Search More · GCI-TPs

Graphs show a maximum of 100 compounds. Use downloads for complete results.

Upstream Precursor

UPMVPDSZPOOATN-ULZUWYFZSA-N

7-(((2R)-aminophenylacetyl)amino)-3-chloro-8-oxo-5-Thia-1-azabicyclo(4.2.0)oct-3-ene-2-carboxylic acid, (6R,7R)-

C1=CC=C(C=C1)[C@H](C(=O)N[C@H]2[C@@H]3N(C2=O)C(C(=CS3)Cl)C(=O)O)N

Environmental

Product

ZOPJRIFNLLZUOI-UHFFFAOYSA-N

7-[(2-Amino-2-phenylacetyl)amino]-3-hydroxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(=C(CS3)O)C(=O)O)N

Upstream Precursor

QYIYFLOTGYLRGG-GPCCPHFNSA-N

Cefaclor

C1C(=C(N2[C@H](S1)[C@@H](C2=O)NC(=O)[C@@H](C3=CC=CC=C3)N)C(=O)O)Cl

Environmental

Product

ZOPJRIFNLLZUOI-UHFFFAOYSA-N

7-[(2-Amino-2-phenylacetyl)amino]-3-hydroxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(=C(CS3)O)C(=O)O)N

Upstream Precursor

DVTWTJLWDODKJS-UHFFFAOYSA-N

C1C(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=CC=C3)N)C(=O)O)(Cl)O

Abiotic

Product

ZOPJRIFNLLZUOI-UHFFFAOYSA-N

7-[(2-Amino-2-phenylacetyl)amino]-3-hydroxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(=C(CS3)O)C(=O)O)N

Upstream Precursor

DVTWTJLWDODKJS-UHFFFAOYSA-N

C1C(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=CC=C3)N)C(=O)O)(Cl)O

Environmental

Product

ZOPJRIFNLLZUOI-UHFFFAOYSA-N

7-[(2-Amino-2-phenylacetyl)amino]-3-hydroxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(=C(CS3)O)C(=O)O)N

Upstream Precursor

DVTWTJLWDODKJS-UHFFFAOYSA-N

C1C(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=CC=C3)N)C(=O)O)(Cl)O

Abiotic

Product

ZOPJRIFNLLZUOI-UHFFFAOYSA-N

7-[(2-Amino-2-phenylacetyl)amino]-3-hydroxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(=C(CS3)O)C(=O)O)N

Upstream Precursor

DHFQYIAEICFKKY-UHFFFAOYSA-N

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(C(CS3=O)(Cl)O)C(=O)O)N

Abiotic

Product

ZOPJRIFNLLZUOI-UHFFFAOYSA-N

7-[(2-Amino-2-phenylacetyl)amino]-3-hydroxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(=C(CS3)O)C(=O)O)N

Upstream Precursor

VMHBVADHXLQFPX-UHFFFAOYSA-N

C1=CC=C(C=C1)C(C(=O)NC2C3[N+](C2=O)(C(C(CS3)(Cl)O)C(=O)O)[O-])N

Environmental

Product

ZOPJRIFNLLZUOI-UHFFFAOYSA-N

7-[(2-Amino-2-phenylacetyl)amino]-3-hydroxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(=C(CS3)O)C(=O)O)N

Upstream Precursor

AMCBNCWNALNIJH-UHFFFAOYSA-O

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(C(C[S+]3Cl)(Cl)O)C(=O)O)N

Abiotic

Product

ZOPJRIFNLLZUOI-UHFFFAOYSA-N

7-[(2-Amino-2-phenylacetyl)amino]-3-hydroxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(=C(CS3)O)C(=O)O)N

Upstream Precursor

HCAZDJKHIPWHJO-UHFFFAOYSA-N

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(C(=CS3=O)Cl)C(=O)O)N

Environmental

Product

ZOPJRIFNLLZUOI-UHFFFAOYSA-N

7-[(2-Amino-2-phenylacetyl)amino]-3-hydroxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(=C(CS3)O)C(=O)O)N

Upstream Precursor

HCAZDJKHIPWHJO-UHFFFAOYSA-N

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(C(=CS3=O)Cl)C(=O)O)N

Abiotic

Product

ZOPJRIFNLLZUOI-UHFFFAOYSA-N

7-[(2-Amino-2-phenylacetyl)amino]-3-hydroxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(=C(CS3)O)C(=O)O)N

Previewing top 10 entries. If you want the full results, please use the download button above.

