Search More · GCI-TPs

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

Precursor

ZCACQPQQMFRMSQ-UHFFFAOYSA-N

Benzenepropanoic acid, alpha-[[(2E)-3-(4-nitrophenyl)-1-oxo-2-propenyl]oxy]-, (alphaS)-

C1=CC=C(C=C1)CC(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)[N+](=O)[O-]

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

ZCACQPQQMFRMSQ-UHFFFAOYSA-N

Benzenepropanoic acid, alpha-[[(2E)-3-(4-nitrophenyl)-1-oxo-2-propenyl]oxy]-, (alphaS)-

C1=CC=C(C=C1)CC(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)[N+](=O)[O-]

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

ZCACQPQQMFRMSQ-UHFFFAOYSA-N

Benzenepropanoic acid, alpha-[[(2E)-3-(4-nitrophenyl)-1-oxo-2-propenyl]oxy]-, (alphaS)-

C1=CC=C(C=C1)CC(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)[N+](=O)[O-]

4 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

ZCACQPQQMFRMSQ-UHFFFAOYSA-N

Benzenepropanoic acid, alpha-[[(2E)-3-(4-nitrophenyl)-1-oxo-2-propenyl]oxy]-, (alphaS)-

C1=CC=C(C=C1)CC(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)[N+](=O)[O-]

5 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

ZCACQPQQMFRMSQ-UHFFFAOYSA-N

Benzenepropanoic acid, alpha-[[(2E)-3-(4-nitrophenyl)-1-oxo-2-propenyl]oxy]-, (alphaS)-

C1=CC=C(C=C1)CC(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)[N+](=O)[O-]

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

ZCACQPQQMFRMSQ-UHFFFAOYSA-N

Benzenepropanoic acid, alpha-[[(2E)-3-(4-nitrophenyl)-1-oxo-2-propenyl]oxy]-, (alphaS)-

C1=CC=C(C=C1)CC(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)[N+](=O)[O-]

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

ZCACQPQQMFRMSQ-UHFFFAOYSA-N

Benzenepropanoic acid, alpha-[[(2E)-3-(4-nitrophenyl)-1-oxo-2-propenyl]oxy]-, (alphaS)-

C1=CC=C(C=C1)CC(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)[N+](=O)[O-]

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

ZCACQPQQMFRMSQ-UHFFFAOYSA-N

Benzenepropanoic acid, alpha-[[(2E)-3-(4-nitrophenyl)-1-oxo-2-propenyl]oxy]-, (alphaS)-

C1=CC=C(C=C1)CC(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)[N+](=O)[O-]

14 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

ZCACQPQQMFRMSQ-UHFFFAOYSA-N

Benzenepropanoic acid, alpha-[[(2E)-3-(4-nitrophenyl)-1-oxo-2-propenyl]oxy]-, (alphaS)-

C1=CC=C(C=C1)CC(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)[N+](=O)[O-]

14 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

ZCACQPQQMFRMSQ-UHFFFAOYSA-N

Benzenepropanoic acid, alpha-[[(2E)-3-(4-nitrophenyl)-1-oxo-2-propenyl]oxy]-, (alphaS)-

C1=CC=C(C=C1)CC(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)[N+](=O)[O-]

6 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

C([N+](=O)[O-])([O-])=O

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

Precursor

ZCACQPQQMFRMSQ-UHFFFAOYSA-N

Benzenepropanoic acid, alpha-[[(2E)-3-(4-nitrophenyl)-1-oxo-2-propenyl]oxy]-, (alphaS)-

C1=CC=C(C=C1)CC(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)[N+](=O)[O-]

Abiotic

Downstream Successor

VOXXWSYKYCBWHO-UHFFFAOYSA-N

(+-)-3-Phenyllactic acid

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

Precursor

ZCACQPQQMFRMSQ-UHFFFAOYSA-N

Benzenepropanoic acid, alpha-[[(2E)-3-(4-nitrophenyl)-1-oxo-2-propenyl]oxy]-, (alphaS)-

C1=CC=C(C=C1)CC(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)[N+](=O)[O-]

