Compounds
| ID | Spectrum Quality | Annotated Name |
|---|
COMPOUND NPA001252
PROPERTIES
| NPAID | NPA001252 |
|---|---|
| CLUSTER ID | 835 |
| NODE ID | 724 |
| NAME | (S)-banchromene |
| FORMULA | C17H22N2O4 |
| MOLECULAR WEIGHT (Da) | 318.3730 |
| ACCURATE MASS (Da) | 318.1580 |
| ORIGIN ORGANISM TYPE | Fungus |
| ORIGIN GENUS | Fusarium |
| ORIGIN SPECIES | sp. strain CAMKT24b1 |
| InChIKey | JWWKBOBMBFAOAR-NSHDSACASA-N |
| InChI | InChI=1S/C17H22N2O4/c1-10(21)19-11(9-20)8-14(22)12-4-5-15-13(16(12)18)6-7-17(2,3)23-15/h4-7,11,20H,8-9,18H2,1-3H3,(H,19,21)/t11-/m0/s1 |
| SMILES | CC(=O)N[C@@H](CC(=O)C1=C(C2=C(C=C1)OC(C=C2)(C)C)N)CO |
ORIGINAL ISOLATION REFERENCE
| CITATION | Kongue Tatong, Michel D.; Talontsi, Ferdinand M.; Abdel Rahim, Hamdi M.D.; Islam, Md. Tofazzal; Oswald, Rainer B.; Laatsch, Hartmut Banchromene and other secondary metabolites from the endophytic fungus Fusarium sp. obtained from Piper guineense inhibit the motility of phytopathogenic Plasmopara viticola zoospores Tetrahedron Letters 2014 55 (30) 4057-4061. | ||
|---|---|---|---|
| DOI | 10.1016/j.tetlet.2014.06.001 | PMID | - |
