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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
6 produced by Streptomyces collinus contains a cyclohexanecarboxylic acid (CHC) derived moiety.
7 containing both E- and Z-double bonds from a cyclohexanecarboxylic acid (CHC) primer.
8 enin A from Streptomyces collinus contains a cyclohexanecarboxylic acid (CHC)-derived moiety.
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
11              These were trans-4-(aminomethyl)cyclohexanecarboxylic acid (t-AMCHA), proline, 4-aminobu
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
16 ctive steps in the pathway that provides the cyclohexanecarboxylic acid from shikimic acid.
17 ro-furan-2-yl)-9H- purin-2-yl]- prop-2-ynyl}-cyclohexanecarboxylic acid methyl ester (ATL146e).
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
21 ctivity and the ability to synthesize either cyclohexanecarboxylic acid or ansatrienin.
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
25 reductive steps involved in the formation of cyclohexanecarboxylic acid.

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