5-bromo-N-[2,10-dihydroxy-7-(2-methylpropyl)-5,8-dioxo-4-propan-2-yl-3-oxa-6,9-diazatricyclo[7.3.0.02,6]dodecan-4-yl]-7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide
- InChIKey: NZGWOMCNZDKBSR-UHFFFAOYSA-N
- InChI: InChI=1S/C32H40BrN5O6/c1-15(2)11-23-29(41)37-24(9-10-25(37)39)32(43)38(23)30(42)31(44-32,16(3)4)35-28(40)17-12-19-18-7-6-8-21-26(18)20(27(33)34-21)13-22(19)36(5)14-17/h6-8,12,15-17,22-25,34,39,43H,9-11,13-14H2,1-5H3,(H,35,40)
- SMILES: CC(C)CC1C(=O)N2C(CCC2O)C3(N1C(=O)C(O3)(C(C)C)NC(=O)C4CN(C5CC6=C(NC7=CC=CC(=C67)C5=C4)Br)C)O
- Exact Mass: 669.21620
- Molecular Formula: C32H40BrN5O6
-
Compound CID:
154699832
154699832
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.