Graphs show a maximum of 100 compounds. Use downloads for complete results.
Depiction
Upstream Precursor
KHSLVOXXCDXGFS-STVHZKCLSA-N
3-Hydroxy-4-((4-((hydroxyimino)methyl)phenyl)azo)-N-(4-methoxyphenyl)naphthalene-2-carboxamide
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)/C=N/O
Environmental
Depiction
Product
MUTNGISPWUDFLF-UHFFFAOYSA-N
4-[[2-Hydroxy-3-[(4-methoxyphenyl)carbamoyl]naphthalen-1-yl]diazenyl]benzoic acid
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C(O)=O
Depiction
Upstream Precursor
KHSLVOXXCDXGFS-STVHZKCLSA-N
3-Hydroxy-4-((4-((hydroxyimino)methyl)phenyl)azo)-N-(4-methoxyphenyl)naphthalene-2-carboxamide
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)/C=N/O
Environmental
Depiction
Product
MUTNGISPWUDFLF-UHFFFAOYSA-N
4-[[2-Hydroxy-3-[(4-methoxyphenyl)carbamoyl]naphthalen-1-yl]diazenyl]benzoic acid
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C(O)=O
Depiction
Upstream Precursor
NMOCMTZCYDRHQB-UHFFFAOYSA-N
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C#N
Abiotic
Depiction
Product
MUTNGISPWUDFLF-UHFFFAOYSA-N
4-[[2-Hydroxy-3-[(4-methoxyphenyl)carbamoyl]naphthalen-1-yl]diazenyl]benzoic acid
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C(O)=O
Depiction
Upstream Precursor
NMOCMTZCYDRHQB-UHFFFAOYSA-N
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C#N
Environmental
Depiction
Product
MUTNGISPWUDFLF-UHFFFAOYSA-N
4-[[2-Hydroxy-3-[(4-methoxyphenyl)carbamoyl]naphthalen-1-yl]diazenyl]benzoic acid
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C(O)=O
Depiction
Upstream Precursor
NMOCMTZCYDRHQB-UHFFFAOYSA-N
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C#N
Environmental
Depiction
Product
MUTNGISPWUDFLF-UHFFFAOYSA-N
4-[[2-Hydroxy-3-[(4-methoxyphenyl)carbamoyl]naphthalen-1-yl]diazenyl]benzoic acid
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C(O)=O
Depiction
Upstream Precursor
ZVAUTSHJTQRZFO-UHFFFAOYSA-N
4-[(4-carbamoylphenyl)diazenyl]-3-hydroxy-N-(4-methoxyphenyl)naphthalene-2-carboxamide
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C(N)=O
Abiotic
Depiction
Product
MUTNGISPWUDFLF-UHFFFAOYSA-N
4-[[2-Hydroxy-3-[(4-methoxyphenyl)carbamoyl]naphthalen-1-yl]diazenyl]benzoic acid
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C(O)=O
Depiction
Upstream Precursor
ZVAUTSHJTQRZFO-UHFFFAOYSA-N
4-[(4-carbamoylphenyl)diazenyl]-3-hydroxy-N-(4-methoxyphenyl)naphthalene-2-carboxamide
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C(N)=O
Environmental
Depiction
Product
MUTNGISPWUDFLF-UHFFFAOYSA-N
4-[[2-Hydroxy-3-[(4-methoxyphenyl)carbamoyl]naphthalen-1-yl]diazenyl]benzoic acid
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C(O)=O
Depiction
Upstream Precursor
XEMZWLDNUIFPEI-UHFFFAOYSA-N
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C=O
Abiotic
Depiction
Product
MUTNGISPWUDFLF-UHFFFAOYSA-N
4-[[2-Hydroxy-3-[(4-methoxyphenyl)carbamoyl]naphthalen-1-yl]diazenyl]benzoic acid
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C(O)=O
Depiction
Upstream Precursor
XEMZWLDNUIFPEI-UHFFFAOYSA-N
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C=O
Environmental
Depiction
Product
MUTNGISPWUDFLF-UHFFFAOYSA-N
4-[[2-Hydroxy-3-[(4-methoxyphenyl)carbamoyl]naphthalen-1-yl]diazenyl]benzoic acid
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C(O)=O

Previewing top 9 entries. If you want the full results, please use the download button above.

