Structure
Loading the model…
- Class
- Organic compound
- Formula
- C5H8O5
- Mass
- 148.114 g/mol
- Charge
- 0
- InChIKey
- XXBSUZSONOQQGK-FLRLBIABSA-N
- SMILES
- O=C1OC[C@@H](O)[C@H](O)[C@H]1O
- Look it up
- ChEBIPubChemBy InChIKey
Identity from ChEBI, geometry from PubChem. Not evidence.
What it touches on the way
Mechanistic reach
1 entity
1 entities reached.
0 reported hops1 assembled from the scaffold
What the reference databases state
Statements
7 statements
7 statements · 1 reference database · Subject: D-xylono-1,5-lactone · Sources: Rhea
- D-xylono-1,5-lactone is converted to D-xyloseCompoundRhea RHEA:22000Inferred only
- D-xylono-1,5-lactone is converted to D-xyloseCompoundRhea RHEA:13861Inferred only
- D-xylose is converted to D-xylono-1,5-lactoneCompoundRhea RHEA:13861Inferred only
- D-xylose is converted to D-xylono-1,5-lactoneCompoundRhea RHEA:22000Inferred only
- D-xylose is converted to D-xylono-1,5-lactoneCompoundRhea RHEA:59324Inferred only
- D-xylono-1,5-lactone is converted to D-xyloseCompoundRhea RHEA:59324Inferred only
- D-xylono-1,5-lactone is a substrate of DHDHProteinRhea RHEA:22000Inferred only
Reactions
5 reactions
MAM01758c+NADP(3-)D-xylono-1,5-lactone+proton+NADPH(4-)
Catalysed by DHDH
Reaction pageLeft to rightBalancedEC 1.1.1.179cytosol
Human-GEM MAR04594CC BY 4.0Reference data
D-xylose+NAD(1-)D-xylono-1,5-lactone+NADH(2-)+hydron
Reaction pageDirection not assertedBalanced
Rhea RHEA:13861CC BY 4.0Reference data
D-xylose+NADP(3-)D-xylono-1,5-lactone+NADPH(4-)+hydron
Catalysed by DHDH
Reaction pageDirection not assertedBalanced
Rhea RHEA:22000CC BY 4.0Reference data
D-xylose+dioxygenD-xylono-1,5-lactone+hydrogen peroxide
Reaction pageDirection not assertedBalanced
Rhea RHEA:59324CC BY 4.0Reference data
D-xylono-1,5-lactone+waterCHEBI:17746+hydron
Reaction pageDirection not assertedBalanced
Rhea RHEA:59328CC BY 4.0Reference data
Other names
2 names
Resolves to: D-xylono-1,5-lactone
- Also called
- D-Xylonolactone
- Systematic name
- (3R,4S,5R)-3,4,5-trihydroxytetrahydro-2H-pyran-2-one