Search More · GCI-TPs

Graphs show a maximum of 100 compounds. Use downloads for complete results.

Precursor

ACAXIUADIABHTE-UHFFFAOYSA-N

Benzoic acid, 4-butyl-, 4-[(4-butylphenoxy)carbonyl]phenyl ester

CCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)C(=O)OC3=CC=C(C=C3)CCCC

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

ACAXIUADIABHTE-UHFFFAOYSA-N

Benzoic acid, 4-butyl-, 4-[(4-butylphenoxy)carbonyl]phenyl ester

CCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)C(=O)OC3=CC=C(C=C3)CCCC

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

ACAXIUADIABHTE-UHFFFAOYSA-N

Benzoic acid, 4-butyl-, 4-[(4-butylphenoxy)carbonyl]phenyl ester

CCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)C(=O)OC3=CC=C(C=C3)CCCC

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

ACAXIUADIABHTE-UHFFFAOYSA-N

Benzoic acid, 4-butyl-, 4-[(4-butylphenoxy)carbonyl]phenyl ester

CCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)C(=O)OC3=CC=C(C=C3)CCCC

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

C(=O)(C(O)=O)O

Precursor

ACAXIUADIABHTE-UHFFFAOYSA-N

Benzoic acid, 4-butyl-, 4-[(4-butylphenoxy)carbonyl]phenyl ester

CCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)C(=O)OC3=CC=C(C=C3)CCCC

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

ACAXIUADIABHTE-UHFFFAOYSA-N

Benzoic acid, 4-butyl-, 4-[(4-butylphenoxy)carbonyl]phenyl ester

CCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)C(=O)OC3=CC=C(C=C3)CCCC

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

ACAXIUADIABHTE-UHFFFAOYSA-N

Benzoic acid, 4-butyl-, 4-[(4-butylphenoxy)carbonyl]phenyl ester

CCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)C(=O)OC3=CC=C(C=C3)CCCC

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

C(CCC(=O)C(=O)O)(=O)C(O)=O

Precursor

ACAXIUADIABHTE-UHFFFAOYSA-N

Benzoic acid, 4-butyl-, 4-[(4-butylphenoxy)carbonyl]phenyl ester

CCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)C(=O)OC3=CC=C(C=C3)CCCC

11 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

C(CC(C(O)O)O)O

Precursor

ACAXIUADIABHTE-UHFFFAOYSA-N

Benzoic acid, 4-butyl-, 4-[(4-butylphenoxy)carbonyl]phenyl ester

CCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)C(=O)OC3=CC=C(C=C3)CCCC

11 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

But-1-ene-1,1,4-triol

C(CC=C(O)O)O

Precursor

ACAXIUADIABHTE-UHFFFAOYSA-N

Benzoic acid, 4-butyl-, 4-[(4-butylphenoxy)carbonyl]phenyl ester

CCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)C(=O)OC3=CC=C(C=C3)CCCC

8 steps

Dead-End Product

WCJLIWFWHPOTAC-UHFFFAOYSA-N

Rhodizonic acid

c1(c(c(=O)c(c(c1=O)O)O)=O)=O

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

Precursor

ACAXIUADIABHTE-UHFFFAOYSA-N

Benzoic acid, 4-butyl-, 4-[(4-butylphenoxy)carbonyl]phenyl ester

CCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)C(=O)OC3=CC=C(C=C3)CCCC

PriorBiotransformation

Downstream Successor

ISWSIDIOOBJBQZ-UHFFFAOYSA-N

