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The trifluoroethylamine function as peptide bond replacement
被引:135
作者
:
Sani, Monica
论文数:
0
引用数:
0
h-index:
0
Sani, Monica
Volonterio, Alessandro
论文数:
0
引用数:
0
h-index:
0
Volonterio, Alessandro
Zanda, Matteo
论文数:
0
引用数:
0
h-index:
0
Zanda, Matteo
机构
:
来源
:
CHEMMEDCHEM
|
2007年
/ 2卷
/ 12期
关键词
:
D O I
:
10.1002/cmdc.200700156
中图分类号
:
R914 [药物化学];
学科分类号
:
100701 ;
摘要
:
引用
收藏
页码:1693 / 1700
页数:8
相关论文
共 27 条
[1]
The consequences of lysosomotropism on the design of selective cathepsin K inhibitors
[J].
Black, W. Cameron
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Dept Med Chem & Biochem, Pointe Claire, PQ H9R 4P8, Canada
Black, W. Cameron
;
Percival, M. David
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Dept Med Chem & Biochem, Pointe Claire, PQ H9R 4P8, Canada
Percival, M. David
.
CHEMBIOCHEM,
2006,
7
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:1525
-1535
[2]
Trifluoroethylamines as amide isosteres in inhibitors of cathepsin K
[J].
Black, WC
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0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Black, WC
;
Bayly, CI
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Bayly, CI
;
Davis, DE
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Davis, DE
;
Desmarais, S
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Desmarais, S
;
Falgueyret, JP
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0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Falgueyret, JP
;
Léger, S
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0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Léger, S
;
Li, CS
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0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Li, CS
;
Massé, F
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Massé, F
;
McKay, DJ
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
McKay, DJ
;
Palmer, JT
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Palmer, JT
;
Percival, MD
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Percival, MD
;
Robichaud, J
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Robichaud, J
;
Tsou, N
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Tsou, N
;
Zamboni, R
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
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BIOORGANIC & MEDICINAL CHEMISTRY LETTERS,
2005,
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Optimal recognition of neutral endopeptidase and angiotensin-converting enzyme active sites by mercaptoacyldipeptides as a means to design potent dual inhibitors
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机构:
Coric, P
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Turcaud, S
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UNIV PARIS 05, FAC PHARM, UFR SCI PHARMACEUT & BIOL, DEPT PHARMACOCHIM MOLEC & STRUCT, F-75270 PARIS 06, FRANCE
UNIV PARIS 05, FAC PHARM, UFR SCI PHARMACEUT & BIOL, DEPT PHARMACOCHIM MOLEC & STRUCT, F-75270 PARIS 06, FRANCE
Turcaud, S
;
论文数:
引用数:
h-index:
机构:
Meudal, H
;
Roques, BP
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0
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UNIV PARIS 05, FAC PHARM, UFR SCI PHARMACEUT & BIOL, DEPT PHARMACOCHIM MOLEC & STRUCT, F-75270 PARIS 06, FRANCE
UNIV PARIS 05, FAC PHARM, UFR SCI PHARMACEUT & BIOL, DEPT PHARMACOCHIM MOLEC & STRUCT, F-75270 PARIS 06, FRANCE
Roques, BP
;
FournieZaluski, MC
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0
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UNIV PARIS 05, FAC PHARM, UFR SCI PHARMACEUT & BIOL, DEPT PHARMACOCHIM MOLEC & STRUCT, F-75270 PARIS 06, FRANCE
UNIV PARIS 05, FAC PHARM, UFR SCI PHARMACEUT & BIOL, DEPT PHARMACOCHIM MOLEC & STRUCT, F-75270 PARIS 06, FRANCE
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[J].
DADO, GP
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0
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UNIV WISCONSIN,DEPT CHEM,SM MCELVAIN LAB ORGAN CHEM,1101 UNIV AVE,MADISON,WI 53706
UNIV WISCONSIN,DEPT CHEM,SM MCELVAIN LAB ORGAN CHEM,1101 UNIV AVE,MADISON,WI 53706
DADO, GP
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GELLMAN, SH
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UNIV WISCONSIN,DEPT CHEM,SM MCELVAIN LAB ORGAN CHEM,1101 UNIV AVE,MADISON,WI 53706
UNIV WISCONSIN,DEPT CHEM,SM MCELVAIN LAB ORGAN CHEM,1101 UNIV AVE,MADISON,WI 53706
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.
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CAMBRIDGE CRYSTALLOG DATA CTR,CAMBRIDGE CB2 1EZ,ENGLAND
Dunitz, JD
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CAMBRIDGE CRYSTALLOG DATA CTR,CAMBRIDGE CB2 1EZ,ENGLAND
CAMBRIDGE CRYSTALLOG DATA CTR,CAMBRIDGE CB2 1EZ,ENGLAND
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Univ Bath, Sch Chem, Bath BA2 7AY, Avon, England
Univ Bath, Sch Chem, Bath BA2 7AY, Avon, England
Fletcher, MD
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Campbell, MM
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UNIV PARIS 05,UFR SCI PHARMACEUT & BIOL,CNRS,URA D1500,INSERM,U266,UNITE PHARMACOCHIM MOLEC,F-75270 PARIS 06,FRANCE
ROQUES, BP
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UNIV PARIS 05,UFR SCI PHARMACEUT & BIOL,CNRS,URA D1500,INSERM,U266,UNITE PHARMACOCHIM MOLEC,F-75270 PARIS 06,FRANCE
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UNIV WISCONSIN,DEPT CHEM,MADISON,WI 53706
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UNIV WISCONSIN,DEPT CHEM,MADISON,WI 53706
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UNIV WISCONSIN,DEPT CHEM,MADISON,WI 53706
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Hughes, Greg
;
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0
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机构:
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Naber, John R.
