ライフサイエンスコーパス: conjugate base

1 complexes that are kappa(2)-chelated by the conjugate base.

2 complex and a chiral phosphoric acid or its conjugate base.

3 f their higher charge density at the anionic conjugate base.

4 to oxidize H2 in the presence of a suitable conjugate base.

5 ected viability rather than the pH itself or conjugate bases.

6 d cocrystallizes with two of its monoanionic conjugated bases.

7 resonance stabilization of the corresponding conjugate bases 1, 2 and 3, respectively.

8 2 and the lithium salt of the corresponding conjugate base 3 were decomposed by photolysis.

9 the identity proton transfer of 3H-O to its conjugate base (3(-)-O) and of 3H-S to 3(-)-S have been

10 The respective conjugate bases, 3--O and 3--S, represent benzofuran and

11 Both 3a and its conjugate base 3a(-) are present in aqueous solution und

12 on of base to 2 at -85 degrees C elicits its conjugate base 6 with a novel O horizontal lineFe(IV)-O-

13 by tetramethylcyclam via protonation of its conjugate base and characterized it in detail using vari

14 boxylic acids, which adsorb as their anionic conjugate bases, and proceeds indirectly by dissolution

15 the importance of the chemical stability of conjugate base anions in attaining high acidity and sugg

16 the kinetic and thermodynamic effects of the conjugate base are not accounted for properly.

17 ole occurs through the formation of a chiral conjugate base/bicyclic quaternary N-acyliminium ion pai

18 lization of the charged oxygen center in the conjugate base by three hydrogen bonds and another 6.3 k

19 Based on natural population analysis, the conjugate bases can be thought of as salts between a pol

20 Its conjugate base, CHB(11)Cl(11)(-), was found by photoelec

21 ions is generally believed to be HOCl or its conjugate base, ClO-.

22 e ligands in the 5-, 6-, 7-, or 8-coordinate conjugate base complex of the hydride or dihydrogen comp

23 preferentially at the phenolic site, and the conjugate base consists of a 70:30 mixture of phenoxide

24 Since the radical anion conjugate base does not undergo ring opening as fast as

25 irreversible first-order elimination from a conjugate base (E1cB(I)) mechanism with acetoxy ester 3,

26 of not only acid strength but also inherent conjugate base electron density.

27 Various polymer-drug conjugates based, for example, on polyethylene glycol (P

28 hift in the equilibrium between the acid and conjugate base forms of glutamic acid due to other amino

29 H6X6) (where X = chlorine or bromine), whose conjugate base is the exceptionally inert CB11H6X6- carb

30 ute interactions of the excited acid and its conjugate base leads to a pronounced fluorosolvatochromi

31 be replaced by an arginine, disfavoring the conjugate base mechanism, distinguishing between these t

32 d within a cationic Ru complex by the chiral conjugate base of (R)-1-phenylethanol.

33 ts the greater aromatic stabilization of the conjugate base of 6H-S (thiophene derivative) compared t

34 adiabatic electron detachment energy of the conjugate base of a small covalent polyol model compound

35 th an initially less stable anion (i.e., the conjugate base of a weaker acid), and is negligible for

36 elimination of the C1-mesyloxy group by the conjugate base of adenine or thymine to give two diaster

37 er transform mass spectrometer to afford the conjugate base of benzocyclobutadiene (1a).

38 give thiocarbamate-S-oxide (H2NC(=O)SO-, the conjugate base of carbamothioperoxoic acid) via a mechan

39 zed in good yields, by Michael addition of a conjugate base of core-substituted phenylacetones to sub

40 exchange experiments were carried out on the conjugate base of cysteine with four different deuterate

41 nucleophilic substitution reaction where the conjugate base of Pro-1 functions as the nucleophile and

42 d ring opening followed by alkylation of the conjugate base of Pro-1.

43 rst modified by deposition of a layer of the conjugate base of sulfanilic acid and then with quaterni

44 cals appear to remain H-bonded to the chiral conjugate base of the Bronsted acid during the course of

45 e of synthesis and low molecular weight, the conjugate base of triethylurea (TEU(-)) was of primary f

46 The computed relative stabilities of the conjugate bases of 1 are as follows: beta > gamma > alph

47 y basic anions (A(-)), many of which are the conjugate bases of known strong acids and superacids.

48 addition, PB microcubes will react with the conjugate bases of metal oxide based weak acids, generat

49 (3) Conjugate bases of organolithiums are stable with respec

50 The dissociated anionic conjugate bases of PFCAs have negligible air-water parti

51 The structures of the conjugate bases of saccharin and iso-saccharin were also

52 at total concentrations (uncharged acid plus conjugate base) of 257 and 27.1 mM, respectively.

53 ation of a novel, targeted, nanobiopolymeric conjugate based on biodegradable, nontoxic, and nonimmun

54 We have synthesized new protein conjugates based on 4-(2-pyridylazo) ligands.

55 E. coli ATCC 33475 (ent-) revealed that six conjugates based on L-Ent having relatively small cargos

56 approach may lead to a new class of antibody conjugates based on peptide-tags that have minimal effec

57 A survey of several antibody drug conjugates based on the same IgG framework and small mol

58 and the carbonate radical anion form an acid/conjugate base pair.

59 ion to benzene and of cyclopentadiene to its conjugate base, reflecting the smaller aromatic stabiliz

60 more easily cleaved from DNA by AlkA (their conjugate bases should be better leaving groups).

61 the neutral inorganic halamines, the anionic conjugate base species, and the cationic conjugate acid

62 igned to the catalytic base Tyr-411 with the conjugate base stabilized by interaction with the guanid

63 from these three tautomers produces the same conjugate base structure.

64 critical requirement is the strength of the conjugate base such that an equilibrium exists between p

65 citation energies of the poly-ynes and their conjugate bases suggest that the alkynyl groups are inte

66 We report here a novel conjugate-based targeting method to enhance tissue-speci

67 the triplet excited state and yields the pHP conjugate base that, upon reprotonation, regenerates the

68 found to be easily distinguishable from its conjugate base, the N1-deprotonated radical, G*(-H)*.

69 ution," and "Unimolecular elimination by the conjugate base." They were associated with the most ance

70 the reaction that leads to the most aromatic conjugate base (thiophene derivative) has a lower intrin

71 Herein, we report a coumarin-quinoline (CQ) conjugate-based turn-on near-infrared (NIR) fluorescence

72 ost likely residue to which the ubiquitin is conjugated, based upon fitting atomic structures of acti

73 ic acid as well as its water-soluble anionic conjugate base valproate.

74 nts of the carbon acids and their respective conjugate bases were also determined which helped in und

75 se of stronger acids, which form more stable conjugate bases with lower charge densities.

76 reactions between 21 acids, Y-X-H, and their conjugate bases, (-)X-Y, were studied according to the r

77 ic oxides (those having weaker corresponding conjugate bases) yield stronger surface organometallic e