Compounds
| ID | Spectrum Quality | Annotated Name |
|---|
COMPOUND NPA001484
PROPERTIES
| NPAID | NPA001484 |
|---|---|
| CLUSTER ID | 46 |
| NODE ID | 11 |
| NAME | 9'-hydroxyaloesaponarin II |
| FORMULA | C15H10O5 |
| MOLECULAR WEIGHT (Da) | 270.2400 |
| ACCURATE MASS (Da) | 270.0528 |
| ORIGIN ORGANISM TYPE | Bacterium |
| ORIGIN GENUS | Streptomyces |
| ORIGIN SPECIES | lividans K4-114 |
| InChIKey | FVKAMXQJMZSFNK-UHFFFAOYSA-N |
| InChI | InChI=1S/C15H10O5/c16-6-7-4-8(17)5-10-12(7)15(20)13-9(14(10)19)2-1-3-11(13)18/h1-5,16-18H,6H2 |
| SMILES | C1=CC2=C(C(=C1)O)C(=O)C3=C(C=C(C=C3C2=O)O)CO |
ORIGINAL ISOLATION REFERENCE
| CITATION | Kalaitzis, John A.; Moore, Bradley S. Heterologous biosynthesis of truncated hexaketides derived from the actinorhodin polyketide synthase Journal of Natural Products 2004 67 (8) 1419-1422. | ||
|---|---|---|---|
| DOI | 10.1021/np0499564 | PMID | 15332868 |
SYNTHESES
| CITATION 1 | Elkazaz S; Jones PB Photochemical hydroxylation of 1-methyl-9,10-anthraquinones: synthesis of 9'-hydroxyaloesaponarin II. Journal of Organic Chemistry 2010 75 (2) 412-416. DOI: 10.1021/jo902247v PMID: 20000650 | ||
|---|---|---|---|
