Compounds
| ID | Spectrum Quality | Annotated Name |
|---|
COMPOUND NPA021316
PROPERTIES
| NPAID | NPA021316 |
|---|---|
| CLUSTER ID | 258 |
| NODE ID | 235 |
| NAME | Strobilurin G |
| FORMULA | C26H34O6 |
| MOLECULAR WEIGHT (Da) | 442.5520 |
| ACCURATE MASS (Da) | 442.2355 |
| ORIGIN ORGANISM TYPE | Fungus |
| ORIGIN GENUS | Bolinea |
| ORIGIN SPECIES | lutea Sacc. |
| InChIKey | CGBAOGDKJZIWTF-BDONDIIXSA-N |
| InChI | InChI=1S/C26H34O6/c1-18(2)13-14-30-24-17-31-22-12-11-20(15-23(22)32-26(24,4)5)10-8-9-19(3)21(16-28-6)25(27)29-7/h8-13,15-16,24H,14,17H2,1-7H3/b10-8+,19-9-,21-16+/t24-/m0/s1 |
| SMILES | CO/C=C(C(=O)OC)\C(C)=C/C=C/C1=CC2=C(C=C1)OC[C@H](OCC=C(C)C)C(C)(C)O2 |
ORIGINAL ISOLATION REFERENCE
| CITATION | Fredenhagen A; Kuhn A; Peter HH; Cuomo V; Giuliano U Strobilurins F, G and H, three new antifungal metabolites from Bolinea lutea. I. Fermentation, isolation and biological activity. Journal of Antibiotics 1990 43 (6) 655-660. | ||
|---|---|---|---|
| DOI | 10.7164/antibiotics.43.655 | PMID | 2380111 |
REVISIONS
| VERSION | SMILES | CITATION | ||
|---|---|---|---|---|
| Original Isolation | CC(=CCOC1COC2=C(C=C(C=C2)/C=C/C=C(/C)\C(=C/OC)\C(=O)OC)OC1(C)C)C | Fredenhagen A; Kuhn A; Peter HH; Cuomo V; Giuliano U Strobilurins F, G and H, three new antifungal metabolites from Bolinea lutea. I. Fermentation, isolation and biological activity. Journal of Antibiotics 1990 43 (6) 655-660. DOI: 10.7164/antibiotics.43.655 PMID: 2380111 | ||
| 2 | CO/C=C(C(=O)OC)\C(C)=C/C=C/C1=CC2=C(C=C1)OC[C@H](OCC=C(C)C)C(C)(C)O2 | Kroiß, Stefan; Steglich, Wolfgang Total syntheses of the strobilurins G, M, and N Tetrahedron 2004 60 (22) 4921-4929. DOI: 10.1016/j.tet.2004.03.092 | ||
