Graphs show a maximum of 100 compounds. Use downloads for complete results.
Depiction
Upstream Precursor
3-Methyl-1-(4-methylphenyl)sulfonyl-4-phenylpiperidine-4-carboxylic acid
CC1CN(CCC1(C(O)=O)C2=CC=CC=C2)S(=O)(=O)C3=CC=C(C=C3)C
Environmental
Depiction
Product
CC1CN(CCC1(C2=CC=CC=C2)C(=O)O)S(=O)(=O)C3=CC=C(C(=C3O)O)C
Depiction
Upstream Precursor
3-Methyl-1-(4-methylphenyl)sulfonyl-4-phenylpiperidine-4-carboxylic acid
CC1CN(CCC1(C(O)=O)C2=CC=CC=C2)S(=O)(=O)C3=CC=C(C=C3)C
Environmental
Depiction
Product
CC1CN(CCC1(C2=CC=CC=C2)C(=O)O)S(=O)(=O)C3=CC=C(C(=C3O)O)C
Depiction
Upstream Precursor
Benzyl 3-methyl-4-phenyl-1-(p-tolylsulphonyl)piperidine-4-carboxylate
CC1CN(CCC1(C2=CC=CC=C2)C(=O)OCC3=CC=CC=C3)S(=O)(=O)C4=CC=C(C=C4)C
Abiotic
Depiction
Product
CC1CN(CCC1(C2=CC=CC=C2)C(=O)O)S(=O)(=O)C3=CC=C(C(=C3O)O)C
Depiction
Upstream Precursor
Benzyl 3-methyl-4-phenyl-1-(p-tolylsulphonyl)piperidine-4-carboxylate
CC1CN(CCC1(C2=CC=CC=C2)C(=O)OCC3=CC=CC=C3)S(=O)(=O)C4=CC=C(C=C4)C
Abiotic
Depiction
Product
CC1CN(CCC1(C2=CC=CC=C2)C(=O)O)S(=O)(=O)C3=CC=C(C(=C3O)O)C
Depiction
Upstream Precursor
Benzyl 3-methyl-4-phenyl-1-(p-tolylsulphonyl)piperidine-4-carboxylate
CC1CN(CCC1(C2=CC=CC=C2)C(=O)OCC3=CC=CC=C3)S(=O)(=O)C4=CC=C(C=C4)C
PriorBiotransformation
Depiction
Product
CC1CN(CCC1(C2=CC=CC=C2)C(=O)O)S(=O)(=O)C3=CC=C(C(=C3O)O)C
Depiction
Upstream Precursor
trans-(1)-3-Methyl-4-phenyl-1-(p-tolylsulphonyl)piperidine-4-carbonyl chloride
C[C@H]1CN(CC[C@]1(C2=CC=CC=C2)C(=O)Cl)S(=O)(=O)C3=CC=C(C=C3)C
Abiotic
Depiction
Product
CC1CN(CCC1(C2=CC=CC=C2)C(=O)O)S(=O)(=O)C3=CC=C(C(=C3O)O)C
Depiction
Upstream Precursor
trans-(1)-3-Methyl-4-phenyl-1-(p-tolylsulphonyl)piperidine-4-carbonyl chloride
C[C@H]1CN(CC[C@]1(C2=CC=CC=C2)C(=O)Cl)S(=O)(=O)C3=CC=C(C=C3)C
Environmental
Depiction
Product
CC1CN(CCC1(C2=CC=CC=C2)C(=O)O)S(=O)(=O)C3=CC=C(C(=C3O)O)C
Depiction
Upstream Precursor
trans-(1)-3-Methyl-4-phenyl-1-(p-tolylsulphonyl)piperidine-4-carbonyl chloride
C[C@H]1CN(CC[C@]1(C2=CC=CC=C2)C(=O)Cl)S(=O)(=O)C3=CC=C(C=C3)C
Environmental
Depiction
Product
CC1CN(CCC1(C2=CC=CC=C2)C(=O)O)S(=O)(=O)C3=CC=C(C(=C3O)O)C
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
or Explore another compound
Higher depth reveals distant relationships but increases loading time.