Search More · GCI-TPs

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

Precursor

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

3 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

3 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

9 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

9 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

9 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

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

Abiotic

Product

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

Upstream Precursor

KNIVRMVIFVLVCN-UHFFFAOYSA-N

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)CCl

Abiotic

Product

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

Previewing top 2 entries. If you want the full results, please use the download button above.

Precursor

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

Abiotic

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

PriorBiotransformation

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

Abiotic

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

PriorBiotransformation

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

Abiotic

Downstream Successor

AEMRFAOFKBGASW-UHFFFAOYSA-N

Glycolic Acid

C(=O)(CO)O

Precursor

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

PriorBiotransformation

Downstream Successor

AEMRFAOFKBGASW-UHFFFAOYSA-N

Glycolic Acid

C(=O)(CO)O

Precursor

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

Abiotic

Downstream Successor

AEMRFAOFKBGASW-UHFFFAOYSA-N

Glycolic Acid

C(=O)(CO)O

Precursor

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

PriorBiotransformation

Downstream Successor

AEMRFAOFKBGASW-UHFFFAOYSA-N

Glycolic Acid

C(=O)(CO)O

Precursor

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

PriorBiotransformation

Downstream Successor

HHLFWLYXYJOTON-UHFFFAOYSA-N

Glyoxylic Acid

C(=O)(C=O)O

Precursor

AKATWDMRLRLIRX-UHFFFAOYSA-N

Dodecyl (4-(1,3-dioxobutyl)phenoxy)acetate

CCCCCCCCCCCCOC(=O)COC1=CC=C(C=C1)C(=O)CC(=O)C

Abiotic

Downstream Successor

HHLFWLYXYJOTON-UHFFFAOYSA-N

Glyoxylic Acid

C(=O)(C=O)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.

Search with another depth

Depth:

or Explore another compound

Higher depth reveals distant relationships but increases loading time.