Biophysical fragment screening of the β1-adrenergic receptor: identification of high affinity arylpiperazine leads using structure-based drug design.
Biophysical fragment screening of the β1-adrenergic receptor: identification of high affinity arylpiperazine leads using structure-based drug design.
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DOI:
10.1021/jm400140q
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发表时间:
2013-05-09
影响因子:
7.3
通讯作者:
Congreve, Miles
中科院分区:
文献类型:
--
作者:
Christopher, John A.;Brown, Jason;Dore, Andrew S.;Errey, James C.;Koglin, Markus;Marshall, Fiona H.;Myszka, David G.;Rich, Rebecca L.;Tate, Christopher G.;Tehan, Benjamin;Warne, Tony;Congreve, Miles
Biophysical fragment screening of a thermostabilized β1-adrenergic receptor (β1AR) using surface plasmon resonance (SPR) enabled the identification of moderate affinity, high ligand efficiency (LE) arylpiperazine hits 7 and 8. Subsequent hit to lead follow-up confirmed the activity of the chemotype, and a structure-based design approach using protein–ligand crystal structures of the β1AR resulted in the identification of several fragments that bound with higher affinity, including indole 19 and quinoline 20. In the first example of GPCR crystallography with ligands derived from fragment screening, structures of the stabilized β1AR complexed with 19 and 20 were determined at resolutions of 2.8 and 2.7 Å, respectively.
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DOI:
10.1107/s0907444905036693
发表时间:
2006-01-01
影响因子:
2.2
作者:
Evans, P
通讯作者:
Evans, P
影响因子:
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作者:
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通讯作者:
GOODFORD, PJ
影响因子:
14.9
作者:
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Richardson DC
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64.8
作者:
Granier, Sebastien;Manglik, Aashish;Kruse, Andrew C.;Kobilka, Tong Sun;Thian, Foon Sun;Weis, William I.;Kobilka, Brian K.
通讯作者:
Kobilka, Brian K.
DOI:
10.1021/ci0498719
发表时间:
2004-09-01
期刊:
JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES
影响因子:
--
作者:
Bender, A;Mussa, HY;Reiling, S
通讯作者:
Reiling, S