Search More · GCI-TPs

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

Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

2 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

6 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

C(=O)(C(O)=O)O

Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

C(CCC(=O)C(=O)O)(=O)C(O)=O

Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

14 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

C(CC(C(O)O)O)O

Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

14 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

But-1-ene-1,1,4-triol

C(CC=C(O)O)O

Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

7 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

C([N+](=O)[O-])([O-])=O

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

Upstream Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

Abiotic

Product

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

Upstream Precursor

ZUMBBWMZQCENOR-UHFFFAOYSA-N

CCCS(=O)(=O)Nc1c(ccc(c1)C(=O)c2ccccc2)N=O

Environmental

Product

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

Upstream Precursor

MEKVOGWLDVTFOC-UHFFFAOYSA-N

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N(O)O

Abiotic

Product

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

Upstream Precursor

WQXIPRCOZBWMNU-UHFFFAOYSA-N

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)NO

Abiotic

Product

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

Upstream Precursor

WQXIPRCOZBWMNU-UHFFFAOYSA-N

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)NO

Environmental

Product

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

Previewing top 5 entries. If you want the full results, please use the download button above.

Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

Abiotic

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

Environmental

Downstream Successor

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

Environmental

Downstream Successor

JBEBGTMCZIGUTK-UHFFFAOYSA-N

2-Hydroxyhexa-2,4-diendioic acid

C(=CC=CC(=O)O)(C(O)=O)O

Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

Environmental

Downstream Successor

NBBJYMSMWIIQGU-UHFFFAOYSA-N

Propanal

CCC=O

Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

Environmental

Downstream Successor

WQPMYSHJKXVTME-UHFFFAOYSA-N

1-Propanesulfonic acid, 3-hydroxy-

OCCCS(=O)(=O)O

Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

Environmental

Downstream Successor

KCXFHTAICRTXLI-UHFFFAOYSA-N

1-Propanesulfonic acid

CCCS(=O)(=O)O

Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

Abiotic

Downstream Successor

KCXFHTAICRTXLI-UHFFFAOYSA-N

1-Propanesulfonic acid

CCCS(=O)(=O)O

Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

Environmental

Downstream Successor

KCXFHTAICRTXLI-UHFFFAOYSA-N

1-Propanesulfonic acid

CCCS(=O)(=O)O

Precursor

ANPFMRPEXKODMN-UHFFFAOYSA-N

N-(2-Amino-5-benzoylphenyl)propane-1-sulphonamide

CCCS(=O)(=O)NC1=C(C=CC(=C1)C(=O)C2=CC=CC=C2)N

Environmental

Downstream Successor

GTIBQOVZWUVLOF-UHFFFAOYSA-N

Methanone, (4-amino-3-hydroxyphenyl)phenyl-

NC1=CC=C(C=C1O)C(=O)C2=CC=CC=C2

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.

Search with another depth

Depth:

or Explore another compound

Higher depth reveals distant relationships but increases loading time.