Authors:
Harmat, V
Bocskei, Z
Naray-Szabo, G
Bata, I
Csutor, AS
Hermecz, I
Aranyi, P
Szabo, B
Liliom, K
Vertessy, BG
Ovadi, J
Citation: V. Harmat et al., A new potent calmodulin antagonist with arylalkylamine structure: Crystallographic, spectroscopic and functional studies, J MOL BIOL, 297(3), 2000, pp. 747-755
Authors:
Podanyi, B
Bokotey, S
Kanai, K
Feher, M
Hermecz, I
Citation: B. Podanyi et al., Investigations on a flexible prolyl-endopeptidase inhibitor in solution byNMR techniques, MAGN RES CH, 37(5), 1999, pp. 346-352
Authors:
Csikos, E
Gonczi, C
Podanyi, B
Toth, G
Hermecz, I
Citation: E. Csikos et al., Regioselectivity in preparation of unsymmetrically substituted 3-aminoquinoxalin-2(1H)-ones, J CHEM S P1, (13), 1999, pp. 1789-1793
Citation: I. Hermecz, Chemistry of benzologs of pyrido[1,2-a]pyrimidines: Part V of series on pyrido-oxazines, -diazines, and -thiazines, ADV HETERO, 73, 1999, pp. 177-274
Citation: I. Hermecz, Chemistry of pyrido[2,1-b][1,3]oxazines, pyrido[2,1-b][1,3]thiazines, and their benzologs, part IV, ADV HETERO, 72, 1999, pp. 225-281
Citation: M. Balogh et al., Reaction with N-benzylideneanilines with methyl 3-aminocrotonate catalyzedby inorganic solids, HETEROCYC C, 4(5), 1998, pp. 403-410
Citation: I. Hermecz, Chemistry of pyrido[1,2-c][1,3]oxazines, pyrido[1,2-c][1,3]thiazines, pyrido[1,2-c]pyrimidines, and their benzologs: Part II, ADV HETERO, 70, 1998, pp. 1-88
Citation: I. Hermecz, Chemistry of pyrido[2,1-c][1,4]oxazines, pyrido[2,1-c][1,4]thiazines, pyrido[1,2-a]pyrazines and their benzologues, ADV HETERO, 71, 1998, pp. 145-289