7î±-sulfenic-spironolactone
- Other Name: 7alpha-Sulfenic-spironolactone
- InChIKey: VUJBLXDJUZTUBQ-BIPXHUIRSA-N
- InChI: InChI=1S/C22H30O4S/c1-20-7-3-14(23)11-13(20)12-17(27-25)19-15(20)4-8-21(2)16(19)5-9-22(21)10-6-18(24)26-22/h11,15-17,19,25H,3-10,12H2,1-2H3/t15-,16-,17+,19+,20+,21+,22+/m0/s1
- SMILES: C[C@@]12CCC(=O)C=C1C[C@H]([C@@H]3[C@@H]2CC[C@@]4([C@H]3CC[C@@]45CCC(=O)O5)C)SO
- Exact Mass: 390.18648
- Molecular Formula: C22H30O4S
-
Compound CID:
169502192
169502192
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.