Search More · GCI-TPs

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

Precursor

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

12 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

6 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

12 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

12 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

13 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

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

Abiotic

Product

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

Upstream Precursor

YKYJNERLWHRIJX-UHFFFAOYSA-N

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2Cl)O)C(=O)C4=CC=CC=C4C3=O)N

Abiotic

Product

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

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

Precursor

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

Abiotic

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

Abiotic

Downstream Successor

QUXBARPXUAPKDG-UHFFFAOYSA-N

1-Amino-2,4-dihydroxyanthraquinone

c1ccc2c(c1)C(=O)c3c(C2=O)c(c(cc3O)O)N

Precursor

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

Abiotic

Downstream Successor

WXLUODUSDHPLDZ-UHFFFAOYSA-N

c1(c(c2c(c(c1O)N)C(=O)c3ccccc3C2=O)O)O

Precursor

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

Abiotic

Downstream Successor

UKUGEEQHAAGTQQ-UHFFFAOYSA-N

C1=CC=C2C(=C1)C(=O)C(C(C2=O)=C(N)C(=O)O)=C(O)C(O)=O

Precursor

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

Abiotic

Downstream Successor

UAPBFUWSWSOLAS-UHFFFAOYSA-N

C1=CC=C2C(=C1)C(=O)C(=C(C2=O)C(=O)O)C(=CC(O)=O)O

Precursor

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

Abiotic

Downstream Successor

DUEVINLJBYASEY-UHFFFAOYSA-N

C(=C(C1=C(C(=O)c2ccccc2C1=O)C(=O)O)N)(C(O)=O)O

Precursor

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

Abiotic

Downstream Successor

GHNJKICEUXEXBG-UHFFFAOYSA-N

c1c(cc2c(c1)C(=O)c3c(C2=O)c(c(cc3O)O)N)O

Precursor

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

Abiotic

Downstream Successor

KZKWOOQDVFFAHC-UHFFFAOYSA-N

c1(ccc2c(c1)C(=O)c3c(C2=O)c(c(cc3O)O)N)O

Precursor

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

Abiotic

Downstream Successor

IUBBRSCHPHPBPQ-UHFFFAOYSA-N

Oc1c(c2c(c(c1Cl)O)C(=O)c3ccccc3C2=O)N

Precursor

FMJLZDIPOPILLS-UHFFFAOYSA-N

1-Amino-4-hydroxy-2-(4-pentylphenoxy)-9,10-anthracenedione

CCCCCC1=CC=C(C=C1)OC2=C(C3=C(C(=C2)O)C(=O)C4=CC=CC=C4C3=O)N

Abiotic

Downstream Successor

BBNQQADTFFCFGB-UHFFFAOYSA-N

Purpurin anthraquinone

C1(=C2C(=C(C=C1O)O)C(=O)C3=CC=CC=C3C2=O)O

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

No Original Precursors

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