saikogenin f-27-oic acid
- Other Name: (1S,2S,4R,5R,8R,9R,10S,13S,14R,17S,18R)-2,10-dihydroxy-9-(hydroxymethyl)-5,9,13,20,20-pentamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-ene-4-carboxylic acid
- InChIKey: DTPHURDVMCZDLM-CRHPDMSDSA-N
- InChI: InChI=1S/C30H46O6/c1-24(2)12-13-28-17-36-30(20(28)14-24)11-7-19-25(3)9-8-21(32)26(4,16-31)18(25)6-10-27(19,5)29(30,23(34)35)15-22(28)33/h7,11,18-22,31-33H,6,8-10,12-17H2,1-5H3,(H,34,35)/t18-,19-,20-,21+,22+,25+,26+,27-,28-,29-,30+/m1/s1
- SMILES: C[C@]12CC[C@@H]([C@@]([C@@H]1CC[C@@]3([C@@H]2C=C[C@@]45[C@]3(C[C@@H]([C@@]6([C@H]4CC(CC6)(C)C)CO5)O)C(=O)O)C)(C)CO)O
- Exact Mass: 502.32944
- Molecular Formula: C30H46O6
-
Compound CID:
118753425
118753425
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.