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Results 1 - 10 of 30 > >>
EC Number
Substrates
Commentary Substrates
Organism
Products
Commentary (Products)
Reversibility
caffeoyl-CoA + malonyl-CoA
8% of activity with 4-coumaroyl-CoA
3,3',4',5-tetrahydroxystilbene + CoA + CO2
-
?
3-coumaroyl-CoA + malonyl-CoA
9% of activity with 4-coumaroyl-CoA
3,3',5-trihydroxystilbene + CoA + CO2
-
?
feruloyl-CoA + malonyl-CoA
6% of activity with 4-coumaroyl-CoA
3,4',5-trihydroxy-3'-methoxystilbene + CoA + CO2
-
?
dihydro-4-coumaroyl-CoA + malonyl-CoA
13% of activity with 4-coumaroyl-CoA
3,4',5-trihydroxybibenzyl + CoA + CO2
-
?
4-coumaroyl-CoA + malonyl-CoA
-
3,4',5-trihydroxystilbene + CoA + CO2
-
?
4-coumaroyl-CoA + malonyl-CoA
-
3,4',5-trihydroxystilbene + CoA + CO2
-
?
4-coumaroyl-CoA + malonyl-CoA
-
3,4',5-trihydroxystilbene + CoA + CO2
79% resveratrol, side products: 10% p-coumaroyltriacetic acid lactone, 8.6% bisnoryangonin and 1.7% naringenin
-
4-coumaroyl-CoA + malonyl-CoA
-
3,4',5-trihydroxystilbene + CoA + CO2
side products: smaller amounts of bisnoryangonin-type and p-coumaroyltriacetic acid lactone-type pyrones
?
4-coumaroyl-CoA + malonyl-CoA
malonyl-CoA cannot be replaced by related compounds e.g. acetyl-CoA
3,4',5-trihydroxystilbene + CoA + CO2
trivial name resveratrol
?
4-coumaroyl-CoA + malonyl-CoA
key enzyme of stilbene synthesis
3,4',5-trihydroxystilbene + CoA + CO2
-
?
Results 1 - 10 of 30 > >>