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Citation: A. Hilgeroth et A. Langner, Bioanalysis of syn dimeric HIV-1 protease inhibitor N-benzyl 4-aryl-1,4-dihydropyridine H19: Metabolic and cytotoxic properties in Hep G2 cells, ARCH PHARM, 333(6), 2000, pp. 195-197
Citation: A. Hilgeroth et A. Langner, First bioanalytical evaluation of nonpeptidic cage dimeric HIV-1 protease inhibitor N-benzyl 4-aryl-1,4-dihydropyridine H17: Biotransformation and toxicity on Hep G2 cells, ARCH PHARM, 333(1), 2000, pp. 32-34
Citation: A. Hilgeroth et A. Langner, Plasma protein binding properties of dimeric 4-aryl-1,4-dihydropyridines as novel non peptidic HIV-1 protease inhibitors, PHARMAZIE, 55(7), 2000, pp. 542-543
Authors:
Hilgeroth, A
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Citation: A. Hilgeroth et al., Dimeric 4-aryl-1,4-dihydropyridines as novel HIV-1 protease inhibitors - affinities to intestinal P-glycoprotein, PHARMAZIE, 55(10), 2000, pp. 784-785
Authors:
Hilgeroth, A
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Citation: A. Hilgeroth et al., Solid-state photodimerization of 4-aryl-1,4-dihydropyridines studied by C-13 CPMAS NMR spectroscopy, SOL ST NUCL, 13(4), 1999, pp. 231-243
Authors:
Hilgeroth, A
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Heinemann, FW
Citation: A. Hilgeroth et al., Comparison of azacyclic urea A-98881 as HIV-1 protease inhibitor with cagedimeric N-benzyl 4-(4-methoxyphenyl)-1,4-dihydropyridine as representativeof a novel class of HIV-1 protease inhibitors: A molecular modeling study, J COMPUT A, 13(3), 1999, pp. 233-242
Authors:
Hilgeroth, A
Hempel, G
Baumeister, U
Reichert, D
Citation: A. Hilgeroth et al., Solid-state formation of centrosymmetric cage dimeric 4-aryl-1,4-dihydropyridines via non-symmetric syn-dimers studied by C-13 cross-polarization magic angle spinning NMR spectroscopy, MAGN RES CH, 37(5), 1999, pp. 376-381
Citation: A. Hilgeroth et al., Rotameric properties of novel N-acyl and N-acyloxy dimeric 4-phenyl-1,4-dihydropridines derived from developed solid-state synthesis, HETEROCYCLE, 51(10), 1999, pp. 2367-2376
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Citation: A. Hilgeroth et A. Billich, Cage dimeric 4-aryl-1,4-dihydropyridines as promising lead structures for the development of a novel class of HIV-1 protease inhibitors, ARCH PHARM, 332(1), 1999, pp. 3-5
Citation: A. Hilgeroth et al., Topochemical investigations of dimerizing 4-aryl-1,4-dihydropyridines by X-ray crystal structure analysis., J MOL STRUC, 474, 1999, pp. 267-274
Citation: A. Hilgeroth et al., Synthesis and biological evaluation of the first N-alkyl cage dimeric 4-aryl-1,4-dihydropyridines as novel nonpeptidic HIV-1 protease inhibitors, J MED CHEM, 42(22), 1999, pp. 4729-4732