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Depiction
Precursor
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
4 steps
Depiction
Dead-End Product
Oxalic Acid
C(=O)(C(O)=O)O
Depiction
Precursor
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
5 steps
Depiction
Dead-End Product
CID 22568690
C([N+](=O)[O-])([O-])=O
Depiction
Upstream Precursor
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
Abiotic
Depiction
Product
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
Depiction
Upstream Precursor
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)CCl
Abiotic
Depiction
Product
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
Depiction
Upstream Precursor
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)CCl
Environmental
Depiction
Product
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
Depiction
Upstream Precursor
C(C(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C)Cl
Environmental
Depiction
Product
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
Depiction
Upstream Precursor
C(C(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C)Cl
Abiotic
Depiction
Product
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
Depiction
Upstream Precursor
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)CCl
Environmental
Depiction
Product
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
Depiction
Upstream Precursor
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)CCl
Abiotic
Depiction
Product
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
Depiction
Upstream Precursor
C(C(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C)Cl
Environmental
Depiction
Product
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
Depiction
Upstream Precursor
C(C(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C)Cl
Abiotic
Depiction
Product
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
Depiction
Upstream Precursor
C(C(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)CCl)Cl
Abiotic
Depiction
Product
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
Depiction
Precursor
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
Environmental
Depiction
Downstream Successor
Acetic Acid
CC(=O)O
Depiction
Precursor
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
Environmental
Depiction
Downstream Successor
Chloroacetate
[O-]C(=O)CCl
Depiction
Precursor
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
Abiotic
Depiction
Downstream Successor
Chloroacetate
[O-]C(=O)CCl
Depiction
Precursor
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
Environmental
Depiction
Downstream Successor
Glycolic Acid
C(=O)(CO)O
Depiction
Precursor
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
Abiotic
Depiction
Downstream Successor
Glycolic Acid
C(=O)(CO)O
Depiction
Precursor
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
Environmental
Depiction
Downstream Successor
Uracil
OC1=NC=CC(=O)N1
Depiction
Precursor
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
Environmental
Depiction
Downstream Successor
5-Iodouracil
N1C=C(C(=O)NC1=O)I
Depiction
Precursor
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
Environmental
Depiction
Downstream Successor
CC(=O)OCC1C(CC(O1)O)OC(=O)CCl
Depiction
Precursor
[(2R,3S,5R)-3-(acetyloxy)-5-(5-iodo-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methyl acetate
CC(=O)OCC1C(CC(O1)N2C=C(C(=O)NC2=O)I)OC(=O)C
Abiotic
Depiction
Downstream Successor
CC(=O)OCC1C(CC(O1)O)OC(=O)CCl
No Original Precursors

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