Hyoscyamine

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q27181620
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Hyoscyamine

Summary

Hyoscyamine is a group of stereoisomers[1].

Key Facts

  • Hyoscyamine's instance of is recorded as group of stereoisomers[2].
  • Hyoscyamine's canonical SMILES is recorded as CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3[3].
  • Hyoscyamine's InChI is recorded as InChI=1S/C17H23NO3/c1-18-13-7-8-14(18)10-15(9-13)21-17(20)16(11-19)12-5-3-2-4-6-12/h2-6,13-16,19H,7-11H2,1H3[4].
  • Hyoscyamine's InChIKey is recorded as RKUNBYITZUJHSG-UHFFFAOYSA-N[5].
  • Hyoscyamine's chemical formula is recorded as C₁₇H₂₃NO₃[6].
  • Hyoscyamine's subclass of is recorded as carboxylate ester[7].
  • Hyoscyamine's subclass of is recorded as tropane alkaloids[8].
  • Hyoscyamine's ChEMBL ID is recorded as CHEMBL9751[9].
  • Hyoscyamine's ChemSpider ID is recorded as 3534[10].
  • Hyoscyamine's PubChem CID is recorded as 3661[11].
  • Hyoscyamine's ChEBI ID is recorded as 104243[12].
  • Hyoscyamine's found in taxon is recorded as Datura quercifolia[13].
  • Hyoscyamine's found in taxon is recorded as Duboisia arenitensis[14].
  • Hyoscyamine's found in taxon is recorded as Anthotroche pannosa[15].
  • Hyoscyamine's found in taxon is recorded as Anthotroche myoporoides[16].
  • Hyoscyamine's found in taxon is recorded as Anthotroche walcottii[17].
  • Hyoscyamine's found in taxon is recorded as Datura discolor[18].
  • Hyoscyamine's found in taxon is recorded as Datura innoxia[19].
  • Hyoscyamine's found in taxon is recorded as Datura innoxia[20].
  • Hyoscyamine's found in taxon is recorded as Datura arborea[21].
  • Hyoscyamine's found in taxon is recorded as Datura alba[22].
  • Hyoscyamine's found in taxon is recorded as Scopolia lurida[23].
  • Hyoscyamine's found in taxon is recorded as Scopolia parviflora[24].
  • Hyoscyamine's found in taxon is recorded as Scopolia japonica[25].
  • Hyoscyamine's found in taxon is recorded as Duboisia myoporoides[26].

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] . PubChem. Retrieved . wikidata.org.
  5. [6] . PubChem. Retrieved . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . ChEMBL. Retrieved . wikidata.org.
  9. [10] . Q2311683. Retrieved . wikidata.org.
  10. [11] . PubChem. Retrieved . wikidata.org.
  11. [12] . ChEBI. Retrieved . wikidata.org.
  12. [13] . Fatal Datura poisoning: identification of atropine and scopolamine by high performance liquid chromatography/photodiode array/mass spectrometry. wikidata.org.
  13. [14] . The alkaloids of Duboisia leichhardtii: butropine and valtropine. wikidata.org.
  14. [15] . Isolation of ( - )-hyoscyamine from Anthotroche pannosa Endl. wikidata.org.
  15. [16] . Isolation of ( - )-hyoscyamine from Anthotroche pannosa Endl. wikidata.org.
  16. [17] . Isolation of ( - )-hyoscyamine from Anthotroche pannosa Endl. wikidata.org.
  17. [18] . Fatal Datura poisoning: identification of atropine and scopolamine by high performance liquid chromatography/photodiode array/mass spectrometry. wikidata.org.
  18. [19] . Fatal Datura poisoning: identification of atropine and scopolamine by high performance liquid chromatography/photodiode array/mass spectrometry. wikidata.org.
  19. [20] . Fatal Datura poisoning: identification of atropine and scopolamine by high performance liquid chromatography/photodiode array/mass spectrometry. wikidata.org.
  20. [21] . Fatal Datura poisoning: identification of atropine and scopolamine by high performance liquid chromatography/photodiode array/mass spectrometry. wikidata.org.
  21. [22] . Ueber Datura alba (Nees) und das Hyoscin. wikidata.org.
  22. [23] . Über die Bestandteile derScopolia atropoides. wikidata.org.
  23. [24] . Production of tropane alkaloids during de-differentiation of Scopolia parviflora calli. wikidata.org.
  24. [25] . Production of tropane alkaloids during de-differentiation of Scopolia parviflora calli. wikidata.org.
  25. [26] . The alkaloids of Duboisia leichhardtii: butropine and valtropine. 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). Hyoscyamine. Retrieved May 3, 2026, from https://4ort.xyz/entity/hyoscyamine-q27181620
MLA “Hyoscyamine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hyoscyamine-q27181620.
BibTeX @misc{4ortxyz_hyoscyamine-q27181620_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Hyoscyamine}}, year = {2026}, url = {https://4ort.xyz/entity/hyoscyamine-q27181620}, note = {Accessed: 2026-05-03}}
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