C23H38N7O17P3S
Acetyl-CoA
809.1258
17220838
ChemSpider
937
ChemSpider
6.0
439153
PubChem-compound
1.0
Trifunctional enzyme subunit alpha, mitochondrial
Enoyl-CoA hydratase, mitochondrial
3-oxooctanoyl-CoA
1.0
C33H58N7O17P3S
Lauroyl-CoA
949.2823
38795-33-4
CAS
HMDB0001070
HMDB
Trans-2-enoyl-CoA reductase, mitochondrial
HMDB0006404
HMDB
HMDB0006402
HMDB
1.0
1.0
1.0
CPD-196
BioCyc
1.0
Acetyl-CoA
2.0
CHEBI:16474
ChEBI
11966197
PubChem-compound
1.0
Lauroyl-CoA
HMDB0001088
HMDB
7-METHYL-3-OXOOCTANOYL-COA
BioCyc
1.0
1010
ChemSpider
SMILES
CC(C)(COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N)[C@@H](O)C(=O)NCCC(=O)NCCS
Tetradecanoyl-CoA
C33H56N7O17P3S
(2E)-Dodecenoyl-CoA
947.2666
C27H46N7O17P3S
Hexanoyl-CoA
865.18835
LAUROYLCOA-CPD
BioCyc
53477508
PubChem-compound
3-oxohexadecanoyl-CoA
Acetyl-CoA acyltransferase
C00249
KEGG Compound
C00006
KEGG Compound
3-ketoacyl-CoA thiolase, mitochondrial
CHEBI:18009
ChEBI
C00001
KEGG Compound
C00005
KEGG Compound
C00004
KEGG Compound
C00003
KEGG Compound
P42765
UniProt
CHEBI:28276
ChEBI
3-hydroxyoctanoyl-CoA
1.0
3130-72-1
CAS
389502
ChemSpider
C29H50N7O17P3S
Octanoyl-CoA
893.21967
389501
ChemSpider
389500
ChemSpider
C21H27N7O14P2
NAD
663.10913
389506
ChemSpider
389504
ChemSpider
C00010
KEGG Compound
HMDB0000902
HMDB
11966160
PubChem-compound
C00136
KEGG Compound
3-oxohexanoyl-CoA
3-ketoacyl-CoA thiolase, mitochondrial
NAD(P)
BioCyc
CHEBI:10723
ChEBI
3-hydroxyacyl-CoA dehydrogenase type-2
389508
ChemSpider
CHEBI:28264
ChEBI
Palmitoyl-protein thioesterase 1
H
Hydrogen Ion
1.007825
C25H42N7O17P3S
Butyryl-CoA
837.15704
4.0
53-84-9
CAS
4.0
389510
ChemSpider
C00024
KEGG Compound
1264-57-9
CAS
3-hydroxyacyl-CoA dehydrogenase type-2
3-Hydroxyhexanoyl-CoA
CHEBI:28493
ChEBI
4460-95-1
CAS
72059-49-5
CAS
C37H66N7O18P3S
3-Hydroxyhexadecanoyl-CoA
1021.3398
C00154
KEGG Compound
C35H62N7O18P3S
3-Hydroxytetradecanoyl-CoA
993.3085
C35H60N7O18P3S
3-oxotetradecanoyl-CoA
991.29285
SMILES
NC(=O)C1=CN(C=CC1)[C@@H]1O[C@H](CO[P@](O)(=O)O[P@](O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C(N)N=CN=C23)[C@@H](O)[C@H]1O
1.0
35106-50-4
CAS
1.0
16061159
PubChem-compound
CPD-12174
BioCyc
SMILES
CCCCCCCC(=O)CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
SMILES
[H][C@](O)(CCCCC)CC(=O)SCCNC(=O)CCNC(=O)[C@]([H])(O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H](C(O)[C@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
SMILES
CCCCCC(=O)CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
SMILES
CCC[C@H](O)CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
C02593
KEGG Compound
SMILES
CCCCCCCCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
SMILES
