Main compound image
[(1r)-2-hydroxy-1-methyl-ethyl]n-[(2s)-7-cyano-4-(2-pyridylmethyl)-2,3-dihydro-1h-cyclopenta[b]indol-2-yl]carbamate
  • Other Name: Carbamic acid, N-((2S)-7-cyano-1,2,3,4-tetrahydro-4-(2-pyridinylmethyl)cyclopent(b)indol-2-yl)-, (1R)-2-hydroxy-1-methylethyl ester
  • InChIKey: FBKLHMXRQOSWPP-PBHICJAKSA-N
  • InChI: InChI=1S/C22H22N4O3/c1-14(13-27)29-22(28)25-17-9-19-18-8-15(11-23)5-6-20(18)26(21(19)10-17)12-16-4-2-3-7-24-16/h2-8,14,17,27H,9-10,12-13H2,1H3,(H,25,28)/t14-,17+/m1/s1
  • SMILES: C[C@H](CO)OC(=O)N[C@H]1CC2=C(C1)N(C3=C2C=C(C=C3)C#N)CC4=CC=CC=N4
  • Exact Mass: 390.16919
  • Molecular Formula: C22H22N4O3
  • Compound CID: pubchemlite118753373 pubchem118753373
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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