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AK-toxin I

chemical compound
ChemicalSubstance group_of_stereoisomers Q27149778
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AK-toxin I

Summary

AK-toxin I is a group of stereoisomers[1].

Key Facts

  • AK-toxin I's instance of is recorded as group of stereoisomers[2].
  • AK-toxin I's CAS Registry Number is recorded as 85146-09-4[3].
  • AK-toxin I's canonical SMILES is recorded as CC(C1=CC=CC=C1)C(C(=O)OC(C=CC=CC=CC(=O)O)C2(CO2)C)NC(=O)C[4].
  • AK-toxin I's InChI is recorded as InChI=1S/C23H27NO6/c1-16(18-11-7-6-8-12-18)21(24-17(2)25)22(28)30-19(23(3)15-29-23)13-9-4-5-10-14-20(26)27/h4-14,16,19,21H,15H2,1-3H3,(H,24,25)(H,26,27)/b5-4-,13-9+,14-10+[5].
  • AK-toxin I's InChIKey is recorded as HGSOUJPIFSDBKJ-OUYMFVGOSA-N[6].
  • AK-toxin I's chemical formula is recorded as C₂₃H₂₇NO₆[7].
  • AK-toxin I's subclass of is recorded as chemical compound[8].
  • AK-toxin I's ChemSpider ID is recorded as 30791746[9].
  • AK-toxin I's PubChem CID is recorded as 46173828[10].
  • AK-toxin I's KEGG ID is recorded as C16787[11].
  • AK-toxin I's ChEBI ID is recorded as 80727[12].
  • AK-toxin I's found in taxon is recorded as Alternaria alternata[13].
  • AK-toxin I's found in taxon is recorded as Alternaria gaisen[14].
  • AK-toxin I's found in taxon is recorded as Alternaria kikuchiana[15].
  • AK-toxin I's isomeric SMILES is recorded as CC(C1=CC=CC=C1)C(C(=O)OC(/C=C/C=C\C=C\C(=O)O)C2(CO2)C)NC(=O)C[16].
  • AK-toxin I's Human Metabolome Database ID is recorded as HMDB0030401[17].
  • AK-toxin I's KNApSAcK ID is recorded as C00024781[18].
  • AK-toxin I's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+413.183838'}[19].
  • AK-toxin I's Natural Product Atlas ID is recorded as NPA008756[20].
  • AK-toxin I's UniChem compound ID is recorded as 1070758[21].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . ChEBI. Retrieved . 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] ↑ . Q2311683. Retrieved . wikidata.org.
  9. [10] ↑ . PubChem. Retrieved . wikidata.org.
  10. [11] ↑ . ChEBI. Retrieved . wikidata.org.
  11. [12] ↑ . ChEBI. Retrieved . wikidata.org.
  12. [13] ↑ . Complex regulation of secondary metabolism controlling pathogenicity in the phytopathogenic fungus Alternaria alternata. wikidata.org.
  13. [14] ↑ . Isolation and structures of AK-toxin I and II. Host-specific phytotoxic metabolites produced by Alternaria alternata Japanese pear pathotype.. wikidata.org.
  14. [15] ↑ . Isolation and structures of AK-toxin I and II. Host-specific phytotoxic metabolites produced by Alternaria alternata Japanese pear pathotype.. wikidata.org.
  15. [16] ↑ . PubChem. Retrieved . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . ChEBI. Retrieved . wikidata.org.
  18. [19] ↑ . PubChem. Retrieved . wikidata.org.
  19. [20] ↑ . wikidata.org.
  20. [21] ↑ . 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). AK-toxin I. Retrieved May 3, 2026, from https://4ort.xyz/entity/ak-toxin-i
MLA “AK-toxin I.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/ak-toxin-i.
BibTeX @misc{4ortxyz_ak-toxin-i_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{AK-toxin I}}, year = {2026}, url = {https://4ort.xyz/entity/ak-toxin-i}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): AK-toxin I — https://4ort.xyz/entity/ak-toxin-i (retrieved 2026-05-03)

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