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1 educing termini with aromatic amines such as 2-aminobenzamide.
4 hroughput method for the characterization of 2-aminobenzamide (2-AB)-labeled N-glycans from recombina
6 s are derivatized at their reducing end with 2-aminobenzamide (2AB) and separated on a RP column with
7 ed to develop a method for the separation of 2-aminobenzamide (AB)-labeled neutral and anionic oligos
8 ere released by hydrazinolysis, labeled with 2-aminobenzamide, and analyzed by fluorometric, high-per
9 ecedented condensation reaction with various 2-aminobenzamide derivatives in boiling water to afford
10 dienediolate 1 with 2-aminobenzoic acid- and 2-aminobenzamide-derived imines to furnish highly substi
11 released oligosaccharides were labeled with 2-aminobenzamide, digested with Endoglycosidases F2 and
12 spectrometry (MS) and 2) derivatization with 2-aminobenzamide followed by separation by high-performa
13 t stem cells, to determine the efficacy of a 2-aminobenzamide HDACi (109) as a modulator of FXN gene
15 s time consuming than a previously published 2-aminobenzamide labeling method for analyzing GSL-deriv
16 compared with those derived from a ladder of 2-aminobenzamide-labelled arabinose oligomers instead of
17 ondensation of isatin (indole-2,3-dione) and 2-aminobenzamide led to the spirocyclic molecule, spiro[
18 These indol-4-one and indazol-4-one derived 2-aminobenzamides showed strong binding affinity to Hsp9
19 ately potent and highly lipophilic series of 2-aminobenzamides was identified through focused screeni
21 cular iodine catalyzed oxidative coupling of 2-aminobenzamides with aryl methyl ketones produced 2-ar
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