Main compound image
thioridazine glutathione conjugate
  • Other Name: 2-Amino-5-[[1-(carboxymethylamino)-3-[10-[2-(1-methylpiperidin-2-yl)ethyl]-8-methylsulfanylphenothiazin-3-yl]sulfanyl-1-oxopropan-2-yl]amino]-5-oxopentanoic acid
  • InChIKey: OJCZHARCPHEHPT-UHFFFAOYSA-N
  • InChI: InChI=1S/C31H41N5O6S3/c1-35-13-4-3-5-19(35)12-14-36-24-9-6-21(16-27(24)45-26-10-7-20(43-2)15-25(26)36)44-18-23(30(40)33-17-29(38)39)34-28(37)11-8-22(32)31(41)42/h6-7,9-10,15-16,19,22-23H,3-5,8,11-14,17-18,32H2,1-2H3,(H,33,40)(H,34,37)(H,38,39)(H,41,42)
  • SMILES: CN1CCCCC1CCN2C3=C(C=C(C=C3)SCC(C(=O)NCC(=O)O)NC(=O)CCC(C(=O)O)N)SC4=C2C=C(C=C4)SC
  • Exact Mass: 675.22190
  • Molecular Formula: C31H41N5O6S3
  • Compound CID: pubchemlite118753610 pubchem118753610
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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