Cluster scaffolds:

OH

1

Putative metabolites:


Name Rank Metabolite Score Similarity MCS Score Post-Mod Score Post-Mod Info Source Link Smiles Molview Full Name Figure
Argimycin PIII 0 0.61 0.59 0.77 0.0 5-Ring:0/1 MIBiG Source C/C=C/C=C/C=C/C1=NCCCC1 view Argimycin PIII N
myxalamid 1 0.49 0.45 0.65 0.0 5-Ring:0/1 MIBiG Source CC(/C=C/C=C\C=C\C=C(/C)C(=O)N[C@@H](C)CO)=C\[C@@H](C)[C@@H](O)/C(C)=C/C(C)C view myxalamid O NH OH OH
APE Ec 2 0.43 0.47 0.51 0.0 5-Ring:0/1 MIBiG Source COC(=O)/C=C/C=C/C=C/C=C/C=C/C=C/c1ccc(O)c(C)c1 view APE Ec O O OH
APE Vf 3 0.43 0.46 0.51 0.0 5-Ring:0/1 MIBiG Source COC(=O)/C=C/C=C/C=C/C=C/C=C/C=C/c1cc(C)c(O)c(C)c1 view APE Vf O O OH
fostriecin 4 0.42 0.47 0.49 0.0 5-Ring:0/1 MIBiG Source C[C@@](O)(/C=C/[C@@H]1CC=CC(=O)O1)[C@@H](C[C@@H](O)/C=C\C=C/C=C/CO)OP(=O)(O)O view fostriecin OH O O OH HO O P O HO OH