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Depiction
Precursor
N-[[4-[2-[4-[(hexylamino)methyl]-2-methoxyphenoxy]ethoxy]-3-methoxyphenyl]methyl]hexan-1-amine
CCCCCCNCC1=CC(=C(C=C1)OCCOC2=C(C=C(C=C2)CNCCCCCC)OC)OC
8 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Precursor
N-[[4-[2-[4-[(hexylamino)methyl]-2-methoxyphenoxy]ethoxy]-3-methoxyphenyl]methyl]hexan-1-amine
CCCCCCNCC1=CC(=C(C=C1)OCCOC2=C(C=C(C=C2)CNCCCCCC)OC)OC
13 steps
Depiction
Dead-End Product
1,2,4-Butantriol Alkohol
C(CC(C(O)O)O)O
Depiction
Precursor
N-[[4-[2-[4-[(hexylamino)methyl]-2-methoxyphenoxy]ethoxy]-3-methoxyphenyl]methyl]hexan-1-amine
CCCCCCNCC1=CC(=C(C=C1)OCCOC2=C(C=C(C=C2)CNCCCCCC)OC)OC
13 steps
Depiction
Dead-End Product
But-1-ene-1,1,4-triol
C(CC=C(O)O)O
Depiction
Precursor
N-[[4-[2-[4-[(hexylamino)methyl]-2-methoxyphenoxy]ethoxy]-3-methoxyphenyl]methyl]hexan-1-amine
CCCCCCNCC1=CC(=C(C=C1)OCCOC2=C(C=C(C=C2)CNCCCCCC)OC)OC
9 steps
Depiction
Dead-End Product
Rhodizonic acid
c1(c(c(=O)c(c(c1=O)O)O)=O)=O
Depiction
Precursor
N-[[4-[2-[4-[(hexylamino)methyl]-2-methoxyphenoxy]ethoxy]-3-methoxyphenyl]methyl]hexan-1-amine
CCCCCCNCC1=CC(=C(C=C1)OCCOC2=C(C=C(C=C2)CNCCCCCC)OC)OC
Environmental
Depiction
Downstream Successor
Hexanal
C(CCC)CC=O
Depiction
Precursor
N-[[4-[2-[4-[(hexylamino)methyl]-2-methoxyphenoxy]ethoxy]-3-methoxyphenyl]methyl]hexan-1-amine
CCCCCCNCC1=CC(=C(C=C1)OCCOC2=C(C=C(C=C2)CNCCCCCC)OC)OC
Environmental
Depiction
Downstream Successor
Hexanal
C(CCC)CC=O
Depiction
Precursor
N-[[4-[2-[4-[(hexylamino)methyl]-2-methoxyphenoxy]ethoxy]-3-methoxyphenyl]methyl]hexan-1-amine
CCCCCCNCC1=CC(=C(C=C1)OCCOC2=C(C=C(C=C2)CNCCCCCC)OC)OC
Environmental
Depiction
Downstream Successor
Hexanoic Acid
CCCCCC(=O)O
Depiction
Precursor
N-[[4-[2-[4-[(hexylamino)methyl]-2-methoxyphenoxy]ethoxy]-3-methoxyphenyl]methyl]hexan-1-amine
CCCCCCNCC1=CC(=C(C=C1)OCCOC2=C(C=C(C=C2)CNCCCCCC)OC)OC
Environmental
Depiction
Downstream Successor
Hexylamine
NCCCCCC
No Original Precursors

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No All Precursors

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