ライフサイエンスコーパス: acid dissociation constant

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1 indicator pKa (the negative logarithm of the acid dissociation constant).

2 d based on selected reduction potentials and acid dissociation constants.

3 lationships between reduction potentials and acid dissociation constants are presented to model n=1 a

4 ynamic quantities of ionization reaction for acid dissociation constants as a function of temperature

5 LC peak retention time-based method, the two acid dissociation constants associated with the carboxyl

6 Our approach combines pK(a) (logarithmic acid dissociation constant) calculations from all-atom c

7 to simultaneously measure the difference in acid dissociation constants (delta pKa) of two or more c

8 While the pKa (the negative log of the acid dissociation constant) for this dissociation is app

9 Mixed-mode acid dissociation constants (hydrogen ion in terms of ac

10 The acid dissociation constant in water for a monorhamnolipi

11 ized nucleophiles (pKa < 25, where Ka is the acid dissociation constant) in palladium-catalysed asymm

12 relationship between cofactor efficiency and acid dissociation constants is consistent with a mechani

13 he CPO-II ferryl [pKa > 8.2 (where Ka is the acid dissociation constant)] is attributable to strong e

14 (LAC for short) allows the estimation of the acid dissociation constant Ka(LAC) of diamagnetic transi

15 on because it has a pK(a) (where K(a) is the acid dissociation constant) near physiological pH.

16 1.2 pH units higher, respectively, than the acid dissociation constants obtained for the phosphate g

17 The acid dissociation constant of each cysteine residue in e

18 om the ferric iron atom in metmyoglobin, the acid dissociation constant of HCN inside the protein (K*

19 We hypothesize that the reduction in the acid dissociation constant of the imidazolium ring resul

20 Studies were conducted to determine the acid dissociation constant of TPT's phenolic -OH and int

21 In this study, we measured acid dissociation constants of glutamate residues on tro

22 etermination of residue-specific, side-chain acid dissociation constants of peptides that contain mul

23 Acid dissociation constants of side-chain acidic groups

24 ted to increase the pK(a) (where K(a) is the acid dissociation constant) of compound II, an iron(IV)h

25 ower pH than His37 in AM2, indicating larger acid-dissociation constants or lower pKa's.

26 A hydrogen-bonded, pKa (where Ka is the acid dissociation constant)-perturbed pair of conserved

27 This peptide has a thiol acid dissociation constant (pK(a) = 8.7) that is lower t

28 The acid dissociation constant (pK(a)) of g(j)-pH(i) depende

29 fected by volume ratios, we use the apparent acid dissociation constant, pK', as a proxy for intersys

30 inally, theoretical results indicate aqueous acid dissociation constant (pKa) values of 1.5 +/- 1 for

31 he deprotonation of carboxyl groups with low acid dissociation constants (pKa) as the main contributo

32 The acid dissociation constants (pKas) of perfluoroalkyl car

33 The unusual pK(a) (where K(a) is the acid dissociation constant) required for A2486 to perfor

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