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psi-Taraxasterol

group of stereoisomers with the chemical formula C₃₀H₅₀O
ChemicalSubstance group_of_stereoisomers Q105178870
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psi-Taraxasterol

Summary

psi-Taraxasterol is a group of stereoisomers[1].

Key Facts

  • psi-Taraxasterol's instance of is recorded as group of stereoisomers[2].
  • psi-Taraxasterol's canonical SMILES is recorded as OC1CCC2(C)C(CCC3(C)C2CCC4C5C(C(=CCC5(C)CCC43C)C)C)C1(C)C[3].
  • psi-Taraxasterol's InChI is recorded as InChI=1S/C30H50O/c1-19-11-14-27(5)17-18-29(7)21(25(27)20(19)2)9-10-23-28(6)15-13-24(31)26(3,4)22(28)12-16-30(23,29)8/h11,20-25,31H,9-10,12-18H2,1-8H3/t20-,21?,22?,23?,24+,25?,27-,28+,29-,30-/m1/s1[4].
  • psi-Taraxasterol's InChIKey is recorded as NGFFRJBGMSPDMS-VPUBHQHASA-N[5].
  • psi-Taraxasterol's chemical formula is recorded as C₃₀H₅₀O[6].
  • psi-Taraxasterol's subclass of is recorded as taraxastane / ursane triterpenoid[7].
  • psi-Taraxasterol's PubChem CID is recorded as 5270605[8].
  • psi-Taraxasterol's found in taxon is recorded as Atractylodes lancea[9].
  • psi-Taraxasterol's found in taxon is recorded as Camellia japonica[10].
  • psi-Taraxasterol's found in taxon is recorded as Camellia sasanqua[11].
  • psi-Taraxasterol's found in taxon is recorded as Taraxacum japonicum[12].
  • psi-Taraxasterol's found in taxon is recorded as Camellia oleifera[13].
  • psi-Taraxasterol's isomeric SMILES is recorded as CC1=CC[C@]2(C)CC[C@]3(C)C(CCC4[C@@]5(C)CCC@HC(C)(C)C5CC[C@]43C)C2[C@@H]1CC@HC(C)(C)C5CC[C@]43C)C2[C@@H]1C">[14].
  • psi-Taraxasterol's Human Metabolome Database ID is recorded as HMDB0302321[15].
  • psi-Taraxasterol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+426.38616622'}[16].
  • psi-Taraxasterol's SureChEMBL ID is recorded as 29985785[17].
  • psi-Taraxasterol's UniChem compound ID is recorded as 44925571[18].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . Phytochemical and Pharmacological Studies on Chinese Changzhu. wikidata.org.
  9. [10] ↑ . Triterpene Alcohols from Camellia and Sasanqua Oils and Their Anti-inflammatory Effects. wikidata.org.
  10. [11] ↑ . Triterpene Alcohols from Camellia and Sasanqua Oils and Their Anti-inflammatory Effects. wikidata.org.
  11. [12] ↑ . Anti-carcinogenic activity of Taraxacum plant. II.. wikidata.org.
  12. [13] ↑ . Triterpene Alcohols from Camellia and Sasanqua Oils and Their Anti-inflammatory Effects. wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). psi-Taraxasterol. Retrieved May 3, 2026, from https://4ort.xyz/entity/psi-taraxasterol
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BibTeX @misc{4ortxyz_psi-taraxasterol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{psi-Taraxasterol}}, year = {2026}, url = {https://4ort.xyz/entity/psi-taraxasterol}, note = {Accessed: 2026-05-03}}
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