succinyl-CoA

chemical compound
Class type of: fatty acyl-CoA Q419560

Facts

8 properties
Instance of
group of stereoisomers
Subclass of
fatty acyl-CoA
Part of
succinyl-CoA metabolic process, methionine catabolic process to succinyl-CoA, succinyl-CoA catabolic process, succinyl-CoA biosynthetic process, tetrapyrrole biosynthetic process from glycine and succinyl-CoA
Canonical SMILES
CC(C)(COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)N2C=NC3=C2N=CN=C3N)O)OP(=O)(O)O)C(C(=O)NCCC(=O)NCCSC(=O)CCC(=O)O)O
Chemical formula
C₂₅H₄₀N₇O₁₉P₃S
Isomeric SMILES
CC(C)(COP(=O)(O)OP(=O)(O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)N2C=NC3=C2N=CN=C3N)O)OP(=O)(O)O)[C@H](C(=O)NCCC(=O)NCCSC(=O)CCC(=O)O)O
Mass
+867.131
🏷️ Also known as
en S-(hydrogen succinyl)-CoA en Succinyl-Coenzyme A en Succinyl coenzyme A en succinyl-CoA en SUCC-CoA en S-(Hydrogen succinyl)coenzyme A en Coenzyme A, S-(hydrogen butanedioate) en S-(3-carboxy-propionyl)-CoA en S-(3-carboxypropionyl)-coenzyme-A ar سكسينيل-مرافق الإنزيم A cs Sukcinyl-CoA cs Sukcinylkoenzym A cs Sukcinyl-koenzym A cs Sukcinyl CoA de Succinyl-Coenzym A es Succinil-coA fa سوکینیل-کوآ fi Sukkinyylikoentsyymi-A fr Succinyl-CoA he סוקציניל קואנזים A
🔖 Identifiers · 26
CAS Registry Number
604-98-8
ChEBI ID
15380
ChemSpider ID
83179
DSSTOX compound identifier
DTXCID501403202
DSSTox substance ID
DTXSID40975809
DrugBank ID
DB03699
EC number
210-079-5
ECHA Substance Infocard ID
100.009.163
Encyclopædia Britannica Online ID
science/succinyl-coenzyme-A
Freebase ID
/m/03bzwv
Human Metabolome Database ID
HMDB0001022
Show all 26 identifiers +14
KEGG ID
C00091
KNApSAcK ID
C00019546
LIPID MAPS ID
LMFA07050370
Microsoft Academic ID (discontinued)
2780516146
PDB ligand ID
SCA
PDB structure ID
5E3Q, 4REQ, 3FSY, 2BWO, 2VZZ, 1KGT
Probes And Drugs ID
PD059511
PubChem CID
92133
Reaxys registry number
78365
SureChEMBL ID
50744
UM-BBD compound ID
c0344
UniChem compound ID
645910

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🔗 Connections
Found in taxon 2
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Summary

succinyl-CoA is a group of stereoisomers[1]. succinyl-CoA is a type of fatty acyl-CoA[2].

Key Facts

  • Canonical SMILES: CC(C)(COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)N2C=NC3=C2N=CN=C3N)O)OP(=O)(O)O)C(C(=O)NCCC(=O)NCCSC(=O)CCC(=O)O)O[3]
  • Chemical formula: C₂₅H₄₀N₇O₁₉P₃S[4]
  • Part of: succinyl-CoA metabolic process[5], methionine catabolic process to succinyl-CoA[6], succinyl-CoA catabolic process[7], succinyl-CoA biosynthetic process[8], tetrapyrrole biosynthetic process from glycine and succinyl-CoA[9]
  • Found in taxon: Streptomyces cinnamonensis[10], Homo sapiens[11], Caenorhabditis elegans[12]
  • Isomeric SMILES: CC(C)(COP(=O)(O)OP(=O)(O)OC[C@@H]1C@HOP(=O)(O)O)C@HOC@HOP(=O)(O)O)C@HO">[13]
  • Mass: 867.131 dalton[14]

References

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

Direct Wikidata claims

  1. [3] ↑ . PubChem. Retrieved . wikidata.org.
  2. [4] ↑ . PubChem. Retrieved . wikidata.org.
  3. [2] ↑ . wikidata.org.
  4. [5] ↑ . Gene Ontology release 2019-11-16. wikidata.org.
  5. [6] ↑ . Gene Ontology release 2019-11-16. wikidata.org.
  6. [7] ↑ . Gene Ontology release 2019-11-16. wikidata.org.
  7. [8] ↑ . Gene Ontology release 2019-11-16. wikidata.org.
  8. [9] ↑ . Gene Ontology release 2020-05-02. wikidata.org.
  9. [10] ↑ . Insertional Inactivation of Methylmalonyl Coenzyme A (CoA) Mutase and Isobutyryl-CoA Mutase Genes in Streptomyces cinnamonensis: Influence on Polyketide Antibiotic Biosynthesis. wikidata.org.
  10. [11] ↑ . Recon 2.2: from reconstruction to model of human metabolism. wikidata.org.
  11. [12] ↑ . Metabotyping of the C. elegans sir-2.1 Mutant Using in Vivo Labeling and 13C-Heteronuclear Multidimensional NMR Metabolomics. wikidata.org.
  12. [13] ↑ . PubChem. Retrieved . wikidata.org.
  13. [14] ↑ . PubChem. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). succinyl-CoA. Retrieved November 4, 2026, from https://4ort.xyz/entity/succinyl-coa
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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 20w ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Instance of → group of stereoisomers
    Part of → —
    Subclass of → —
    Aliases → —
    + 5 other properties edited (see Wikidata diff for full list)
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