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

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

Depiction
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
Depiction
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
Depiction
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
Depiction
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
Depiction
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
Depiction
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
Depiction
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
Depiction
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
Depiction
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
Depiction
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
Depiction
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
Depiction
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

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.

Search with another depth
or Explore another compound
Higher depth reveals distant relationships but increases loading time.