5-[4-(acetylamino)benzenesulf-onyloxy]sulfapyridine acetate
- Other Name: 5-[4-(Acetylamino)benzenesulfonyloxy]sulfapyridine Acetate
- InChIKey: JPIUMBXLXMOUNV-UHFFFAOYSA-N
- InChI: InChI=1S/C21H20N4O7S2/c1-14(26)23-16-3-8-19(9-4-16)33(28,29)25-21-12-7-18(13-22-21)32-34(30,31)20-10-5-17(6-11-20)24-15(2)27/h3-13H,1-2H3,(H,22,25)(H,23,26)(H,24,27)
- SMILES: CC(=O)NC1=CC=C(C=C1)S(=O)(=O)NC2=NC=C(C=C2)OS(=O)(=O)C3=CC=C(C=C3)NC(=O)C
- Exact Mass: 504.07734
- Molecular Formula: C21H20N4O7S2
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Compound CID:
125378864
125378864
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.