Search More · GCI-TPs

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

Precursor

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

12 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

20 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

9 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

8 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

12 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

12 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

16 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

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

Precursor

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

6 steps

Dead-End Product

UACFYXXWBXHZFO-UHFFFAOYSA-N

C=1(C2C(=O)C(=C(C(=O)C2=C(C(C1O)=O)O)C(=O)O)C(=CC(O)=O)O)O

Precursor

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

5 steps

Dead-End Product

UZBXUKOBHSHYGO-UHFFFAOYSA-N

C(=C(C1=C(C(=O)C2=CC(C(=C(C2C1=O)O)O)=O)C(=O)O)O)C(O)=O

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

Upstream Precursor

FWEQPMZEKHHFTB-UHFFFAOYSA-N

Benzamide, N-(5-amino-9,10-dihydro-9,10-dioxo-1-anthracenyl)-

Nc1cccc2c1C(=O)c3c(C2=O)c(ccc3)NC(c4ccccc4)=O

Abiotic

Product

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

Upstream Precursor

FWEQPMZEKHHFTB-UHFFFAOYSA-N

Benzamide, N-(5-amino-9,10-dihydro-9,10-dioxo-1-anthracenyl)-

Nc1cccc2c1C(=O)c3c(C2=O)c(ccc3)NC(c4ccccc4)=O

Environmental

Product

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

Upstream Precursor

VWBVCOPVKXNMMZ-UHFFFAOYSA-N

1,5-Diaminoanthraquinone

NC1=CC=CC2=C1C(=O)C3=C(C2=O)C(=CC=C3)N

Abiotic

Product

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

Upstream Precursor

GYKJKBJCGCBQTE-UHFFFAOYSA-N

Nc1cccc2c1C(=O)c3c(C2=O)c(ccc3)NC(c4ccc(cc4)O)=O

Abiotic

Product

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

Upstream Precursor

GYKJKBJCGCBQTE-UHFFFAOYSA-N

Nc1cccc2c1C(=O)c3c(C2=O)c(ccc3)NC(c4ccc(cc4)O)=O

Environmental

Product

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

Upstream Precursor

CRZSPFNSBLLXFJ-UHFFFAOYSA-N

9,10-Anthracenedione, 1-amino-4,5-dinitro-

NC1=C2C(=C(C=C1)[N+](=O)[O-])C(=O)C3=C(C2=O)C=CC=C3[N+](=O)[O-]

Abiotic

Product

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

Upstream Precursor

CRZSPFNSBLLXFJ-UHFFFAOYSA-N

9,10-Anthracenedione, 1-amino-4,5-dinitro-

NC1=C2C(=C(C=C1)[N+](=O)[O-])C(=O)C3=C(C2=O)C=CC=C3[N+](=O)[O-]

Environmental

Product

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

Upstream Precursor

GSNYCCVPEQDXNU-UHFFFAOYSA-N

N-(5-amino-9,10-dioxoanthracen-1-yl)-2,3,4,5-tetrachlorobenzamide

C1=CC2=C(C(=C1)NC(=O)C3=CC(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)C4=C(C2=O…

Abiotic

Product

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

Upstream Precursor

GSNYCCVPEQDXNU-UHFFFAOYSA-N

N-(5-amino-9,10-dioxoanthracen-1-yl)-2,3,4,5-tetrachlorobenzamide

C1=CC2=C(C(=C1)NC(=O)C3=CC(=C(C(=C3Cl)Cl)Cl)Cl)C(=O)C4=C(C2=O…

Environmental

Product

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

Upstream Precursor

AUTVNGXRBJKDPL-UHFFFAOYSA-N

C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C=C(C=C3)C(NC4=CC=CC5=C4C(=O)C6=…

Abiotic

Product

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

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

Precursor

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

Abiotic

Downstream Successor

DOGUOZGKCCVTAE-UHFFFAOYSA-N

Nc1c2c(c(cc1)O)C(=O)C(C(=CC(=O)O)N)=C(C2=O)C(O)=O

Precursor

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

Abiotic

Downstream Successor

HSYLKWSCFRLSKB-UHFFFAOYSA-N

1,5-Diamino-4,8-dihydroxyanthraquinone

NC1=C2C(=C(C=C1)O)C(=O)C3=C(C2=O)C(=CC=C3N)O

Precursor

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

Abiotic

Downstream Successor

CBVYVWGKYWSTHC-UHFFFAOYSA-N

4,8-Diamino-2-chloro-1,5-dihydroxyanthracene-9,10-dione

NC1=C2C(=C(C=C1)O)C(=O)C3=C(C=C(C(=C3C2=O)O)Cl)N

Precursor

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

Abiotic

Downstream Successor

CAELQZMPHVGBEU-UHFFFAOYSA-N

NC=1C(C=C(C2C(=O)C3=C(C=CC(=C3C(=O)C12)O)N)O)=O

Precursor

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

Abiotic

Downstream Successor

ICRPMHQBDMEAPH-UHFFFAOYSA-N

4,8-Diamino-1,2-dihydroxyanthracene-9,10-dione

Nc1c2c(c(c(c1)O)O)C(=O)c3c(C2=O)cccc3N

Precursor

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

Environmental

Downstream Successor

ICRPMHQBDMEAPH-UHFFFAOYSA-N

4,8-Diamino-1,2-dihydroxyanthracene-9,10-dione

Nc1c2c(c(c(c1)O)O)C(=O)c3c(C2=O)cccc3N

Precursor

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

Environmental

Downstream Successor

BKVKMZPWOBAUHC-UHFFFAOYSA-N

C1=C2C3=C(C(=C1)N)C(=O)C4=C(C3=O)C(=CC(=C4O)O)N2

Precursor

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

Abiotic

Downstream Successor

BKVKMZPWOBAUHC-UHFFFAOYSA-N

C1=C2C3=C(C(=C1)N)C(=O)C4=C(C3=O)C(=CC(=C4O)O)N2

Precursor

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

Abiotic

Downstream Successor

OXQYGVSMUGQPDF-UHFFFAOYSA-N

1,4-Dihydroxy-5-aminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C=CC(=C3C2=O)O)O

Precursor

KJDPNZKJMSKKDY-UHFFFAOYSA-N

1-Hydroxy-4,8-diaminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C2=O)C(=CC=C3O)N

Environmental

Downstream Successor

OXQYGVSMUGQPDF-UHFFFAOYSA-N

1,4-Dihydroxy-5-aminoanthraquinone

C1=CC2=C(C(=C1)N)C(=O)C3=C(C=CC(=C3C2=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.