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Depiction
Upstream Precursor
Dibenzo(i,t)(1,4,7,12,15,18)hexaazacyclodocosine-5,13,18,26(6H,19H)-tetrone, 7,8,9,10,11,12,20,21,22,23,24,25-dodecahydro-
C1CNC(=O)C2=CC=CC=C2C(=O)NCCNCCNC(=O)C3=CC=CC=C3C(=O)NCCN1
Abiotic
Depiction
Product
2-[2-[2-[[2-[2-(2-Aminoethylamino)ethylcarbamoyl]benzoyl]amino]ethylamino]ethylcarbamoyl]benzoic acid
C(CNC(=O)C1=CC=CC=C1C(=O)NCCNCCNC(=O)C2=CC=CC=C2C(=O)O)NCCN
Depiction
Upstream Precursor
Dibenzo(i,t)(1,4,7,12,15,18)hexaazacyclodocosine-5,13,18,26(6H,19H)-tetrone, 7,8,9,10,11,12,20,21,22,23,24,25-dodecahydro-
C1CNC(=O)C2=CC=CC=C2C(=O)NCCNCCNC(=O)C3=CC=CC=C3C(=O)NCCN1
Environmental
Depiction
Product
2-[2-[2-[[2-[2-(2-Aminoethylamino)ethylcarbamoyl]benzoyl]amino]ethylamino]ethylcarbamoyl]benzoic acid
C(CNC(=O)C1=CC=CC=C1C(=O)NCCNCCNC(=O)C2=CC=CC=C2C(=O)O)NCCN
Depiction
Precursor
2-[2-[2-[[2-[2-(2-Aminoethylamino)ethylcarbamoyl]benzoyl]amino]ethylamino]ethylcarbamoyl]benzoic acid
C(CNC(=O)C1=CC=CC=C1C(=O)NCCNCCNC(=O)C2=CC=CC=C2C(=O)O)NCCN
Environmental
Depiction
Downstream Successor
Glycine
C(CN)(O)=O
Depiction
Precursor
2-[2-[2-[[2-[2-(2-Aminoethylamino)ethylcarbamoyl]benzoyl]amino]ethylamino]ethylcarbamoyl]benzoic acid
C(CNC(=O)C1=CC=CC=C1C(=O)NCCNCCNC(=O)C2=CC=CC=C2C(=O)O)NCCN
Environmental
Depiction
Downstream Successor
Aminoacetaldehyde
NCC=O
Depiction
Precursor
2-[2-[2-[[2-[2-(2-Aminoethylamino)ethylcarbamoyl]benzoyl]amino]ethylamino]ethylcarbamoyl]benzoic acid
C(CNC(=O)C1=CC=CC=C1C(=O)NCCNCCNC(=O)C2=CC=CC=C2C(=O)O)NCCN
Environmental
Depiction
Downstream Successor
Ethylenediamine
NCCN
Depiction
Precursor
2-[2-[2-[[2-[2-(2-Aminoethylamino)ethylcarbamoyl]benzoyl]amino]ethylamino]ethylcarbamoyl]benzoic acid
C(CNC(=O)C1=CC=CC=C1C(=O)NCCNCCNC(=O)C2=CC=CC=C2C(=O)O)NCCN
Environmental
Depiction
Downstream Successor
Phthalic Acid
C1=CC=C(C(=C1)C(O)=O)C(O)=O
Depiction
Precursor
2-[2-[2-[[2-[2-(2-Aminoethylamino)ethylcarbamoyl]benzoyl]amino]ethylamino]ethylcarbamoyl]benzoic acid
C(CNC(=O)C1=CC=CC=C1C(=O)NCCNCCNC(=O)C2=CC=CC=C2C(=O)O)NCCN
Abiotic
Depiction
Downstream Successor
Phthalic Acid
C1=CC=C(C(=C1)C(O)=O)C(O)=O
Depiction
Precursor
2-[2-[2-[[2-[2-(2-Aminoethylamino)ethylcarbamoyl]benzoyl]amino]ethylamino]ethylcarbamoyl]benzoic acid
C(CNC(=O)C1=CC=CC=C1C(=O)NCCNCCNC(=O)C2=CC=CC=C2C(=O)O)NCCN
Abiotic
Depiction
Downstream Successor
Diethylenetriamine
C(CN)NCCN
Depiction
Precursor
2-[2-[2-[[2-[2-(2-Aminoethylamino)ethylcarbamoyl]benzoyl]amino]ethylamino]ethylcarbamoyl]benzoic acid
C(CNC(=O)C1=CC=CC=C1C(=O)NCCNCCNC(=O)C2=CC=CC=C2C(=O)O)NCCN
Environmental
Depiction
Downstream Successor
Diethylenetriamine
C(CN)NCCN
Depiction
Precursor
2-[2-[2-[[2-[2-(2-Aminoethylamino)ethylcarbamoyl]benzoyl]amino]ethylamino]ethylcarbamoyl]benzoic acid
C(CNC(=O)C1=CC=CC=C1C(=O)NCCNCCNC(=O)C2=CC=CC=C2C(=O)O)NCCN
Environmental
Depiction
Downstream Successor
2-((2-Aminoethyl)amino)acetaldehyde
C(CN)NCC=O
Depiction
Precursor
2-[2-[2-[[2-[2-(2-Aminoethylamino)ethylcarbamoyl]benzoyl]amino]ethylamino]ethylcarbamoyl]benzoic acid
C(CNC(=O)C1=CC=CC=C1C(=O)NCCNCCNC(=O)C2=CC=CC=C2C(=O)O)NCCN
Abiotic
Depiction
Downstream Successor
2-((2-Aminoethyl)amino)acetaldehyde
C(CN)NCC=O
Depiction
Precursor
2-[2-[2-[[2-[2-(2-Aminoethylamino)ethylcarbamoyl]benzoyl]amino]ethylamino]ethylcarbamoyl]benzoic acid
C(CNC(=O)C1=CC=CC=C1C(=O)NCCNCCNC(=O)C2=CC=CC=C2C(=O)O)NCCN
Environmental
Depiction
Downstream Successor
N-(2-Hydroxyethyl)ethylenediamine
NCCNCCO
No Original Precursors

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No Dead-Ends

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