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Depiction
Precursor
LWPNEFYVMBUAID-UHFFFAOYSA-N
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
MUBZPKHOEPUJKR-UHFFFAOYSA-N
Oxalic Acid
C(=O)(C(O)=O)O
Depiction
Precursor
LWPNEFYVMBUAID-UHFFFAOYSA-N
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
HEPCJCVNHBXRBO-UHFFFAOYSA-N
Succinyl-carboxylic acid
C(CCC(=O)C(=O)O)(=O)C(O)=O
Depiction
Precursor
LWPNEFYVMBUAID-UHFFFAOYSA-N
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
LJDZFAPLPVPTBD-UHFFFAOYSA-M
CID 22568690
C([N+](=O)[O-])([O-])=O
Depiction
Precursor
LWPNEFYVMBUAID-UHFFFAOYSA-N
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
WCJLIWFWHPOTAC-UHFFFAOYSA-N
Rhodizonic acid
c1(c(c(=O)c(c(c1=O)O)O)=O)=O
Depiction
Precursor
LWPNEFYVMBUAID-UHFFFAOYSA-N
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
HJEBWCDVXVPBRC-UHFFFAOYSA-N
C(=C(C(=C(O)C(=O)O)O)O)([N+](=O)[O-])C(O)=O

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Depiction
Upstream Precursor
FCYWMOPNCXDTLZ-UHFFFAOYSA-N
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=C(C(=C(C=C1)NC(=O)C2=CC=C…
Depth 1
Depiction
Product
LWPNEFYVMBUAID-UHFFFAOYSA-N
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
CVLLJFMPUMPBNZ-UHFFFAOYSA-N
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=CC(=C(C=C1Cl)NC(=O)C2=CC=CO2)O
Depth 1
Depiction
Product
LWPNEFYVMBUAID-UHFFFAOYSA-N
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
OYYCXBLRJWZNPS-UHFFFAOYSA-N
CCCCCCCCCCCCCC=CCC(CC(=O)O)C(=O)NC1=C(C(=C(C=C1Cl)NC(=O)C2=CC…
Depth 2
Depiction
Product
LWPNEFYVMBUAID-UHFFFAOYSA-N
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

Previewing top 3 entries. If you want the full results, please use the download button above.

Depiction
Precursor
LWPNEFYVMBUAID-UHFFFAOYSA-N
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
Depth 3
Depiction
Downstream Successor
BVKZGUZCCUSVTD-UHFFFAOYSA-N
Carbonic Acid
C(=O)(O)O
Depiction
Precursor
LWPNEFYVMBUAID-UHFFFAOYSA-N
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
Depth 2
Depiction
Downstream Successor
MUBZPKHOEPUJKR-UHFFFAOYSA-N
Oxalic Acid
C(=O)(C(O)=O)O
Depiction
Precursor
LWPNEFYVMBUAID-UHFFFAOYSA-N
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
Depth 3
Depiction
Downstream Successor
FOCAUTSVDIKZOP-UHFFFAOYSA-M
Chloroacetate
[O-]C(=O)CCl
Depiction
Precursor
LWPNEFYVMBUAID-UHFFFAOYSA-N
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
Depth 3
Depiction
Downstream Successor
DLKZGMNZEDNHKO-UHFFFAOYSA-N
3-Hydroxyhexa-2,4-dienedioic acid
C(C=CC(=O)O)(=CC(O)=O)O
Depiction
Precursor
LWPNEFYVMBUAID-UHFFFAOYSA-N
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
Depth 3
Depiction
Downstream Successor
KDHUXRBROABJBC-UHFFFAOYSA-N
4-Aminocatechol
OC1=C(C=CC(=C1)N)O
Depiction
Precursor
LWPNEFYVMBUAID-UHFFFAOYSA-N
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
Depth 2
Depiction
Downstream Successor
KDYFGRWQOYBRFD-UHFFFAOYSA-N
Succinic Acid
C(CC(O)=O)C(O)=O
Depiction
Precursor
LWPNEFYVMBUAID-UHFFFAOYSA-N
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
Depth 3
Depiction
Downstream Successor
AOGYCOYQMAVAFD-UHFFFAOYSA-N
Chloroformic acid
C(O)(Cl)=O
Depiction
Precursor
LWPNEFYVMBUAID-UHFFFAOYSA-N
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
Depth 2
Depiction
Downstream Successor
XQRUEDXXCQDNOT-UHFFFAOYSA-N
2,5-Diaminophenol
Nc1c(cc(cc1)N)O

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

No Original Precursors

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