Depiction
Precursor
MUTNGISPWUDFLF-UHFFFAOYSA-N
4-[[2-Hydroxy-3-[(4-methoxyphenyl)carbamoyl]naphthalen-1-yl]diazenyl]benzoic acid
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C(O)=O
Environmental
Depiction
Downstream Successor
FJKROLUGYXJWQN-UHFFFAOYSA-N
4-Hydroxybenzoic Acid
C(=O)(C1=CC=C(O)C=C1)O
Depiction
Precursor
MUTNGISPWUDFLF-UHFFFAOYSA-N
4-[[2-Hydroxy-3-[(4-methoxyphenyl)carbamoyl]naphthalen-1-yl]diazenyl]benzoic acid
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C(O)=O
Abiotic
Depiction
Downstream Successor
FJKROLUGYXJWQN-UHFFFAOYSA-N
4-Hydroxybenzoic Acid
C(=O)(C1=CC=C(O)C=C1)O
Depiction
Precursor
MUTNGISPWUDFLF-UHFFFAOYSA-N
4-[[2-Hydroxy-3-[(4-methoxyphenyl)carbamoyl]naphthalen-1-yl]diazenyl]benzoic acid
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C(O)=O
Environmental
Depiction
Downstream Successor
KDHUXRBROABJBC-UHFFFAOYSA-N
4-Aminocatechol
OC1=C(C=CC(=C1)N)O
Depiction
Precursor
MUTNGISPWUDFLF-UHFFFAOYSA-N
4-[[2-Hydroxy-3-[(4-methoxyphenyl)carbamoyl]naphthalen-1-yl]diazenyl]benzoic acid
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C(O)=O
Abiotic
Depiction
Downstream Successor
KDHUXRBROABJBC-UHFFFAOYSA-N
4-Aminocatechol
OC1=C(C=CC(=C1)N)O
Depiction
Precursor
MUTNGISPWUDFLF-UHFFFAOYSA-N
4-[[2-Hydroxy-3-[(4-methoxyphenyl)carbamoyl]naphthalen-1-yl]diazenyl]benzoic acid
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C(O)=O
Environmental
Depiction
Downstream Successor
ALYNCZNDIQEVRV-UHFFFAOYSA-N
4-Aminobenzoic Acid
c1cc(ccc1C(O)=O)N
Depiction
Precursor
MUTNGISPWUDFLF-UHFFFAOYSA-N
4-[[2-Hydroxy-3-[(4-methoxyphenyl)carbamoyl]naphthalen-1-yl]diazenyl]benzoic acid
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C(O)=O
Abiotic
Depiction
Downstream Successor
ALYNCZNDIQEVRV-UHFFFAOYSA-N
4-Aminobenzoic Acid
c1cc(ccc1C(O)=O)N
Depiction
Precursor
MUTNGISPWUDFLF-UHFFFAOYSA-N
4-[[2-Hydroxy-3-[(4-methoxyphenyl)carbamoyl]naphthalen-1-yl]diazenyl]benzoic acid
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C(O)=O
Environmental
Depiction
Downstream Successor
ALYNCZNDIQEVRV-UHFFFAOYSA-N
4-Aminobenzoic Acid
c1cc(ccc1C(O)=O)N
Depiction
Precursor
MUTNGISPWUDFLF-UHFFFAOYSA-N
4-[[2-Hydroxy-3-[(4-methoxyphenyl)carbamoyl]naphthalen-1-yl]diazenyl]benzoic acid
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C(O)=O
Abiotic
Depiction
Downstream Successor
ALYNCZNDIQEVRV-UHFFFAOYSA-N
4-Aminobenzoic Acid
c1cc(ccc1C(O)=O)N
Depiction
Precursor
MUTNGISPWUDFLF-UHFFFAOYSA-N
4-[[2-Hydroxy-3-[(4-methoxyphenyl)carbamoyl]naphthalen-1-yl]diazenyl]benzoic acid
COC1=CC=C(C=C1)NC(=O)C2=CC3=CC=CC=C3C(=C2O)N=NC4=CC=C(C=C4)C(O)=O
Abiotic
Depiction
Downstream Successor
BHAAPTBBJKJZER-UHFFFAOYSA-N
P-Anisidine
C1=C(C=CC(=C1)N)OC

Previewing top 10 entries. If you want the full results, please use the download button above.

No Original Precursors

No entries were found for this section with the current query and depth.

No Dead-Ends

No entries were found for this section with the current query and depth.

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