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NF449 -: The first subnanomolar P2 antagonist selective for recombinant rat P2X1 receptors
被引:0
|
作者
:
Braun, K
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Frankfurt, Dept Pharmacol, Bioctr Niederursel, D-60439 Frankfurt, Germany
Univ Frankfurt, Dept Pharmacol, Bioctr Niederursel, D-60439 Frankfurt, Germany
Braun, K
[
1
]
Rettinger, J
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Frankfurt, Dept Pharmacol, Bioctr Niederursel, D-60439 Frankfurt, Germany
Univ Frankfurt, Dept Pharmacol, Bioctr Niederursel, D-60439 Frankfurt, Germany
Rettinger, J
[
1
]
Ganso, M
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Frankfurt, Dept Pharmacol, Bioctr Niederursel, D-60439 Frankfurt, Germany
Univ Frankfurt, Dept Pharmacol, Bioctr Niederursel, D-60439 Frankfurt, Germany
Ganso, M
[
1
]
Hildebrandt, C
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Frankfurt, Dept Pharmacol, Bioctr Niederursel, D-60439 Frankfurt, Germany
Univ Frankfurt, Dept Pharmacol, Bioctr Niederursel, D-60439 Frankfurt, Germany
Hildebrandt, C
[
1
]
Nickel, P
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Frankfurt, Dept Pharmacol, Bioctr Niederursel, D-60439 Frankfurt, Germany
Univ Frankfurt, Dept Pharmacol, Bioctr Niederursel, D-60439 Frankfurt, Germany
Nickel, P
[
1
]
Schmalzing, G
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Frankfurt, Dept Pharmacol, Bioctr Niederursel, D-60439 Frankfurt, Germany
Univ Frankfurt, Dept Pharmacol, Bioctr Niederursel, D-60439 Frankfurt, Germany
Schmalzing, G
[
1
]
Lambrecht, G
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Frankfurt, Dept Pharmacol, Bioctr Niederursel, D-60439 Frankfurt, Germany
Univ Frankfurt, Dept Pharmacol, Bioctr Niederursel, D-60439 Frankfurt, Germany
Lambrecht, G
[
1
]
机构
:
[1]
Univ Frankfurt, Dept Pharmacol, Bioctr Niederursel, D-60439 Frankfurt, Germany
来源
:
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY
|
2001年
/ 363卷
/ 04期
关键词
:
D O I
:
暂无
中图分类号
:
R9 [药学];
学科分类号
:
1007 ;
摘要
:
127
引用
收藏
页码:R35 / R35
页数:1
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NF449:: a subnanomolar potency antagonist at recombinant rat P2X1 receptors
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NF449: a subnanomolar potency antagonist at recombinant rat P2X1 receptors
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NF449, a novel picomolar potency antagonist at human P2X1 receptors
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Profiling at recombinant homomeric and heteromeric rat P2X receptors identifies the suramin analogue NF449 as a highly potent P2X1 receptor antagonist
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Structure-activity relationships of analogues of NF449 confirm NF449 as the most potent and selective known P2X1 receptor antagonist
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