What the reference databases state
Chemical structure
- D-arabinitol is the enantiomer of L-arabinitolCompoundChEBI CHEBI:18333Inferred only
Statements
2 statements
2 statements · 1 reference database · Subject: D-arabinitol · Sources: Human-GEM
- D-arabinitol is converted to L-xyluloseCompoundHuman-GEM MAR09992Inferred only
- L-xylulose is converted to D-arabinitolCompoundHuman-GEM MAR09992Inferred only
Reactions
9 reactions
Reaction pageReversibleBalancedEC 3.1.1.4GO:0005615, GO:0005829
Human-GEM MAR09990CC BY 4.0Reference data
proton+D-arabinitolproton+D-arabinitol
Reaction pageReversibleBalancedEC 3.1.1.4GO:0005615, GO:0005829
Human-GEM MAR09991CC BY 4.0Reference data
NAD(+)+D-arabinitolproton+L-xylulose+NADH(2-)
Reaction pageReversibleBalancedEC 3.1.1.4GO:0005829
Human-GEM MAR09992CC BY 4.0Reference data
Reaction pageReversibleBalance undeterminableGO:0005615
Human-GEM MAR10429CC BY 4.0Reference data
D-arabinitol+NADP(3-)D-ribulose+NADPH(4-)+hydron
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:11868CC BY 4.0Reference data
D-arabinitol+NAD(1-)D-ribulose+NADH(2-)+hydron
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:17389CC BY 4.0Reference data
D-arabinitol+NAD(1-)D-xylulose+NADH(2-)+hydron
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:17921CC BY 4.0Reference data
D-arabinitol+NADP(3-)D-xylulose+NADPH(4-)+hydron
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:21276CC BY 4.0Reference data
D-arabinitol+dioxygenCHEBI:46994+hydrogen peroxide
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:59776CC BY 4.0Reference data