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stigmast-5-en-3-ol

group of stereoisomers with the chemical formula C₂₉H₅₀O
ChemicalSubstance group_of_stereoisomers Q104415282
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stigmast-5-en-3-ol

Summary

stigmast-5-en-3-ol is a group of stereoisomers[1].

Key Facts

  • stigmast-5-en-3-ol's instance of is recorded as group of stereoisomers[2].
  • stigmast-5-en-3-ol's canonical SMILES is recorded as OC1CC2=CCC3C(CCC4(C)C(CCC34)C(C)CCC(CC)C(C)C)C2(C)CC1[3].
  • stigmast-5-en-3-ol's InChI is recorded as InChI=1S/C29H50O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h10,19-21,23-27,30H,7-9,11-18H2,1-6H3/t20-,21-,23?,24+,25-,26+,27+,28+,29-/m1/s1[4].
  • stigmast-5-en-3-ol's InChIKey is recorded as KZJWDPNRJALLNS-BWRKXDIJSA-N[5].
  • stigmast-5-en-3-ol's chemical formula is recorded as C₂₉H₅₀O[6].
  • stigmast-5-en-3-ol's subclass of is recorded as stigmastan-type steroid[7].
  • stigmast-5-en-3-ol's PubChem CID is recorded as 22012[8].
  • stigmast-5-en-3-ol's found in taxon is recorded as Cyrtocarpa[9].
  • stigmast-5-en-3-ol's found in taxon is recorded as Qualea labouriauana[10].
  • stigmast-5-en-3-ol's found in taxon is recorded as Ocimum gratissimum[11].
  • stigmast-5-en-3-ol's found in taxon is recorded as Senna polyphylla[12].
  • stigmast-5-en-3-ol's found in taxon is recorded as Ageratina altissima[13].
  • stigmast-5-en-3-ol's found in taxon is recorded as Monteverdia retusa[14].
  • stigmast-5-en-3-ol's found in taxon is recorded as Cinnamomum triplinerve[15].
  • stigmast-5-en-3-ol's found in taxon is recorded as Sonchus[16].
  • stigmast-5-en-3-ol's found in taxon is recorded as Phanera integrifolia[17].
  • stigmast-5-en-3-ol's found in taxon is recorded as Andrographis[18].
  • stigmast-5-en-3-ol's found in taxon is recorded as Taraxacum croceum[19].
  • stigmast-5-en-3-ol's found in taxon is recorded as Phanera vahlii[20].
  • stigmast-5-en-3-ol's found in taxon is recorded as Taraxacum lapponicum[21].
  • stigmast-5-en-3-ol's found in taxon is recorded as Patrinia villosa[22].
  • stigmast-5-en-3-ol's found in taxon is recorded as Leptogorgia rubroflavescens[23].
  • stigmast-5-en-3-ol's isomeric SMILES is recorded as CCC@HC(C)CC@HC(C)C">[24].
  • stigmast-5-en-3-ol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+414.38616622'}[25].
  • stigmast-5-en-3-ol's SureChEMBL ID is recorded as 3128216[26].

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] ↑ . Anti-ulcer activity of Cyrtocarpa procera analogous to that of Amphipterygium adstringens, both assayed on the experimental gastric injury in rats. wikidata.org.
  9. [10] ↑ . C-methyl phenolics from Qualea species. wikidata.org.
  10. [11] ↑ . Chemical Composition and Biological Activity of the Tanzanian Plant Ocimum Suave. wikidata.org.
  11. [12] ↑ . Anthraquinones of Cassia marginata seeds. wikidata.org.
  12. [13] ↑ . Further heliangolides and guaianolides from Eupatorium altissimum. wikidata.org.
  13. [14] ↑ . 3-Oxo-friedelan-20α-OIC acid from gymnosporia emarginata. wikidata.org.
  14. [15] ↑ . Oxoaporphine Alkaloids from the Wood of Phoebe cinnamomifolia. wikidata.org.
  15. [16] ↑ . Herbal remedies of the Maritime Indians: phytosterols and triterpenes of 67 plants. wikidata.org.
  16. [17] ↑ . β-Sitosterol and flavonoids isolated from Bauhinia malabarica found during screening for Wnt signaling inhibitory activity. wikidata.org.
  17. [18] ↑ . The role of leucine in isoprenoid metabolism. Incorporation of [3-13C]leucine and of [2-3H,4-14C]-β,β-dimethylacrylic acid into phytosterols by tissue cultures of Andrographis paniculata. wikidata.org.
  18. [19] ↑ . Supercritical fluid extraction of dandelion leaves. wikidata.org.
  19. [20] ↑ . β-Sitosterol and flavonoids isolated from Bauhinia malabarica found during screening for Wnt signaling inhibitory activity. wikidata.org.
  20. [21] ↑ . Supercritical fluid extraction of dandelion leaves. wikidata.org.
  21. [22] ↑ . Chemical composition and antioxidant activity of volatiles from Patrinia Villosa Juss obtained by optimized supercritical fluid extraction. wikidata.org.
  22. [23] ↑ . Sterol composition of some gorgonians from the Senegalese coast. wikidata.org.
  23. [24] ↑ . wikidata.org.
  24. [25] ↑ . wikidata.org.
  25. [26] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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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). stigmast-5-en-3-ol. Retrieved May 3, 2026, from https://4ort.xyz/entity/stigmast-5-en-3-ol
MLA “stigmast-5-en-3-ol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/stigmast-5-en-3-ol.
BibTeX @misc{4ortxyz_stigmast-5-en-3-ol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{stigmast-5-en-3-ol}}, year = {2026}, url = {https://4ort.xyz/entity/stigmast-5-en-3-ol}, note = {Accessed: 2026-05-03}}
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