Graph preview: 0 of up to 100 nodes shown.
Graph preview: 0 of up to 100 nodes shown.

Tab counts show list preview rows. Graph preview may show more nodes, up to 100. Export generates the full dataset subject to format and size limits.

Depiction
Precursor
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
8 steps
Depiction
Dead-End Product
Oxalic Acid
C(=O)(C(O)=O)O
Depiction
Precursor
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
4 steps
Depiction
Dead-End Product
CID 22568690
C([N+](=O)[O-])([O-])=O
Depiction
Precursor
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
5 steps
Depiction
Dead-End Product
Thiophene oxide
c1cs(cc1)=O
Depiction
Precursor
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
5 steps
Depiction
Dead-End Product
1-Oxothiophen-2-ol
Oc1cccs1=O
Depiction
Precursor
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
3 steps
Depiction
Dead-End Product
Methylthiophenone
c1cs(c(c1)C)=O
Depiction
Upstream Precursor
C1C(=C(N2C(S1=O)C(C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
Depth 1
Depiction
Product
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
Depiction
Upstream Precursor
C1C(=C([N+]2(C(S1)C(C2=O)NC(=O)CC3=CC=CS3)[O-])C(=O)O)COC(=O)N
Depth 1
Depiction
Product
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
Depiction
Upstream Precursor
C1C(=C(N2C([S+]1Cl)C(C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
Depth 2
Depiction
Product
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
Depiction
Upstream Precursor
C1C(=C([N+]2(C(S1=O)C(C2=O)NC(=O)CC3=CC=CS3)[O-])C(=O)O)COC(=O)N
Depth 2
Depiction
Product
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
Depiction
Upstream Precursor
C1C(=C(N2C(S1(=O)=O)C(C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
Depth 2
Depiction
Product
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
Depiction
Upstream Precursor
C1C(=C([N+]2(C([S+]1Cl)C(C2=O)NC(=O)CC3=CC=CS3)[O-])C(=O)O)COC(=O)N
Depth 3
Depiction
Product
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
Depiction
Precursor
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
Depth 1
Depiction
Downstream Successor
Carbamic Acid
OC(=O)N
Depiction
Precursor
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
Depth 2
Depiction
Downstream Successor
Hydroxycarbamic acid
OC(=O)NO
Depiction
Precursor
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
Depth 1
Depiction
Downstream Successor
2-Thiopheneacetic acid
OC(=O)CC1=CC=CS1
Depiction
Precursor
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
Depth 1
Depiction
Downstream Successor
Thiophen-2-acetamide
NC(=O)CC1=CC=CS1
Depiction
Precursor
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
Depth 2
Depiction
Downstream Successor
2-Thiophenecarboxaldehyde
C(=O)c1cccs1
Depiction
Precursor
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
Depth 3
Depiction
Downstream Successor
Dihydroxycarbamic acid
C(=O)(N(O)O)O
Depiction
Precursor
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
Depth 2
Depiction
Downstream Successor
C1=CS(C(=C1)CC(O)=O)=O
Depiction
Precursor
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
Depth 3
Depiction
Downstream Successor
2-Thiophenecarboxylic acid
C(C1=CC=CS1)(O)=O
Depiction
Precursor
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
Depth 2
Depiction
Downstream Successor
7-Amino-3-formyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
C1C(=C(N2C(S1)C(C2=O)N)C(=O)O)C=O
Depiction
Precursor
(6R-trans)-3-((Carbamoyloxy)methyl)-8-oxo-7-(2-thienylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid
C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)CC3=CC=CS3)C(=O)O)COC(=O)N
Depth 2
Depiction
Downstream Successor
2-Thiophenemethanol
OCC1=CC=CS1
No Original Precursors

No entries were found for this section with the current query and depth.

Search with another depth
or Explore another compound
Higher depth reveals distant relationships but increases loading time.