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1 determined that OA and trans-4-(aminomethyl)cyclohexanecarboxylic acid (AMCHA) (K(a) approximately 5
2 s of similar size such as trans-(aminomethyl)cyclohexanecarboxylic acid (AMCHA) and p-benzylaminesulf
3 tanoic acid (7-AHpA), and trans-(aminomethyl)cyclohexanecarboxylic acid (AMCHA) to each of these muta
4 3 for the lysine analogue trans-(aminomethyl)cyclohexanecarboxylic acid (AMCHA) was investigated from
5 amma-amino acid (1R,2R,3S)-2-(1-aminopropyl)-cyclohexanecarboxylic acid (APCH), which is constrained
9 de (4a), using various acids in place of the cyclohexanecarboxylic acid (CHCA, 2a) in the reaction sc
10 azo[4,5-b]pyridin-1-yl-3-phenyl-acryloyloxy)-cyclohexanecarboxylic acid (compound A) with a 50% inhib
12 mer, (+/-)-cis-2-(3,5-dichlorphenylcarbamoyl)cyclohexanecarboxylic acid (VU0155041), contained the ma
13 uran-1(3H),9'-(9H)xanthen]-3-one), and M119 (cyclohexanecarboxylic acid [2-(4,5,6-trihydroxy-3-oxo-3H
14 e, we demonstrate that this inhibitor, M119 (cyclohexanecarboxylic acid [2-(4,5,6-trihydroxy-3-oxo-3H
15 e molecular framework of 2 from 3,4-AHBA and cyclohexanecarboxylic acid apparently does not involve f
18 ahydrofuran-2-yl)-9H-pu rin-2-yl]prop-2-ynyl}cyclohexanecarboxylic acid methyl ester (ATL146e; EC(50)
19 dro-furan-2-yl)-9H- purin-2-yl]-prop-2-ynyl]-cyclohexanecarboxylic acid methyl ester, which is rapidl
20 ich is essential for the biosynthesis of the cyclohexanecarboxylic acid moiety of ansatrienin from sh
22 ts, an "upper" polyketide chain initiated by cyclohexanecarboxylic acid, a "lower" polyketide chain i
23 dro-furan-2-yl)-9H- purin-2-yl]-prop-2-ynyl]-cyclohexanecarboxylic acid, which has similar affinity f
24 the penultimate step is hydroxylation of the cyclohexanecarboxylic acid-derived side chain of Plm B b
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