Home › Entities › type_of_chemical_entity › 3β-androstanediol

3β-androstanediol

chemical compound
ChemicalSubstance type_of_chemical_entity Q4641516
Press Enter · cited answer in seconds

3β-androstanediol

Summary

3β-androstanediol is a type of chemical entity[1]. 3β-androstanediol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (15 views/month).[2]

Key Facts

  • 3β-androstanediol's instance of is recorded as type of chemical entity[3].
  • 3β-androstanediol's chemical structure is recorded as 3beta-Androstanediol.svg[4].
  • 3β-androstanediol's CAS Registry Number is recorded as 571-20-0[5].
  • 3β-androstanediol's EC number is recorded as 209-334-3[6].
  • 3β-androstanediol's canonical SMILES is recorded as CC12CCC(CC1CCC3C2CCC4(C3CCC4O)C)O[7].
  • 3β-androstanediol's InChI is recorded as InChI=1S/C19H32O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12-17,20-21H,3-11H2,1-2H3/t12-,13-,14-,15-,16-,17-,18-,19-/m0/s1[8].
  • 3β-androstanediol's InChIKey is recorded as CBMYJHIOYJEBSB-YSZCXEEOSA-N[9].
  • 3β-androstanediol's chemical formula is recorded as C₁₉H₃₂O₂[10].
  • 3β-androstanediol's subclass of is recorded as (1S,3aS,3bR,5aS,9aS,9bS,11aS)-9a,11a-dimethyl-tetradecahydro-1H-cyclopenta[a]phenanthrene-1,7-diol[11].
  • 3β-androstanediol's part of is recorded as 5alpha-androstane-3beta,17beta-diol dehydrogenase activity[12].
  • 3β-androstanediol's ChEMBL ID is recorded as CHEMBL316048[13].
  • 3β-androstanediol's PDB structure ID is recorded as 3KM0[14].
  • 3β-androstanediol's PDB structure ID is recorded as 1LHO[15].
  • 3β-androstanediol's PDB structure ID is recorded as 3UZX[16].
  • 3β-androstanediol's Freebase ID is recorded as /m/02kckx7[17].
  • 3β-androstanediol's UNII is recorded as 6J0K4253QD[18].
  • 3β-androstanediol's ChemSpider ID is recorded as 211834[19].
  • 3β-androstanediol's PubChem CID is recorded as 242332[20].
  • 3β-androstanediol's KEGG ID is recorded as C12525[21].
  • 3β-androstanediol's ChEBI ID is recorded as 18329[22].
  • 3β-androstanediol's found in taxon is recorded as Daphnia magna[23].
  • 3β-androstanediol's DrugBank ID is recorded as DB03882[24].
  • 3β-androstanediol's Reaxys registry number is recorded as 2559488[25].
  • 3β-androstanediol's isomeric SMILES is recorded as C[C@]12CCC@@HOC@@HO">[26].
  • 3β-androstanediol's Human Metabolome Database ID is recorded as HMDB0000493[27].

Why It Matters

3β-androstanediol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (15 views/month).[2] 3β-androstanediol is known by 14 alternative names across languages and contexts.[28]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  11. [13] ↑ . ChEMBL. Retrieved . wikidata.org.
  12. [14] ↑ . Protein Data Bank. Retrieved . wikidata.org.
  13. [15] ↑ . Protein Data Bank. Retrieved . wikidata.org.
  14. [16] ↑ . Protein Data Bank. Retrieved . wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  17. [19] ↑ . Q2311683. Retrieved . wikidata.org.
  18. [20] ↑ . PubChem. Retrieved . wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . ChEMBL. Retrieved . wikidata.org.
  21. [23] ↑ . Changes in the metabolic elimination profile of testosterone following exposure of the crustacean Daphnia magna to tributyltin. wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . ChEBI. Retrieved . wikidata.org.
  24. [26] ↑ . PubChem. Retrieved . wikidata.org.
  25. [27] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] ↑ . Wikidata aliases. wikidata.org.

📑 Cite this page

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). 3β-androstanediol. Retrieved October 7, 2026, from https://4ort.xyz/entity/3-androstanediol
MLA “3β-androstanediol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 7 Oct. 2026, https://4ort.xyz/entity/3-androstanediol.
BibTeX @misc{4ortxyz_3-androstanediol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{3β-androstanediol}}, year = {2026}, url = {https://4ort.xyz/entity/3-androstanediol}, note = {Accessed: 2026-10-07}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 3β-androstanediol — https://4ort.xyz/entity/3-androstanediol (retrieved 2026-10-07)

Canonical URL: https://4ort.xyz/entity/3-androstanediol · Last refreshed:

Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 23w ago · KaleemBot bot · 2026-04-30 view diff on Wikidata ↗
    Subclass of → (1S,3aS,3bR,5aS,9aS,9bS,11aS)-9a,11a-dimethyl-tetradecahydro-1H-cyclopenta[a]phenanthrene-1,7-diol
    Found in taxon → Daphnia magna
    Mass → {'unit': 'Q483261', 'amount': '+292.24'}
    Part of → 5alpha-androstane-3beta,17beta-diol dehydrogenase activity
    + 6 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ Added [[wikipedia:ur:3-بیٹا-اینڈرو اسٹین ڈائی اول]]"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.