Search More · GCI-TPs

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

Precursor

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

10 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

10 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

10 steps

Dead-End Product

WCJLIWFWHPOTAC-UHFFFAOYSA-N

Rhodizonic acid

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

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Upstream Precursor

TWAOKHHZKFMFMD-UHFFFAOYSA-N

2-Ethylhexyl 4-Phenylbenzophenone-2'-Carboxylate

CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3

Abiotic

Product

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

Upstream Precursor

TWAOKHHZKFMFMD-UHFFFAOYSA-N

2-Ethylhexyl 4-Phenylbenzophenone-2'-Carboxylate

CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3

PriorBiotransformation

Product

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

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

Precursor

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

Environmental

Downstream Successor

BPNFIJXKGJIUHO-UHFFFAOYSA-N

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

Precursor

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

Abiotic

Downstream Successor

LYXOWKPVTCPORE-UHFFFAOYSA-N

4-Benzoylbiphenyl

C1=CC=C(C=C1)C2=CC=C(C=C2)C(C3=CC=CC=C3)=O

Precursor

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

Environmental

Downstream Successor

LYXOWKPVTCPORE-UHFFFAOYSA-N

4-Benzoylbiphenyl

C1=CC=C(C=C1)C2=CC=C(C=C2)C(C3=CC=CC=C3)=O

Precursor

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

Environmental

Downstream Successor

KEFWJRLUBJXDHP-UHFFFAOYSA-N

C1=CC(=C(C(=C1)C2=CC=C(C=C2)C(=O)C3=CC=CC=C3C(=O)O)O)O

Precursor

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

Environmental

Downstream Successor

QWGQMOFEDMIMPS-UHFFFAOYSA-N

C1(=CC=C(C=C1O)C2=CC=C(C=C2)C(=O)C3=CC=CC=C3C(=O)O)O

Precursor

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

Environmental

Downstream Successor

GHJWHNNDCYPBTA-UHFFFAOYSA-N

(2,3-Dihydroxyphenyl)-(4-phenylphenyl)methanone

c1ccc(c(c1O)O)C(=O)c2ccc(cc2)-c3ccccc3

Precursor

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

Abiotic

Downstream Successor

GHJWHNNDCYPBTA-UHFFFAOYSA-N

(2,3-Dihydroxyphenyl)-(4-phenylphenyl)methanone

c1ccc(c(c1O)O)C(=O)c2ccc(cc2)-c3ccccc3

Precursor

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

Environmental

Downstream Successor

GHJWHNNDCYPBTA-UHFFFAOYSA-N

(2,3-Dihydroxyphenyl)-(4-phenylphenyl)methanone

c1ccc(c(c1O)O)C(=O)c2ccc(cc2)-c3ccccc3

Precursor

NBYNVBRXIUUSIG-UHFFFAOYSA-N

Benzoic acid, 2-((1,1'-biphenyl)-4-ylcarbonyl)-

C(=O)(C1=CC=CC=C1C(=O)C2=CC=C(C=C2)C3=CC=CC=C3)O

Environmental

Downstream Successor

CEWNMFFRCJSLBZ-UHFFFAOYSA-N

C1=CC(=C(C(=C1)C2=CC=C(C=C2)C(=O)C3=CC(=CC=C3C(=O)O)O)O)O

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No Original Precursors

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