Search More · GCI-TPs

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

Precursor

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

10 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

10 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Previewing top 9 entries. If you want the full results, please use the download button above.

Upstream Precursor

FCGVBHISQBBIQF-UHFFFAOYSA-N

Rhodamine 123 free base

COC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

Abiotic

Product

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

Upstream Precursor

FCGVBHISQBBIQF-UHFFFAOYSA-N

Rhodamine 123 free base

COC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

Environmental

Product

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

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

Precursor

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

Environmental

Downstream Successor

BPNFIJXKGJIUHO-UHFFFAOYSA-N

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

Precursor

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

Environmental

Downstream Successor

WYFMQURTUZVEHK-UHFFFAOYSA-N

C(=O)(C1=CC(=C(C=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N)O)O)O

Precursor

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

Abiotic

Downstream Successor

CZXUAXZMLJBDBQ-UHFFFAOYSA-N

C(=O)(C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C(=C(C(=C4)N)O)O)O

Precursor

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

Environmental

Downstream Successor

CZXUAXZMLJBDBQ-UHFFFAOYSA-N

C(=O)(C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C(=C(C(=C4)N)O)O)O

Precursor

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

Environmental

Downstream Successor

SGKQVYDWDRSORR-UHFFFAOYSA-N

C(=O)(C1=C(C(=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N)O)O)O

Precursor

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

Environmental

Downstream Successor

KAVFPHLKWAFTDD-UHFFFAOYSA-N

C(=O)(C1=CC=C(C(=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N)O)O)O

Precursor

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

Abiotic

Downstream Successor

JAGRRJPZIAUJMX-UHFFFAOYSA-N

C1=CC=C(C(=C1)C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4O)N)C(=O)O

Precursor

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

Environmental

Downstream Successor

ADSYIBNHEZRYOC-UHFFFAOYSA-N

c1(cccc(c1O)-c2c-3ccc(=N)cc3oc4c2ccc(c4)N)O

Precursor

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

Abiotic

Downstream Successor

ADSYIBNHEZRYOC-UHFFFAOYSA-N

c1(cccc(c1O)-c2c-3ccc(=N)cc3oc4c2ccc(c4)N)O

Precursor

UPZKDDJKJWYWHQ-UHFFFAOYSA-N

xanthylium, 3,6-diamino-9-(2-carboxyphenyl)-, inner salt

OC(=O)C1=CC=CC=C1C2=C3C=CC(=N)C=C3OC4=C2C=CC(=C4)N

Environmental

Downstream Successor

ADSYIBNHEZRYOC-UHFFFAOYSA-N

c1(cccc(c1O)-c2c-3ccc(=N)cc3oc4c2ccc(c4)N)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.

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