aloin

group of stereoisomers with the chemical formula C₂₁H₂₂O₉
ChemicalSubstance group_of_stereoisomers Q104667246
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aloin

Summary

aloin is a group of stereoisomers[1].

Key Facts

  • aloin's instance of is recorded as group of stereoisomers[2].
  • aloin's CAS Registry Number is recorded as 73649-93-1[3].
  • aloin's canonical SMILES is recorded as O=C1C=2C(O)=CC=CC2C(C3=CC(=CC(O)=C13)CO)C4OC(CO)C(O)C(O)C4O[4].
  • aloin's InChI is recorded as InChI=1S/C21H22O9/c22-6-8-4-10-14(21-20(29)19(28)17(26)13(7-23)30-21)9-2-1-3-11(24)15(9)18(27)16(10)12(25)5-8/h1-5,13-14,17,19-26,28-29H,6-7H2[5].
  • aloin's InChIKey is recorded as AFHJQYHRLPMKHU-UHFFFAOYSA-N[6].
  • aloin's chemical formula is recorded as C₂₁H₂₂O₉[7].
  • aloin's subclass of is recorded as anthrone polyketide[8].
  • aloin's PubChem CID is recorded as 313325[9].
  • aloin's found in taxon is recorded as Aloe barbadensis[10].
  • aloin's found in taxon is recorded as Aloe arborescens[11].
  • aloin's found in taxon is recorded as Aloe microdonta[12].
  • aloin's Human Metabolome Database ID is recorded as HMDB0035219[13].
  • aloin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+418.126382284'}[14].
  • aloin's SureChEMBL ID is recorded as 29832551[15].
  • aloin's SureChEMBL ID is recorded as 13990758[16].
  • aloin's DSSTox substance ID is recorded as DTXSID70859643[17].
  • aloin's MassBank accession ID is recorded as MSBNK-IPB_Halle-PB005501[18].
  • aloin's MassBank accession ID is recorded as MSBNK-IPB_Halle-PB006161[19].
  • aloin's MassBank accession ID is recorded as MSBNK-IPB_Halle-PB006162[20].
  • aloin's UniChem compound ID is recorded as 562216[21].
  • aloin's Probes And Drugs ID is recorded as PD055198[22].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . Chemical Abstracts Service. Retrieved . 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] . Hypotensive Effect of Chemical Constituents fromAloe barbadensis. wikidata.org.
  10. [11] . Anti-inflammatory Active Constituents ofAloe arborescensMiller. wikidata.org.
  11. [12] . Microdontin A and B: Two New Aloin Derivatives from Aloe microdonta. wikidata.org.
  12. [13] . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . wikidata.org.
  17. [18] . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  18. [19] . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  19. [20] . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  20. [21] . UniChem. wikidata.org.
  21. [22] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. 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). aloin. Retrieved May 3, 2026, from https://4ort.xyz/entity/aloin
MLA “aloin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/aloin.
BibTeX @misc{4ortxyz_aloin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{aloin}}, year = {2026}, url = {https://4ort.xyz/entity/aloin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): aloin — https://4ort.xyz/entity/aloin (retrieved 2026-05-03)

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