Compounds
| ID | Spectrum Quality | Annotated Name |
|---|
COMPOUND NPA020360
PROPERTIES
| NPAID | NPA020360 |
|---|---|
| CLUSTER ID | 6445 |
| NODE ID | 4457 |
| NAME | Taromycin A |
| FORMULA | C70H91Cl2N17O25 |
| MOLECULAR WEIGHT (Da) | 1641.4980 |
| ACCURATE MASS (Da) | 1639.5749 |
| ORIGIN ORGANISM TYPE | Bacterium |
| ORIGIN GENUS | Saccharomonospora |
| ORIGIN SPECIES | sp. CNQ-490 |
| InChIKey | SDWVVLSMGFBQOZ-WLQCZBCJSA-N |
| InChI | InChI=1S/C70H91Cl2N17O25/c1-6-7-8-9-10-13-51(92)82-43(20-35-28-76-42-22-37(72)14-16-38(35)42)65(108)84-44(24-50(75)91)66(109)86-47(27-57(101)102)67(110)89-59-34(5)114-70(113)48(23-49(90)39-17-15-36(71)21-40(39)74)87-69(112)58(31(2)19-54(95)96)88-61(104)32(3)79-52(93)29-77-62(105)45(25-55(97)98)83-60(103)33(4)80-64(107)46(26-56(99)100)85-63(106)41(12-11-18-73)81-53(94)30-78-68(59)111/h8-10,13-17,21-22,28,31-34,41,43-48,58-59,76H,6-7,11-12,18-20,23-27,29-30,73-74H2,1-5H3,(H2,75,91)(H,77,105)(H,78,111)(H,79,93)(H,80,107)(H,81,94)(H,82,92)(H,83,103)(H,84,108)(H,85,106)(H,86,109)(H,87,112)(H,88,104)(H,89,110)(H,95,96)(H,97,98)(H,99,100)(H,101,102)/b9-8+,13-10+/t31-,32-,33-,34-,41+,43+,44-,45+,46+,47+,48+,58+,59+/m1/s1 |
| SMILES | CCC/C=C/C=C/C(=N[C@@H](CC1=CNC2=C1C=CC(=C2)Cl)C(=N[C@H](CC(=N)O)C(=N[C@@H](CC(=O)O)C(=N[C@H]3[C@H](OC(=O)[C@@H](N=C([C@@H](N=C([C@H](N=C(CN=C([C@@H](N=C([C@H](N=C([C@@H](N=C([C@@H](N=C(CN=C3O)O)CCCN)O)CC(=O)O)O)C)O)CC(=O)O)O)O)C)O)[C@H](C)CC(=O)O)O)CC(=O)C4=C(C=C(C=C4)Cl)N)C)O)O)O)O |
ORIGINAL ISOLATION REFERENCE
| CITATION | Yamanaka K; Reynolds KA; Kersten RD; Ryan KS; Gonzalez DJ; Nizet V; Dorrestein PC; Moore BS Direct cloning and refactoring of a silent lipopeptide biosynthetic gene cluster yields the antibiotic taromycin A. Proceedings of the National Academy of Sciences of the United States of America 2014 111 (5) 1957-1962. | ||
|---|---|---|---|
| DOI | 10.1073/pnas.1319584111 | PMID | 24449899 |
