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Depiction
Precursor
N-[4-({4-[(Cyclohexylcarbamoyl)amino]phenyl}methyl)phenyl]-N'-octadecylurea
CCCCCCCCCCCCCCCCCCNC(=O)NC1=CC=C(C=C1)CC2=CC=C(C=C2)NC(=O)NC3CCCCC3
13 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Precursor
N-[4-({4-[(Cyclohexylcarbamoyl)amino]phenyl}methyl)phenyl]-N'-octadecylurea
CCCCCCCCCCCCCCCCCCNC(=O)NC1=CC=C(C=C1)CC2=CC=C(C=C2)NC(=O)NC3CCCCC3
18 steps
Depiction
Dead-End Product
1,2,4-Butantriol Alkohol
C(CC(C(O)O)O)O
Depiction
Precursor
N-[4-({4-[(Cyclohexylcarbamoyl)amino]phenyl}methyl)phenyl]-N'-octadecylurea
CCCCCCCCCCCCCCCCCCNC(=O)NC1=CC=C(C=C1)CC2=CC=C(C=C2)NC(=O)NC3CCCCC3
18 steps
Depiction
Dead-End Product
But-1-ene-1,1,4-triol
C(CC=C(O)O)O
Depiction
Precursor
N-[4-({4-[(Cyclohexylcarbamoyl)amino]phenyl}methyl)phenyl]-N'-octadecylurea
CCCCCCCCCCCCCCCCCCNC(=O)NC1=CC=C(C=C1)CC2=CC=C(C=C2)NC(=O)NC3CCCCC3
4 steps
Depiction
Dead-End Product
CID 22568690
C([N+](=O)[O-])([O-])=O
Depiction
Precursor
N-[4-({4-[(Cyclohexylcarbamoyl)amino]phenyl}methyl)phenyl]-N'-octadecylurea
CCCCCCCCCCCCCCCCCCNC(=O)NC1=CC=C(C=C1)CC2=CC=C(C=C2)NC(=O)NC3CCCCC3
Depth 3
Depiction
Downstream Successor
Stearic Acid
C(CCCCCCCCCCCCCCCCC)(O)=O
Depiction
Precursor
N-[4-({4-[(Cyclohexylcarbamoyl)amino]phenyl}methyl)phenyl]-N'-octadecylurea
CCCCCCCCCCCCCCCCCCNC(=O)NC1=CC=C(C=C1)CC2=CC=C(C=C2)NC(=O)NC3CCCCC3
Depth 3
Depiction
Downstream Successor
Hydroxycarbamic acid
OC(=O)NO
Depiction
Precursor
N-[4-({4-[(Cyclohexylcarbamoyl)amino]phenyl}methyl)phenyl]-N'-octadecylurea
CCCCCCCCCCCCCCCCCCNC(=O)NC1=CC=C(C=C1)CC2=CC=C(C=C2)NC(=O)NC3CCCCC3
Depth 3
Depiction
Downstream Successor
N-oxocarbamate
C(N=O)([O-])=O
Depiction
Precursor
N-[4-({4-[(Cyclohexylcarbamoyl)amino]phenyl}methyl)phenyl]-N'-octadecylurea
CCCCCCCCCCCCCCCCCCNC(=O)NC1=CC=C(C=C1)CC2=CC=C(C=C2)NC(=O)NC3CCCCC3
Depth 1
Depiction
Downstream Successor
Stearyl Alcohol
CCCCCCCCCCCCCCCCCCO
Depiction
Precursor
N-[4-({4-[(Cyclohexylcarbamoyl)amino]phenyl}methyl)phenyl]-N'-octadecylurea
CCCCCCCCCCCCCCCCCCNC(=O)NC1=CC=C(C=C1)CC2=CC=C(C=C2)NC(=O)NC3CCCCC3
Depth 1
Depiction
Downstream Successor
N-cyclohexylcarbamate
C(NC1CCCCC1)(=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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