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Compound class

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Activity

Antibiotics Enzyme Ligands 1. Oxidoreductases 1.13 Acting on single donors with incorporation of molecular oxygen (oxygenases) 1.13.11 With incorporation of two atoms of oxygen 1.13.11.1 catechol 1,2-dioxygenase 1.13.11.10 7,8-dihydroxykynurenate 8,8a-dioxygenase 1.13.11.11 tryptophan 2,3-dioxygenase 1.13.11.12 lipoxygenase 1.13.11.13 ascorbate 2,3-dioxygenase 1.13.11.15 3,4-dihydroxyphenylacetate 2,3-dioxygenase 1.13.11.16 3-carboxyethylcatechol 2,3-dioxygenase 1.13.11.17 indole 2,3-dioxygenase 1.13.11.18 sulfur dioxygenase 1.13.11.19 cysteamine dioxygenase 1.13.11.2 catechol 2,3-dioxygenase 1.13.11.20 cysteine dioxygenase 1.13.11.24 quercetin 2,3-dioxygenase 1.13.11.25 3,4-dihydroxy-9,10-secoandrosta-1,3,5(10)-triene-9,17-dione 1.13.11.29 stizolobate synthase 1.13.11.3 protocatechuate 3,4-dioxygenase 1.13.11.30 stizolobinate synthase 1.13.11.31 arachidonate 12-lipoxygenase 1.13.11.32 2-nitropropane dioxygenase 1.13.11.34 arachidonate 5-lipoxygenase 1.13.11.36 chloridazon-catechol dioxygenase 1.13.11.37 hydroxyquinol 1,2-dioxygenase 1.13.11.38 1-hydroxy-2-naphthoate 1,2-dioxygenase 1.13.11.4 gentisate 1,2-dioxygenase 1.13.11.43 lignostilbene alpha,beta-dioxygenase 1.13.11.5 homogentisate 1,2-dioxygenase 1.13.11.6 3-hydroxyanthranilate 3,4-dioxygenase 1.13.11.8 protocatechuate 4,5-dioxygenase 1.13.11.9 2,5-dihydroxypyridine 5,6-dioxygenase Enzyme Substrates GPCR Ligands Ion Channel Ligands Nuclear Receptor Ligands Transporter Substrates
Compound classification data were obtained from KEGG database.
BiSSCat v1.06.20 http://bisscat.org/
Developed by Masaaki Kotera, Department of Biochemistry, Trinity College Dublin.
Science Foundation of Ireland is gratefully acknowledged.