14-Hydroxy-6-O-methylerythromycins A, active metabolites of 6-O-methylerythromycin A in human.

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14-Hydroxy-6-O-methylerythromycins A, active metabolites of 6-O-methylerythromycin A in human.

(14R)-14-Hydroxy-6-O-methylerythromycin A and (14S)-epimer have been isolated as active metabolites from human urine after oral administration of 6-O-methylerythromycin A (TE-031, A-56268). The structures of these metabolites were determined by means of mass, 1H and 13C NMR spectroscopies. Antimicrobial activities of (14R)-14-hydroxy-6-O-methylerythromycin A, a major metabolite, were comparable...

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Poly[(6-carboxy­picolinato-κ3 O 2,N,O 6)(μ3-pyridine-2,6-dicarboxyl­ato-κ5 O 2,N,O 6:O 2′:O 6′)dysprosium(III)]

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Chemical modification of erythromycins. IV. Synthesis and biological properties of 6-O-methylerythromycin B.

6-O-Methylerythromycin B has been synthesized from erythromycin B via regioselective methylation of the 6-hydroxyl group in 71% overall yield. This compound shows in vitro antibacterial activity comparable to erythromycins A and B and exhibits superior in vivo activity with improved pharmacokinetic properties.

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Poly[[tetra­aqua­(μ3-naphthalene-1,6-disulfonato-κ4 O 1:O 6,O 6′:O 6′′)strontium(II)] monohydrate]

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ژورنال

عنوان ژورنال: The Journal of Antibiotics

سال: 1988

ISSN: 0021-8820,1881-1469

DOI: 10.7164/antibiotics.41.966