moronic acid

chemical compound
ChemicalSubstance type_of_chemical_entity Q6913266
Press Enter · cited answer in seconds

Summary

moronic acid is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (39 views/month).[2]

Key Facts

  • moronic acid's instance of is recorded as type of chemical entity[3].
  • moronic acid's canonical SMILES is recorded as CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C(=O)O)C[4].
  • moronic acid's chemical formula is recorded as C₃₀H₄₆O₃[5].
  • moronic acid is a type of oleanane triterpenoid[6].
  • moronic acid is a type of carboxylic acid[7].
  • moronic acid's found in taxon is recorded as Orthopterygium[8].
  • moronic acid's found in taxon is recorded as Chisocheton macrophyllus[9].
  • moronic acid's found in taxon is recorded as Salvia pomifera[10].
  • moronic acid's found in taxon is recorded as Boronia inornata[11].
  • moronic acid's found in taxon is recorded as Waltheria viscosissima[12].
  • moronic acid's found in taxon is recorded as Acridocarpus vivy[13].
  • moronic acid's found in taxon is recorded as Xyris pterygoblephara[14].
  • moronic acid's found in taxon is recorded as Croton betulaster[15].
  • moronic acid's found in taxon is recorded as Phoradendron reichenbachianum[16].
  • moronic acid's found in taxon is recorded as Rhus chinensis[17].
  • moronic acid's found in taxon is recorded as Brucea javanica[18].
  • moronic acid's isomeric SMILES is recorded as C[C@@]12CC[C@]3(CCC(C=C3[C@H]1CC[C@H]4[C@]2(CC[C@@H]5[C@@]4(CCC(=O)C5(C)C)C)C)(C)C)C(=O)O[19].
  • moronic acid's mass is recorded as {'unit': 'dalton', 'amount': '+454.344695'}[20].

Why It Matters

moronic acid ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (39 views/month).[2] It is known by 3 alternative names across languages and contexts.[21]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . PubChem. Retrieved . wikidata.org.
  3. [5] ↑ . PubChem. Retrieved . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . 3-oxo-6β-hydroxyolean-18-en-28-oic acid from orthopterygium huancuy. wikidata.org.
  7. [9] ↑ . Phytochemical Studies on Meliaceous Plants. VIII. Structures and Inhibitory Effects on Epstein-Barr Virus Activation of Triterpenoids from Leaves of Chisocheton macrophyllus King.. wikidata.org.
  8. [10] ↑ . Di- and triterpenoids of Salvia pomifera. wikidata.org.
  9. [11] ↑ . Terpenoids, alkaloids and coumarins from Boronia inornata and Boronia gracilipes. wikidata.org.
  10. [12] ↑ . Four known triterpenoids isolated from three Brazilian plants:1H and13C chemical shift assignments. wikidata.org.
  11. [13] ↑ . Cytotoxic triterpenoids from Acridocarpus vivy from the Madagascar rain forest.. wikidata.org.
  12. [14] ↑ . Dihydroisocoumarin from Xyris pterygoblephara active against dermatophyte fungi. wikidata.org.
  13. [15] ↑ . Triterpenes of Croton betulaster (Euphorbiaceae). wikidata.org.
  14. [16] ↑ . Cytotoxic activity of moronic acid and identification of the new triterpene 3,4-seco-olean-18-ene-3,28-dioic acid from Phoradendron reichenbachianum. wikidata.org.
  15. [17] ↑ . A new benzofuranone and anti-HIV constituents from the stems of Rhus chinensis. wikidata.org.
  16. [18] ↑ . Separation and Determination of Chemical Constituents in the Roots ofRhus JavanicaL. Var.Roxburghiana. wikidata.org.
  17. [19] ↑ . PubChem. Retrieved . wikidata.org.
  18. [20] ↑ . PubChem. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [21] ↑ . 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). moronic acid. Retrieved October 16, 2026, from https://4ort.xyz/entity/moronic-acid
MLA “moronic acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 16 Oct. 2026, https://4ort.xyz/entity/moronic-acid.
BibTeX @misc{4ortxyz_moronic-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{moronic acid}}, year = {2026}, url = {https://4ort.xyz/entity/moronic-acid}, note = {Accessed: 2026-10-16}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): moronic acid — https://4ort.xyz/entity/moronic-acid (retrieved 2026-10-16)

Canonical URL: https://4ort.xyz/entity/moronic-acid · 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. 17w ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Instance of → type of chemical entity
    Subclass of → —
    Aliases → —
    Found in taxon → Orthopterygium, Chisocheton macrophyllus, Salvia pomifera +8
    + 3 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||tr */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/37300|batch #37300]]"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.