Main compound image
(2s)-2-amino-5-[[(2r)-1-(carboxymethylamino)-3-[[3-(2-chloroethyl)-2-(2-chloroethylamino)-2-oxo-1,3,2lambda5-oxazaphosphinan-4-yl]oxysulfanyl]-1-oxopropan-2-yl]amino]-5-oxopentanoic acid
  • Other Name: (2S)-2-amino-5-[[(2R)-1-(carboxymethylamino)-3-[[3-(2-chloroethyl)-2-(2-chloroethylamino)-2-oxo-1,3,2lambda5-oxazaphosphinan-4-yl]oxysulfanyl]-1-oxopropan-2-yl]amino]-5-oxopentanoic acid
  • InChIKey: DSLZNGNGALUIJI-LGUIJYROSA-N
  • InChI: InChI=1S/C17H30Cl2N5O9PS/c18-4-6-22-34(31)24(7-5-19)14(3-8-32-34)33-35-10-12(16(28)21-9-15(26)27)23-13(25)2-1-11(20)17(29)30/h11-12,14H,1-10,20H2,(H,21,28)(H,22,31)(H,23,25)(H,26,27)(H,29,30)/t11-,12-,14?,34?/m0/s1
  • SMILES: C1COP(=O)(N(C1OSC[C@@H](C(=O)NCC(=O)O)NC(=O)CC[C@@H](C(=O)O)N)CCCl)NCCCl
  • Exact Mass: 581.08789
  • Molecular Formula: C17H30Cl2N5O9PS
  • Compound CID: pubchemlite154699572 pubchem154699572
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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