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(4bS)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol

group of stereoisomers with the chemical formula C₂₀H₃₀O
ChemicalSubstance group_of_stereoisomers Q105229734
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(4bS)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol

Summary

(4bS)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol is a group of stereoisomers[1].

Key Facts

  • (4bS)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol's instance of is recorded as group of stereoisomers[2].
  • (4bS)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol's canonical SMILES is recorded as OC=1C=C2C(=CC1C(C)C)CCC3C2(C)CCCC3(C)C[3].
  • (4bS)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol's InChI is recorded as InChI=1S/C20H30O/c1-13(2)15-11-14-7-8-18-19(3,4)9-6-10-20(18,5)16(14)12-17(15)21/h11-13,18,21H,6-10H2,1-5H3/t18?,20-/m1/s1[4].
  • (4bS)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol's InChIKey is recorded as QXNWVJOHUAQHLM-ROPPNANJSA-N[5].
  • (4bS)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol's chemical formula is recorded as C₂₀H₃₀O[6].
  • (4bS)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol's subclass of is recorded as abietane diterpenoid[7].
  • (4bS)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol's PubChem CID is recorded as 403773[8].
  • (4bS)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol's found in taxon is recorded as Harpagophytum procumbens[9].
  • (4bS)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol's found in taxon is recorded as Salvia kronenburgii[10].
  • (4bS)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol's found in taxon is recorded as Salvia ceratophylla[11].
  • (4bS)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol's found in taxon is recorded as Salvia prionitis[12].
  • (4bS)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol's isomeric SMILES is recorded as CC(C)c1cc2c(cc1O)[C@@]1(C)CCCC(C)(C)C1CC2[13].
  • (4bS)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+286.22966558'}[14].
  • (4bS)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol's SureChEMBL ID is recorded as 13423521[15].
  • (4bS)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol's UniChem compound ID is recorded as 33998940[16].

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] ↑ . Identification of major and minor constituents of Harpagophytum procumbens (Devil's claw) using HPLC-SPE-NMR and HPLC-ESIMS/APCIMS.. wikidata.org.
  9. [10] ↑ . Terpenoids from Salvia nemorosa. wikidata.org.
  10. [11] ↑ . Diterpenoids from Salvia ceratophylla.. wikidata.org.
  11. [12] ↑ . Diterpenoids from Salvia prionitis. wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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MLA “(4bS)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/-4bs-2-isopropyl-4b-8-8-trimethyl-5-6-7-8a-9-10-hexahydrophenanthren-3-ol.
BibTeX @misc{4ortxyz_-4bs-2-isopropyl-4b-8-8-trimethyl-5-6-7-8a-9-10-hexahydrophenanthren-3-ol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(4bS)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol}}, year = {2026}, url = {https://4ort.xyz/entity/-4bs-2-isopropyl-4b-8-8-trimethyl-5-6-7-8a-9-10-hexahydrophenanthren-3-ol}, note = {Accessed: 2026-05-03}}
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