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Depiction
Upstream Precursor
COC1=CC=CC=C1N2CCN(CC2)CC[NH+](C3=CC=CC=N3)C(=O)C4CCCCC4
Depth 1
Depiction
Product
Cyclohexanecarboxylic acid {2-[4-(2-hydroxy-phenyl)-piperazin-1-yl]-ethyl}-pyridin-2-yl-amide
C1(=CC=CC=C1N2CCN(CC2)CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)O
Depiction
Upstream Precursor
C1(=C(C=CC=C1N2CCN(CC2)CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)Cl)O
Depth 1
Depiction
Product
Cyclohexanecarboxylic acid {2-[4-(2-hydroxy-phenyl)-piperazin-1-yl]-ethyl}-pyridin-2-yl-amide
C1(=CC=CC=C1N2CCN(CC2)CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)O
Depiction
Upstream Precursor
C1(=CC=C(C=C1N2CCN(CC2)CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)Cl)O
Depth 1
Depiction
Product
Cyclohexanecarboxylic acid {2-[4-(2-hydroxy-phenyl)-piperazin-1-yl]-ethyl}-pyridin-2-yl-amide
C1(=CC=CC=C1N2CCN(CC2)CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)O
Depiction
Upstream Precursor
C1(=CC=CC=C1[N+]2(CCN(CC2)CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)[O-])O
Depth 1
Depiction
Product
Cyclohexanecarboxylic acid {2-[4-(2-hydroxy-phenyl)-piperazin-1-yl]-ethyl}-pyridin-2-yl-amide
C1(=CC=CC=C1N2CCN(CC2)CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)O
Depiction
Upstream Precursor
C1(=CC=CC=C1N2CCN(CC2)CC[N+](C3=CC=CC=N3)(C(=O)C4CCCCC4)[O-])O
Depth 1
Depiction
Product
Cyclohexanecarboxylic acid {2-[4-(2-hydroxy-phenyl)-piperazin-1-yl]-ethyl}-pyridin-2-yl-amide
C1(=CC=CC=C1N2CCN(CC2)CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)O
Depiction
Upstream Precursor
C1(=CC=CC=C1N2CC[N+](CC2)(CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)[O-])O
Depth 1
Depiction
Product
Cyclohexanecarboxylic acid {2-[4-(2-hydroxy-phenyl)-piperazin-1-yl]-ethyl}-pyridin-2-yl-amide
C1(=CC=CC=C1N2CCN(CC2)CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)O
Depiction
Upstream Precursor
COC1=CC=CC=C1[N+]2(CCN(CC2)CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)[O-]
Depth 2
Depiction
Product
Cyclohexanecarboxylic acid {2-[4-(2-hydroxy-phenyl)-piperazin-1-yl]-ethyl}-pyridin-2-yl-amide
C1(=CC=CC=C1N2CCN(CC2)CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)O
Depiction
Upstream Precursor
COC1=CC=CC=C1N2CCN(CC2)CC[N+](C3=CC=CC=N3)(C(=O)C4CCCCC4)[O-]
Depth 2
Depiction
Product
Cyclohexanecarboxylic acid {2-[4-(2-hydroxy-phenyl)-piperazin-1-yl]-ethyl}-pyridin-2-yl-amide
C1(=CC=CC=C1N2CCN(CC2)CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)O
Depiction
Upstream Precursor
COC1=CC=CC=C1N2CC[N+](CC2)(CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)[O-]
Depth 2
Depiction
Product
Cyclohexanecarboxylic acid {2-[4-(2-hydroxy-phenyl)-piperazin-1-yl]-ethyl}-pyridin-2-yl-amide
C1(=CC=CC=C1N2CCN(CC2)CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)O
Depiction
Upstream Precursor
COC1=CC=CC=C1[N+]2(CCN(CC2)CC[N+](C3=CC=CC=N3)(C(=O)C4CCCCC4)…
Depth 3
Depiction
Product
Cyclohexanecarboxylic acid {2-[4-(2-hydroxy-phenyl)-piperazin-1-yl]-ethyl}-pyridin-2-yl-amide
C1(=CC=CC=C1N2CCN(CC2)CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)O
Depiction
Precursor
Cyclohexanecarboxylic acid {2-[4-(2-hydroxy-phenyl)-piperazin-1-yl]-ethyl}-pyridin-2-yl-amide
C1(=CC=CC=C1N2CCN(CC2)CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)O
Depth 3
Depiction
Downstream Successor
Chloroacetate
[O-]C(=O)CCl
Depiction
Precursor
Cyclohexanecarboxylic acid {2-[4-(2-hydroxy-phenyl)-piperazin-1-yl]-ethyl}-pyridin-2-yl-amide
C1(=CC=CC=C1N2CCN(CC2)CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)O
Depth 2
Depiction
Downstream Successor
2-Hydroxyhexa-2,4-diendioic acid
C(=CC=CC(=O)O)(C(O)=O)O
Depiction
Precursor
Cyclohexanecarboxylic acid {2-[4-(2-hydroxy-phenyl)-piperazin-1-yl]-ethyl}-pyridin-2-yl-amide
C1(=CC=CC=C1N2CCN(CC2)CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)O
Depth 1
Depiction
Downstream Successor
2,4-Hexadienedioic acid, (2Z,4Z)-
C(C=CC=CC(=O)O)(O)=O
Depiction
Precursor
Cyclohexanecarboxylic acid {2-[4-(2-hydroxy-phenyl)-piperazin-1-yl]-ethyl}-pyridin-2-yl-amide
C1(=CC=CC=C1N2CCN(CC2)CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)O
Depth 2
Depiction
Downstream Successor
3-Hydroxyhexa-2,4-dienedioic acid
C(C=CC(=O)O)(=CC(O)=O)O
Depiction
Precursor
Cyclohexanecarboxylic acid {2-[4-(2-hydroxy-phenyl)-piperazin-1-yl]-ethyl}-pyridin-2-yl-amide
C1(=CC=CC=C1N2CCN(CC2)CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)O
Depth 2
Depiction
Downstream Successor
Succinic Acid
C(CC(O)=O)C(O)=O
Depiction
Precursor
Cyclohexanecarboxylic acid {2-[4-(2-hydroxy-phenyl)-piperazin-1-yl]-ethyl}-pyridin-2-yl-amide
C1(=CC=CC=C1N2CCN(CC2)CCN(C3=CC=CC=N3)C(=O)C4CCCCC4)O
Depth 2
Depiction
Downstream Successor
CID 417
C(C=C(C=CC(O)=O)Cl)(O)=O
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.

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