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Depiction
Precursor
benzyl-[3-[[(Z,12R)-12-hydroxyoctadec-9-enoyl]amino]propyl]-dimethylazanium
CCCCCC[C@H](C/C=C\CCCCCCCC(=O)NCCC[N+](C)(C)CC1=CC=CC=C1)O
7 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Precursor
benzyl-[3-[[(Z,12R)-12-hydroxyoctadec-9-enoyl]amino]propyl]-dimethylazanium
CCCCCC[C@H](C/C=C\CCCCCCCC(=O)NCCC[N+](C)(C)CC1=CC=CC=C1)O
10 steps
Depiction
Dead-End Product
Rhodizonic acid
c1(c(c(=O)c(c(c1=O)O)O)=O)=O
Depiction
Precursor
benzyl-[3-[[(Z,12R)-12-hydroxyoctadec-9-enoyl]amino]propyl]-dimethylazanium
CCCCCC[C@H](C/C=C\CCCCCCCC(=O)NCCC[N+](C)(C)CC1=CC=CC=C1)O
Abiotic
Depiction
Downstream Successor
3-(Dimethylamino)propylazanium
NCCC[NH+](C)C
Depiction
Precursor
benzyl-[3-[[(Z,12R)-12-hydroxyoctadec-9-enoyl]amino]propyl]-dimethylazanium
CCCCCC[C@H](C/C=C\CCCCCCCC(=O)NCCC[N+](C)(C)CC1=CC=CC=C1)O
Environmental
Depiction
Downstream Successor
3-(Dimethylamino)propylazanium
NCCC[NH+](C)C
Depiction
Precursor
benzyl-[3-[[(Z,12R)-12-hydroxyoctadec-9-enoyl]amino]propyl]-dimethylazanium
CCCCCC[C@H](C/C=C\CCCCCCCC(=O)NCCC[N+](C)(C)CC1=CC=CC=C1)O
Abiotic
Depiction
Downstream Successor
3-(Dimethylamino)-1-propanol
OCCCN(C)C
Depiction
Precursor
benzyl-[3-[[(Z,12R)-12-hydroxyoctadec-9-enoyl]amino]propyl]-dimethylazanium
CCCCCC[C@H](C/C=C\CCCCCCCC(=O)NCCC[N+](C)(C)CC1=CC=CC=C1)O
Environmental
Depiction
Downstream Successor
3-(Dimethylamino)-1-propanol
OCCCN(C)C
Depiction
Precursor
benzyl-[3-[[(Z,12R)-12-hydroxyoctadec-9-enoyl]amino]propyl]-dimethylazanium
CCCCCC[C@H](C/C=C\CCCCCCCC(=O)NCCC[N+](C)(C)CC1=CC=CC=C1)O
Abiotic
Depiction
Downstream Successor
12-Hydroxyoctadec-9-enoic acid
C(=O)(CCCCCCCC=CCC(CCCCCC)O)O
Depiction
Precursor
benzyl-[3-[[(Z,12R)-12-hydroxyoctadec-9-enoyl]amino]propyl]-dimethylazanium
CCCCCC[C@H](C/C=C\CCCCCCCC(=O)NCCC[N+](C)(C)CC1=CC=CC=C1)O
Environmental
Depiction
Downstream Successor
12-Hydroxyoctadec-9-enoic acid
C(=O)(CCCCCCCC=CCC(CCCCCC)O)O
Depiction
Precursor
benzyl-[3-[[(Z,12R)-12-hydroxyoctadec-9-enoyl]amino]propyl]-dimethylazanium
CCCCCC[C@H](C/C=C\CCCCCCCC(=O)NCCC[N+](C)(C)CC1=CC=CC=C1)O
Environmental
Depiction
Downstream Successor
12-Hydroxystearic acid
CCCCCCC(CCCCCCCCCCC(=O)O)O
No Original Precursors

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

No All Precursors

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

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