Main compound image
Formyl-H4MPT
  • InChIKey: RMPHWTMYCVTPKB-LJNCEWCUSA-K
  • InChI: InChI=1S/C31H45N6O17P/c1-13(22-14(2)34-27-23(37(22)12-38)28(46)36-31(32)35-27)33-16-5-3-15(4-6-16)9-17(39)24(43)18(40)10-51-30-26(45)25(44)20(53-30)11-52-55(49,50)54-19(29(47)48)7-8-21(41)42/h3-6,12-14,17-20,22,24-26,30,33,39-40,43-45H,7-11H2,1-2H3,(H,41,42)(H,47,48)(H,49,50)(H4,32,34,35,36,46)/p-3/t13?,14?,17?,18?,19?,20-,22?,24?,25-,26-,30+/m1/s1
  • SMILES: CC1C(N(C2=C(N1)N=C(NC2=O)N)C=O)C(C)NC3=CC=C(C=C3)CC(C(C(CO[C@@H]4[C@@H]([C@@H]([C@H](O4)COP(=O)([O-])OC(CCC(=O)[O-])C(=O)[O-])O)O)O)O)O
  • Exact Mass: 801.23441
  • Molecular Formula: C31H42N6O17P-3
  • Compound CID: pubchemlite135527503 pubchem135527503
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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