lopinavir m5 metabolite
- Other Name: Lopinavir M5 metabolite
- InChIKey: VPEYYVJRGQGLCF-JKAXMSHYSA-N
- InChI: InChI=1S/C37H48N4O6/c1-24(2)34(41-17-11-16-38-37(41)46)36(45)39-29(20-27-12-7-5-8-13-27)22-32(43)31(21-28-14-9-6-10-15-28)40-33(44)23-47-35-25(3)18-30(42)19-26(35)4/h5-10,12-15,18-19,24,29,31-32,34,42-43H,11,16-17,20-23H2,1-4H3,(H,38,46)(H,39,45)(H,40,44)/t29-,31-,32-,34-/m0/s1
- SMILES: CC1=CC(=CC(=C1OCC(=O)N[C@@H](CC2=CC=CC=C2)[C@H](C[C@H](CC3=CC=CC=C3)NC(=O)[C@H](C(C)C)N4CCCNC4=O)O)C)O
- Exact Mass: 644.35739
- Molecular Formula: C37H48N4O6
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Compound CID:
169502185
169502185
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.