Main compound image
(r)-2-(4-aminophenethylamino)-1-phenylethanol hydrochloride
  • Other Name: 2-((4-Aminophenethyl)amino)-1-phenylethanol hydrochloride, (R)-
  • InChIKey: QILVTBCJVNFIDP-NTISSMGPSA-N
  • InChI: InChI=1S/C16H20N2O.ClH/c17-15-8-6-13(7-9-15)10-11-18-12-16(19)14-4-2-1-3-5-14;/h1-9,16,18-19H,10-12,17H2;1H/t16-;/m0./s1
  • SMILES: C1=CC=C(C=C1)[C@H](CNCCC2=CC=C(C=C2)N)O.Cl
  • Exact Mass: 292.13424
  • Molecular Formula: C16H21ClN2O
  • Compound CID: pubchemlite52953007 pubchem52953007
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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