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1 involving both sensitizers were shown to be exergonic.
2 to phosphate, a reaction that is 15 kcal/mol exergonic.
3 ubstituted tetraenes undergo facile but less exergonic 8pi electrocyclization due to a steric clash t
5 ial energy-conserving mechanism that couples exergonic and endergonic reactions of methanogenesis.
8 formation of the [3 + 2] phosphorus-ylide is exergonic, and hence, the [3 + 2] cycloaddition is kinet
10 pending on the pH, the aqueous reactions are exergonic by deltaG = -20 to -27 kcal mol(-1), based on
11 Thermodynamic calculations suggest that the exergonic character of the formation of the Michael addu
12 se superfamily, catalyzes the Mn2+-dependent exergonic dehydration of 2-succinyl-6R-hydroxy-2,4-cyclo
13 ber of the enolase superfamily, catalyzes an exergonic dehydration reaction in the menaquinone biosyn
15 brium being driven forward by the subsequent exergonic dimerization of the aminoborane Me(2)N horizon
17 s we reported recently, endergonic to mildly exergonic electron transfer between neutral aromatics (b
18 electron-transfer reactions are often highly exergonic, for which Marcus theory predicts reduced elec
20 tion of mixed tetramers and resulted in less exergonic free energies of mixed dimer and mixed trimer
21 roline to form L-glutamate is coupled to the exergonic hydrolysis of ATP to ADP and inorganic phospha
23 t synthesis reactions of 11 amino acids were exergonic in the hydrothermal solution, but all were end
24 s-cis to one s-trans butadiene is facile and exergonic, leading to the observed 1Z,4Z,8E-cyclodecatri
27 bifurcating [FeFe] hydrogenase in which the exergonic oxidation of ferredoxin (midpoint potential, -
29 Although ion solvation in liquid media is an exergonic reaction overall, we find it is also associate
31 lectron transfer from NADH, and couples this exergonic reaction to the translocation of protons again
32 d/or physical environment or catalysis of an exergonic reaction, drives the system away from equilibr
36 Acidaminococcus fermentans, which couple the exergonic reduction of crotonyl-CoA to butyryl-CoA to th
37 with a limiting rate constant k(lim) in the exergonic region, followed, near the thermoneutral point
40 ction of ferredoxin with NADPH driven by the exergonic transhydrogenation from NADPH onto NAD(+).
41 ns are pumped in conjunction with the highly exergonic, two-electron reduction of Fe(III)- (-)O-O (-)
42 ton is pumped in conjunction with the weakly exergonic, two-electron reduction of Fe-bound O 2 to the
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