Search More · GCI-TPs

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

Precursor

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

4 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

3 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

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.

Upstream Precursor

FEJMLRXCJBNRFC-CUPIEXAXSA-N

tetrakis[(2S)-octan-2-yl] benzene-1,2,4,5-tetracarboxylate

CCCCCC[C@H](C)OC(=O)C1=CC(=C(C=C1C(=O)O[C@@H](C)CCCCCC)C(=O)O…

Abiotic

Product

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

Upstream Precursor

KXRSNXMHCPUIPF-UHFFFAOYSA-N

CCCCCCC(C)OC(=O)C1=CC(=C(C=C1C(=O)OC(C)CCCCCC)C(=O)OC(C)CCCCC…

Abiotic

Product

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

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

Precursor

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

PriorBiotransformation

Downstream Successor

MWRVRCAFWBBXTL-UHFFFAOYSA-N

4-Hydroxyphthalic acid

C(=O)(c1c(cc(cc1)O)C(=O)O)O

Precursor

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

Abiotic

Downstream Successor

ARCGXLSVLAOJQL-UHFFFAOYSA-N

Trimellitic acid

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

Precursor

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

PriorBiotransformation

Downstream Successor

ARCGXLSVLAOJQL-UHFFFAOYSA-N

Trimellitic acid

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

Precursor

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

PriorBiotransformation

Downstream Successor

KKEYFWRCBNTPAC-UHFFFAOYSA-N

Terephthalic Acid

C(=O)(c1ccc(cc1)C(=O)O)O

Precursor

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

PriorBiotransformation

Downstream Successor

SJWFXCIHNDVPSH-UHFFFAOYSA-N

2-Octanol

C(C)(CCCCCC)O

Precursor

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

Abiotic

Downstream Successor

SJWFXCIHNDVPSH-UHFFFAOYSA-N

2-Octanol

C(C)(CCCCCC)O

Precursor

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

PriorBiotransformation

Downstream Successor

BCEQKAQCUWUNML-UHFFFAOYSA-N

4-Hydroxyisophthalic acid

c1cc(cc(c1O)C(O)=O)C(=O)O

Precursor

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

PriorBiotransformation

Downstream Successor

FBOCZYIJDQZQFE-UHFFFAOYSA-N

4,5-Dihydroxy-1,3-benzenedicarboxylic acid

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

Precursor

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

PriorBiotransformation

Downstream Successor

BOPPPUCSDSHZEZ-UHFFFAOYSA-N

5-Hydroxybenzene-1,2,4-tricarboxylic acid

C(=O)(c1cc(c(cc1C(=O)O)C(=O)O)O)O

Precursor

UVCNQUKPQSCICG-UHFFFAOYSA-N

1,2,4-Benzenetricarboxylic acid, 1,2,4-tris(1-methylheptyl) ester

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

Abiotic

Downstream Successor

BOPPPUCSDSHZEZ-UHFFFAOYSA-N

5-Hydroxybenzene-1,2,4-tricarboxylic acid

C(=O)(c1cc(c(cc1C(=O)O)C(=O)O)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.