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🧪 2-Oxoglutaryl-CoA

Appears in: 2 pathways
Produces: 1 compound
Produced by: 2 transformations

Chemical Structure

2-Oxoglutaryl-CoA

📋 Properties

SMILES:
O=C([O-])CCC(=O)C(=O)SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP(=O)(O)OP(=O)(O)OCC1OC(N2C=NC=3C(=NC=NC32)N)C(O)C1OP(=O)(O)O
InChI:
InChI=1S/C26H40N7O20P3S/c1-26(2,20(39)23(40)29-6-5-15(35)28-7-8-57-25(41)13(34)3-4-16(36)37)10-50-56(47,48)53-55(45,46)49-9-14-19(52-54(42,43)44)18(38)24(51-14)33-12-32-17-21(27)30-11-31-22(17)33/h11-12,14,18-20,24,38-39H,3-10H2,1-2H3,(H,28,35)(H,29,40)(H,36,37)(H,45,46)(H,47,48)(H2,27,30,31)(H2,42,43,44)/p-1
Database ID:
376
External:
View on PubChem ↗

🔬 Reactant

Reactant 2-Oxoglutaryl-CoA → Product 2-Oxoglutarate
2-oxoglutaryl-CoA thioesterase (Eawag BBD reaction r1238)       (EC 3.1.2.-)
In pathway: Thiophene-2-carboxylate

🔬 Product

Reactant 5-Hydroxy-2-furoyl-CoA → Product 2-Oxoglutaryl-CoA
5-oxo-dihydro-2-furoyl-CoA hydrolase (Eawag BBD reaction r1357)       (EC 3.1.1.-)
In pathway: Furfural
Reactant (2Z)-5-Carboxy-2-sulfanylpent-2-enoyl-CoA → Product 2-Oxoglutaryl-CoA
thiol hydrolase (Eawag BBD reaction r1237)       (EC 3.13.1.-)
In pathway: Thiophene-2-carboxylate

🗺️ All Pathways Containing This Compound

Furfural Thiophene-2-carboxylate
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