

  • lupeol's instance of is recorded as group of stereoisomers[2].
  • lupeol's canonical SMILES is recorded as OC1CCC2(C)C(CCC3(C)C2CCC4C5C(C(=C)C)CCC5(C)CCC43C)C1(C)C[3].
  • lupeol's InChI is recorded as InChI=1S/C30H50O/c1-19(2)20-11-14-27(5)17-18-29(7)21(25(20)27)9-10-23-28(6)15-13-24(31)26(3,4)22(28)12-16-30(23,29)8/h20-25,31H,1,9-18H2,2-8H3/t20-,21+,22-,23+,24-,25+,27+,28-,29?,30+/m0/s1[4].
  • lupeol's InChIKey is recorded as MQYXUWHLBZFQQO-JGGBMTAGSA-N[5].
  • lupeol's chemical formula is recorded as C₃₀H₅₀O[6].
  • lupeol's subclass of is recorded as lupane[7].
  • lupeol's PubChem CID is recorded as 73040[8].
  • lupeol's isomeric SMILES is recorded as C=C(C)[C@@H]1CC[C@]2(C)CCC3(C)C@H[C@@H]12C@H[C@@H]12">[9].
  • lupeol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+426.38616621999995'}[10].
  • lupeol's SureChEMBL ID is recorded as 561024[11].
  • lupeol's UniChem compound ID is recorded as 23614952[12].
  • lupeol's Probes And Drugs ID is recorded as PD118162[13].

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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). lupeol. Retrieved May 3, 2026, from https://4ort.xyz/entity/lupeol-q105170364
MLA “lupeol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/lupeol-q105170364.
BibTeX @misc{4ortxyz_lupeol-q105170364_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{lupeol}}, year = {2026}, url = {https://4ort.xyz/entity/lupeol-q105170364}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): lupeol — https://4ort.xyz/entity/lupeol-q105170364 (retrieved 2026-05-03)

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