Compounds
| ID | Spectrum Quality | Annotated Name |
|---|
COMPOUND NPA004350
PROPERTIES
| NPAID | NPA004350 |
|---|---|
| CLUSTER ID | 46 |
| NODE ID | 11 |
| NAME | Landomycin A |
| FORMULA | C55H74O22 |
| MOLECULAR WEIGHT (Da) | 1087.1750 |
| ACCURATE MASS (Da) | 1086.4672 |
| ORIGIN ORGANISM TYPE | Bacterium |
| ORIGIN GENUS | Streptomyces |
| ORIGIN SPECIES | sp. |
| InChIKey | YMSZNAXJMXNNPT-OPAYXXSESA-N |
| InChI | InChI=1S/C55H74O22/c1-21-14-28-16-32(59)47-49(45(28)31(58)15-21)53(65)46-30(57)8-10-36(48(46)52(47)64)73-42-18-34(61)55(27(7)71-42)77-44-20-38(51(63)25(5)69-44)75-40-13-11-35(23(3)67-40)72-41-17-33(60)54(26(6)70-41)76-43-19-37(50(62)24(4)68-43)74-39-12-9-29(56)22(2)66-39/h8,10,14-15,22-27,29,32-35,37-44,50-51,54-63H,9,11-13,16-20H2,1-7H3/t22-,23-,24+,25+,26+,27+,29-,32+,33+,34+,35-,37+,38+,39-,40-,41-,42-,43-,44-,50+,51+,54+,55+/m0/s1 |
| SMILES | C[C@H]1[C@H](CC[C@@H](O1)O[C@@H]2C[C@@H](O[C@@H]([C@H]2O)C)O[C@@H]3[C@H](O[C@H](C[C@H]3O)O[C@H]4CC[C@@H](O[C@H]4C)O[C@@H]5C[C@@H](O[C@@H]([C@H]5O)C)O[C@@H]6[C@H](O[C@H](C[C@H]6O)OC7=C8C(=C(C=C7)O)C(=O)C9=C(C8=O)[C@@H](CC1=CC(=CC(=C19)O)C)O)C)C)O |
ORIGINAL ISOLATION REFERENCE
| CITATION | Henkel, T; Rohr, J; Beale, J M; Schwenen, L Landomycins, new angucycline antibiotics from Streptomyces sp. I. Structural studies on landomycins A-D Journal of Antibiotics 1990 43 (5) 492. | ||
|---|---|---|---|
| DOI | 10.7164/antibiotics.43.492 | PMID | 2358402 |
SYNTHESES
| CITATION 1 | Yang X; Fu B; Yu B Total synthesis of landomycin A, a potent antitumor angucycline antibiotic. Journal of the American Chemical Society 2011 133 (32) 12433-12435. DOI: 10.1021/ja205339p PMID: 21780843 | ||
|---|---|---|---|