Abiotic

Downstream Successor

VOXXWSYKYCBWHO-UHFFFAOYSA-N

(+-)-3-Phenyllactic acid

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

Precursor

ZCACQPQQMFRMSQ-UHFFFAOYSA-N

Benzenepropanoic acid, alpha-[[(2E)-3-(4-nitrophenyl)-1-oxo-2-propenyl]oxy]-, (alphaS)-

C1=CC=C(C=C1)CC(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)[N+](=O)[O-]

PriorBiotransformation

Downstream Successor

VOXXWSYKYCBWHO-UHFFFAOYSA-N

(+-)-3-Phenyllactic acid

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

Precursor

ZCACQPQQMFRMSQ-UHFFFAOYSA-N

Benzenepropanoic acid, alpha-[[(2E)-3-(4-nitrophenyl)-1-oxo-2-propenyl]oxy]-, (alphaS)-

C1=CC=C(C=C1)CC(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)[N+](=O)[O-]

Abiotic

Downstream Successor

PAFLSMZLRSPALU-UHFFFAOYSA-N

3-(3,4-Dihydroxyphenyl)-2-hydroxypropanoic acid

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

Precursor

ZCACQPQQMFRMSQ-UHFFFAOYSA-N

Benzenepropanoic acid, alpha-[[(2E)-3-(4-nitrophenyl)-1-oxo-2-propenyl]oxy]-, (alphaS)-

C1=CC=C(C=C1)CC(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)[N+](=O)[O-]

PriorBiotransformation

Downstream Successor

PAFLSMZLRSPALU-UHFFFAOYSA-N

3-(3,4-Dihydroxyphenyl)-2-hydroxypropanoic acid

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

Precursor

ZCACQPQQMFRMSQ-UHFFFAOYSA-N

Benzenepropanoic acid, alpha-[[(2E)-3-(4-nitrophenyl)-1-oxo-2-propenyl]oxy]-, (alphaS)-

C1=CC=C(C=C1)CC(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)[N+](=O)[O-]

PriorBiotransformation

Downstream Successor

WRMNZCZEMHIOCP-UHFFFAOYSA-N

2-Phenylethanol

c1ccccc1CCO

Precursor

ZCACQPQQMFRMSQ-UHFFFAOYSA-N

Benzenepropanoic acid, alpha-[[(2E)-3-(4-nitrophenyl)-1-oxo-2-propenyl]oxy]-, (alphaS)-

C1=CC=C(C=C1)CC(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)[N+](=O)[O-]

Abiotic

Downstream Successor

WRMNZCZEMHIOCP-UHFFFAOYSA-N

2-Phenylethanol

c1ccccc1CCO

Precursor

ZCACQPQQMFRMSQ-UHFFFAOYSA-N

Benzenepropanoic acid, alpha-[[(2E)-3-(4-nitrophenyl)-1-oxo-2-propenyl]oxy]-, (alphaS)-

C1=CC=C(C=C1)CC(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)[N+](=O)[O-]

PriorBiotransformation

Downstream Successor

JVGVDSSUAVXRDY-UHFFFAOYSA-N

(+-)-3-(4-Hydroxyphenyl)lactic acid

C(C(=O)O)(CC1=CC=C(C=C1)O)O

Precursor

ZCACQPQQMFRMSQ-UHFFFAOYSA-N

Benzenepropanoic acid, alpha-[[(2E)-3-(4-nitrophenyl)-1-oxo-2-propenyl]oxy]-, (alphaS)-

C1=CC=C(C=C1)CC(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)[N+](=O)[O-]

Abiotic

Downstream Successor

JVGVDSSUAVXRDY-UHFFFAOYSA-N

(+-)-3-(4-Hydroxyphenyl)lactic acid

C(C(=O)O)(CC1=CC=C(C=C1)O)O

Precursor

ZCACQPQQMFRMSQ-UHFFFAOYSA-N

Benzenepropanoic acid, alpha-[[(2E)-3-(4-nitrophenyl)-1-oxo-2-propenyl]oxy]-, (alphaS)-

C1=CC=C(C=C1)CC(C(=O)O)OC(=O)C=CC2=CC=C(C=C2)[N+](=O)[O-]

Abiotic

Downstream Successor

QAIPRVGONGVQAS-UHFFFAOYSA-N

3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid

C1=C(C(=CC(=C1)C=CC(=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.

No All 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.