Search More · GCI-TPs

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

Upstream Precursor

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Abiotic

Product

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Upstream Precursor

FJHBVJOVLFPMQE-UHFFFAOYSA-N

7-Ethyl-10-hydroxy camptothecin, (rac)-

CCC1=C2CN3C(=CC4=C(C3=O)COC(=O)C4(CC)O)C2=NC5=C1C=C(C=C5)O

Abiotic

Product

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Upstream Precursor

FJHBVJOVLFPMQE-UHFFFAOYSA-N

7-Ethyl-10-hydroxy camptothecin, (rac)-

CCC1=C2CN3C(=CC4=C(C3=O)COC(=O)C4(CC)O)C2=NC5=C1C=C(C=C5)O

PriorBiotransformation

Product

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Upstream Precursor

BQTSIJRYWOMMII-UHFFFAOYSA-N

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C(=C(C=C4)O)Cl

Environmental

Product

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Upstream Precursor

BQTSIJRYWOMMII-UHFFFAOYSA-N

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C(=C(C=C4)O)Cl

Abiotic

Product

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Upstream Precursor

BQTSIJRYWOMMII-UHFFFAOYSA-N

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C(=C(C=C4)O)Cl

Abiotic

Product

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Upstream Precursor

BQTSIJRYWOMMII-UHFFFAOYSA-N

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C(=C(C=C4)O)Cl

Environmental

Product

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Upstream Precursor

QUYXFCMRCNFYDH-UHFFFAOYSA-N

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C(=C4)Cl)O

Abiotic

Product

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Upstream Precursor

QUYXFCMRCNFYDH-UHFFFAOYSA-N

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C(=C4)Cl)O

Environmental

Product

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Upstream Precursor

UWKQSNNFCGGAFS-XIFFEERXSA-N

Irinotecan

CCC1=C2CN3C(=CC4=C(C3=O)COC(=O)[C@@]4(CC)O)C2=NC5=C1C=C(C=C5)…

Abiotic

Product

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

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

Precursor

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Abiotic

Downstream Successor

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Precursor

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Abiotic

Downstream Successor

QALLNVYTLTXTJE-UHFFFAOYSA-N

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C(=C4)O)O

Precursor

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Abiotic

Downstream Successor

ALTQEKOCEJGCEE-UHFFFAOYSA-N

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C(=C(C=C4)O)O

Precursor

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Abiotic

Downstream Successor

ALTQEKOCEJGCEE-UHFFFAOYSA-N

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C(=C(C=C4)O)O

Precursor

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Abiotic

Downstream Successor

OWTGGBXVHQGAGB-UHFFFAOYSA-N

CCC1=C2CNC(=CC(=C(C(=O)O)CO)C(C(O)=O)(CC)O)C2=NC3=C1C=C(C=C3)O

Precursor

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Abiotic

Downstream Successor

GQGOKRSNQPJLPE-UHFFFAOYSA-N

CCc1c2Cn3c(cc(c(c3=O)CO)C(C(O)=O)(CC)O)-c2nc(c1C=C(O)C(=O)O)C(O)=O

Precursor

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Abiotic

Downstream Successor

GQGOKRSNQPJLPE-UHFFFAOYSA-N

CCc1c2Cn3c(cc(c(c3=O)CO)C(C(O)=O)(CC)O)-c2nc(c1C=C(O)C(=O)O)C(O)=O

Precursor

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Abiotic

Downstream Successor

FTPYUJBQXCOULJ-UHFFFAOYSA-N

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=[N+](C4=C1C=C(C=…

Precursor

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Abiotic

Downstream Successor

BQTSIJRYWOMMII-UHFFFAOYSA-N

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C(=C(C=C4)O)Cl

Precursor

IRKZFHZUIBLGKU-UHFFFAOYSA-N

2-[12-ethyl-2-hydroxy-8-(hydroxymethyl)-9-oxo-11H-indolizino[1,2-b]quinolin-7-yl]-2-hydroxybutanoic acid

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C=C4)O

Abiotic

Downstream Successor

QUYXFCMRCNFYDH-UHFFFAOYSA-N

CCC1=C2CN3C(=CC(=C(C3=O)CO)C(C(O)=O)(CC)O)C2=NC4=C1C=C(C(=C4)Cl)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 Dead-Ends

No entries were found for this section with the current query and depth.

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