Compounds
ID | Spectrum Quality | Annotated Name |
---|---|---|
CCMSLIB00000571854 | Bronze | MoNA:2346618&Phosphramidon |
CCMSLIB00000571856 | Bronze | MoNA:2346766&Phosphramidon |
CCMSLIB00000571965 | Bronze | MoNA:2299216&Phosphramidon |
CCMSLIB00000572043 | Bronze | MoNA:2308910&Phosphramidon |
CCMSLIB00000572117 | Bronze | MoNA:2346631&Phosphramidon |
CCMSLIB00000573021 | Bronze | MoNA:2346618&Phosporamidon |
CCMSLIB00000567373 | Bronze | MoNA:2475098&N-Alpha-L-Rhamnopyranosyloxy(Hydroxyphosphinyl)-L-Leucyl-L-Tryptophan |
CCMSLIB00005729621 | Gold | 3 |
CCMSLIB00005729346 | Gold | 3 |
CCMSLIB00005728969 | Gold | 3 |
CCMSLIB00005729652 | Gold | 3 |
CCMSLIB00005729117 | Gold | 3 |
CCMSLIB00000220291 | Gold | 3!CCMSLIB00000220293 |
COMPOUND NPA021178
PROPERTIES
NPAID | NPA021178 |
---|---|
CLUSTER ID | 539 |
NODE ID | 481 |
NAME | Phosphoramidon |
FORMULA | C23H34N3O10P |
MOLECULAR WEIGHT (Da) | 543.5100 |
ACCURATE MASS (Da) | 543.1982 |
ORIGIN ORGANISM TYPE | Bacterium |
ORIGIN GENUS | Streptomyces |
ORIGIN SPECIES | tanashiensis MD706-Y4 |
InChIKey | ZPHBZEQOLSRPAK-IWOPNAARSA-N |
InChI | InChI=1S/C23H34N3O10P/c1-11(2)8-16(26-37(33,34)36-23-20(29)19(28)18(27)12(3)35-23)21(30)25-17(22(31)32)9-13-10-24-15-7-5-4-6-14(13)15/h4-7,10-12,16-20,23-24,27-29H,8-9H2,1-3H3,(H,25,30)(H,31,32)(H2,26,33,34)/t12-,16+,17+,18+,19-,20+,23+/m1/s1 |
SMILES | C[C@@H]1[C@@H]([C@H]([C@@H]([C@@H](O1)OP(=O)(N[C@@H](CC(C)C)C(=O)N[C@@H](CC2=CNC3=CC=CC=C32)C(=O)O)O)O)O)O |
ORIGINAL ISOLATION REFERENCE
CITATION | Suda H; Aoyagi T; Takeuchi T; Umezawa H A thermolysin inhibitor produced by Actinomycetes: phospholamidon. Journal of Antibiotics 1973 26 (10) 621-623. | ||
---|---|---|---|
DOI | 10.7164/antibiotics.26.621 | PMID | 4792110 |