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Depiction
Upstream Precursor
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CC[NH+](CC2)C3=CC=CC=C3OC
Abiotic
Depiction
Product
1,3,5-Trimethyl-6-[[3-[4-(2-hydroxyphenyl)-1-piperazinyl]propyl]amino]-2,4(1H,3H)-pyrimidinedione
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC=C3O
Depiction
Upstream Precursor
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CC[NH+](CC2)C3=CC=CC=C3OC
Environmental
Depiction
Product
1,3,5-Trimethyl-6-[[3-[4-(2-hydroxyphenyl)-1-piperazinyl]propyl]amino]-2,4(1H,3H)-pyrimidinedione
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC=C3O
Depiction
Upstream Precursor
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CC[NH+](CC2)C3=CC=CC=C3OC
Abiotic
Depiction
Product
1,3,5-Trimethyl-6-[[3-[4-(2-hydroxyphenyl)-1-piperazinyl]propyl]amino]-2,4(1H,3H)-pyrimidinedione
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC=C3O
Depiction
Upstream Precursor
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CC[NH+](CC2)C3=CC=CC=C3OC
Environmental
Depiction
Product
1,3,5-Trimethyl-6-[[3-[4-(2-hydroxyphenyl)-1-piperazinyl]propyl]amino]-2,4(1H,3H)-pyrimidinedione
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC=C3O
Depiction
Upstream Precursor
1,3,5-Trimethyl-6-[[3-[4-(2-hydroxyphenyl)-1-piperazinyl]propyl]amino]-2,4(1H,3H)-pyrimidinedione
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC=C3O
Abiotic
Depiction
Product
1,3,5-Trimethyl-6-[[3-[4-(2-hydroxyphenyl)-1-piperazinyl]propyl]amino]-2,4(1H,3H)-pyrimidinedione
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC=C3O
Depiction
Upstream Precursor
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC(=C3O)Cl
Abiotic
Depiction
Product
1,3,5-Trimethyl-6-[[3-[4-(2-hydroxyphenyl)-1-piperazinyl]propyl]amino]-2,4(1H,3H)-pyrimidinedione
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC=C3O
Depiction
Upstream Precursor
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC(=C3O)Cl
Environmental
Depiction
Product
1,3,5-Trimethyl-6-[[3-[4-(2-hydroxyphenyl)-1-piperazinyl]propyl]amino]-2,4(1H,3H)-pyrimidinedione
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC=C3O
Depiction
Upstream Precursor
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC(=C3O)Cl
Environmental
Depiction
Product
1,3,5-Trimethyl-6-[[3-[4-(2-hydroxyphenyl)-1-piperazinyl]propyl]amino]-2,4(1H,3H)-pyrimidinedione
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC=C3O
Depiction
Upstream Precursor
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC(=C3O)Cl
Abiotic
Depiction
Product
1,3,5-Trimethyl-6-[[3-[4-(2-hydroxyphenyl)-1-piperazinyl]propyl]amino]-2,4(1H,3H)-pyrimidinedione
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC=C3O
Depiction
Upstream Precursor
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CC[N+](CC2)(C3=CC=CC=C3O)[O-]
Environmental
Depiction
Product
1,3,5-Trimethyl-6-[[3-[4-(2-hydroxyphenyl)-1-piperazinyl]propyl]amino]-2,4(1H,3H)-pyrimidinedione
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC=C3O
Depiction
Precursor
1,3,5-Trimethyl-6-[[3-[4-(2-hydroxyphenyl)-1-piperazinyl]propyl]amino]-2,4(1H,3H)-pyrimidinedione
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC=C3O
Abiotic
Depiction
Downstream Successor
2-Hydroxyhexa-2,4-diendioic acid
C(=CC=CC(=O)O)(C(O)=O)O
Depiction
Precursor
1,3,5-Trimethyl-6-[[3-[4-(2-hydroxyphenyl)-1-piperazinyl]propyl]amino]-2,4(1H,3H)-pyrimidinedione
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC=C3O
Abiotic
Depiction
Downstream Successor
2,4-Hexadienedioic acid, (2Z,4Z)-
C(C=CC=CC(=O)O)(O)=O
Depiction
Precursor
1,3,5-Trimethyl-6-[[3-[4-(2-hydroxyphenyl)-1-piperazinyl]propyl]amino]-2,4(1H,3H)-pyrimidinedione
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC=C3O
Environmental
Depiction
Downstream Successor
3-Hydroxyhexa-2,4-dienedioic acid
C(C=CC(=O)O)(=CC(O)=O)O
Depiction
Precursor
1,3,5-Trimethyl-6-[[3-[4-(2-hydroxyphenyl)-1-piperazinyl]propyl]amino]-2,4(1H,3H)-pyrimidinedione
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC=C3O
Abiotic
Depiction
Downstream Successor
Succinic Acid
C(CC(O)=O)C(O)=O
Depiction
Precursor
1,3,5-Trimethyl-6-[[3-[4-(2-hydroxyphenyl)-1-piperazinyl]propyl]amino]-2,4(1H,3H)-pyrimidinedione
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC=C3O
Environmental
Depiction
Downstream Successor
Piperazine
C1CNCCN1
Depiction
Precursor
1,3,5-Trimethyl-6-[[3-[4-(2-hydroxyphenyl)-1-piperazinyl]propyl]amino]-2,4(1H,3H)-pyrimidinedione
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC=C3O
Abiotic
Depiction
Downstream Successor
CID 417
C(C=C(C=CC(O)=O)Cl)(O)=O
Depiction
Precursor
1,3,5-Trimethyl-6-[[3-[4-(2-hydroxyphenyl)-1-piperazinyl]propyl]amino]-2,4(1H,3H)-pyrimidinedione
CC1=C(N(C(=O)N(C1=O)C)C)NCCCN2CCN(CC2)C3=CC=CC=C3O
Environmental
Depiction
Downstream Successor
2-Piperazin-4-ium-1-ylphenol
C1C[NH+](CCN1)C2=CC=CC=C2O
No Original Precursors

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

No Dead-Ends

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