ranolazine metabolite cvt-5031-sulfate
- Other Name: Ranolazine metabolite CVT-5031-sulfate
- InChIKey: NCYBGJQUZOABLC-UHFFFAOYSA-N
- InChI: InChI=1S/C24H33N3O8S/c1-17-6-4-7-18(2)23(17)25-22(29)15-27-12-10-26(11-13-27)14-19(28)16-34-24-20(33-3)8-5-9-21(24)35-36(30,31)32/h4-9,19,28H,10-16H2,1-3H3,(H,25,29)(H,30,31,32)
- SMILES: CC1=C(C(=CC=C1)C)NC(=O)CN2CCN(CC2)CC(COC3=C(C=CC=C3OS(=O)(=O)O)OC)O
- Exact Mass: 523.19884
- Molecular Formula: C24H33N3O8S
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Compound CID:
169501999
169501999
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.