Phenol

Oc1ccccc1

Precursor

ACAXIUADIABHTE-UHFFFAOYSA-N

Benzoic acid, 4-butyl-, 4-[(4-butylphenoxy)carbonyl]phenyl ester

CCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)C(=O)OC3=CC=C(C=C3)CCCC

Abiotic

Downstream Successor

FJKROLUGYXJWQN-UHFFFAOYSA-N

4-Hydroxybenzoic Acid

C(=O)(C1=CC=C(O)C=C1)O

Precursor

ACAXIUADIABHTE-UHFFFAOYSA-N

Benzoic acid, 4-butyl-, 4-[(4-butylphenoxy)carbonyl]phenyl ester

CCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)C(=O)OC3=CC=C(C=C3)CCCC

PriorBiotransformation

Downstream Successor

FJKROLUGYXJWQN-UHFFFAOYSA-N

4-Hydroxybenzoic Acid

C(=O)(C1=CC=C(O)C=C1)O

Precursor

ACAXIUADIABHTE-UHFFFAOYSA-N

Benzoic acid, 4-butyl-, 4-[(4-butylphenoxy)carbonyl]phenyl ester

CCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)C(=O)OC3=CC=C(C=C3)CCCC

PriorBiotransformation

Downstream Successor

YQUVCSBJEUQKSH-UHFFFAOYSA-N

Protocatechuic Acid

C(C1=CC(=C(C=C1)O)O)(O)=O

Precursor

ACAXIUADIABHTE-UHFFFAOYSA-N

Benzoic acid, 4-butyl-, 4-[(4-butylphenoxy)carbonyl]phenyl ester

CCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)C(=O)OC3=CC=C(C=C3)CCCC

PriorBiotransformation

Downstream Successor

QIGBRXMKCJKVMJ-UHFFFAOYSA-N

Hydroquinone

C1(=CC=C(C=C1)O)O

Precursor

ACAXIUADIABHTE-UHFFFAOYSA-N

Benzoic acid, 4-butyl-, 4-[(4-butylphenoxy)carbonyl]phenyl ester

CCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)C(=O)OC3=CC=C(C=C3)CCCC

PriorBiotransformation

Downstream Successor

KJOVGYUGXHIVAY-UHFFFAOYSA-N

Buta-1,3-diene-1,2,4-tricarboxylic acid

OC(=O)C(=CC(O)=O)C=CC(O)=O

Precursor

ACAXIUADIABHTE-UHFFFAOYSA-N

Benzoic acid, 4-butyl-, 4-[(4-butylphenoxy)carbonyl]phenyl ester

CCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)C(=O)OC3=CC=C(C=C3)CCCC

PriorBiotransformation

Downstream Successor

QGNLHMKIGMZKJX-UHFFFAOYSA-N

3-Chloro-4-hydroxybenzoic acid

OC1=C(C=C(C=C1)C(=O)O)Cl

Precursor

ACAXIUADIABHTE-UHFFFAOYSA-N

Benzoic acid, 4-butyl-, 4-[(4-butylphenoxy)carbonyl]phenyl ester

CCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)C(=O)OC3=CC=C(C=C3)CCCC

PriorBiotransformation

Downstream Successor

AJPXTSMULZANCB-UHFFFAOYSA-N

Chlorohydroquinone

c1(cc(c(cc1)O)Cl)O

Precursor

ACAXIUADIABHTE-UHFFFAOYSA-N

Benzoic acid, 4-butyl-, 4-[(4-butylphenoxy)carbonyl]phenyl ester

CCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)C(=O)OC3=CC=C(C=C3)CCCC

PriorBiotransformation

Downstream Successor

CYYZDBDROVLTJU-UHFFFAOYSA-N

4-Butylphenol

CCCCc1ccc(cc1)O

Precursor

ACAXIUADIABHTE-UHFFFAOYSA-N

Benzoic acid, 4-butyl-, 4-[(4-butylphenoxy)carbonyl]phenyl ester

CCCCC1=CC=C(C=C1)C(=O)OC2=CC=C(C=C2)C(=O)OC3=CC=C(C=C3)CCCC

Abiotic

Downstream Successor

CYYZDBDROVLTJU-UHFFFAOYSA-N

4-Butylphenol

CCCCc1ccc(cc1)O

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 All Precursors

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

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