Precursor

ZOPJRIFNLLZUOI-UHFFFAOYSA-N

7-[(2-Amino-2-phenylacetyl)amino]-3-hydroxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(=C(CS3)O)C(=O)O)N

Abiotic

Downstream Successor

FAQJJMHZNSSFSM-UHFFFAOYSA-N

Phenylglyoxylic Acid

c1cccc(c1)C(C(O)=O)=O

Precursor

ZOPJRIFNLLZUOI-UHFFFAOYSA-N

7-[(2-Amino-2-phenylacetyl)amino]-3-hydroxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(=C(CS3)O)C(=O)O)N

Environmental

Downstream Successor

FAQJJMHZNSSFSM-UHFFFAOYSA-N

Phenylglyoxylic Acid

c1cccc(c1)C(C(O)=O)=O

Precursor

ZOPJRIFNLLZUOI-UHFFFAOYSA-N

7-[(2-Amino-2-phenylacetyl)amino]-3-hydroxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(=C(CS3)O)C(=O)O)N

Environmental

Downstream Successor

ZGUNAGUHMKGQNY-ZETCQYMHSA-N

L-Phenylglycine

C1=CC=C(C=C1)[C@@H](C(=O)O)N

Precursor

ZOPJRIFNLLZUOI-UHFFFAOYSA-N

7-[(2-Amino-2-phenylacetyl)amino]-3-hydroxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(=C(CS3)O)C(=O)O)N

Abiotic

Downstream Successor

ZGUNAGUHMKGQNY-ZETCQYMHSA-N

L-Phenylglycine

C1=CC=C(C=C1)[C@@H](C(=O)O)N

Precursor

ZOPJRIFNLLZUOI-UHFFFAOYSA-N

7-[(2-Amino-2-phenylacetyl)amino]-3-hydroxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(=C(CS3)O)C(=O)O)N

Environmental

Downstream Successor

KIYRSYYOVDHSPG-SSDOTTSWSA-N

(2R)-2-Amino-2-phenylacetamide

C1=CC=C(C=C1)[C@H](C(=O)N)N

Precursor

ZOPJRIFNLLZUOI-UHFFFAOYSA-N

7-[(2-Amino-2-phenylacetyl)amino]-3-hydroxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(=C(CS3)O)C(=O)O)N

Abiotic

Downstream Successor

APHFQZJMZZWSNW-UHFFFAOYSA-N

C=1C(C=CC(C(C(=O)O)N)C1)=O

Precursor

ZOPJRIFNLLZUOI-UHFFFAOYSA-N

7-[(2-Amino-2-phenylacetyl)amino]-3-hydroxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(=C(CS3)O)C(=O)O)N

Environmental

Downstream Successor

APHFQZJMZZWSNW-UHFFFAOYSA-N

C=1C(C=CC(C(C(=O)O)N)C1)=O

Precursor

ZOPJRIFNLLZUOI-UHFFFAOYSA-N

7-[(2-Amino-2-phenylacetyl)amino]-3-hydroxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(=C(CS3)O)C(=O)O)N

Environmental

Downstream Successor

JJVODHIRRAFJDE-UHFFFAOYSA-N

2-(Hydroxyamino)-2-phenylacetic acid

c1ccccc1C(C(=O)O)NO

Precursor

ZOPJRIFNLLZUOI-UHFFFAOYSA-N

7-[(2-Amino-2-phenylacetyl)amino]-3-hydroxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(=C(CS3)O)C(=O)O)N

Abiotic

Downstream Successor

JJVODHIRRAFJDE-UHFFFAOYSA-N

2-(Hydroxyamino)-2-phenylacetic acid

c1ccccc1C(C(=O)O)NO

Precursor

ZOPJRIFNLLZUOI-UHFFFAOYSA-N

7-[(2-Amino-2-phenylacetyl)amino]-3-hydroxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

C1=CC=C(C=C1)C(C(=O)NC2C3N(C2=O)C(=C(CS3)O)C(=O)O)N

Environmental

Downstream Successor

BQSKWCILIORCGZ-UHFFFAOYSA-N

C=1C(C=CC(C(C(=O)N)N)C1)=O

Previewing top 10 entries. If you want the full results, please use the download button above.

No Original Precursors

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

No Dead-Ends

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

Search with another depth

Depth:

or Explore another compound

Higher depth reveals distant relationships but increases loading time.