Tenuazonic acid

chemical compound
ChemicalSubstance group_of_stereoisomers Q27108395
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Tenuazonic acid

Summary

Tenuazonic acid is a group of stereoisomers[1].

Key Facts

  • Tenuazonic acid's instance of is recorded as group of stereoisomers[2].
  • Tenuazonic acid's CAS Registry Number is recorded as 27778-66-1[3].
  • Tenuazonic acid's canonical SMILES is recorded as CCC(C)C1C(=O)C(C(=O)N1)C(=O)C[4].
  • Tenuazonic acid's InChI is recorded as InChI=1S/C10H15NO3/c1-4-5(2)8-9(13)7(6(3)12)10(14)11-8/h5,7-8H,4H2,1-3H3,(H,11,14)/t5-,7?,8-/m0/s1[5].
  • Tenuazonic acid's InChIKey is recorded as KLBSRSYHIIAQTG-PZICIZFRSA-N[6].
  • Tenuazonic acid's chemical formula is recorded as C₁₀H₁₅NO₃[7].
  • Tenuazonic acid's subclass of is recorded as pyrrolidine alkaloid[8].
  • Tenuazonic acid's MeSH descriptor ID is recorded as D013720[9].
  • Tenuazonic acid's ChemSpider ID is recorded as 390249[10].
  • Tenuazonic acid's PubChem CID is recorded as 441580[11].
  • Tenuazonic acid's KEGG ID is recorded as C08511[12].
  • Tenuazonic acid's MeSH tree code is recorded as D03.383.773.812.900[13].
  • Tenuazonic acid's MeSH tree code is recorded as D23.946.587.915[14].
  • Tenuazonic acid's ChEBI ID is recorded as 9440[15].
  • Tenuazonic acid's found in taxon is recorded as Alternaria alternata[16].
  • Tenuazonic acid's found in taxon is recorded as Alternaria tenuis[17].
  • Tenuazonic acid's found in taxon is recorded as Pyricularia oryzae[18].
  • Tenuazonic acid's different from is recorded as L-tenuazonic acid[19].
  • Tenuazonic acid's isomeric SMILES is recorded as CCC@H[C@H]1C(=O)C(C(=O)N1)C(=O)CC@H[C@H]1C(=O)C(C(=O)N1)C(=O)C">[20].
  • Tenuazonic acid's KNApSAcK ID is recorded as C00001554[21].
  • Tenuazonic acid's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+197.105193'}[22].
  • Tenuazonic acid's subject has role is recorded as antineoplastic antibiotics[23].
  • Tenuazonic acid's subject has role is recorded as antiviral agent[24].
  • Tenuazonic acid's UMLS CUI is recorded as C0039531[25].
  • Tenuazonic acid's DSSTox substance ID is recorded as DTXSID30893265[26].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . ChEBI. 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] . wikidata.org.
  9. [10] . Q2311683. Retrieved . wikidata.org.
  10. [11] . PubChem. Retrieved . wikidata.org.
  11. [12] . ChEBI. Retrieved . wikidata.org.
  12. [13] . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . ChEBI. Retrieved . wikidata.org.
  15. [16] . Biosynthesis and preparation of fiveAlternaria metabolites. wikidata.org.
  16. [17] . Studies in the biochemistry of micro-organisms. 106. Metabolites of Alternaria tenuis auct.: the structure of tenuazonic acid. wikidata.org.
  17. [18] . Structures of Two Novel Pyriculol-related Compounds and Identification of Naturally Produced Epipyriculol from Pyricularia oryzae.. wikidata.org.
  18. [19] . wikidata.org.
  19. [20] . PubChem. Retrieved . wikidata.org.
  20. [21] . ChEBI. Retrieved . wikidata.org.
  21. [22] . PubChem. Retrieved . wikidata.org.
  22. [23] . Medical Subject Headings. Retrieved . wikidata.org.
  23. [24] . Medical Subject Headings. Retrieved . wikidata.org.
  24. [25] . UMLS 2023. Retrieved . wikidata.org.
  25. [26] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). Tenuazonic acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/tenuazonic-acid
MLA “Tenuazonic acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/tenuazonic-acid.
BibTeX @misc{4ortxyz_tenuazonic-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Tenuazonic acid}}, year = {2026}, url = {https://4ort.xyz/entity/tenuazonic-acid}, note = {Accessed: 2026-05-03}}
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