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Depiction
Precursor
2-[4-[5-(4-Chlorophenyl)-3,4-dihydropyrazol-2-yl]phenyl]sulfonylethanesulfonic acid
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)(CCS(=O)(=O)O)=O
7 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Upstream Precursor
2-[4-[5-(4-Chlorophenyl)-3,4-dihydropyrazol-2-yl]phenyl]sulfonylethanesulfonic acid
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)(CCS(=O)(=O)O)=O
Abiotic
Depiction
Product
2-[4-[5-(4-Chlorophenyl)-3,4-dihydropyrazol-2-yl]phenyl]sulfonylethanesulfonic acid
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)(CCS(=O)(=O)O)=O
Depiction
Upstream Precursor
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)SCCS(=O)(=O)O
Abiotic
Depiction
Product
2-[4-[5-(4-Chlorophenyl)-3,4-dihydropyrazol-2-yl]phenyl]sulfonylethanesulfonic acid
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)(CCS(=O)(=O)O)=O
Depiction
Upstream Precursor
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)SCCS(=O)(=O)O
Environmental
Depiction
Product
2-[4-[5-(4-Chlorophenyl)-3,4-dihydropyrazol-2-yl]phenyl]sulfonylethanesulfonic acid
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)(CCS(=O)(=O)O)=O
Depiction
Upstream Precursor
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)CCS(=O)(=O)O
Abiotic
Depiction
Product
2-[4-[5-(4-Chlorophenyl)-3,4-dihydropyrazol-2-yl]phenyl]sulfonylethanesulfonic acid
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)(CCS(=O)(=O)O)=O
Depiction
Upstream Precursor
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)CCS(=O)(=O)O
Environmental
Depiction
Product
2-[4-[5-(4-Chlorophenyl)-3,4-dihydropyrazol-2-yl]phenyl]sulfonylethanesulfonic acid
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)(CCS(=O)(=O)O)=O
Depiction
Upstream Precursor
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)CCS(=O)(=O)O
Environmental
Depiction
Product
2-[4-[5-(4-Chlorophenyl)-3,4-dihydropyrazol-2-yl]phenyl]sulfonylethanesulfonic acid
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)(CCS(=O)(=O)O)=O
Depiction
Upstream Precursor
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)CCS(=O)(=O)O
Abiotic
Depiction
Product
2-[4-[5-(4-Chlorophenyl)-3,4-dihydropyrazol-2-yl]phenyl]sulfonylethanesulfonic acid
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)(CCS(=O)(=O)O)=O
Depiction
Precursor
2-[4-[5-(4-Chlorophenyl)-3,4-dihydropyrazol-2-yl]phenyl]sulfonylethanesulfonic acid
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)(CCS(=O)(=O)O)=O
Environmental
Depiction
Downstream Successor
C(C(=C(O)C(=O)O)Cl)=CC(O)=O
Depiction
Precursor
2-[4-[5-(4-Chlorophenyl)-3,4-dihydropyrazol-2-yl]phenyl]sulfonylethanesulfonic acid
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)(CCS(=O)(=O)O)=O
Environmental
Depiction
Downstream Successor
C(CS(=O)(=O)C1=CC=C(C=C1)N2CCC(=N2)C3=CC=C(C=C3)Cl)=O
Depiction
Precursor
2-[4-[5-(4-Chlorophenyl)-3,4-dihydropyrazol-2-yl]phenyl]sulfonylethanesulfonic acid
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)(CCS(=O)(=O)O)=O
Abiotic
Depiction
Downstream Successor
C1CN(N=C1C2=CC(=C(C=C2)O)O)C3=CC=C(C=C3)S(=O)(=O)CCS(=O)(=O)O
Depiction
Precursor
2-[4-[5-(4-Chlorophenyl)-3,4-dihydropyrazol-2-yl]phenyl]sulfonylethanesulfonic acid
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)(CCS(=O)(=O)O)=O
Environmental
Depiction
Downstream Successor
C1CN(N=C1C2=CC(=C(C=C2)O)O)C3=CC=C(C=C3)S(=O)(=O)CCS(=O)(=O)O
Depiction
Precursor
2-[4-[5-(4-Chlorophenyl)-3,4-dihydropyrazol-2-yl]phenyl]sulfonylethanesulfonic acid
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)(CCS(=O)(=O)O)=O
Environmental
Depiction
Downstream Successor
C1CN(N=C1C2=CC=C(C=C2)O)C3=CC=C(C=C3)S(=O)(=O)CC=O
Depiction
Precursor
2-[4-[5-(4-Chlorophenyl)-3,4-dihydropyrazol-2-yl]phenyl]sulfonylethanesulfonic acid
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)(CCS(=O)(=O)O)=O
Environmental
Depiction
Downstream Successor
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C(=C3O)O)S(=O)(=O)CC=O
Depiction
Precursor
2-[4-[5-(4-Chlorophenyl)-3,4-dihydropyrazol-2-yl]phenyl]sulfonylethanesulfonic acid
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)(CCS(=O)(=O)O)=O
Environmental
Depiction
Downstream Successor
O=CCS(=O)C1=CC=C(C=C1)N2CCC(=N2)C3=CC=C(C=C3)Cl
Depiction
Precursor
2-[4-[5-(4-Chlorophenyl)-3,4-dihydropyrazol-2-yl]phenyl]sulfonylethanesulfonic acid
C1CN(N=C1C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)S(=O)(CCS(=O)(=O)O)=O
Abiotic
Depiction
Downstream Successor
O=CCS(=O)C1=CC=C(C=C1)N2CCC(=N2)C3=CC=C(C=C3)Cl
No Original Precursors

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