hemanthidine

chemical compound
ChemicalSubstance group_of_stereoisomers Q27896532
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hemanthidine

Summary

hemanthidine is a group of stereoisomers[1].

Key Facts

  • hemanthidine's instance of is recorded as group of stereoisomers[2].
  • hemanthidine's CAS Registry Number is recorded as 466-73-9[3].
  • hemanthidine's canonical SMILES is recorded as COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O[4].
  • hemanthidine's InChI is recorded as InChI=1S/C17H19NO5/c1-21-9-2-3-17-11-6-13-12(22-8-23-13)5-10(11)16(20)18(7-15(17)19)14(17)4-9/h2-3,5-6,9,14-16,19-20H,4,7-8H2,1H3/t9-,14+,15+,16+,17+/m1/s1[5].
  • hemanthidine's InChIKey is recorded as ZSTPNQLNQBRLQF-UAQFGPKRSA-N[6].
  • hemanthidine's chemical formula is recorded as C₁₇H₁₉NO₅[7].
  • hemanthidine's subclass of is recorded as 5,10b-ethanophenanthridine alkaloid[8].
  • hemanthidine's ChEMBL ID is recorded as CHEMBL465820[9].
  • hemanthidine's UNII is recorded as 6DB9318OGJ[10].
  • hemanthidine's PubChem CID is recorded as 3002914[11].
  • hemanthidine's found in taxon is recorded as Sternbergia sicula[12].
  • hemanthidine's found in taxon is recorded as Sternbergia lutea[13].
  • hemanthidine's found in taxon is recorded as Hymenocallis littoralis[14].
  • hemanthidine's found in taxon is recorded as Pancratium trianthum[15].
  • hemanthidine's found in taxon is recorded as George lily, Scarborough lily[16].
  • hemanthidine's found in taxon is recorded as Scadoxus multiflorus[17].
  • hemanthidine's found in taxon is recorded as Hymenocallis latifolia var. latifolia[18].
  • hemanthidine's isomeric SMILES is recorded as CO[C@H]1C[C@H]2[C@@]3(C=C1)C@HOC@HO">[19].
  • hemanthidine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+317.126322708'}[20].
  • hemanthidine's SureChEMBL ID is recorded as 29372967[21].
  • hemanthidine's DSSTox substance ID is recorded as DTXSID70963613[22].
  • hemanthidine's DSSTOX compound identifier is recorded as DTXCID201391357[23].
  • hemanthidine's UniChem compound ID is recorded as 490858[24].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [4] . PubChem. Retrieved . wikidata.org.
  4. [5] . PubChem. Retrieved . wikidata.org.
  5. [6] . PubChem. Retrieved . wikidata.org.
  6. [7] . PubChem. Retrieved . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . ChEMBL. Retrieved . wikidata.org.
  9. [10] . Global Substance Registration System. Retrieved . wikidata.org.
  10. [11] . PubChem. Retrieved . wikidata.org.
  11. [12] . Four New Crinine-Type Alkaloids from Sternbergia Species. wikidata.org.
  12. [13] . Four New Crinine-Type Alkaloids from Sternbergia Species. wikidata.org.
  13. [14] . Lycorine alkaloids from Hymenocallis littoralis. wikidata.org.
  14. [15] . Alkaloid composition ofPancratium trianthum. wikidata.org.
  15. [16] . Alkaloids from Cyrtanthus elatus. wikidata.org.
  16. [17] . Isocarbostyril alkaloids from Haemanthus kalbreyeri. wikidata.org.
  17. [18] . Cytotoxicity of Hymenocallis expansa alkaloids. wikidata.org.
  18. [19] . PubChem. Retrieved . wikidata.org.
  19. [20] . wikidata.org.
  20. [21] . wikidata.org.
  21. [22] . wikidata.org.
  22. [23] . wikidata.org.
  23. [24] . 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). hemanthidine. Retrieved May 3, 2026, from https://4ort.xyz/entity/hemanthidine
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BibTeX @misc{4ortxyz_hemanthidine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hemanthidine}}, year = {2026}, url = {https://4ort.xyz/entity/hemanthidine}, note = {Accessed: 2026-05-03}}
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