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moronic acid

chemical compound
ChemicalSubstance type_of_chemical_entity Q6913266
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moronic acid

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 (15 views/month).[2]

Key Facts

  • moronic acid's instance of is recorded as type of chemical entity[3].
  • moronic acid's chemical structure is recorded as Moronic acid structure.png[4].
  • moronic acid's CAS Registry Number is recorded as 6713-27-5[5].
  • 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[6].
  • moronic acid's InChI is recorded as InChI=1S/C30H46O3/c1-25(2)14-16-30(24(32)33)17-15-28(6)19(20(30)18-25)8-9-22-27(5)12-11-23(31)26(3,4)21(27)10-13-29(22,28)7/h18-19,21-22H,8-17H2,1-7H3,(H,32,33)/t19-,21+,22-,27+,28-,29-,30+/m1/s1[7].
  • moronic acid's InChIKey is recorded as UMYJVVZWBKIXQQ-QALSDZMNSA-N[8].
  • moronic acid's chemical formula is recorded as C₃₀H₄₆O₃[9].
  • moronic acid's subclass of is recorded as oleanane triterpenoid[10].
  • moronic acid's subclass of is recorded as carboxylic acid[11].
  • moronic acid's ChEMBL ID is recorded as CHEMBL472646[12].
  • moronic acid's Freebase ID is recorded as /m/0d_xd7[13].
  • moronic acid's UNII is recorded as XW8W7HC4JK[14].
  • moronic acid's ChemSpider ID is recorded as 429156[15].
  • moronic acid's PubChem CID is recorded as 489941[16].
  • moronic acid's ChEBI ID is recorded as 30815[17].
  • moronic acid's found in taxon is recorded as Orthopterygium[18].
  • moronic acid's found in taxon is recorded as Chisocheton macrophyllus[19].
  • moronic acid's found in taxon is recorded as Salvia pomifera[20].
  • moronic acid's found in taxon is recorded as Boronia inornata[21].
  • moronic acid's found in taxon is recorded as Waltheria viscosissima[22].
  • moronic acid's found in taxon is recorded as Acridocarpus vivy[23].
  • moronic acid's found in taxon is recorded as Xyris pterygoblephara[24].
  • moronic acid's found in taxon is recorded as Croton betulaster[25].
  • moronic acid's found in taxon is recorded as Phoradendron reichenbachianum[26].
  • moronic acid's found in taxon is recorded as Rhus chinensis[27].

Why It Matters

moronic acid ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (15 views/month).[2] It is known by 3 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] ↑ . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . PubChem. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . ChEMBL. Retrieved . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . Q2311683. Retrieved . wikidata.org.
  14. [16] ↑ . PubChem. Retrieved . wikidata.org.
  15. [17] ↑ . ChEBI. Retrieved . wikidata.org.
  16. [18] ↑ . 3-oxo-6β-hydroxyolean-18-en-28-oic acid from orthopterygium huancuy. wikidata.org.
  17. [19] ↑ . 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.
  18. [20] ↑ . Di- and triterpenoids of Salvia pomifera. wikidata.org.
  19. [21] ↑ . Terpenoids, alkaloids and coumarins from Boronia inornata and Boronia gracilipes. wikidata.org.
  20. [22] ↑ . Four known triterpenoids isolated from three Brazilian plants:1H and13C chemical shift assignments. wikidata.org.
  21. [23] ↑ . Cytotoxic triterpenoids from Acridocarpus vivy from the Madagascar rain forest.. wikidata.org.
  22. [24] ↑ . Dihydroisocoumarin from Xyris pterygoblephara active against dermatophyte fungi. wikidata.org.
  23. [25] ↑ . Triterpenes of Croton betulaster (Euphorbiaceae). wikidata.org.
  24. [26] ↑ . 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.
  25. [27] ↑ . A new benzofuranone and anti-HIV constituents from the stems of Rhus chinensis. 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). moronic acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/moronic-acid
MLA “moronic acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 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: 2026-05-03}}
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 2026-05-03)

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