Cluster scaffolds:
2 |
1 |
Putative metabolites:
| Name | Rank | Metabolite Score | Similarity | MCS Score | Post-Mod Score | Post-Mod Info | Source | Link | Smiles | Molview | Full Name | Figure | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Soraphen | 0 | 0.65 | 0.53 | 0.81 | 0.4 | Glyco:0/3 * 6-Ring:1/1 | MIBiG | Source | *[C@@H]1/C=C\C(C)[C@@H]2O[C@@](O)([C@H](C)C(=O)O[C@H](c3ccccc3)CCCC[C@@H]1*)[C@H](*)[C@@H](O)[C@@H]2C | view | Soraphen | ||
| chaxamycin C | 1 | 0.58 | 0.51 | 0.77 | 0.0 | Glyco:0/3 * 6-Ring:0/1 | MIBiG | Source | CC1=C2NC(=O)/C=C\C=C/[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](O)[C@H](C)[C@@H](O)[C@@H](CO)/C=C(/C)C(=O)c3c(O)c(C)c(O)c(c3C1=O)C2=O | view | chaxamycin C | ||
| phenalamide | 2 | 0.57 | 0.5 | 0.77 | 0.0 | Glyco:0/3 * 6-Ring:0/1 | MIBiG | Source | CC(/C=C/C=C/C=C/C=C(\C)C(=O)NC(C)CO)=C\C(C)C(O)/C(C)=C/C(C)CCc1ccccc1 | view | phenalamide | ||
| Hapalosin | 3 | 0.5 | 0.54 | 0.6 | 0.0 | Glyco:0/3 * 6-Ring:0/1 | MIBiG | Source | CCCCCCC[C@H]1OC(=O)C[C@@H](O)[C@H](Cc2ccccc2)N(C)C(=O)[C@H](C(C)C)OC(=O)[C@H]1C | view | Hapalosin | ||
| cytochalasin K | 4 | 0.49 | 0.5 | 0.61 | 0.0 | Glyco:0/3 * 6-Ring:0/1 | MIBiG | Source | CC1=C(C)[C@H]2[C@H](Cc3ccccc3)NC(=O)[C@]23OC(=O)O/C=C\[C@@](C)(O)C(=O)[C@@H](C)C/C=C\[C@H]3[C@@H]1O | view | cytochalasin K |