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Targeting nucleic acid secondary structures with polyamides using an optimized dynamic combinatorial approach
被引:46
作者
:
Ladame, S
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Cambridge, Chem Lab, Cambridge CB2 1EW, England
Univ Cambridge, Chem Lab, Cambridge CB2 1EW, England
Ladame, S
[
1
]
Whitney, AM
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Cambridge, Chem Lab, Cambridge CB2 1EW, England
Univ Cambridge, Chem Lab, Cambridge CB2 1EW, England
Whitney, AM
[
1
]
论文数:
引用数:
h-index:
机构:
Balasubramanian, S
[
1
]
机构
:
[1]
Univ Cambridge, Chem Lab, Cambridge CB2 1EW, England
来源
:
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
|
2005年
/ 44卷
/ 35期
基金
:
英国生物技术与生命科学研究理事会;
关键词
:
combinatorial chemistry;
DNA recognition;
DNA structures;
nucleic acids;
template synthesis;
D O I
:
10.1002/anie.200501450
中图分类号
:
O6 [化学];
学科分类号
:
0703 ;
摘要
:
(Chemical Equation Presented) Reversible disulfide chemistry is used to identify ligands that stabilize either duplex or quadruplex DNA secondary structures from a dynamic combinatorial library of polyamide building blocks (example structure shown). Double-stranded DNA induces a larger amplification than quadruplex DNA, in accordance with the selectivity of the ligands for each DNA target. © 2005 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:5736 / 5739
页数:4
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