ライフサイエンスコーパス: alpha-cyano-4-hydroxycinnamic acid

1 lls (approximately 5 mg) cocrystallized with alpha-cyano-4-hydroxycinnamic acid.

2 and uses the same matrix compounds, such as alpha-cyano-4-hydroxycinnamic acid.

3 y for detection of acidic glycopeptides over alpha-cyano-4-hydroxycinnamic acid.

4 elded a far superior signal in comparison to alpha-cyano-4-hydroxycinnamic acid, 2,5-dihydrobenzoic a

5 in comparison to classical matrices such as alpha-cyano-4-hydroxycinnamic acid, 2,5-dihydroxybenzoic

6 Probenecid (1 mM), alpha-cyano-4-hydroxycinnamic acid (4 mM) or basolateral

7 e was inhibited by phloretin, mercurials and alpha-cyano-4-hydroxycinnamic acid (4-CHC), but not by t

8 ed the lactate transport blockers quercetin, alpha-cyano-4-hydroxycinnamic acid (4-CIN), and p-chloro

9 Finally, we showed that alpha-cyano-4-hydroxycinnamic acid, a classic inhibitor

10 The matrix mixture consisted of 5 mg/mL alpha-cyano-4-hydroxycinnamic acid, acetonitrile, ethano

11 Encapsulation of an anticancer therapeutic, alpha-cyano-4-hydroxycinnamic acid (alpha-CHC), and subs

12 A mixture of alpha-cyano-4-hydroxycinnamic acid and 2,5-dihydroxybenz

13 Comparisons with other UV matrixes (alpha-cyano-4-hydroxycinnamic acid and sinapinic acid) a

14 ch as DHB (2,5-dihydroxybenzoic acid), CHCA (alpha-cyano-4-hydroxycinnamic acid), and 2-mercaptobenzo

15 5-dihydroxybenzoic acid and in thin films of alpha-cyano-4-hydroxycinnamic acid as well as a complex

16 combination of TBA (tributylamine) and CHCA (alpha-Cyano-4-hydroxycinnamic acid) as extraction solven

17 ds (2,5-dihydroxybenzoic acid + pyridine and alpha-cyano-4-hydroxycinnamic acid + butylamine) were in

18 The use of two MALDI matrixes, alpha-cyano-4-hydroxycinnamic acid (CHCA) and 2,5-dihydr

19 s than did two other commonly used matrixes, alpha-cyano-4-hydroxycinnamic acid (CHCA) and 2,5-dihydr

20 mparison to its well-established predecessor alpha-cyano-4-hydroxycinnamic acid (CHCA) is significant

21 nvolved applying layers of finely ground dry alpha-cyano-4-hydroxycinnamic acid (CHCA) to the surface

22 Two ILs derived from alpha-cyano-4-hydroxycinnamic acid (CHCA) were synthesiz

23 roxybenzoic acid (DHB), sinapinic acid (SA), alpha-cyano-4-hydroxycinnamic acid (CHCA), 2,6-dihydroxy

24 s were measured in three different matrixes, alpha-cyano-4-hydroxycinnamic acid (CHCA), 3,5-dimethoxy

25 roxybenzoic acid (DHB), 4-nitroaniline (NA), alpha-cyano-4-hydroxycinnamic acid (CHCA), and sinapic a

26 Different MALDI matrixes like alpha-cyano-4-hydroxycinnamic acid (CHCA), dihyroxy benz

27 I-mass spectrometry (MS) bacteria profiling, alpha-cyano-4-hydroxycinnamic acid (CHCA), sinapinic aci

28 atrices, 2,5-dihydroxybenzoic acid (DHB) and alpha-cyano-4-hydroxycinnamic acid (CHCA).

29 tly to a tissue blot covered with the matrix alpha-cyano-4-hydroxycinnamic acid (CHCA).

30 D(4)-alpha-Cyano-4-hydroxycinnamic acid (D(4)-CHCA) has been

31 and durability, as compared to conventional alpha-cyano-4-hydroxycinnamic acid dried-droplet prepara

32 c liquid matrix (ILM), a guanidinium salt of alpha-cyano-4-hydroxycinnamic acid, facilitates direct U

33 that have low aqueous solubilities, such as alpha-cyano-4-hydroxycinnamic acid, ferulic acid, and 2,

34 drogen citrate proved to be much better than alpha-cyano-4-hydroxycinnamic acid for the detection of

35 dried-droplet MALDI matrix consisting of 1:1 alpha-cyano-4-hydroxycinnamic acid/fructose proves to be

36 Although alpha-cyano-4-hydroxycinnamic acid functions as an excel

37 matrixes 2,5-dihydroxybenzoic acid (DHB) and alpha-cyano-4-hydroxycinnamic acid (HCCA) as well as fiv

38 Subsequently, the MALDI matrix alpha-cyano-4-hydroxycinnamic acid in methanol and 10% t

39 intact molecules from "hot"matrixes such as alpha-cyano-4-hydroxycinnamic acid is possible.

40 The LC eluent was mixed with alpha-cyano-4-hydroxycinnamic acid matrix solution and d

41 he sample deposition method, and the matrix, alpha-cyano-4-hydroxycinnamic acid, served as the intern

42 ., sinapinic acid,2,5-dihydroxybenzoic acid, alpha-cyano-4-hydroxycinnamic acid) were found to be sup

43 The latter, exemplified by alpha-cyano-4-hydroxycinnamic acid, were typically proce

44 A matrix composition of alpha-cyano-4-hydroxycinnamic acid with fructose yields