non-aromatic ring hydroxynebivolol-glucuronide
- Other Name: Non-aromatic ring hydroxynebivolol-glucuronide
- InChIKey: KIYRCCCXPCDMSE-UHFFFAOYSA-N
- InChI: InChI=1S/C28H33F2NO11/c29-13-2-5-18-12(7-13)1-4-20(39-18)16(32)10-31-11-17(33)22-9-21(15-8-14(30)3-6-19(15)40-22)41-28-25(36)23(34)24(35)26(42-28)27(37)38/h2-3,5-8,16-17,20-26,28,31-36H,1,4,9-11H2,(H,37,38)
- SMILES: C1CC2=C(C=CC(=C2)F)OC1C(CNCC(C3CC(C4=C(O3)C=CC(=C4)F)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O
- Exact Mass: 597.20217
- Molecular Formula: C28H33F2NO11
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Compound CID:
169501952
169501952
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.