Main compound image
6'-exomethylene lovastatin (acid form)
  • Other Name: 1-Naphthaleneheptanoic acid, 1,2,6,7,8,8a-hexahydro-beta,delta-dihydroxy-2-methyl-6-methylene-8-(2-methyl-1-oxobutoxy)-, [1S-[1alpha(betaS*,deltaS*),2alpha,8beta(R*),8aalpha]]-
  • InChIKey: VOCGRWFQWIIZEJ-HGQWONQESA-N
  • InChI: InChI=1S/C24H36O6/c1-5-15(3)24(29)30-21-11-14(2)10-17-7-6-16(4)20(23(17)21)9-8-18(25)12-19(26)13-22(27)28/h6-7,10,15-16,18-21,23,25-26H,2,5,8-9,11-13H2,1,3-4H3,(H,27,28)/t15-,16-,18+,19+,20-,21-,23-/m0/s1
  • SMILES: CC[C@H](C)C(=O)O[C@H]1CC(=C)C=C2[C@H]1[C@H]([C@H](C=C2)C)CC[C@H](C[C@H](CC(=O)O)O)O
  • Exact Mass: 420.25119
  • Molecular Formula: C24H36O6
  • Compound CID: pubchemlite118753582 pubchem118753582
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.
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.

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