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3-O-Acetylhamayne

chemical compound
ChemicalSubstance group_of_stereoisomers Q27114151
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3-O-Acetylhamayne

Summary

3-O-Acetylhamayne is a group of stereoisomers[1].

Key Facts

  • 3-O-Acetylhamayne's instance of is recorded as group of stereoisomers[2].
  • 3-O-Acetylhamayne's canonical SMILES is recorded as CC(=O)OC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O[3].
  • 3-O-Acetylhamayne's chemical formula is recorded as C₁₈H₁₉NO₅[4].
  • 3-O-Acetylhamayne is a type of 5,10b-ethanophenanthridine alkaloid[5].
  • 3-O-Acetylhamayne's found in taxon is recorded as Crinum moorei[6].
  • 3-O-Acetylhamayne's found in taxon is recorded as Crinum macowanii[7].
  • 3-O-Acetylhamayne's found in taxon is recorded as Crinum bulbispermum[8].
  • 3-O-Acetylhamayne's found in taxon is recorded as Crossyne flava[9].
  • 3-O-Acetylhamayne's found in taxon is recorded as Brunsvigia josephinae[10].
  • 3-O-Acetylhamayne's found in taxon is recorded as Crinum latifolium[11].
  • 3-O-Acetylhamayne's found in taxon is recorded as Crinum asiaticum[12].
  • 3-O-Acetylhamayne's found in taxon is recorded as Crinum yemense[13].
  • 3-O-Acetylhamayne's found in taxon is recorded as Crinum album[14].
  • 3-O-Acetylhamayne's isomeric SMILES is recorded as CC(=O)O[C@@H]1C[C@H]2[C@@]3(C=C1)C@HOC@HO">[15].
  • 3-O-Acetylhamayne's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+329.126323'}[16].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . PubChem. Retrieved . wikidata.org.
  3. [4] ↑ . PubChem. Retrieved . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . Variation among three Crinum species in alkaloid content. wikidata.org.
  6. [7] ↑ . Variation among three Crinum species in alkaloid content. wikidata.org.
  7. [8] ↑ . Variation among three Crinum species in alkaloid content. wikidata.org.
  8. [9] ↑ . Alkaloids from Boophane flava. wikidata.org.
  9. [10] ↑ . Alkaloids from Brunsvigia josephinæ. wikidata.org.
  10. [11] ↑ . Alkaloidal constituents of Crinum latifolium and Crinum bulbispermum (amaryllidaceae).. wikidata.org.
  11. [12] ↑ . Chemical constituents of Crinum asiaticum L. var. sinicum Baker and their cytotoxic activities. wikidata.org.
  12. [13] ↑ . New crinine-type alkaloids with inhibitory effect on induction of inducible nitric oxide synthase from Crinum yemense.. wikidata.org.
  13. [14] ↑ . New crinine-type alkaloids with inhibitory effect on induction of inducible nitric oxide synthase from Crinum yemense.. wikidata.org.
  14. [15] ↑ . PubChem. Retrieved . wikidata.org.
  15. [16] ↑ . PubChem. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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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. 12w ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Isomeric smiles → CC(=O)O[C@@H]1C[C@H]2[C@@]3(C=C1)[C@H](CN2CC4=CC5=C(C=C34)OC
    Found in taxon → Crinum moorei, Crinum macowanii, Crinum bulbispermum +6
    Subclass of → 5,10b-ethanophenanthridine alkaloid
    Instance of → group of stereoisomers
    + 13 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]]"
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