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Depiction
Precursor
N-[4-[(4-hydroxy-9,10-dioxoanthracen-1-yl)amino]phenyl]butanamide
CCCC(=O)NC1=CC=C(C=C1)NC2=C3C(=C(C=C2)O)C(=O)C4=CC=CC=C4C3=O
7 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Upstream Precursor
N-[4-[(4-hydroxy-9,10-dioxoanthracen-1-yl)amino]phenyl]butanamide
CCCC(=O)NC1=CC=C(C=C1)NC2=C3C(=C(C=C2)O)C(=O)C4=CC=CC=C4C3=O
Abiotic
Depiction
Product
N-[4-[(4-hydroxy-9,10-dioxoanthracen-1-yl)amino]phenyl]butanamide
CCCC(=O)NC1=CC=C(C=C1)NC2=C3C(=C(C=C2)O)C(=O)C4=CC=CC=C4C3=O
Depiction
Upstream Precursor
CCCC(=O)NC1=CC=C(C=C1)NC2=C3C(=C(C(=C2)Cl)O)C(=O)C4=CC=CC=C4C3=O
Environmental
Depiction
Product
N-[4-[(4-hydroxy-9,10-dioxoanthracen-1-yl)amino]phenyl]butanamide
CCCC(=O)NC1=CC=C(C=C1)NC2=C3C(=C(C=C2)O)C(=O)C4=CC=CC=C4C3=O
Depiction
Upstream Precursor
CCCC(=O)NC1=CC=C(C=C1)NC2=C3C(=C(C(=C2)Cl)O)C(=O)C4=CC=CC=C4C3=O
Abiotic
Depiction
Product
N-[4-[(4-hydroxy-9,10-dioxoanthracen-1-yl)amino]phenyl]butanamide
CCCC(=O)NC1=CC=C(C=C1)NC2=C3C(=C(C=C2)O)C(=O)C4=CC=CC=C4C3=O
Depiction
Upstream Precursor
CCCC(=O)NC1=CC=C(C=C1)NC2=C3C(=C(C(=C2)Cl)O)C(=O)C4=CC=CC=C4C3=O
Abiotic
Depiction
Product
N-[4-[(4-hydroxy-9,10-dioxoanthracen-1-yl)amino]phenyl]butanamide
CCCC(=O)NC1=CC=C(C=C1)NC2=C3C(=C(C=C2)O)C(=O)C4=CC=CC=C4C3=O
Depiction
Upstream Precursor
CCCC(=O)NC1=CC=C(C=C1)NC2=C3C(=C(C(=C2)Cl)O)C(=O)C4=CC=CC=C4C3=O
Environmental
Depiction
Product
N-[4-[(4-hydroxy-9,10-dioxoanthracen-1-yl)amino]phenyl]butanamide
CCCC(=O)NC1=CC=C(C=C1)NC2=C3C(=C(C=C2)O)C(=O)C4=CC=CC=C4C3=O
Depiction
Precursor
N-[4-[(4-hydroxy-9,10-dioxoanthracen-1-yl)amino]phenyl]butanamide
CCCC(=O)NC1=CC=C(C=C1)NC2=C3C(=C(C=C2)O)C(=O)C4=CC=CC=C4C3=O
Abiotic
Depiction
Downstream Successor
C1=CC=C2C(=C1)C(=O)C(=C(C2=O)C(=CC(=O)O)N)C(O)=O
Depiction
Precursor
N-[4-[(4-hydroxy-9,10-dioxoanthracen-1-yl)amino]phenyl]butanamide
CCCC(=O)NC1=CC=C(C=C1)NC2=C3C(=C(C=C2)O)C(=O)C4=CC=CC=C4C3=O
Abiotic
Depiction
Downstream Successor
C1=CC=C2C(=C1)C(=O)C(=C(C2=O)C(=O)O)C(=CC(O)=O)O
No Original Precursors

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