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(3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

group of stereoisomers with the chemical formula C₂₉H₄₈O₂
ChemicalSubstance group_of_stereoisomers Q105196224
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(3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

Summary

(3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol is a group of stereoisomers[1].

Key Facts

  • (3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol's instance of is recorded as group of stereoisomers[2].
  • (3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol's canonical SMILES is recorded as OC1CC2=CCC3C(CCC4(C)C(CCC34)C(C)CCC(O)(C=C)C(C)C)C2(C)CC1[3].
  • (3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol's InChI is recorded as InChI=1S/C29H48O2/c1-7-29(31,19(2)3)17-12-20(4)24-10-11-25-23-9-8-21-18-22(30)13-15-27(21,5)26(23)14-16-28(24,25)6/h7-8,19-20,22-26,30-31H,1,9-18H2,2-6H3/t20?,22-,23?,24?,25?,26?,27?,28?,29?/m0/s1[4].
  • (3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol's InChIKey is recorded as OPGVEUGCNGNPSX-FHOLUHAZSA-N[5].
  • (3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol's chemical formula is recorded as C₂₉H₄₈O₂[6].
  • (3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol's subclass of is recorded as stigmastan-type steroid[7].
  • (3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol's PubChem CID is recorded as 5321131[8].
  • (3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol's found in taxon is recorded as Tydemania expeditionis[9].
  • (3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol's found in taxon is recorded as hijiki[10].
  • (3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol's isomeric SMILES is recorded as C=CC(O)(CCC(C)C1CCC2C3CC=C4CC@@HCCC4(C)C3CCC12C)C(C)C[11].
  • (3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+428.365430776'}[12].
  • (3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol's UniChem compound ID is recorded as 51155403[13].

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] ↑ . Steroids with inhibitory activity against the prostate cancer cells and chemical diversity of marine alga Tydemania expeditionis. wikidata.org.
  9. [10] ↑ . 24(S)-Saringosterol from edible marine seaweed Sargassum fusiforme is a novel selective LXRβ agonist.. wikidata.org.
  10. [11] ↑ . wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). (3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol. Retrieved May 3, 2026, from https://4ort.xyz/entity/-3s-17-5-hydroxy-5-propan-2-ylhept-6-en-2-yl-10-13-dimethyl-2-3-4-7-8-9-11-12-14-15-16-17-dodecahydro-1h-cyclopenta-a-phenanthren-3-ol
MLA “(3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/-3s-17-5-hydroxy-5-propan-2-ylhept-6-en-2-yl-10-13-dimethyl-2-3-4-7-8-9-11-12-14-15-16-17-dodecahydro-1h-cyclopenta-a-phenanthren-3-ol.
BibTeX @misc{4ortxyz_-3s-17-5-hydroxy-5-propan-2-ylhept-6-en-2-yl-10-13-dimethyl-2-3-4-7-8-9-11-12-14-15-16-17-dodecahydro-1h-cyclopenta-a-phenanthren-3-ol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol}}, year = {2026}, url = {https://4ort.xyz/entity/-3s-17-5-hydroxy-5-propan-2-ylhept-6-en-2-yl-10-13-dimethyl-2-3-4-7-8-9-11-12-14-15-16-17-dodecahydro-1h-cyclopenta-a-phenanthren-3-ol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (3S)-17-(5-hydroxy-5-propan-2-ylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol — https://4ort.xyz/entity/-3s-17-5-hydroxy-5-propan-2-ylhept-6-en-2-yl-10-13-dimethyl-2-3-4-7-8-9-11-12-14-15-16-17-dodecahydro-1h-cyclopenta-a-phenanthren-3-ol (retrieved 2026-05-03)

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