Main compound image
(s)-2-amino-5-((r)-1-(carboxymethylamino)-3-(4-fluoro-2-hydroxy-5-((4-(4-(5-(2-hydroxypropan-2-yl)pyridin-2-yl)piperazin-1-yl)phthalazin-1-yl)methyl)phenylthio)-1-oxopropan-2-ylamino)-5-oxopentanoic acid
  • Other Name: (2S)-2-amino-5-[[(2R)-1-(carboxymethylamino)-3-[4-fluoro-2-hydroxy-5-[[4-[4-[5-(2-hydroxypropan-2-yl)-2-pyridinyl]piperazin-1-yl]phthalazin-1-yl]methyl]phenyl]sulfanyl-1-oxopropan-2-yl]amino]-5-oxopentanoic acid
  • InChIKey: RPQNGGOQJLHDBQ-XCZPVHLTSA-N
  • InChI: InChI=1S/C37H43FN8O8S/c1-37(2,54)22-7-9-31(40-18-22)45-11-13-46(14-12-45)34-24-6-4-3-5-23(24)27(43-44-34)15-21-16-30(29(47)17-25(21)38)55-20-28(35(51)41-19-33(49)50)42-32(48)10-8-26(39)36(52)53/h3-7,9,16-18,26,28,47,54H,8,10-15,19-20,39H2,1-2H3,(H,41,51)(H,42,48)(H,49,50)(H,52,53)/t26-,28-/m0/s1
  • SMILES: CC(C)(C1=CN=C(C=C1)N2CCN(CC2)C3=NN=C(C4=CC=CC=C43)CC5=CC(=C(C=C5F)O)SC[C@@H](C(=O)NCC(=O)O)NC(=O)CC[C@@H](C(=O)O)N)O
  • Exact Mass: 778.29086
  • Molecular Formula: C37H43FN8O8S
  • Compound CID: pubchemlite118753300 pubchem118753300
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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