ライフサイエンスコーパス: 2-aminobenzamide

1 educing termini with aromatic amines such as 2-aminobenzamide.

2 The N-glycan pool was labeled with a 2-aminobenzamide (2-AB) fluorescence tag and separated u

3 y were released by PNGase F and labeled with 2-aminobenzamide (2-AB) fluorescent tag.

4 ells or intestinal tissues were labeled with 2-aminobenzamide (2-AB), 2-aminobenzoic acid (2-AA), or

5 hroughput method for the characterization of 2-aminobenzamide (2-AB)-labeled N-glycans from recombina

6 absorption and subsequent dissociation than 2-aminobenzamide (2-AB).

7 s are derivatized at their reducing end with 2-aminobenzamide (2AB) and separated on a RP column with

8 2-Aminobenzamide (2AB) labeling derivatization, includin

9 ed to develop a method for the separation of 2-aminobenzamide (AB)-labeled neutral and anionic oligos

10 e clusters for monazomycin, oasomycin A, and 2-aminobenzamide-actiphenol.

11 of synthesizing quinazolinone directly from 2-aminobenzamide and alcohols.

12 he dehydrogenative coupling of alcohols with 2-aminobenzamides and 2-aminobenzonitriles, respectively

13 ere released by hydrazinolysis, labeled with 2-aminobenzamide, and analyzed by fluorometric, high-per

14 f O-propargylated 2-hydroxybenzaldehydes and 2-aminobenzamides delivered oxazepino[5,4-b]quinazolin-9

15 ecedented condensation reaction with various 2-aminobenzamide derivatives in boiling water to afford

16 dienediolate 1 with 2-aminobenzoic acid- and 2-aminobenzamide-derived imines to furnish highly substi

17 released oligosaccharides were labeled with 2-aminobenzamide, digested with Endoglycosidases F2 and

18 spectrometry (MS) and 2) derivatization with 2-aminobenzamide followed by separation by high-performa

19 nulative coupling of sulfoxonium ylides with 2-aminobenzamides has been disclosed.

20 t stem cells, to determine the efficacy of a 2-aminobenzamide HDACi (109) as a modulator of FXN gene

21 g reaction in the presence of I(2)/DMSO with 2-aminobenzamide is described herein.

22 As a result, 2-aminobenzamide-labeled glucose homopolymer (Glcs) was

23 an orthogonal technique such as the HPLC of 2-aminobenzamide-labeled glycans.

24 s time consuming than a previously published 2-aminobenzamide labeling method for analyzing GSL-deriv

25 We found that 2-aminobenzamide labeling of glycans with 2-picoline bor

26 compared with those derived from a ladder of 2-aminobenzamide-labelled arabinose oligomers instead of

27 ondensation of isatin (indole-2,3-dione) and 2-aminobenzamide led to the spirocyclic molecule, spiro[

28 These indol-4-one and indazol-4-one derived 2-aminobenzamides showed strong binding affinity to Hsp9

29 s heterochromatin, we previously showed that 2-aminobenzamide-type histone deacetylase inhibitors (HD

30 ately potent and highly lipophilic series of 2-aminobenzamides was identified through focused screeni

31 tively aminated with 2-aminobenzoic acid and 2-aminobenzamide were compared.

32 cular iodine catalyzed oxidative coupling of 2-aminobenzamides with aryl methyl ketones produced 2-ar