Compounds
| ID | Spectrum Quality | Annotated Name |
|---|
COMPOUND NPA001223
PROPERTIES
| NPAID | NPA001223 |
|---|---|
| CLUSTER ID | 819 |
| NODE ID | 711 |
| NAME | Oximidine III |
| FORMULA | C23H24N2O6 |
| MOLECULAR WEIGHT (Da) | 424.4530 |
| ACCURATE MASS (Da) | 424.1634 |
| ORIGIN ORGANISM TYPE | Bacterium |
| ORIGIN GENUS | Pseudomonas |
| ORIGIN SPECIES | sp. QN05727 |
| InChIKey | AHOWOFTYCJCPEK-QEMVUTTGSA-N |
| InChI | InChI=1S/C23H24N2O6/c1-29-25-14-6-12-21(27)24-13-5-9-17-15-20-19(31-20)11-3-2-7-16-8-4-10-18(26)22(16)23(28)30-17/h2-8,10-14,17,19-20,26H,9,15H2,1H3,(H,24,27)/b7-2+,11-3?,12-6-,13-5+,25-14-/t17-,19+,20-/m0/s1 |
| SMILES | CO/N=C\C=C/C(=O)N/C=C/C[C@H]1C[C@H]2[C@H](O2)C=C/C=C/C3=C(C(=CC=C3)O)C(=O)O1 |
ORIGINAL ISOLATION REFERENCE
| CITATION | Hayakawa, Yoichi; Tomikawa, Taijiro; Shin-Ya, Kazuo; Arao, Nakako; Nagai, Koji; Suzuki, Ken-Ichi Oximidine III, a new antitumor antibiotic against transformed cells from Pseudomonas sp. I. Taxonomy, fermentation, isolation, physico-chemical properties and biological activity Journal of Antibiotics 2003 56 (11) 899-904. | ||
|---|---|---|---|
| DOI | 10.7164/antibiotics.56.899 | PMID | 14763554 |
SYNTHESES
| CITATION 1 | Wang X; Bowman EJ; Bowman BJ; Porco JA Total synthesis of the salicylate enamide macrolide oximidine III: application of relay ring-closing metathesis. Angewandte Chemie International Edition 2004 43 (27) 3601-3605. DOI: 10.1002/anie.200460042 PMID: 15293258 | ||
|---|---|---|---|
