6' beta-hydroxy lovastatin (acid form)
- Other Name: (3R,5R)-7-[(1S,2S,6S,8S,8aR)-6-hydroxy-2,6-dimethyl-8-[(2S)-2-methylbutanoyl]oxy-2,7,8,8a-tetrahydro-1H-naphthalen-1-yl]-3,5-dihydroxyheptanoic acid
- InChIKey: ULAAPVRVEVCSJH-QOPMPQMQSA-N
- InChI: InChI=1S/C24H38O7/c1-5-14(2)23(29)31-20-13-24(4,30)12-16-7-6-15(3)19(22(16)20)9-8-17(25)10-18(26)11-21(27)28/h6-7,12,14-15,17-20,22,25-26,30H,5,8-11,13H2,1-4H3,(H,27,28)/t14-,15-,17+,18+,19-,20-,22-,24+/m0/s1
- SMILES: CC[C@H](C)C(=O)O[C@H]1C[C@](C=C2[C@H]1[C@H]([C@H](C=C2)C)CC[C@H](C[C@H](CC(=O)O)O)O)(C)O
- Exact Mass: 438.26175
- Molecular Formula: C24H38O7
-
Compound CID:
118753580
118753580
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.