Flopristin
Appearance
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Names | |
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IUPAC name
(7R,10R,11R,12Z,17Z,19Z,21S,23R)-23-fluoro-21-hydroxy-11,19-dimethyl-10-propan-2-yl-9,26-dioxa-3,15,28-triazatricyclo[23.2.1.03,7]octacosa-1(27),12,17,19,25(28)-pentaene-2,8,14-trione
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Other names
(16R)-16-Desoxy-16-fluoropristinamycin IIB; RPR 132552; RPR 132552A
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.218.104 |
EC Number |
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PubChemCID
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UNII | |
CompTox Dashboard(EPA)
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Properties | |
C28H38FN3O6 | |
Molar mass | 531.625g·mol−1 |
Hazards | |
GHSlabelling: | |
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Warning | |
H302,H312,H317,H332,H341 | |
P201,P202,P261,P264,P270,P271,P272,P280,P281,P301+P312,P302+P352,P304+P312,P304+P340,P308+P313,P312,P321,P322,P330,P333+P313,P363,P405,P501 | |
Except where otherwise noted, data are given for materials in theirstandard state(at 25 °C [77 °F], 100 kPa).
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Flopristinis asemi-syntheticantibioticof thestreptogramin Aclass. It is afluorinatedderivativeofpristinamycin IIB.[citation needed]
Flopristin is one of the components of the experimental drugNXL103.[1]
References[edit]
- ^Pankuch, Glenn A.; Kelly, Linda M.; Lin, Gengrong; Bryskier, Andre; Couturier, Catherine; Jacobs, Michael R.; Appelbaum, Peter C. (2003)."Activities of a new oral streptogramin, XRP 2868, compared to those of other agents against Streptococcus pneumoniae and Haemophilus species".Antimicrobial Agents and Chemotherapy.47(10): 3270–3274.doi:10.1128/AAC.47.10.3270-3274.2003.PMC201162.PMID14506040.