BiSSCat: Acyl amide

F451000 Acyl amideCLASS:    Nitrogen / Amide
COMPOUND: 44910
          KEGG: 1866
          NCI:  43044
ENZYME:   190
          (Show enzyme(s))
RELATED:  6
          F102421 N-acetyl
          F450000 Amide
          F451100 N-terminal acyl amide
          F451200 N-alkyl acyl amide
          F451300 N,n-dialkyl acyl amide

1631. C05266 (S)-3-Hydroxyoctanoyl-CoA (Molfile)(InChI)(KEGG)

map00062 Fatty acid elongation in mitochondria
map00071 Fatty acid metabolism

1632. C00356 (S)-3-Hydroxy-3-methylglutaryl-CoA (Molfile)(InChI)(KEGG)

1.1.1.34 hydroxymethylglutaryl-CoA reductase (NADPH)
1.1.1.88 hydroxymethylglutaryl-CoA reductase
2.3.3.10 hydroxymethylglutaryl-CoA synthase
2.8.3.13 succinate-hydroxymethylglutarate CoA-transferase
3.1.2.5 hydroxymethylglutaryl-CoA hydrolase
4.1.3.4 hydroxymethylglutaryl-CoA lyase
4.2.1.18 methylglutaconyl-CoA hydratase

1633. C00223 4-Coumaroyl-CoA (Molfile)(InChI)(KEGG)

2.3.1.133 shikimate O-hydroxycinnamoyltransferase
2.3.1.170 6'-deoxychalcone synthase
2.3.1.173 flavonol-3-O-triglucoside O-coumaroyltransferase
2.3.1.64 agmatine N4-coumaroyltransferase
2.3.1.74 naringenin-chalcone synthase
2.3.1.95 trihydroxystilbene synthase
6.2.1.12 4-coumarate-CoA ligase

1634. C07118 Benzoyl acetyl coenzyme A (Molfile)(InChI)(KEGG)

map00642 Ethylbenzene degradation

1635. C07909 Rapamycin (Molfile)(InChI)(KEGG)

map01052 Type I polyketide structures

1636. C11929 Perillyl-CoA (Molfile)(InChI)(KEGG)

map00903 Limonene and pinene degradation

1637. C12324 3,5-Dihydroxyphenylacetyl-CoA (Molfile)(InChI)(KEGG)

map01055 Biosynthesis of vancomycin group antibiotics

1638. C01920 Geranoyl-CoA (Molfile)(InChI)(KEGG)

6.4.1.5 geranoyl-CoA carboxylase

1639. C11945 trans-2-Methyl-5-isopropylhexa-2,5-dienoyl-CoA (Molfile)(InChI)(KEGG)

map00903 Limonene and pinene degradation

1640. C11946 cis-2-Methyl-5-isopropylhexa-2,5-dienoyl-CoA (Molfile)(InChI)(KEGG)

map00903 Limonene and pinene degradation

BiSSCat v1.06.20 http://bisscat.org/
Developed by Masaaki Kotera, Department of Biochemistry, Trinity College Dublin.
Science Foundation of Ireland is gratefully acknowledged.

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