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beta-Amyrone

group of stereoisomers with the chemical formula C₃₀H₄₈O
ChemicalSubstance group_of_stereoisomers Q72443179
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beta-Amyrone

Summary

beta-Amyrone is a group of stereoisomers[1].

Key Facts

  • beta-Amyrone's instance of is recorded as group of stereoisomers[2].
  • beta-Amyrone's CAS Registry Number is recorded as 638-97-1[3].
  • beta-Amyrone's canonical SMILES is recorded as O=C1CCC2(C)C(CCC3(C)C2CC=C4C5CC(C)(C)CCC5(C)CCC43C)C1(C)C[4].
  • beta-Amyrone's InChI is recorded as InChI=1S/C30H48O/c1-25(2)15-16-27(5)17-18-29(7)20(21(27)19-25)9-10-23-28(6)13-12-24(31)26(3,4)22(28)11-14-30(23,29)8/h9,21-23H,10-19H2,1-8H3/t21-,22?,23-,27-,28+,29-,30-/m1/s1[5].
  • beta-Amyrone's InChIKey is recorded as LIIFBMGUDSHTOU-GCNWHLNUSA-N[6].
  • beta-Amyrone's chemical formula is recorded as C₃₀H₄₈O[7].
  • beta-Amyrone's subclass of is recorded as oleanane triterpenoid[8].
  • beta-Amyrone's PubChem CID is recorded as 6454747[9].
  • beta-Amyrone's found in taxon is recorded as Diospyros morrisiana[10].
  • beta-Amyrone's found in taxon is recorded as Salvia palaefolia[11].
  • beta-Amyrone's found in taxon is recorded as Adiantum capillus-veneris[12].
  • beta-Amyrone's isomeric SMILES is recorded as CC1(C)CC[C@]2(C)CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CCC(=O)C(C)(C)C5CC[C@]43C)[C@H]2C1[13].
  • beta-Amyrone's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+424.370516156'}[14].
  • beta-Amyrone's SureChEMBL ID is recorded as 2453965[15].
  • beta-Amyrone's DSSTox substance ID is recorded as DTXSID20980370[16].
  • beta-Amyrone's DSSTOX compound identifier is recorded as DTXCID701407648[17].
  • beta-Amyrone's UniChem compound ID is recorded as 31458220[18].

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] ↑ . wikidata.org.
  8. [9] ↑ . PubChem. Retrieved . wikidata.org.
  9. [10] ↑ . Cytotoxic components of Diospyros morrisiana. wikidata.org.
  10. [11] ↑ . Study of Salvia palaefolia: Absolute Configuration of Glechomafuran. wikidata.org.
  11. [12] ↑ . Fern Constituents: Triterpenoids from Adiantum capillus-veneris.. wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . UniChem. 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). beta-Amyrone. Retrieved May 3, 2026, from https://4ort.xyz/entity/beta-amyrone
MLA “beta-Amyrone.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/beta-amyrone.
BibTeX @misc{4ortxyz_beta-amyrone_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{beta-Amyrone}}, year = {2026}, url = {https://4ort.xyz/entity/beta-amyrone}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): beta-Amyrone — https://4ort.xyz/entity/beta-amyrone (retrieved 2026-05-03)

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