CCCCCCCCC[C@H](O)CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
C37H64N7O18P3S
3-oxohexadecanoyl-CoA
1019.32416
SMILES
CCCCCCCCCC(=O)CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
SMILES
CCCCCCC[C@H](O)CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
C31H54N7O17P3S
Decanoyl-CoA
921.251
1.0
7732-18-5
CAS
54684-64-9
CAS
1.0
3-OXOPALMITOYL-COA
BioCyc
NAD
HMDB0001487
HMDB
2140-48-9
CAS
3-oxodecanoyl-CoA
57-10-3
CAS
26330706
ChemSpider
165436
PubChem-compound
3-Hydroxydecanoyl-CoA
962
PubChem-compound
(2E)-Octenoyl-CoA
C03221
KEGG Compound
Palmitoyl-protein thioesterase 1
1.0
C00080
KEGG Compound
3-oxododecanoyl-CoA
1.0
P50897
UniProt
Palmitic acid
1.0
HMDB0002111
HMDB
(2E)-Dodecenoyl-CoA
6245-70-1
CAS
NADP
960
ChemSpider
HMDB0003571
HMDB
1264-52-4
CAS
(2E)-Tetradecenoyl-CoA
985
PubChem-compound
444493
PubChem-compound
1.0
Palmitoyl-CoA
Q9BV79
UniProt
SMILES
CCCC(=O)CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
SMILES
CCC\C=C\C(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
SMILES
CCCCCCCCCCCCC\C=C\C(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
22833512
PubChem-compound
1.0
ACETYL-COA
BioCyc
SMILES
CCCCCCCCCCC\C=C\C(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
H2O
Water
18.010565
SMILES
CCCCCCC\C=C\C(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
SMILES
CCCCC\C=C\C(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
P55084
UniProt
NADH
BioCyc
NAD
BioCyc
1.0
NADPH
HMDB0059597
HMDB
(2E)-Decenoyl-CoA
SMILES
CCCCCCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
ReactionCatalysis278
ACTIVATION
ReactionCatalysis279
ACTIVATION
Reaction759
false
3-Hydroxydodecanoyl-CoA + NAD ↔ 3-oxododecanoyl-CoA + Hydrogen Ion + NADH
REVERSIBLE
ReactionCatalysis276
ACTIVATION
17215925
ChemSpider
ReactionCatalysis277
ACTIVATION
1.3.1.38
false
1.3.1.38
(2E)-Decenoyl-CoA + NADPH → Decanoyl-CoA + NADP
LEFT_TO_RIGHT
ReactionCatalysis274
ACTIVATION
Trans-2-enoyl-CoA reductase, mitochondrial
2.3.1.16
false
2.3.1.16
Acetyl-CoA + Decanoyl-CoA → 3-oxododecanoyl-CoA + Coenzyme A
LEFT_TO_RIGHT
ReactionCatalysis275
ACTIVATION
Reaction755
false
3-Hydroxydecanoyl-CoA + NAD ↔ 3-oxodecanoyl-CoA + Hydrogen Ion + NADH
REVERSIBLE
ReactionCatalysis272
ACTIVATION
65113
PubChem-compound
4.2.1.17
false
4.2.1.17
3-Hydroxydecanoyl-CoA ↔ (2E)-Decenoyl-CoA + Water
REVERSIBLE
ReactionCatalysis273
ACTIVATION
78303-19-2
CAS
ReactionCatalysis270
ACTIVATION
Trifunctional enzyme subunit beta, mitochondrial
ReactionCatalysis271
ACTIVATION
3-Hydroxydodecanoyl-CoA
Enoyl-CoA hydratase, mitochondrial
10140190
ChemSpider
SMILES
O
1.3.1.38
false
1.3.1.38
(2E)-Octenoyl-CoA + NADPH → NADP + Octanoyl-CoA
