Search More · GCI-TPs

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

Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

2 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

3 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

11 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

11 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

7 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.

Upstream Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

Abiotic

Product

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

Upstream Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

Abiotic

Product

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

Upstream Precursor

PUIOZFWQIHBVOH-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfinylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)S(C)=O

Abiotic

Product

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

Upstream Precursor

PUIOZFWQIHBVOH-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfinylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)S(C)=O

Abiotic

Product

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

Upstream Precursor

FJKBFUKGZAZVSI-UHFFFAOYSA-N

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)[…

Abiotic

Product

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

Upstream Precursor

DRWDJTSTOZGLPD-UHFFFAOYSA-N

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)S…

Abiotic

Product

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

Previewing top 6 entries. If you want the full results, please use the download button above.

Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

Abiotic

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

PriorBiotransformation

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

PriorBiotransformation

Downstream Successor

WPYMKLBDIGXBTP-UHFFFAOYSA-N

Benzoic Acid

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

Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

Abiotic

Downstream Successor

WPYMKLBDIGXBTP-UHFFFAOYSA-N

Benzoic Acid

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

Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

Abiotic

Downstream Successor

ISWSIDIOOBJBQZ-UHFFFAOYSA-N

Phenol

Oc1ccccc1

Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

PriorBiotransformation

Downstream Successor

ISWSIDIOOBJBQZ-UHFFFAOYSA-N

Phenol

Oc1ccccc1

Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

Abiotic

Downstream Successor

FJKROLUGYXJWQN-UHFFFAOYSA-N

4-Hydroxybenzoic Acid

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

Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

PriorBiotransformation

Downstream Successor

FJKROLUGYXJWQN-UHFFFAOYSA-N

4-Hydroxybenzoic Acid

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

Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

PriorBiotransformation

Downstream Successor

FRJCLFVLGNIIPX-UHFFFAOYSA-N

4-Oxocyclohex-2,5-dienecarboxylate

OC(=O)C1C=CC(=O)C=C1

Precursor

CDAHGMWZPIRCKK-UHFFFAOYSA-N

[4-[2-[4-(4-Methoxyphenyl)butan-2-ylamino]acetyl]-2-methylsulfanylphenyl] benzoate

CC(CCC1=CC=C(C=C1)OC)NCC(=O)C2=CC(=C(C=C2)OC(=O)C3=CC=CC=C3)SC

Abiotic

Downstream Successor

FRJCLFVLGNIIPX-UHFFFAOYSA-N

4-Oxocyclohex-2,5-dienecarboxylate

OC(=O)C1C=CC(=O)C=C1

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

No Original Precursors

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