Josamycin propionate structure
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Common Name | Josamycin propionate | ||
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| CAS Number | 31674-19-8 | Molecular Weight | 884.05800 | |
| Density | 1.19g/cm3 | Boiling Point | 946.1ºC at 760 mmHg | |
| Molecular Formula | C45H73NO16 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 526ºC | |
Use of Josamycin propionateJosamycin propionate is a macrolide antibiotic. It is synthesized from strains of Streptomyces narbonensis var. josamyceticus var. nova |
| Name | [6-[6-[[(11Z,13E)-4-acetyloxy-10-hydroxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)-1-oxacyclohexadeca-11,13-dien-6-yl]oxy]-4-(dimethylamino)-2-methyl-5-propanoyloxyoxan-3-yl]oxy-4-hydroxy-2,4-dimethyloxan-3-yl] 3-methylbutanoate |
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| Synonym | More Synonyms |
| Density | 1.19g/cm3 |
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| Boiling Point | 946.1ºC at 760 mmHg |
| Molecular Formula | C45H73NO16 |
| Molecular Weight | 884.05800 |
| Flash Point | 526ºC |
| Exact Mass | 883.49300 |
| PSA | 212.12000 |
| LogP | 3.97430 |
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Application of liquid chromatography-ion trap mass spectrometry to the characterization of the 16-membered ring macrolide josamycin propionate.
J. Mass Spectrom. 39(4) , 437-46, (2004) Coupled liquid chromatography and ion trap mass spectrometry (LC/MS) was used for the characterization of the semi-synthetic 16-membered ring macrolide josamycin propionate. On-line identification of ... |
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A rapid and sensitive high-pressure liquid chromatographic method for monitoring josamycin levels in plasma.
Int. J. Clin. Pharmacol. Res. 4(3) , 195-9, (1984) In this study a new high-pressure liquid chromatographic method for monitoring plasma levels of josamycin is described. Josamycin propionate was used as the internal standard. After being extracted fr... |
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Clinical multicentre trial with josamycin propionate in paediatric patients.
Int. J. Clin. Pharmacol. Res. 4(3) , 201-7, (1984) Josamycin propionate, a tasteless josamycin derivative suitable for the preparation of paediatric oral suspension, was employed in a large, multicentre clinical study aimed at evaluating the effective... |
| 2'-O-Methyl-5-methylcytidine |
| Leucomycin V 3-acetate 4B-(3-methylbutanoate) 2A-propanoate |
| 2'-O-Propionyl-LM-A4 |