Synthesis, biological activity, QSAR and QSPR study of 2-aminobenzimidazole derivatives as potent H3-antagonists.
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Qsar Modeling Of Histamine H3r Antagonists/Inverse Agonists As Future Drugs For Neurodegenerative Diseases.1-Prop-2-ynyl-1H-benzimidazol-2-amineHybrid Steered Molecular Dynamics-Docking: An Efficient Solution to the Problem of Ranking Inhibitor Affinities Against a Flexible Drug Target.Aminosilanes derived from 1H-benzimidazole-2(3H)-thione.Brain pharmacokinetics of non-imidazole biphenyl H3 receptor antagonists: a liquid chromatography/electrospray-mass spectrometry and ex vivo binding study in rats.Synthesis and crystal structure of new heterocycles containing 1,2,4-oxadiazole, 1,2,4-oxadiazolone (thione), hydantoin, and mercaptobenzimidazole units
P2860
Synthesis, biological activity, QSAR and QSPR study of 2-aminobenzimidazole derivatives as potent H3-antagonists.
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2004 nî lūn-bûn
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2004年の論文
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2004年学术文章
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2004年学术文章
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Synthesis, biological activity ...... ives as potent H3-antagonists.
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Synthesis, biological activity ...... ives as potent H3-antagonists.
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type
label
Synthesis, biological activity ...... ives as potent H3-antagonists.
@en
Synthesis, biological activity ...... ives as potent H3-antagonists.
@nl
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Synthesis, biological activity ...... ives as potent H3-antagonists.
@en
Synthesis, biological activity ...... ives as potent H3-antagonists.
@nl
P2093
P1476
Synthesis, biological activity ...... tives as potent H3-antagonists
@en
P2093
Claudia Silva
Elisabetta Barocelli
Fabrizio Bordi
Francesca Magnanini
Mariannina Impicciatore
Mirko Rivara
Pier Vincenzo Plazzi
Silvia Rivara
Simona Bertoni
Valentina Zuliani
P304
P356
10.1016/J.BMC.2003.11.030
P407
P577
2004-02-01T00:00:00Z