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3. Development of FUB 181, a selective histamine H3-receptor antagonist of high oral in vivo potency with 4-(omega-(arylalkyloxy)alkyl)-1H-imidazole structure. Stark H, Hüls A, Ligneau X, Purand K, Pertz H, Arrang JM, Schwartz JC, Schunack W. Arch Pharm (Weinheim); 1998 Jun; 331(6):211-8. PubMed ID: 9713254 [Abstract] [Full Text] [Related]
5. 4-Alkynylphenyl imidazolylpropyl ethers as selective histamine H3-receptor antagonists with high oral central nervous system activity. Krause M, Ligneau X, Stark H, Garbarg M, Schwartz JC, Schunack W. J Med Chem; 1998 Oct 08; 41(21):4171-6. PubMed ID: 9767653 [Abstract] [Full Text] [Related]
8. New histamine H(3)-receptor ligands of the proxifan series: imoproxifan and other selective antagonists with high oral in vivo potency. Sasse A, Sadek B, Ligneau X, Elz S, Pertz HH, Luger P, Ganellin CR, Arrang JM, Schwartz JC, Schunack W, Stark H. J Med Chem; 2000 Aug 24; 43(17):3335-43. PubMed ID: 10966752 [Abstract] [Full Text] [Related]
19. Novel carbamates as potent histamine H3 receptor antagonists with high in vitro and oral in vivo activity. Stark H, Purand K, Ligneau X, Rouleau A, Arrang JM, Garbarg M, Schwartz JC, Schunack W. J Med Chem; 1996 Mar 01; 39(5):1157-63. PubMed ID: 8676353 [Abstract] [Full Text] [Related]