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2-trans-abscisic acid

chemical compound
ChemicalSubstance group_of_stereoisomers Q27131879
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2-trans-abscisic acid

Summary

2-trans-abscisic acid is a group of stereoisomers[1].

Key Facts

  • 2-trans-abscisic acid's instance of is recorded as group of stereoisomers[2].
  • 2-trans-abscisic acid's canonical SMILES is recorded as CC1=CC(=O)CC(C1(C=CC(=CC(=O)O)C)O)(C)C[3].
  • 2-trans-abscisic acid's InChI is recorded as InChI=1S/C15H20O4/c1-10(7-13(17)18)5-6-15(19)11(2)8-12(16)9-14(15,3)4/h5-8,19H,9H2,1-4H3,(H,17,18)/b6-5+,10-7+[4].
  • 2-trans-abscisic acid's InChIKey is recorded as JLIDBLDQVAYHNE-WEYXYWBQSA-N[5].
  • 2-trans-abscisic acid's chemical formula is recorded as C₁₅H₂₀O₄[6].
  • 2-trans-abscisic acid's subclass of is recorded as cyclofarnesoid[7].
  • 2-trans-abscisic acid's ChEMBL ID is recorded as CHEMBL1965138[8].
  • 2-trans-abscisic acid's ChemSpider ID is recorded as 4524740[9].
  • 2-trans-abscisic acid's PubChem CID is recorded as 5375200[10].
  • 2-trans-abscisic acid's ChEBI ID is recorded as 62426[11].
  • 2-trans-abscisic acid's found in taxon is recorded as Vernicia fordii[12].
  • 2-trans-abscisic acid's found in taxon is recorded as Phaseolus vulgaris[13].
  • 2-trans-abscisic acid's found in taxon is recorded as Axinella polypoides[14].
  • 2-trans-abscisic acid's isomeric SMILES is recorded as CC1=CC(=O)CC(C1(/C=C/C(=C/C(=O)O)/C)O)(C)C[15].
  • 2-trans-abscisic acid's Human Metabolome Database ID is recorded as HMDB0036093[16].
  • 2-trans-abscisic acid's KNApSAcK ID is recorded as C00060847[17].
  • 2-trans-abscisic acid's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+264.136'}[18].
  • 2-trans-abscisic acid's SureChEMBL ID is recorded as 2591173[19].
  • 2-trans-abscisic acid's DSSTox substance ID is recorded as DTXSID801033715[20].
  • 2-trans-abscisic acid's UniChem compound ID is recorded as 1103472[21].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . PubChem. Retrieved . wikidata.org.
  3. [4] ↑ . PubChem. Retrieved . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . PubChem. Retrieved . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . ChEMBL. Retrieved . wikidata.org.
  8. [9] ↑ . Q2311683. Retrieved . wikidata.org.
  9. [10] ↑ . PubChem. Retrieved . wikidata.org.
  10. [11] ↑ . ChEBI. Retrieved . wikidata.org.
  11. [12] ↑ . Isolation and Identification of a Growth Inhibitor in Tung Bud Scales1. wikidata.org.
  12. [13] ↑ . Carotenoids and abscisic acid (ABA) biosynthesis in higher plants. wikidata.org.
  13. [14] ↑ . Occurrence, function and potential medicinal applications of the phytohormone abscisic acid in animals and humans.. wikidata.org.
  14. [15] ↑ . PubChem. Retrieved . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . PubChem. Retrieved . wikidata.org.
  18. [19] ↑ . 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). 2-trans-abscisic acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/2-trans-abscisic-acid
MLA “2-trans-abscisic acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/2-trans-abscisic-acid.
BibTeX @misc{4ortxyz_2-trans-abscisic-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{2-trans-abscisic acid}}, year = {2026}, url = {https://4ort.xyz/entity/2-trans-abscisic-acid}, note = {Accessed: 2026-05-03}}
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