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Depiction
Precursor
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
2 steps
Depiction
Dead-End Product
Oxalic Acid
C(=O)(C(O)=O)O
Depiction
Precursor
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
7 steps
Depiction
Dead-End Product
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Precursor
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
15 steps
Depiction
Dead-End Product
CID 22568690
C([N+](=O)[O-])([O-])=O
Depiction
Precursor
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
8 steps
Depiction
Dead-End Product
Rhodizonic acid
c1(c(c(=O)c(c(c1=O)O)O)=O)=O
Depiction
Precursor
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
8 steps
Depiction
Dead-End Product
C(=C(C(=C(O)C(=O)O)O)O)([N+](=O)[O-])C(O)=O
Depiction
Upstream Precursor
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Abiotic
Depiction
Product
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Depiction
Upstream Precursor
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=C(C(=C(C=C1)NC(=O)C2=CC=C…
Abiotic
Depiction
Product
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Depiction
Upstream Precursor
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=C(C(=C(C=C1)NC(=O)C2=CC=C…
Environmental
Depiction
Product
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Depiction
Upstream Precursor
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=C(C(=C(C=C1)NC(=O)C2=CC=C…
Abiotic
Depiction
Product
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Depiction
Upstream Precursor
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=C(C(=C(C=C1)NC(=O)C2=CC=C…
Environmental
Depiction
Product
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Depiction
Upstream Precursor
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1Cl)NC(=O)C2=CC=CO2)O
Abiotic
Depiction
Product
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Depiction
Upstream Precursor
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1Cl)NC(=O)C2=CC=CO2)O
Environmental
Depiction
Product
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Depiction
Upstream Precursor
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1Cl)NC(=O)C2=CC=CO2)O
Abiotic
Depiction
Product
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Depiction
Upstream Precursor
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1Cl)NC(=O)C2=CC=CO2)O
Environmental
Depiction
Product
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Depiction
Upstream Precursor
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=C(C(=C(C=C1Cl)NC(=O)C2=CC…
Environmental
Depiction
Product
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Depiction
Precursor
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Environmental
Depiction
Downstream Successor
Formic Acid
OC=O
Depiction
Precursor
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Environmental
Depiction
Downstream Successor
2-Furancarboxylic acid
C(C1=CC=CO1)(O)=O
Depiction
Precursor
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Abiotic
Depiction
Downstream Successor
2-Furancarboxylic acid
C(C1=CC=CO1)(O)=O
Depiction
Precursor
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Environmental
Depiction
Downstream Successor
2-[(E)-2-hexadecenyl]succinic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)O
Depiction
Precursor
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Abiotic
Depiction
Downstream Successor
2-[(E)-2-hexadecenyl]succinic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)O
Depiction
Precursor
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Abiotic
Depiction
Downstream Successor
2-Furanol
C1(=CC=CO1)O
Depiction
Precursor
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Environmental
Depiction
Downstream Successor
2-Furanol
C1(=CC=CO1)O
Depiction
Precursor
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Abiotic
Depiction
Downstream Successor
N-(4-amino-2-hydroxyphenyl)furan-2-carboxamide
NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Depiction
Precursor
3-[[[4-[(2-Furanylcarbonyl)amino]-3-hydroxyphenyl]amino]carbonyl]-5-nonadecenoic acid
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
Environmental
Depiction
Downstream Successor
N-(4-amino-2-hydroxyphenyl)furan-2-carboxamide
NC1=CC(=C(C=C1)NC(=O)C2=CC=CO2)O
No Original Precursors

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