Main compound image
isopropyl n-[(2s,3s)-7-cyano-3-hydroxy-4-(2-pyridylmethyl)-2,3-dihydro-1h-cyclopenta[b]indol-2-yl]carbamate
  • Other Name: Carbamic acid, N-((2S,3S)-7-cyano-1,2,3,4-tetrahydro-3-hydroxy-4-(2-pyridinylmethyl)cyclopent(b)indol-2-yl)-, 1-methylethyl ester
  • InChIKey: JYLZLLBMSMEHAN-RXVVDRJESA-N
  • InChI: InChI=1S/C22H22N4O3/c1-13(2)29-22(28)25-18-10-17-16-9-14(11-23)6-7-19(16)26(20(17)21(18)27)12-15-5-3-4-8-24-15/h3-9,13,18,21,27H,10,12H2,1-2H3,(H,25,28)/t18-,21-/m0/s1
  • SMILES: CC(C)OC(=O)N[C@H]1CC2=C([C@H]1O)N(C3=C2C=C(C=C3)C#N)CC4=CC=CC=N4
  • Exact Mass: 390.16919
  • Molecular Formula: C22H22N4O3
  • Compound CID: pubchemlite118753417 pubchem118753417
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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