LEFT_TO_RIGHT
371
ChemSpider
2.3.1.16
false
2.3.1.16
Acetyl-CoA + Octanoyl-CoA ↔ 3-oxodecanoyl-CoA + Coenzyme A
REVERSIBLE
Reaction751
false
3-hydroxyoctanoyl-CoA + NAD ↔ 3-oxooctanoyl-CoA + Hydrogen Ion + NADH
REVERSIBLE
4.2.1.17
false
4.2.1.17
3-hydroxyoctanoyl-CoA ↔ (2E)-Octenoyl-CoA + Water
REVERSIBLE
2.3.1.16
false
2.3.1.16
Acetyl-CoA + Hexanoyl-CoA ↔ 3-oxooctanoyl-CoA + Coenzyme A
REVERSIBLE
ReactionCatalysis269
ACTIVATION
P40939
UniProt
ReactionCatalysis267
ACTIVATION
ReactionCatalysis268
ACTIVATION
ReactionCatalysis265
ACTIVATION
ReactionCatalysis266
ACTIVATION
ReactionCatalysis263
ACTIVATION
4.2.1.17
false
4.2.1.17
3-Hydroxyhexadecanoyl-CoA ↔ (2E)-Hexadecenoyl-CoA + Water
REVERSIBLE
ReactionCatalysis264
ACTIVATION
1.3.1.38
false
1.3.1.38
(2E)-Hexadecenoyl-CoA + NADPH → NADP + Palmitoyl-CoA
LEFT_TO_RIGHT
3-hydroxyacyl-CoA dehydrogenase type-2
ReactionCatalysis261
ACTIVATION
2.3.1.16
false
2.3.1.16
Acetyl-CoA + Tetradecanoyl-CoA ↔ 3-oxohexadecanoyl-CoA + Coenzyme A
REVERSIBLE
ReactionCatalysis262
ACTIVATION
CHEBI:57371
ChEBI
Reaction767
false
3-Hydroxyhexadecanoyl-CoA + NAD ↔ 3-oxohexadecanoyl-CoA + Hydrogen Ion + NADH
REVERSIBLE
ReactionCatalysis260
ACTIVATION
HMDB0002845
HMDB
6816
PubChem-compound
HMDB0003934
HMDB
HMDB0003935
HMDB
5060-32-2
CAS
HMDB0003932
HMDB
4.2.1.17
false
4.2.1.17
3-Hydroxytetradecanoyl-CoA ↔ (2E)-Tetradecenoyl-CoA + Water
REVERSIBLE
CHEBI:15846
ChEBI
1.3.1.38
false
1.3.1.38
(2E)-Tetradecenoyl-CoA + NADPH → NADP + Tetradecanoyl-CoA
LEFT_TO_RIGHT
2.3.1.16
false
2.3.1.16
Acetyl-CoA + Lauroyl-CoA → 3-oxotetradecanoyl-CoA + Coenzyme A
LEFT_TO_RIGHT
Reaction763
false
3-Hydroxytetradecanoyl-CoA + NAD ↔ 3-oxotetradecanoyl-CoA + Hydrogen Ion + NADH
REVERSIBLE
4.2.1.17
false
4.2.1.17
3-Hydroxydodecanoyl-CoA ↔ (2E)-Dodecenoyl-CoA + Water
REVERSIBLE
1.3.1.38
false
1.3.1.38
(2E)-Dodecenoyl-CoA + NADPH → Lauroyl-CoA + NADP
LEFT_TO_RIGHT
PALMITYL-COA
BioCyc
1.0
53-59-8
CAS
Hexanoyl-CoA
440608
PubChem-compound
440606
PubChem-compound
HMDB0003938
HMDB
SMILES
CCCCCCCCCCCC(=O)CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
HMDB0003939
HMDB
SMILES
CCCCCCCCCCC[C@H](O)CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
380
PubChem-compound
440604
PubChem-compound
HMDB0003936
HMDB
1038
PubChem-compound
HMDB0003937
HMDB
440603
PubChem-compound
SMILES
CCCCCCCCCCCCC[C@H](O)CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
265
PubChem-compound
440602
PubChem-compound
440601
PubChem-compound
440600
PubChem-compound
HMDB0003941
HMDB
HMDB0003942
HMDB
Fatty Acid Elongation in Mitochondria
HMDB0003940
HMDB
HMDB0001521
HMDB
HMDB0003945
HMDB
HMDB0003946
