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1 reductive steps involved in the formation of cyclohexanecarboxylic acid.
2 uran-1(3H),9'-(9H)xanthen]-3-one), and M119 (cyclohexanecarboxylic acid [2-(4,5,6-trihydroxy-3-oxo-3H
3 e, we demonstrate that this inhibitor, M119 (cyclohexanecarboxylic acid [2-(4,5,6-trihydroxy-3-oxo-3H
4 ts, an "upper" polyketide chain initiated by cyclohexanecarboxylic acid, a "lower" polyketide chain i
5  determined that OA and trans-4-(aminomethyl)cyclohexanecarboxylic acid (AMCHA) (K(a) approximately 5
6 s of similar size such as trans-(aminomethyl)cyclohexanecarboxylic acid (AMCHA) and p-benzylaminesulf
7 tanoic acid (7-AHpA), and trans-(aminomethyl)cyclohexanecarboxylic acid (AMCHA) to each of these muta
8 3 for the lysine analogue trans-(aminomethyl)cyclohexanecarboxylic acid (AMCHA) was investigated from
9 amma-amino acid (1R,2R,3S)-2-(1-aminopropyl)-cyclohexanecarboxylic acid (APCH), which is constrained
10 e molecular framework of 2 from 3,4-AHBA and cyclohexanecarboxylic acid apparently does not involve f
11 produced by Streptomyces collinus contains a cyclohexanecarboxylic acid (CHC) derived moiety.
12 containing both E- and Z-double bonds from a cyclohexanecarboxylic acid (CHC) primer.
13 enin A from Streptomyces collinus contains a cyclohexanecarboxylic acid (CHC)-derived moiety.
14 de (4a), using various acids in place of the cyclohexanecarboxylic acid (CHCA, 2a) in the reaction sc
15 azo[4,5-b]pyridin-1-yl-3-phenyl-acryloyloxy)-cyclohexanecarboxylic acid (compound A) with a 50% inhib
16 the penultimate step is hydroxylation of the cyclohexanecarboxylic acid-derived side chain of Plm B b
17 ctive steps in the pathway that provides the cyclohexanecarboxylic acid from shikimic acid.
18 y experiment to track the decarboxylation of cyclohexanecarboxylic acid in acetonitrile-d(3) over pic
19 ro-furan-2-yl)-9H- purin-2-yl]- prop-2-ynyl}-cyclohexanecarboxylic acid methyl ester (ATL146e).
20 ahydrofuran-2-yl)-9H-pu rin-2-yl]prop-2-ynyl}cyclohexanecarboxylic acid methyl ester (ATL146e; EC(50)
21 dro-furan-2-yl)-9H- purin-2-yl]-prop-2-ynyl]-cyclohexanecarboxylic acid methyl ester, which is rapidl
22 ich is essential for the biosynthesis of the cyclohexanecarboxylic acid moiety of ansatrienin from sh
23 ctivity and the ability to synthesize either cyclohexanecarboxylic acid or ansatrienin.
24              These were trans-4-(aminomethyl)cyclohexanecarboxylic acid (t-AMCHA), proline, 4-aminobu
25 mer, (+/-)-cis-2-(3,5-dichlorphenylcarbamoyl)cyclohexanecarboxylic acid (VU0155041), contained the ma
26 dro-furan-2-yl)-9H- purin-2-yl]-prop-2-ynyl]-cyclohexanecarboxylic acid, which has similar affinity f
27 ual aldehyde C-H bond abstraction leading to cyclohexanecarboxylic acid, which is explained by favora