Compounds
| ID | Spectrum Quality | Annotated Name |
|---|
COMPOUND NPA020098
PROPERTIES
| NPAID | NPA020098 |
|---|---|
| CLUSTER ID | 1486 |
| NODE ID | 11 |
| NAME | 8-O-desmethylanthrotainin |
| FORMULA | C19H15NO9 |
| MOLECULAR WEIGHT (Da) | 401.3270 |
| ACCURATE MASS (Da) | 401.0747 |
| ORIGIN ORGANISM TYPE | Fungus |
| ORIGIN GENUS | Penicillium |
| ORIGIN SPECIES | aethiopicum |
| InChIKey | XZMHEWSQIGGCKG-MOPGFXCFSA-N |
| InChI | InChI=1S/C19H15NO9/c20-17(27)13-10(23)5-18(28)4-7-1-6-2-8(21)3-9(22)11(6)14(24)12(7)15(25)19(18,29)16(13)26/h1-3,21-22,24,26,28-29H,4-5H2,(H2,20,27)/t18-,19+/m1/s1 |
| SMILES | C1C2=C(C(=C3C(=C2)C=C(C=C3O)O)O)C(=O)[C@]4([C@@]1(CC(=O)C(=C4O)C(=O)N)O)O |
ORIGINAL ISOLATION REFERENCE
| CITATION | Chooi YH; Hong YJ; Cacho RA; Tantillo DJ; Tang Y A cytochrome P450 serves as an unexpected terpene cyclase during fungal meroterpenoid biosynthesis. Journal of the American Chemical Society 2013 135 (45) 16805-16808. | ||
|---|---|---|---|
| DOI | 10.1021/ja408966t | PMID | 24161266 |
