For research use only. Not for therapeutic Use.
Mupirocin is a carboxylic acid bacteriostatic/bactericidal antibiotic.</br>Mupirocin inhibits protein synthesis by binding to isoleucyl-tRNA synthetase, an enzyme which conjugates the amino acid isoleucine to its corresponding tRNA.
| Catalog Number | R045886 |
| CAS Number | 73346-79-9 |
| Synonyms | L-talo-Non-2-enonic acid, 5,9-anhydro-2,3,4,8-tetradeoxy-8-[[(2S,3S)-3-[(1S,2S)-2-hydroxy-1-methylpropyl]oxiranyl]methyl]-3-methyl-, 8-carboxyoctyl ester, lithium salt, (2E)- (9CI); L-talo-Non-2-enonic acid, 5,9-anhydro-2,3,4,8-tetradeoxy-8-[[3-(2-hy |
| Molecular Formula | C26H43LiO9 |
| Purity | ≥95% |
| Target | Bacterial |
| Storage | -20°C |
| IUPAC Name | lithium;9-[(E)-4-[(2S,3R,4R,5S)-3,4-dihydroxy-5-[[(2S,3S)-3-[(2S,3S)-3-hydroxybutan-2-yl]oxiran-2-yl]methyl]oxan-2-yl]-3-methylbut-2-enoyl]oxynonanoate |
| InChI | InChI=1S/C26H44O9.Li/c1-16(13-23(30)33-11-9-7-5-4-6-8-10-22(28)29)12-20-25(32)24(31)19(15-34-20)14-21-26(35-21)17(2)18(3)27;/h13,17-21,24-27,31-32H,4-12,14-15H2,1-3H3,(H,28,29);/q;+1/p-1/b16-13+;/t17-,18-,19-,20-,21-,24+,25-,26-;/m0./s1 |
| InChIKey | XFIKMPRBSORKQP-JATHGWPISA-M |
| SMILES | [Li+].CC(C1C(O1)CC2COC(C(C2O)O)CC(=CC(=O)OCCCCCCCCC(=O)[O-])C)C(C)O |
| Reference | <p>Hatfield, S. M., J. J. Leyden, and M. I. Parenti. /Mupirocin: A Topical Antibiotic with a Unique Structure and Mechanism of Action./ <em>PubMed</em> (1987): 761-70. Http://www.ncbi.nlm.nih.gov. Web. 5 Aug. 2012.</p></span></p> |
