Search More · GCI-TPs

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

Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

9 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

4 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

3 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

9 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

9 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

9 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

9 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

12 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.

Upstream Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

Abiotic

Product

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

Upstream Precursor

CKOZWIIROGOMRH-UHFFFAOYSA-N

C1=CC(=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O)Cl

Environmental

Product

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

Upstream Precursor

CKOZWIIROGOMRH-UHFFFAOYSA-N

C1=CC(=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O)Cl

Abiotic

Product

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

Upstream Precursor

MREWALNGILQGRV-UHFFFAOYSA-N

C1(=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O)Cl

Abiotic

Product

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

Upstream Precursor

MREWALNGILQGRV-UHFFFAOYSA-N

C1(=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O)Cl

Environmental

Product

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

Upstream Precursor

CKOZWIIROGOMRH-UHFFFAOYSA-N

C1=CC(=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O)Cl

Abiotic

Product

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

Upstream Precursor

CKOZWIIROGOMRH-UHFFFAOYSA-N

C1=CC(=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O)Cl

Environmental

Product

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

Upstream Precursor

MREWALNGILQGRV-UHFFFAOYSA-N

C1(=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O)Cl

Abiotic

Product

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

Upstream Precursor

MREWALNGILQGRV-UHFFFAOYSA-N

C1(=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O)Cl

Environmental

Product

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

Upstream Precursor

AFHDYXXTSAOBBY-UHFFFAOYSA-N

C1=CC(=C(C(=C1)C(C(=O)O)NCCNC(C2=CC(=CC=C2O)Cl)C(=O)O)O)Cl

Abiotic

Product

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

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

Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

Abiotic

Downstream Successor

TXXHDPDFNKHHGW-UHFFFAOYSA-N

2,4-Hexadienedioic acid, (2Z,4Z)-

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

Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

Abiotic

Downstream Successor

DLKZGMNZEDNHKO-UHFFFAOYSA-N

3-Hydroxyhexa-2,4-dienedioic acid

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

Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

Environmental

Downstream Successor

DLKZGMNZEDNHKO-UHFFFAOYSA-N

3-Hydroxyhexa-2,4-dienedioic acid

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

Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

Abiotic

Downstream Successor

ICMVYBXQDUXEEE-UHFFFAOYSA-N

CID 417

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

Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

Abiotic

Downstream Successor

CQRYARSYNCAZFO-UHFFFAOYSA-N

Salicyl Alcohol

C(c1ccccc1O)O

Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

Environmental

Downstream Successor

CQRYARSYNCAZFO-UHFFFAOYSA-N

Salicyl Alcohol

C(c1ccccc1O)O

Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

Abiotic

Downstream Successor

QQSFIAWCKMCGNN-UHFFFAOYSA-N

2-(2-Hydroxyphenyl)-2-oxoacetic acid

c1ccc(c(c1)C(=O)C(O)=O)O

Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

Environmental

Downstream Successor

QQSFIAWCKMCGNN-UHFFFAOYSA-N

2-(2-Hydroxyphenyl)-2-oxoacetic acid

c1ccc(c(c1)C(=O)C(O)=O)O

Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

Abiotic

Downstream Successor

AQULTZMTCLLZBM-UHFFFAOYSA-N

2-(2,3-Dihydroxyphenyl)-2-hydroxyacetic acid

C(=O)(C(C1=CC=CC(=C1O)O)O)O

Precursor

PZZHMLOHNYWKIK-UHFFFAOYSA-N

Ethylenediaminedi-o-hydroxyphenylacetic acid

C1=CC=C(C(=C1)C(C(=O)O)NCCNC(C2=CC=CC=C2O)C(=O)O)O

Environmental

Downstream Successor

AQULTZMTCLLZBM-UHFFFAOYSA-N

2-(2,3-Dihydroxyphenyl)-2-hydroxyacetic acid

C(=O)(C(C1=CC=CC(=C1O)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.