HMDB
HMDB0003943
HMDB
Q99714
UniProt
HMDB0003944
HMDB
Hydrogen Ion
CHEBI:16908
ChEBI
3.1.2.22
false
3.1.2.22
Palmitoyl-CoA + Water → Coenzyme A + Palmitic acid
LEFT_TO_RIGHT
K-HEXANOYL-COA
BioCyc
ReactionCatalysis287
ACTIVATION
ReactionCatalysis285
ACTIVATION
ReactionCatalysis286
ACTIVATION
ReactionCatalysis283
ACTIVATION
ReactionCatalysis284
ACTIVATION
HMDB0003949
HMDB
ReactionCatalysis281
ACTIVATION
ReactionCatalysis282
ACTIVATION
HMDB0003948
HMDB
ReactionCatalysis280
ACTIVATION
SMILES
CCCCCCCCCCCCCC(=O)CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
1.0
45266564
PubChem-compound
3-Hydroxytetradecanoyl-CoA
SMILES
CCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
HMDB0003712
HMDB
CHEBI:61526
ChEBI
C21H30N7O17P3
NADPH
745.0911
4.0
C16H32O2
Palmitic acid
256.24023
260
ChemSpider
Mitochondrion
C21H28N7O17P3
NADP
743.07544
NADPH
BioCyc
CHEBI:15521
ChEBI
CHEBI:15525
ChEBI
C27H46N7O18P3S
3-Hydroxyhexanoyl-CoA
881.1833
C27H44N7O18P3S
3-oxohexanoyl-CoA
879.16766
C27H44N7O17P3S
(2E)-Hexenoyl-CoA
863.1727
C37H64N7O17P3S
(2E)-Hexadecenoyl-CoA
1003.3292
58-68-4
CAS
C35H60N7O17P3S
(2E)-Tetradecenoyl-CoA
975.2979
Water
Trans-2-enoyl-CoA reductase, mitochondrial
HMDB0001423
HMDB
C31H52N7O17P3S
(2E)-Decenoyl-CoA
919.23535
C29H48N7O17P3S
(2E)-Octenoyl-CoA
891.20404
HMDB0000217
HMDB
CHEBI:28726
ChEBI
10140154
ChemSpider
P30084
UniProt
CHEBI:15533
ChEBI
CHEBI:15532
ChEBI
CHEBI:28706
ChEBI
440615
PubChem-compound
CHEBI:57330
ChEBI
1763-10-6
CAS
TETRADECANOYL-COA
BioCyc
(2E)-Hexadecenoyl-CoA
C05259
KEGG Compound
440610
PubChem-compound
C05258
KEGG Compound
SMILES
NC(=O)C1=C[N+](=CC=C1)[C@@H]1O[C@H](COP([O-])(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](OP(O)(O)=O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)[C@@H](O)[C@H]1O
C05264
KEGG Compound
1.0
HMDB0000221
HMDB
C05263
KEGG Compound
C05266
KEGG Compound
C05265
KEGG Compound
C05260
KEGG Compound
SMILES
NC(=O)C1=CN(C=CC1)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](OP(O)(O)=O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)[C@@H](O)[C@H]1O
C05262
KEGG Compound
SMILES
CCCCCCCCCCCCCCCC(O)=O
CHEBI:27868
ChEBI
C05261
KEGG Compound
SMP0000054
SMPDB
19774-86-8
CAS
3-Hydroxyhexadecanoyl-CoA
C35H62N7O17P3S
Tetradecanoyl-CoA
977.3136
HMDB0000220
HMDB
53-57-6
CAS
C05268
KEGG Compound
(2E)-Hexenoyl-CoA
C05267
KEGG Compound
C05269
KEGG Compound
C05275
KEGG Compound
C05274
KEGG Compound
C05276
KEGG Compound
C21H29N7O14P2
NADH
665.12476
C05271
KEGG Compound
C05270
KEGG Compound
C05273
KEGG Compound
HMDB0001206
HMDB
C05272
KEGG Compound
34619-89-1
CAS
4.2.1.17
false
4.2.1.17
3-Hydroxyhexanoyl-CoA ↔ (2E)-Hexenoyl-CoA + Water
