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3 ical configurations were assigned to the two optical isomers as (-)-(aS)-6 and (+)-(aR)-6 by correlat
6 native JHs and their nonnative geometric and optical isomers for the ability to bind the Drosophila J
7 iral HPLC separation was performed to obtain optical isomers from the corresponding racemic mixtures.
8 f racemic fluoxetine (IC50 = 39 muM) and its optical isomers had a similar IC50 [40 and 47 muM for th
9 nding of EMD 57033 was stereo-selective: the optical isomer of EMD 57033 bound hcTnC much more weakly
11 xplain patterns of selectivity observed with optical isomers of a number of peptoid and nonpeptide li
13 at both the racemic mixtures as well as pure optical isomers of DHS, 7OM and 7OG were more effective
14 elective 5-HT6 receptor agonist EMDT (5) and optical isomers of EMDT-related analog 8, as well as wit
16 e can be used to produce either L(+) or D(-) optical isomers of lactic acid (respectively) at high ti
17 rs of EMDT-related analog 8, as well as with optical isomers of MS-245 (4a)-related and benzenesulfon
18 d as a chiral selector for the separation of optical isomers of organic carboxylates using capillary