Main compound image
5-chloro-3-hydroxy-2,2-dimethyl-n-(8-methyl-8-azabicyclo[3.2.1]octan-3-yl)-3h-1-benzofuran-7-carboxamide
  • Other Name: 5-chloro-3-hydroxy-2,2-dimethyl-N-(8-methyl-8-azabicyclo[3.2.1]octan-3-yl)-3H-1-benzofuran-7-carboxamide
  • InChIKey: NBWGHXIOQAPXMZ-UHFFFAOYSA-N
  • InChI: InChI=1S/C19H25ClN2O3/c1-19(2)17(23)14-6-10(20)7-15(16(14)25-19)18(24)21-11-8-12-4-5-13(9-11)22(12)3/h6-7,11-13,17,23H,4-5,8-9H2,1-3H3,(H,21,24)
  • SMILES: CC1(C(C2=C(O1)C(=CC(=C2)Cl)C(=O)NC3CC4CCC(C3)N4C)O)C
  • Exact Mass: 364.15537
  • Molecular Formula: C19H25ClN2O3
  • Compound CID: pubchemlite10384207 pubchem10384207
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.
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.

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