Glutathione-unsaturated fluorotelomer alcohol conjugate
- InChIKey: SZLFSECIPCQPQO-OQFOIZHKSA-N
- InChI: InChI=1S/C18H20F11N3O7S/c19-14(20,15(21,22)16(23,24)17(25,26)18(27,28)29)9(3-4-33)40-6-8(12(37)31-5-11(35)36)32-10(34)2-1-7(30)13(38)39/h3,7-8,33H,1-2,4-6,30H2,(H,31,37)(H,32,34)(H,35,36)(H,38,39)/b9-3-
- SMILES: C(CC(=O)NC(CS/C(=C\CO)/C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)C(=O)NCC(=O)O)C(C(=O)O)N
- Exact Mass: 631.08463
- Molecular Formula: C18H20F11N3O7S
-
Compound CID:
165362499
165362499
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.
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.