ranolazine metabolite m1
- Other Name: Ranolazine metabolite M1
- InChIKey: BGJLPWKURZVYIE-UHFFFAOYSA-M
- InChI: InChI=1S/C28H39N3O11S/c1-17-6-5-7-18(2)23(17)29-22(33)15-31-12-10-30(11-13-31)14-19(32)16-39-20-8-3-4-9-21(20)40-28-25(35)26(42-43(37)38)24(34)27(36)41-28/h3-9,19,24-28,32,34-36H,10-16H2,1-2H3,(H,29,33)(H,37,38)/p-1
- SMILES: CC1=C(C(=CC=C1)C)NC(=O)CN2CCN(CC2)CC(COC3=CC=CC=C3OC4C(C(C(C(O4)O)O)OS(=O)[O-])O)O
- Exact Mass: 624.22271
- Molecular Formula: C28H38N3O11S-
-
Compound CID:
169502134
169502134
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.