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The Lipophilic Bullet Hits the Targets: Medicinal Chemistry of Adamantane Derivatives
被引:572
作者:
Wanka, Lukas
[1
,2
]
Iqbal, Khalid
[2
]
Schreiner, Peter R.
[1
]
机构:
[1] Univ Giessen, Inst Organ Chem, D-35392 Giessen, Germany
[2] New York State Inst Basic Res Dev Disabil, Dept Neurochem, Staten Isl, NY 10314 USA
关键词:
METHYL-D-ASPARTATE;
SYNTHETIC RETINOID CD437;
DIPEPTIDYL-PEPTIDASE-IV;
HEPATITIS-C VIRUS;
M2 PROTON CHANNEL;
SOLUBLE EPOXIDE HYDROLASE;
NMDA RECEPTOR ANTAGONIST;
INFLUENZA-A VIRUS;
SMALL HETERODIMER PARTNER;
OVARIAN-CARCINOMA CELLS;
D O I:
10.1021/cr100264t
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The article reviews concentrates on the numerous applications in medicinal chemistry and drug development of adamantane derivatives. The aminoadamantanes are synthetic drugs that have not been inspired by natural products like numerous other drugs. There are, however, also isolates from Nature incorporating an adamantane motif, like 'nature's marvel,' tetrodotoxin. Like amantadine, it also blocks an ion channel, the sodium channel. This potent pharmaceutical activity may be, at least in part, attributed to its rigid dioxaadamantane core. The mutations, in turn, destabilize the closed channel, making it easier to open, which counters the effect of the aminoadamantanes. This model could be advantageous for drug design, because drugs that are larger than hydrated ions do have to overcome a higher energetic barrier to find a binding site inside a pore than to bind to the channel complex from the membrane-facing outside.
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页码:3516 / 3604
页数:89
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