Compounds
| ID | Spectrum Quality | Annotated Name |
|---|
COMPOUND NPA020431
PROPERTIES
| NPAID | NPA020431 |
|---|---|
| CLUSTER ID | 46 |
| NODE ID | 11 |
| NAME | Hatomarubigin B |
| FORMULA | C20H16O5 |
| MOLECULAR WEIGHT (Da) | 336.3430 |
| ACCURATE MASS (Da) | 336.0998 |
| ORIGIN ORGANISM TYPE | Bacterium |
| ORIGIN GENUS | Streptomyces |
| ORIGIN SPECIES | sp. 2238-SVT4 |
| InChIKey | IAWMODONDSIOEK-VIFPVBQESA-N |
| InChI | InChI=1S/C20H16O5/c1-9-7-10-3-4-11-16(15(10)13(22)8-9)20(24)17-12(21)5-6-14(25-2)18(17)19(11)23/h3-6,9,21H,7-8H2,1-2H3/t9-/m0/s1 |
| SMILES | C[C@H]1CC2=C(C(=O)C1)C3=C(C=C2)C(=O)C4=C(C=CC(=C4C3=O)O)OC |
ORIGINAL ISOLATION REFERENCE
| CITATION | Hayakawa, Y; Ha, SC; Kim, YJ; Furihata, K; Seta, H Studies on the isotetracenone antibiotics. IV. Hatomarubigins A, B, C and D, new isotetracenone antibiotics effective against multidrug-resistant tumor cells Journal of Antibiotics 1991 44 (11) 1179-1186. | ||
|---|---|---|---|
| DOI | 10.7164/antibiotics.44.1179 | PMID | 1761414 |
SYNTHESES
| CITATION 1 | Caygill GB; Larsen DS; Brooker S Total synthesis of (+)-hatomarubigin B. Journal of Organic Chemistry 2001 66 (22) 7427-31. DOI: 10.1021/jo015839r PMID: 11681957 | ||
|---|---|---|---|
