Search More · GCI-TPs

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

Precursor

JSLKWEGYHJKJRU-UHFFFAOYSA-N

Rel-4-((4-pentylphenyl)ethynyl)phenyl (1s,4r)-4-propylcyclohexane-1-carboxylate

CCCCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C3CCC(CC3)CCC

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

JSLKWEGYHJKJRU-UHFFFAOYSA-N

Rel-4-((4-pentylphenyl)ethynyl)phenyl (1s,4r)-4-propylcyclohexane-1-carboxylate

CCCCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C3CCC(CC3)CCC

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

JSLKWEGYHJKJRU-UHFFFAOYSA-N

Rel-4-((4-pentylphenyl)ethynyl)phenyl (1s,4r)-4-propylcyclohexane-1-carboxylate

CCCCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C3CCC(CC3)CCC

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

JSLKWEGYHJKJRU-UHFFFAOYSA-N

Rel-4-((4-pentylphenyl)ethynyl)phenyl (1s,4r)-4-propylcyclohexane-1-carboxylate

CCCCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C3CCC(CC3)CCC

6 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

JSLKWEGYHJKJRU-UHFFFAOYSA-N

Rel-4-((4-pentylphenyl)ethynyl)phenyl (1s,4r)-4-propylcyclohexane-1-carboxylate

CCCCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C3CCC(CC3)CCC

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

JSLKWEGYHJKJRU-UHFFFAOYSA-N

Rel-4-((4-pentylphenyl)ethynyl)phenyl (1s,4r)-4-propylcyclohexane-1-carboxylate

CCCCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C3CCC(CC3)CCC

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

JSLKWEGYHJKJRU-UHFFFAOYSA-N

Rel-4-((4-pentylphenyl)ethynyl)phenyl (1s,4r)-4-propylcyclohexane-1-carboxylate

CCCCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C3CCC(CC3)CCC

9 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

JSLKWEGYHJKJRU-UHFFFAOYSA-N

Rel-4-((4-pentylphenyl)ethynyl)phenyl (1s,4r)-4-propylcyclohexane-1-carboxylate

CCCCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C3CCC(CC3)CCC

14 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

JSLKWEGYHJKJRU-UHFFFAOYSA-N

Rel-4-((4-pentylphenyl)ethynyl)phenyl (1s,4r)-4-propylcyclohexane-1-carboxylate

CCCCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C3CCC(CC3)CCC

14 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

JSLKWEGYHJKJRU-UHFFFAOYSA-N

Rel-4-((4-pentylphenyl)ethynyl)phenyl (1s,4r)-4-propylcyclohexane-1-carboxylate

CCCCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C3CCC(CC3)CCC

11 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

JSLKWEGYHJKJRU-UHFFFAOYSA-N

Rel-4-((4-pentylphenyl)ethynyl)phenyl (1s,4r)-4-propylcyclohexane-1-carboxylate

CCCCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C3CCC(CC3)CCC

Abiotic

Downstream Successor

QTBSBXVTEAMEQO-UHFFFAOYSA-N

Acetic Acid

CC(=O)O

Precursor

JSLKWEGYHJKJRU-UHFFFAOYSA-N

Rel-4-((4-pentylphenyl)ethynyl)phenyl (1s,4r)-4-propylcyclohexane-1-carboxylate

CCCCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C3CCC(CC3)CCC

PriorBiotransformation

Downstream Successor

QTBSBXVTEAMEQO-UHFFFAOYSA-N

Acetic Acid

CC(=O)O

Precursor

JSLKWEGYHJKJRU-UHFFFAOYSA-N

Rel-4-((4-pentylphenyl)ethynyl)phenyl (1s,4r)-4-propylcyclohexane-1-carboxylate

CCCCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C3CCC(CC3)CCC

Abiotic

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

JSLKWEGYHJKJRU-UHFFFAOYSA-N

Rel-4-((4-pentylphenyl)ethynyl)phenyl (1s,4r)-4-propylcyclohexane-1-carboxylate

CCCCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C3CCC(CC3)CCC

PriorBiotransformation

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

JSLKWEGYHJKJRU-UHFFFAOYSA-N

Rel-4-((4-pentylphenyl)ethynyl)phenyl (1s,4r)-4-propylcyclohexane-1-carboxylate

CCCCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C3CCC(CC3)CCC

Abiotic

Downstream Successor

RGHHSNMVTDWUBI-UHFFFAOYSA-N

4-Hydroxybenzaldehyde

C(=O)c1ccc(cc1)O

Precursor

JSLKWEGYHJKJRU-UHFFFAOYSA-N

Rel-4-((4-pentylphenyl)ethynyl)phenyl (1s,4r)-4-propylcyclohexane-1-carboxylate

CCCCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C3CCC(CC3)CCC

PriorBiotransformation

Downstream Successor

RGHHSNMVTDWUBI-UHFFFAOYSA-N

4-Hydroxybenzaldehyde

C(=O)c1ccc(cc1)O

Precursor

JSLKWEGYHJKJRU-UHFFFAOYSA-N

Rel-4-((4-pentylphenyl)ethynyl)phenyl (1s,4r)-4-propylcyclohexane-1-carboxylate

CCCCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C3CCC(CC3)CCC

Abiotic

Downstream Successor

QCNUKEGGHOLBES-UHFFFAOYSA-N

(1s,4r)-4-Propylcyclohexane-1-carboxylic acid

CCCC1CCC(CC1)C(O)=O

Precursor

JSLKWEGYHJKJRU-UHFFFAOYSA-N

Rel-4-((4-pentylphenyl)ethynyl)phenyl (1s,4r)-4-propylcyclohexane-1-carboxylate

CCCCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C3CCC(CC3)CCC

PriorBiotransformation

Downstream Successor

QCNUKEGGHOLBES-UHFFFAOYSA-N

(1s,4r)-4-Propylcyclohexane-1-carboxylic acid

CCCC1CCC(CC1)C(O)=O

Precursor

JSLKWEGYHJKJRU-UHFFFAOYSA-N

Rel-4-((4-pentylphenyl)ethynyl)phenyl (1s,4r)-4-propylcyclohexane-1-carboxylate

CCCCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C3CCC(CC3)CCC

Abiotic

Downstream Successor

NQVZPRUSNWNSQH-UHFFFAOYSA-N

Benzaldehyde, 4-pentyl-

CCCCCc1ccc(cc1)C=O

Precursor

JSLKWEGYHJKJRU-UHFFFAOYSA-N

Rel-4-((4-pentylphenyl)ethynyl)phenyl (1s,4r)-4-propylcyclohexane-1-carboxylate

CCCCCC1=CC=C(C=C1)C#CC2=CC=C(C=C2)OC(=O)C3CCC(CC3)CCC

PriorBiotransformation

Downstream Successor

NQVZPRUSNWNSQH-UHFFFAOYSA-N

Benzaldehyde, 4-pentyl-

CCCCCc1ccc(cc1)C=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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