Rubrosterone

chemical compound
ChemicalSubstance type_of_chemical_entity Q7376194
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Rubrosterone

Summary

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

Key Facts

  • Rubrosterone's instance of is recorded as type of chemical entity[3].
  • Rubrosterone's chemical structure is recorded as Rubrosterone.svg[4].
  • Rubrosterone's CAS Registry Number is recorded as 19466-41-2[5].
  • Rubrosterone's canonical SMILES is recorded as O=C1C=C2C(CCC3(C(=O)CCC23O)C)C4(C)CC(O)C(O)CC14[6].
  • Rubrosterone's InChI is recorded as InChI=1S/C19H26O5/c1-17-9-15(22)14(21)8-12(17)13(20)7-11-10(17)3-5-18(2)16(23)4-6-19(11,18)24/h7,10,12,14-15,21-22,24H,3-6,8-9H2,1-2H3/t10-,12-,14+,15-,17+,18+,19+/m0/s1[7].
  • Rubrosterone's InChIKey is recorded as OMQCWEJQYPUGJG-DTDIXVHCSA-N[8].
  • Rubrosterone's chemical formula is recorded as C₁₉H₂₆O₅[9].
  • Rubrosterone's subclass of is recorded as 2,3,14-Trihydroxy-10,13-dimethyl-1,2,3,4,5,9,11,12,15,16-decahydrocyclopenta[a]phenanthrene-6,17-dione[10].
  • Rubrosterone's Freebase ID is recorded as /m/0h3qqb4[11].
  • Rubrosterone's UNII is recorded as ND477TPA7H[12].
  • Rubrosterone's PubChem CID is recorded as 12315102[13].
  • Rubrosterone's found in taxon is recorded as Cyanotis arachnoidea[14].
  • Rubrosterone's found in taxon is recorded as Serratula tinctoria[15].
  • Rubrosterone's found in taxon is recorded as Pfaffia glomerata[16].
  • Rubrosterone's found in taxon is recorded as Silene otites[17].
  • Rubrosterone's found in taxon is recorded as Hebanthe pulverulenta[18].
  • Rubrosterone's found in taxon is recorded as Achyranthes aspera var. rubrofusca[19].
  • Rubrosterone's found in taxon is recorded as Leuzea carthamoides[20].
  • Rubrosterone's found in taxon is recorded as Rhaponticum carthamoides[21].
  • Rubrosterone's found in taxon is recorded as Taxus wallichiana[22].
  • Rubrosterone's isomeric SMILES is recorded as O[C@@H]1C@HCC@([H])[C@]3(C)C1C@HCC@([H])[C@]3(C)C1">[23].
  • Rubrosterone's LIPID MAPS ID is recorded as LMST02020137[24].
  • Rubrosterone's mass is recorded as {'unit': 'Q483261', 'amount': '+334.178023932'}[25].
  • Rubrosterone's SureChEMBL ID is recorded as 13649197[26].
  • Rubrosterone's stereoisomer of is recorded as (2S,3R,5R,9S,10R,13S,14R)-2,3,14-trihydroxy-10,13-dimethyl-1,2,3,4,5,9,11,12,15,16-decahydrocyclopenta[a]phenanthrene-6,17-dione[27].

Why It Matters

Rubrosterone ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (3 views/month).[2]

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] . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . PubChem. Retrieved . wikidata.org.
  12. [14] . Phytoecdysteroid constituents from Cyanotis arachnoidea. wikidata.org.
  13. [15] . New Ecdysteroids from Serratula tinctoria. wikidata.org.
  14. [16] . A nortriterpenoid, triterpenoids and ecdysteroids from Pfaffia glomerata. wikidata.org.
  15. [17] . Complex phytoecdysteroid cocktail ofSilene otites(Caryophyllaceae). wikidata.org.
  16. [18] . Pfaffane-type nortriterpenoids from Pfaffia pulverulenta. wikidata.org.
  17. [19] . Inokosterone, an insect metamorphosing substance from Achyranthes fauriei. wikidata.org.
  18. [20] . Minor Ecdysteroid Components of Leuzea carthamoides. wikidata.org.
  19. [21] . Chemistry and pharmacology of Rhaponticum carthamoides: a review.. wikidata.org.
  20. [22] . Non-taxane compounds from the bark of Taxus yunnanensis. wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . LIPID MAPS. Retrieved . lipidmaps.org. Provenance: wikidata.org.
  23. [25] . wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.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). Rubrosterone. Retrieved May 3, 2026, from https://4ort.xyz/entity/rubrosterone
MLA “Rubrosterone.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/rubrosterone.
BibTeX @misc{4ortxyz_rubrosterone_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Rubrosterone}}, year = {2026}, url = {https://4ort.xyz/entity/rubrosterone}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Rubrosterone — https://4ort.xyz/entity/rubrosterone (retrieved 2026-05-03)

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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. 24d ago · KaleemBot bot · 2026-05-01 view diff on Wikidata ↗
    Subclass of 2,3,14-Trihydroxy-10,13-dimethyl-1,2,3,4,5,9,11,12,15,16-decahydrocyclopenta[a]phenanthrene-6,17-dione
    Found in taxon Cyanotis arachnoidea, Serratula tinctoria, Pfaffia glomerata +6
    Mass {'unit': 'Q483261', 'amount': '+334.178023932'}
    Stereoisomer of (2S,3R,5R,9S,10R,13S,14R)-2,3,14-trihydroxy-10,13-dimethyl-1,2,3,4,5,9,11,12,15,16-decahydrocyclopenta[a]phenanthrene-6,17-dione, 3-Epirubrosterone
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ Added [[wikipedia:ur:روبراسٹی رون]]"
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