Main compound image
(s)-3-(3-(aminomethyl)-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-7-yloxy)propanoic acid hydrochloride
  • Other Name: 3-[[(3S)-3-(aminomethyl)-1-hydroxy-3H-2,1-benzoxaborol-7-yl]oxy]propanoic acid;hydrochloride
  • InChIKey: OMNZFUGKQMGAAD-SBSPUUFOSA-N
  • InChI: InChI=1S/C11H14BNO5.ClH/c13-6-9-7-2-1-3-8(11(7)12(16)18-9)17-5-4-10(14)15;/h1-3,9,16H,4-6,13H2,(H,14,15);1H/t9-;/m1./s1
  • SMILES: B1(C2=C(C=CC=C2OCCC(=O)O)[C@H](O1)CN)O.Cl
  • Exact Mass: 287.07318
  • Molecular Formula: C11H15BClNO5
  • Compound CID: pubchemlite118753285 pubchem118753285
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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