Main compound image
(s)-3-(3-(acetamidomethyl)-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-7-yloxy)propanoic acid
  • Other Name: 3-(((3S)-3-((Acetylamino)methyl)-1,3-dihydro-1-hydroxy-2,1-benzoxaborol-7-yl)oxy)propanoic acid
  • InChIKey: IECQEDZZJUTCHL-LLVKDONJSA-N
  • InChI: InChI=1S/C13H16BNO6/c1-8(16)15-7-11-9-3-2-4-10(13(9)14(19)21-11)20-6-5-12(17)18/h2-4,11,19H,5-7H2,1H3,(H,15,16)(H,17,18)/t11-/m1/s1
  • SMILES: B1(C2=C(C=CC=C2OCCC(=O)O)[C@H](O1)CNC(=O)C)O
  • Exact Mass: 293.10707
  • Molecular Formula: C13H16BNO6
  • Compound CID: pubchemlite118753287 pubchem118753287
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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