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π§ͺ Hydrogen (2R,3S)-3-methyloxiran-2-ylphosphonic acid
Appears in:
1 pathway
Produces:
3 compounds
Chemical Structure
π Properties
SMILES:
O=P(O)(O)C1OC1C
InChI:
InChI=1S/C3H7O4P/c1-2-3(7-2)8(4,5)6/h2-3H,1H3,(H2,4,5,6)
Database ID:
967
External:
View on PubChem β
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π
Starting Compound:
This compound serves as the root (starting point) for 1 degradation pathway.
π¬ Reactant
Hydrogen (2R,3S)-3-methyloxiran-2-ylphosphonic acid
β
Hydrogen (1R,2R)-1-glutathio-2-hydroxypropylphosphonic acid
glutathione transferase
(Eawag BBD reaction r1073)
(EC 2.5.1.18)
In pathway:
Fosfomycin
Hydrogen (2R,3S)-3-methyloxiran-2-ylphosphonic acid
β
Hydrogen (1R,2R)-1,2-dihydroxypropylphosphonic acid
epoxide hydrolase
(Eawag BBD reaction r1064)
(EC 3.3.2.10)
In pathway:
Fosfomycin
Hydrogen (2R,3S)-3-methyloxiran-2-ylphosphonic acid
β
Hydrogen (1R,2R)-1- L-cysteine-2-hydroxypropylphosphonic acid
cysteine transferase
(Eawag BBD reaction r1074)
(EC 2.5.1.-)
In pathway:
Fosfomycin
πΊοΈ All Pathways Containing This Compound
Fosfomycin
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