paroxetine metabolite m-ii-glucuronide
- Other Name: Paroxetine metabolite M-II-glucuronide
- InChIKey: VPEIBIYIZBYDPS-DWJNZUPPSA-N
- InChI: InChI=1S/C25H30FNO9/c1-33-19-10-16(34-12-14-11-27-9-8-17(14)13-2-4-15(26)5-3-13)6-7-18(19)35-25-22(30)20(28)21(29)23(36-25)24(31)32/h2-7,10,14,17,20-23,25,27-30H,8-9,11-12H2,1H3,(H,31,32)/t14-,17-,20?,21?,22?,23?,25?/m0/s1
- SMILES: COC1=C(C=CC(=C1)OC[C@@H]2CNCC[C@H]2C3=CC=C(C=C3)F)OC4C(C(C(C(O4)C(=O)O)O)O)O
- Exact Mass: 507.19046
- Molecular Formula: C25H30FNO9
-
Compound CID:
169502184
169502184
Hidden Reactions Filter
Some biological reactions link very small precursors (e.g. CO₂, acetate) to much larger products.
These reactions are correct, but they can create unrealistic shortest paths and connect otherwise separate parts of the graph.
To keep the overview readable, FAIR-TPs hides six such reactions where a <60 Da precursor leads to a >300 Da product in the visualisations.
You can have all these paths in the download output.
You can have all these paths in the download output.
Hidden reaction pairs (precursor → product):
- Acetate → N-(2-benzoyl-4-chlorophenyl)-2-acetamidoacetamide
- Acetate → N-(2-benzoyl-4-chlorophenyl)-2-acetamido-n-methylacetamide
- Carbon dioxide → Formylmethanofuran
- Acrolein → Chembl3706542
- Ethylene oxide → Acetyl-coa
- Formaldehyde → S-hydroxymethylglutathione
Note: In the graph output, up to 100 compounds are displayed for faster visualization. For the full output, please use the export files.
Click on a node or edge to see details here.