Main compound image
(r)-2-(6-carbamoyl-7-methoxyquinolin-4-ylamino)-3-mercaptopropanoic acid
  • Other Name: (2R)-2-[(6-carbamoyl-7-methoxyquinolin-4-yl)amino]-3-sulfanylpropanoic acid
  • InChIKey: YJEAMDJZVMBVHE-NSHDSACASA-N
  • InChI: InChI=1S/C14H15N3O4S/c1-21-12-5-10-7(4-8(12)13(15)18)9(2-3-16-10)17-11(6-22)14(19)20/h2-5,11,22H,6H2,1H3,(H2,15,18)(H,16,17)(H,19,20)/t11-/m0/s1
  • SMILES: COC1=CC2=NC=CC(=C2C=C1C(=O)N)N[C@@H](CS)C(=O)O
  • Exact Mass: 321.07833
  • Molecular Formula: C14H15N3O4S
  • Compound CID: pubchemlite118753340 pubchem118753340
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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