isobutyryl-coenzyme A(4-)

chemical compound
ChemicalSubstance group_of_stereoisomers Q28529703
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Summary

isobutyryl-coenzyme A(4-) is a group of stereoisomers[1].

Key Facts

  • isobutyryl-coenzyme A(4-)'s instance of is recorded as group of stereoisomers[2].
  • isobutyryl-coenzyme A(4-)'s canonical SMILES is recorded as CC(C)C(=O)SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP(=O)([O-])OP(=O)([O-])OCC1OC(n2cnc3c(N)ncnc32)C(O)C1OP(=O)([O-])[O-][3].
  • isobutyryl-coenzyme A(4-)'s InChI is recorded as InChI=1S/C25H42N7O17P3S/c1-13(2)24(37)53-8-7-27-15(33)5-6-28-22(36)19(35)25(3,4)10-46-52(43,44)49-51(41,42)45-9-14-18(48-50(38,39)40)17(34)23(47-14)32-12-31-16-20(26)29-11-30-21(16)32/h11-14,17-19,23,34-35H,5-10H2,1-4H3,(H,27,33)(H,28,36)(H,41,42)(H,43,44)(H2,26,29,30)(H2,38,39,40)/p-4/t14-,17-,18-,19+,23-/m1/s1[4].
  • isobutyryl-coenzyme A(4-)'s InChIKey is recorded as AEWHYWSPVRZHCT-NDZSKPAWSA-J[5].
  • isobutyryl-coenzyme A(4-)'s chemical formula is recorded as C₂₅H₃₈N₇O₁₇P₃S[6].
  • isobutyryl-coenzyme A(4-)'s subclass of is recorded as anion[7].
  • isobutyryl-coenzyme A(4-)'s part of is recorded as isobutyryl-CoA mutase activity[8].
  • isobutyryl-coenzyme A(4-)'s part of is recorded as dihydrolipoyllysine-residue (2-methylpropanoyl)transferase activity[9].
  • isobutyryl-coenzyme A(4-)'s part of is recorded as 3-methyl-2-oxobutanoate dehydrogenase (ferredoxin) activity[10].
  • isobutyryl-coenzyme A(4-)'s part of is recorded as 2-oxoisovalerate dehydrogenase (acylating) activity[11].
  • isobutyryl-coenzyme A(4-)'s PubChem CID is recorded as 45266570[12].
  • isobutyryl-coenzyme A(4-)'s ChEBI ID is recorded as 57338[13].
  • isobutyryl-coenzyme A(4-)'s isomeric SMILES is recorded as CC(C)C(=O)SCCNC(=O)CCNC(=O)C@HC(C)(C)COP([O-])(=O)OP([O-])(=O)OC[C@H]1OC@Hn1cnc2c(N)ncnc12C@HC(C)(C)COP([O-])(=O)OP([O-])(=O)OC[C@H]1OC@Hn1cnc2c(N)ncnc12">[14].
  • isobutyryl-coenzyme A(4-)'s mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+833.1279679656398'}[15].
  • isobutyryl-coenzyme A(4-)'s DSSTox substance ID is recorded as DTXSID90935397[16].
  • isobutyryl-coenzyme A(4-)'s DSSTOX compound identifier is recorded as DTXCID901364028[17].
  • isobutyryl-coenzyme A(4-)'s SwissLipids ID is recorded as SLM:000389506[18].
  • isobutyryl-coenzyme A(4-)'s UniChem compound ID is recorded as 1103856[19].

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] ↑ . wikidata.org.
  4. [5] ↑ . ChEBI release 2020-09-01. wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  8. [9] ↑ . geneontology.org. Retrieved . geneontology.org. Provenance: wikidata.org.
  9. [10] ↑ . geneontology.org. Retrieved . geneontology.org. Provenance: wikidata.org.
  10. [11] ↑ . geneontology.org. Retrieved . geneontology.org. Provenance: wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . ChEBI release 2019-10-02. wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . wikidata.org.
  18. [19] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). isobutyryl-coenzyme A(4-). Retrieved May 3, 2026, from https://4ort.xyz/entity/isobutyryl-coenzyme-a-4-
MLA “isobutyryl-coenzyme A(4-).” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/isobutyryl-coenzyme-a-4-.
BibTeX @misc{4ortxyz_isobutyryl-coenzyme-a-4-_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{isobutyryl-coenzyme A(4-)}}, year = {2026}, url = {https://4ort.xyz/entity/isobutyryl-coenzyme-a-4-}, note = {Accessed: 2026-05-03}}
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