Main compound image
(1-methyl-5-piperazin-1-yl-3-propyl-1h-pyrazolo[4,3-d]pyrimidin-7-yl)-(5-methyl-pyridin-2-yl)-amine
  • Other Name: 1-methyl-N-(5-methyl-2-pyridinyl)-5-piperazin-1-yl-3-propylpyrazolo[4,5-d]pyrimidin-7-amine
  • InChIKey: XEETWKYVVQVUPU-UHFFFAOYSA-N
  • InChI: InChI=1S/C19H26N8/c1-4-5-14-16-17(26(3)25-14)18(22-15-7-6-13(2)12-21-15)24-19(23-16)27-10-8-20-9-11-27/h6-7,12,20H,4-5,8-11H2,1-3H3,(H,21,22,23,24)
  • SMILES: CCCC1=NN(C2=C1N=C(N=C2NC3=NC=C(C=C3)C)N4CCNCC4)C
  • Exact Mass: 366.22804
  • Molecular Formula: C19H26N8
  • Compound CID: pubchemlite46926354 pubchem46926354
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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