Compounds
| ID | Spectrum Quality | Annotated Name |
|---|
COMPOUND NPA002196
PROPERTIES
| NPAID | NPA002196 |
|---|---|
| CLUSTER ID | 46 |
| NODE ID | 11 |
| NAME | Saquayamycin Z |
| FORMULA | C72H102O29 |
| MOLECULAR WEIGHT (Da) | 1431.5790 |
| ACCURATE MASS (Da) | 1430.6507 |
| ORIGIN ORGANISM TYPE | Bacterium |
| ORIGIN GENUS | Micromonospora |
| ORIGIN SPECIES | sp Tü 6368 |
| InChIKey | HXKIEUQACANSNK-SBCHTQRNSA-N |
| InChI | InChI=1S/C72H102O29/c1-31-42(73)13-18-54(85-31)93-46-16-21-57(88-33(46)3)99-68-39(9)92-59(26-45(68)76)100-67-38(8)84-50(25-44(67)75)40-11-12-41-65(80)62-49(98-69(41)66(40)81)23-24-71(82)30-70(10,29-53(77)72(62,71)83)101-58-22-17-48(35(5)89-58)95-61-28-52(64(79)37(7)91-61)97-56-20-15-47(34(4)87-56)94-60-27-51(63(78)36(6)90-60)96-55-19-14-43(74)32(2)86-55/h11-13,18,23-24,31-39,43-48,50-52,54-61,63-64,67-68,74-76,78-79,81-83H,14-17,19-22,25-30H2,1-10H3/t31-,32-,33-,34-,35-,36+,37+,38+,39-,43-,44+,45-,46-,47-,48-,50+,51+,52+,54-,55-,56-,57-,58-,59-,60-,61-,63+,64+,67+,68?,70-,71-,72-/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]3CC[C@@H](O[C@H]3C)O[C@@H]4C[C@@H](O[C@@H]([C@H]4O)C)O[C@H]5CC[C@@H](O[C@H]5C)O[C@]6(CC(=O)[C@@]7(C8=C(C=C[C@@]7(C6)O)OC9=C(C8=O)C=CC(=C9O)[C@H]1C[C@H]([C@@H]([C@H](O1)C)O[C@H]1C[C@@H](C([C@@H](O1)C)O[C@H]1CC[C@@H]([C@@H](O1)C)O[C@H]1C=CC(=O)[C@@H](O1)C)O)O)O)C)O |
ORIGINAL ISOLATION REFERENCE
| CITATION | Antal, Noémi; Fiedler, Hans-Peter; Stackebrandt, Erko; Beil, Winfried; Ströch, Karsten; Zeeck, Axel Retymicin, galtamycin B, saquayamycin Z and ribofuranosyllumichrome, novel secondary metabolites from Micromonospora sp. Tü 6368. I. Taxonomy, fermentation, isolation and biological activities Journal of Antibiotics 2005 58 (2) 95. | ||
|---|---|---|---|
| DOI | 10.1038/ja.2005.12 | PMID | 15835721 |
