(Z)-ajoene

chemical compound
ChemicalSubstance group_of_stereoisomers Q27149741
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(Z)-ajoene

Summary

(Z)-ajoene is a group of stereoisomers[1].

Key Facts

  • (Z)-ajoene's instance of is recorded as group of stereoisomers[2].
  • (Z)-ajoene's chemical structure is recorded as Z-ajoene-2D-skeletal.png[3].
  • (Z)-ajoene's CAS Registry Number is recorded as 92285-00-2[4].
  • (Z)-ajoene's canonical SMILES is recorded as C=CCSSC=CCS(=O)CC=C[5].
  • (Z)-ajoene's InChI is recorded as InChI=1S/C9H14OS3/c1-3-6-11-12-7-5-9-13(10)8-4-2/h3-5,7H,1-2,6,8-9H2/b7-5-[6].
  • (Z)-ajoene's InChIKey is recorded as IXELFRRANAOWSF-ALCCZGGFSA-N[7].
  • (Z)-ajoene's chemical formula is recorded as C₉H₁₄OS₃[8].
  • (Z)-ajoene's subclass of is recorded as chemical compound[9].
  • (Z)-ajoene's ChEMBL ID is recorded as CHEMBL122289[10].
  • (Z)-ajoene's UNII is recorded as J9XLK7547H[11].
  • (Z)-ajoene's ChemSpider ID is recorded as 8056824[12].
  • (Z)-ajoene's PubChem CID is recorded as 9881148[13].
  • (Z)-ajoene's KEGG ID is recorded as C16757[14].
  • (Z)-ajoene's ChEBI ID is recorded as 80707[15].
  • (Z)-ajoene's found in taxon is recorded as Allium sativum[16].
  • (Z)-ajoene's found in taxon is recorded as Allium[17].
  • (Z)-ajoene's isomeric SMILES is recorded as C=CCSS/C=C\CS(=O)CC=C[18].
  • (Z)-ajoene's Human Metabolome Database ID is recorded as HMDB0033566[19].
  • (Z)-ajoene's KNApSAcK ID is recorded as C00052510[20].
  • (Z)-ajoene's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+234.020678'}[21].
  • (Z)-ajoene's SureChEMBL ID is recorded as 3305767[22].
  • (Z)-ajoene's DSSTox substance ID is recorded as DTXSID101318564[23].
  • (Z)-ajoene's UniChem compound ID is recorded as 216690[24].
  • (Z)-ajoene's Probes And Drugs ID is recorded as PD137858[25].

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] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [5] . PubChem. Retrieved . wikidata.org.
  5. [6] . PubChem. Retrieved . wikidata.org.
  6. [7] . PubChem. Retrieved . wikidata.org.
  7. [8] . PubChem. Retrieved . wikidata.org.
  8. [9] . wikidata.org.
  9. [10] . ChEMBL. Retrieved . wikidata.org.
  10. [11] . Global Substance Registration System. Retrieved . wikidata.org.
  11. [12] . Q2311683. Retrieved . wikidata.org.
  12. [13] . PubChem. Retrieved . wikidata.org.
  13. [14] . ChEBI. Retrieved . wikidata.org.
  14. [15] . ChEMBL. Retrieved . wikidata.org.
  15. [16] . Antimicrobial Activity of a Compound Isolated from an Oil-Macerated Garlic Extract. wikidata.org.
  16. [17] . What makes Allium species effective against pathogenic microbes?. wikidata.org.
  17. [18] . PubChem. Retrieved . wikidata.org.
  18. [19] . wikidata.org.
  19. [20] . wikidata.org.
  20. [21] . PubChem. Retrieved . wikidata.org.
  21. [22] . wikidata.org.
  22. [23] . wikidata.org.
  23. [24] . UniChem. wikidata.org.
  24. [25] . 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). (Z)-ajoene. Retrieved May 3, 2026, from https://4ort.xyz/entity/-z-ajoene
MLA “(Z)-ajoene.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/-z-ajoene.
BibTeX @misc{4ortxyz_-z-ajoene_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(Z)-ajoene}}, year = {2026}, url = {https://4ort.xyz/entity/-z-ajoene}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (Z)-ajoene — https://4ort.xyz/entity/-z-ajoene (retrieved 2026-05-03)

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