ライフサイエンスコーパス: acid salt

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1 ind HSO4(-), H2PO4(-), Cl(-), and carboxylic acid salts.

2 ic acid benzyl ester trifuoromethanesulfonic acid salt].

3 d, using the bench-stable ferroceniumboronic acid salt 1 in hexafluoroisopropanol as cosolvent, displ

4 A ferrocenium boronic acid salt activates allylic alcohols to generate transie

5 -poor clay soil, a hydrophilic Aldrich humic acid salt, and water-insoluble leonardite.

6 that exhibit small perturbations in abscisic acid, salt, and cold responses.

7 n metal oxide nanocrystals using metal fatty acid salts as the precursors.

8 receptor-bound agonist to removal with high acid/salt buffer, and leads to receptor desensitization

9 zinyl ]-2-oxoethoxy]phenyl]urea hydrochloric acid salt (BX 471).

10 rtant and useful natural and unnatural amino acid salts can be produced in excellent yields by applyi

11 Antibodies are routinely purified by acid/salt elution from antigen affinity columns.

12 m basic aqueous solution in the ring-opened, acid salt form.

13 rrolidin-1-ylmethyl-ethyl]- amide-l-tartaric acid salt (Genz-123346) lowered glucose and A1C levels a

14 oride salts, including protected alpha-amino acid salts, give excellent yields of the corresponding N

15 not react with the resulting zinc phosphonic acid salt, it could force the newly formed zinc stearate

16 The monoprotonated triflic acid salt of Me2N(CH2)4NMe2 forms a proton-bridged cycli

17 ng the 15N-H dipolar coupling in the triflic acid salt of the completely deuterated diamine (CD3)2N(C

18 ction is the finding that ortho-iodo benzoic acid salts of the chiral copper(II) bis(oxazoline) catal

19 One-pot reactions of sulfinic acid salts (produced from organometallic reagents with S

20 alization or desensitization but did promote acid/salt resistance and high agonist affinity.

21 Nevertheless, arrestin greatly increased acid/salt resistance and the affinity of 4Ala receptor f

22 aStop receptor) abolished arrestin-dependent acid/salt resistance but not the effect of arrestin on a

23 ut still promoted high affinity TRH binding, acid/salt resistance, and desensitization.

24 r site causes increased agonist affinity and acid/salt resistance, but only the proximal phosphosites

25 By correcting the pH shift induced by these acid salts, responses more typical of GABA agonists were

26 inducer of the soxRS system, and to the weak acid salt sodium salicylate (NaSal), an inducer of the m

27 method to transform amino alcohols to amino acid salts using just basic water, without the need of p

28 ures of the hydrochloric and methanesulfonic acid salts were in good agreement with the results obser

29 The sulfinic acid salts were prepared from the reaction of the corres

30 e Lys-Asp salt bridge, and a series of fatty acid salts with varying charge and hydrocarbon length.

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