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Depiction
Upstream Precursor
(4-Methoxyphenyl)methyl 3-(chloromethyl)-8-oxo-7-[(2-phenylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
COC1=CC=C(C=C1)COC(=O)C2=C(CSC3N2C(=O)C3NC(=O)CC4=CC=CC=C4)CCl
Abiotic
Depiction
Product
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Depiction
Upstream Precursor
(4-Methoxyphenyl)methyl 3-(chloromethyl)-8-oxo-7-[(2-phenylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
COC1=CC=C(C=C1)COC(=O)C2=C(CSC3N2C(=O)C3NC(=O)CC4=CC=CC=C4)CCl
PriorBiotransformation
Depiction
Product
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Depiction
Upstream Precursor
(4-Methoxyphenyl)methyl 3-(chloromethyl)-8-oxo-7-[(2-phenylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
COC1=CC=C(C=C1)COC(=O)C2=C(CSC3N2C(=O)C3NC(=O)CC4=CC=CC=C4)CCl
Abiotic
Depiction
Product
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Depiction
Upstream Precursor
(4-Methoxyphenyl)methyl 3-(chloromethyl)-8-oxo-7-[(2-phenylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
COC1=CC=C(C=C1)COC(=O)C2=C(CSC3N2C(=O)C3NC(=O)CC4=CC=CC=C4)CCl
PriorBiotransformation
Depiction
Product
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Depiction
Upstream Precursor
(4-Methoxyphenyl)methyl 3-(chloromethyl)-8-oxo-7-[(2-phenylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
COC1=CC=C(C=C1)COC(=O)C2=C(CSC3N2C(=O)C3NC(=O)CC4=CC=CC=C4)CCl
Abiotic
Depiction
Product
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Depiction
Upstream Precursor
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Abiotic
Depiction
Product
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Depiction
Upstream Precursor
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Environmental
Depiction
Product
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Depiction
Upstream Precursor
OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CCl
Abiotic
Depiction
Product
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Depiction
Upstream Precursor
OC(=O)C1=C(CS(C2N1C(=O)C2NC(=O)CC3=CC=CC=C3)=O)CCl
Abiotic
Depiction
Product
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Depiction
Upstream Precursor
OC(=O)C1=C(CSC2[N+]1(C(=O)C2NC(=O)CC3=CC=CC=C3)[O-])CCl
Environmental
Depiction
Product
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Depiction
Precursor
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Environmental
Depiction
Downstream Successor
Phenylacetic Acid
C(CC1=CC=CC=C1)(O)=O
Depiction
Precursor
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Abiotic
Depiction
Downstream Successor
Phenylacetic Acid
C(CC1=CC=CC=C1)(O)=O
Depiction
Precursor
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Environmental
Depiction
Downstream Successor
Dopac
C1=C(C(=CC(=C1)CC(=O)O)O)O
Depiction
Precursor
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Abiotic
Depiction
Downstream Successor
Dopac
C1=C(C(=CC(=C1)CC(=O)O)O)O
Depiction
Precursor
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Environmental
Depiction
Downstream Successor
Benzeneacetamide
C1=CC=CC(=C1)CC(N)=O
Depiction
Precursor
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Abiotic
Depiction
Downstream Successor
7-Amino-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(C1=C(C(=O)O)N2C(C(C2=O)N)SC1)O
Depiction
Precursor
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Environmental
Depiction
Downstream Successor
7-Amino-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(C1=C(C(=O)O)N2C(C(C2=O)N)SC1)O
Depiction
Precursor
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Environmental
Depiction
Downstream Successor
3-Methyl-8-oxo-7-[(phenylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
CC1=C(N2C(C(C2=O)NC(=O)CC3=CC=CC=C3)SC1)C(=O)O
Depiction
Precursor
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Abiotic
Depiction
Downstream Successor
3-Methyl-8-oxo-7-[(phenylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
CC1=C(N2C(C(C2=O)NC(=O)CC3=CC=CC=C3)SC1)C(=O)O
Depiction
Precursor
3-(Chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C(=O)(C1=C(CSC2N1C(=O)C2NC(=O)CC3=CC=CC=C3)CCl)O
Environmental
Depiction
Downstream Successor
CC1=C(N2C(C(C2=O)O)SC1)C(=O)O
No Original Precursors

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No Dead-Ends

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