REVERSIBLE
1.3.1.38
false
1.3.1.38
(2E)-Hexenoyl-CoA + NADPH → Hexanoyl-CoA + NADP
LEFT_TO_RIGHT
2.3.1.16
false
2.3.1.16
Acetyl-CoA + Butyryl-CoA → 3-oxohexanoyl-CoA + Coenzyme A
LEFT_TO_RIGHT
Reaction747
false
3-Hydroxyhexanoyl-CoA + NAD ↔ 3-oxohexanoyl-CoA + Hydrogen Ion + NADH
REVERSIBLE
CHEBI:15756
ChEBI
Enoyl-CoA hydratase, mitochondrial
1.0
C37H66N7O17P3S
Palmitoyl-CoA
1005.34485
C33H58N7O18P3S
3-Hydroxydodecanoyl-CoA
965.27716
GO:0005739
GENE ONTOLOGY
C33H56N7O18P3S
3-oxododecanoyl-CoA
963.26154
CHEBI:27721
ChEBI
C31H54N7O18P3S
3-Hydroxydecanoyl-CoA
937.2459
Trifunctional enzyme, mitochondrial
C31H52N7O18P3S
3-oxodecanoyl-CoA
935.2302
C29H50N7O18P3S
3-hydroxyoctanoyl-CoA
909.2146
Decanoyl-CoA
C29H48N7O18P3S
3-oxooctanoyl-CoA
907.1989
HMDB0001338
HMDB
1.0
58623
ChemSpider
10018-95-8
CAS
79171-47-4
CAS
SMILES
NC(=O)C1=C[N+](=CC=C1)[C@@H]1O[C@H](COP([O-])(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)[C@@H](O)[C@H]1O
5682
ChemSpider
SMILES
CCCCCCCC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
5280765
PubChem-compound
CHEBI:1146900
ChEBI
CHEBI:28528
ChEBI
5280769
PubChem-compound
50411-91-1
CAS
5280767
PubChem-compound
5280768
PubChem-compound
395736
ChemSpider
CO-A
BioCyc
CPD-8475
BioCyc
5675
ChemSpider
72-89-9
CAS
SMILES
CCCC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
CHEBI:28632
ChEBI
C21H36N7O16P3S
Coenzyme A
767.11523
CHEBI:27668
ChEBI
79171-48-5
CAS
CHEBI:27540
ChEBI
Trifunctional enzyme subunit beta, mitochondrial
C01944
KEGG Compound
1.0
14902
ChemSpider
Coenzyme A
6557
ChemSpider
Homo sapiens
SMILES
CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
388299
ChemSpider
3-oxotetradecanoyl-CoA
CHEBI:27537
ChEBI
SMILES
CCCCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
C01832
KEGG Compound
Octanoyl-CoA
449118
PubChem-compound
122364-86-7
CAS
1.0
CHEBI:27402
ChEBI
CHEBI:27648
ChEBI
1.0
1.0
NADH
9606
TAXONOMY
T2-DECENOYL-COA
BioCyc
PW000022
PathWhiz
392413
ChemSpider
145018
ChemSpider
10018-93-6
CAS
5893
PubChem-compound
CHEBI:28325
ChEBI
1.0
Butyryl-CoA
CHEBI:15377
ChEBI
4.0
CHEBI:15378
ChEBI
SMILES
[H+]
CPD-7222
BioCyc
5886
PubChem-compound
CHEBI:15491
ChEBI
389499
ChemSpider
389498
ChemSpider
CHEBI:27466
ChEBI
Trifunctional enzyme subunit alpha, mitochondrial
26332261
ChemSpider
1.0
4444333
ChemSpider
4444334
ChemSpider
SMILES
CCCCCC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
4444335
ChemSpider
4444331
ChemSpider
1.0
1.0
46173176
PubChem-compound
6244-92-4
CAS
SMILES
CCCCCCCCC\C=C\C(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N
10018-94-7
CAS
1066-12-2
CAS
15667
PubChem-compound
CHEBI:15351
ChEBI
1.0
1.0
85-61-0
CAS