3702
TAXONOMY
CHEBI:10432
ChEBI
SMP0012076
SMPDB
UDP
BioCyc
C19H19O9
1-naphthol 6'-O-malonylglucoside
391.10345
CHEBI:1146900
ChEBI
C16H18O6
1-naphthol glucoside
306.11035
C16H18O6
2-naphthol glucoside
306.11035
1-naphthol glucoside
phenolic glucoside malonyltransferase 1
1.0
CO-A
BioCyc
CHEBI:10319
ChEBI
C21H36N7O16P3S
Coenzyme A
767.11523
1.0
6816
PubChem-compound
C9H14N2O12P2
Uridine 5'-diphosphate
404.0022
10213
ChemSpider
Malonyl-CoA
HMDB0012138
HMDB
6557
ChemSpider
1.0
Arabidopsis thaliana
524-14-1
CAS
1038
PubChem-compound
8341
ChemSpider
90658594
PubChem-compound
GO:0005829
GENE ONTOLOGY
2-naphthol 6'-O-malonylglucoside
2-Naphthol
CPD-13688
BioCyc
135-19-3
CAS
53477679
PubChem-compound
6031
PubChem-compound
CPD-13686
BioCyc
133-89-1
CAS
CPD-13687
BioCyc
90657303
PubChem-compound
CPD-13685
BioCyc
CPD-13683
BioCyc
CPD-8131
BioCyc
1010
ChemSpider
7005
PubChem-compound
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
C10H8O
1-Naphthol
144.05751
SMILES
O[C@H]1[C@@H](O)[C@@H](O[C@@H]1COP(O)(=O)OP(O)(O)=O)N1C=CC(=O)NC1=O
C10H8O
2-Naphthol
144.05751
Uridine 5'-diphosphate
HMDB0000286
HMDB
6739
ChemSpider
CHEBI:91117
ChEBI
Uridine diphosphate glucose
58-98-0
CAS
Cytosol
7573796
PubChem-compound
1-Naphthol
C15H24N2O17P2
Uridine diphosphate glucose
566.055
UDP-GLUCOSE
BioCyc
C00080
KEGG Compound
HMDB0001423
HMDB
C00083
KEGG Compound
2-naphthol glucoside
HMDB0000295
HMDB
5809
ChemSpider
CHEBI:15531
ChEBI
HMDB0012322
HMDB
C24H38N7O19P3S
Malonyl-CoA
853.1156
CHEBI:15378
ChEBI
SMILES
[H+]
4-methylumbelliferyl glucoside
Hydrogen Ion
SMILES
[H][C@]1(COC(=O)CC([O-])=O)O[C@@]([H])(OC2=CC3=C(C=C2)C(C)=CC(=O)O3)[C@]([H])(O)[C@@]([H])(O)[C@]1([H])O
2.3.1.-
false
2.3.1.-
4-methylumbelliferyl glucoside + Malonyl-CoA → 4-methylumbelliferone 6'-O-malonylglucoside + Coenzyme A
LEFT_TO_RIGHT
SMILES
[H][C@]1(COC(=O)CC([O-])=O)O[C@@]([H])(OC2=CC3=CC=CC=C3C=C2)[C@]([H])(O)[C@@]([H])(O)[C@]1([H])O
2.4.1.35
false
2.4.1.35
2-Naphthol + Uridine diphosphate glucose → 2-naphthol glucoside + Hydrogen Ion + Uridine 5'-diphosphate
LEFT_TO_RIGHT
SMILES
[H][C@]1(CO)O[C@@]([H])(OC2=CC=CC3=CC=CC=C23)[C@]([H])(O)[C@@]([H])(O)[C@]1([H])O
PW012938
PathWhiz
Reaction47677
false
2-naphthol glucoside + Malonyl-CoA → 2-naphthol 6'-O-malonylglucoside + Coenzyme A
LEFT_TO_RIGHT
2.4.1.35
false
2.4.1.35
1-Naphthol + Uridine diphosphate glucose → 1-naphthol glucoside + Hydrogen Ion + Uridine 5'-diphosphate
LEFT_TO_RIGHT
Reaction47679
false
1-naphthol glucoside + Malonyl-CoA → 1-naphthol 6'-O-malonylglucoside + Coenzyme A
LEFT_TO_RIGHT
4-methylumbelliferone 6'-O-malonylglucoside
SMILES
CC1=CC(=O)OC2=CC(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=CC=C12
90-15-3
CAS
SMILES
OC1=CC2=CC=CC=C2C=C1
SMILES
OC1=C2C=CC=CC2=CC=C1
1.0
1.0
8663
PubChem-compound
Phenolic Malonylglucosides Biosynthesis
1.0
Coenzyme A
ReactionCatalysis37820
ACTIVATION
1.0
ReactionCatalysis37821
ACTIVATION
C00010
KEGG Compound
C00015
KEGG Compound
10663
PubChem-compound
Q940Z5
UniProt
1.0
SMILES
[H][C@]1(COC(=O)CC([O-])=O)O[C@@]([H])(OC2=CC=CC3=CC=CC=C23)[C@]([H])(O)[C@@]([H])(O)[C@]1([H])O
1.0
phenol beta-glucosyltransferase
SMILES
[H][C@]1(CO)O[C@@]([H])(OC2=CC3=CC=CC=C3C=C2)[C@]([H])(O)[C@@]([H])(O)[C@]1([H])O
1.0
Z0Z000
UniProt
90657742
PubChem-compound
1-naphthol 6'-O-malonylglucoside
1.0
ReactionCatalysis37817
ACTIVATION
SMILES
OC[C@H]1O[C@H](OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=CC(=O)NC2=O)[C@H](O)[C@@H](O)[C@@H]1O
ReactionCatalysis37819
ACTIVATION
ReactionCatalysis37818
ACTIVATION
111141
PubChem-compound
H
Hydrogen Ion
1.007825
C00029
KEGG Compound
CHEBI:17659
ChEBI
2015550
ChemSpider
HMDB0059597
HMDB
1.0
C19H19O9
2-naphthol 6'-O-malonylglucoside
391.10345
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(O)C(=O)NCCC(=O)NCCSC(=O)CC(O)=O
C19H19O11
4-methylumbelliferone 6'-O-malonylglucoside
423.0933
CHEBI:90258
ChEBI
C11713
KEGG Compound
C11714
KEGG Compound
phenol beta-glucosyltransferase
phenolic glucoside malonyltransferase 1
C16H18O8
4-methylumbelliferyl glucoside
338.10016
85-61-0
CAS
MALONYL-COA
BioCyc
HMDB0001175
HMDB
2733779
PubChem-compound
1.0