Main compound image
(r)-2-amino-3-(5-tert-butyl-2-((4,5-dihydro-1h-imidazol-2-yl)methyl)-4-hydroxy-3-methylbenzylthio)propanoic acid
  • Other Name: (2R)-2-amino-3-[[5-tert-butyl-2-(4,5-dihydro-1H-imidazol-2-ylmethyl)-4-hydroxy-3-methylphenyl]methylsulfanyl]propanoic acid
  • InChIKey: UGJKRZCZFCWZDE-HNNXBMFYSA-N
  • InChI: InChI=1S/C19H29N3O3S/c1-11-13(8-16-21-5-6-22-16)12(9-26-10-15(20)18(24)25)7-14(17(11)23)19(2,3)4/h7,15,23H,5-6,8-10,20H2,1-4H3,(H,21,22)(H,24,25)/t15-/m0/s1
  • SMILES: CC1=C(C(=CC(=C1O)C(C)(C)C)CSC[C@@H](C(=O)O)N)CC2=NCCN2
  • Exact Mass: 379.19296
  • Molecular Formula: C19H29N3O3S
  • Compound CID: pubchemlite118753202 pubchem118753202
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.

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