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(4aR/S)-sclareol

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q105343171
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(4aR/S)-sclareol

Summary

(4aR/S)-sclareol is a group of stereoisomers[1].

Key Facts

  • (4aR/S)-sclareol's instance of is recorded as group of stereoisomers[2].
  • (4aR/S)-sclareol's canonical SMILES is recorded as OC(C=C)(C)CCC1C(O)(C)CCC2C(C)(C)CCCC12C[3].
  • (4aR/S)-sclareol's InChI is recorded as InChI=1S/C20H36O2/c1-7-18(4,21)13-9-16-19(5)12-8-11-17(2,3)15(19)10-14-20(16,6)22/h7,15-16,21-22H,1,8-14H2,2-6H3/t15?,16-,18+,19+,20-/m1/s1[4].
  • (4aR/S)-sclareol's InChIKey is recorded as XVULBTBTFGYVRC-FFADBYAMSA-N[5].
  • (4aR/S)-sclareol's chemical formula is recorded as C₂₀H₃₆O₂[6].
  • (4aR/S)-sclareol's subclass of is recorded as labdanes[7].
  • (4aR/S)-sclareol's PubChem CID is recorded as 73114[8].
  • (4aR/S)-sclareol's found in taxon is recorded as Juniperus excelsa[9].
  • (4aR/S)-sclareol's found in taxon is recorded as Cistus creticus[10].
  • (4aR/S)-sclareol's found in taxon is recorded as Nicotiana glutinosa[11].
  • (4aR/S)-sclareol's found in taxon is recorded as Juniperus scopulorum[12].
  • (4aR/S)-sclareol's isomeric SMILES is recorded as C=CC@(O)CC[C@@H]1[C@@]2(C)CCCC(C)(C)C2CC[C@@]1(C)OC@(O)CC[C@@H]1[C@@]2(C)CCCC(C)(C)C2CC[C@@]1(C)O">[13].
  • (4aR/S)-sclareol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+308.271530392'}[14].
  • (4aR/S)-sclareol's SureChEMBL ID is recorded as 1245831[15].
  • (4aR/S)-sclareol's MassBank accession ID is recorded as MSBNK-RIKEN_NPDepo-NGA00933[16].
  • (4aR/S)-sclareol's MassBank accession ID is recorded as MSBNK-RIKEN_NPDepo-NGA00934[17].
  • (4aR/S)-sclareol's MassBank accession ID is recorded as MSBNK-RIKEN_NPDepo-NGA00935[18].
  • (4aR/S)-sclareol's MassBank accession ID is recorded as MSBNK-RIKEN_NPDepo-NGA00936[19].
  • (4aR/S)-sclareol's UniChem compound ID is recorded as 22793435[20].

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] ↑ . Diterpenes from the berries of Juniperus excelsa. wikidata.org.
  9. [10] ↑ . Chemical analysis and antimicrobial activity of the resin Ladano, of its essential oil and of the isolated compounds. wikidata.org.
  10. [11] ↑ . Biosynthesis of labdenediol and sclareol in cell-free extracts from trichomes of Nicotiana glutinosa. wikidata.org.
  11. [12] ↑ . Diterpenes from the berries of Juniperus excelsa. wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  16. [17] ↑ . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  17. [18] ↑ . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  18. [19] ↑ . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  19. [20] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). (4aR/S)-sclareol. Retrieved May 3, 2026, from https://4ort.xyz/entity/-4ar-s-sclareol
MLA “(4aR/S)-sclareol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/-4ar-s-sclareol.
BibTeX @misc{4ortxyz_-4ar-s-sclareol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(4aR/S)-sclareol}}, year = {2026}, url = {https://4ort.xyz/entity/-4ar-s-sclareol}, note = {Accessed: 2026-05-03}}
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