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0
引用数:
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Merck Frosst Canada Inc, Proc Res, Kirkland, PQ H9H 3L1, Canada
Naber, John R.
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0
引用数:
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机构:
Merck Frosst Canada Inc, Proc Res, Kirkland, PQ H9H 3L1, Canada
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Foster, Bruce S.
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0
引用数:
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Merck Frosst Canada Inc, Proc Res, Kirkland, PQ H9H 3L1, Canada
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0
引用数:
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Merck Frosst Canada Inc, Proc Res, Kirkland, PQ H9H 3L1, Canada
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ANGEWANDTE CHEMIE-INTERNATIONAL EDITION,
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46
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:1839
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←
1
2
3
→
共 27 条
[1]
The consequences of lysosomotropism on the design of selective cathepsin K inhibitors
[J].
Black, W. Cameron
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Dept Med Chem & Biochem, Pointe Claire, PQ H9R 4P8, Canada
Black, W. Cameron
;
Percival, M. David
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Dept Med Chem & Biochem, Pointe Claire, PQ H9R 4P8, Canada
Percival, M. David
.
CHEMBIOCHEM,
2006,
7
(10)
:1525
-1535
[2]
Trifluoroethylamines as amide isosteres in inhibitors of cathepsin K
[J].
Black, WC
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Black, WC
;
Bayly, CI
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Bayly, CI
;
Davis, DE
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Davis, DE
;
Desmarais, S
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Desmarais, S
;
Falgueyret, JP
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Falgueyret, JP
;
Léger, S
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Léger, S
;
Li, CS
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Li, CS
;
Massé, F
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Massé, F
;
McKay, DJ
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
McKay, DJ
;
Palmer, JT
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Palmer, JT
;
Percival, MD
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Percival, MD
;
Robichaud, J
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Robichaud, J
;
Tsou, N
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Tsou, N
;
Zamboni, R
论文数:
0
引用数:
0
h-index:
0
机构:
Merck Frosst Ctr Therapeut Res, Pointe Claire, PQ H9R 4P8, Canada
Zamboni, R
.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS,
2005,
15
(21)
:4741
-4744
[3]
Optimal recognition of neutral endopeptidase and angiotensin-converting enzyme active sites by mercaptoacyldipeptides as a means to design potent dual inhibitors
[J].
论文数:
引用数:
h-index:
机构:
Coric, P
;
Turcaud, S
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PARIS 05, FAC PHARM, UFR SCI PHARMACEUT & BIOL, DEPT PHARMACOCHIM MOLEC & STRUCT, F-75270 PARIS 06, FRANCE
UNIV PARIS 05, FAC PHARM, UFR SCI PHARMACEUT & BIOL, DEPT PHARMACOCHIM MOLEC & STRUCT, F-75270 PARIS 06, FRANCE
Turcaud, S
;
论文数:
引用数:
h-index:
机构:
Meudal, H
;
Roques, BP
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PARIS 05, FAC PHARM, UFR SCI PHARMACEUT & BIOL, DEPT PHARMACOCHIM MOLEC & STRUCT, F-75270 PARIS 06, FRANCE
UNIV PARIS 05, FAC PHARM, UFR SCI PHARMACEUT & BIOL, DEPT PHARMACOCHIM MOLEC & STRUCT, F-75270 PARIS 06, FRANCE
Roques, BP
;
FournieZaluski, MC
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PARIS 05, FAC PHARM, UFR SCI PHARMACEUT & BIOL, DEPT PHARMACOCHIM MOLEC & STRUCT, F-75270 PARIS 06, FRANCE
UNIV PARIS 05, FAC PHARM, UFR SCI PHARMACEUT & BIOL, DEPT PHARMACOCHIM MOLEC & STRUCT, F-75270 PARIS 06, FRANCE
FournieZaluski, MC
.
JOURNAL OF MEDICINAL CHEMISTRY,
1996,
39
(06)
:1210
-1219
[4]
STRUCTURAL AND THERMODYNAMIC CHARACTERIZATION OF TEMPERATURE-DEPENDENT CHANGES IN THE FOLDING PATTERN OF A SYNTHETIC TRIAMIDE
[J].
DADO, GP
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV WISCONSIN,DEPT CHEM,SM MCELVAIN LAB ORGAN CHEM,1101 UNIV AVE,MADISON,WI 53706
UNIV WISCONSIN,DEPT CHEM,SM MCELVAIN LAB ORGAN CHEM,1101 UNIV AVE,MADISON,WI 53706
DADO, GP
;
GELLMAN, SH
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV WISCONSIN,DEPT CHEM,SM MCELVAIN LAB ORGAN CHEM,1101 UNIV AVE,MADISON,WI 53706
UNIV WISCONSIN,DEPT CHEM,SM MCELVAIN LAB ORGAN CHEM,1101 UNIV AVE,MADISON,WI 53706
GELLMAN, SH
.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY,
1993,
115
(10)
:4228
-4245
[5]
Organic fluorine hardly ever accepts hydrogen bonds
[J].
Dunitz, JD
论文数:
0
引用数:
0
h-index:
0
机构:
CAMBRIDGE CRYSTALLOG DATA CTR,CAMBRIDGE CB2 1EZ,ENGLAND
CAMBRIDGE CRYSTALLOG DATA CTR,CAMBRIDGE CB2 1EZ,ENGLAND
Dunitz, JD
;
Taylor, R
论文数:
0
引用数:
0
h-index:
0
机构:
CAMBRIDGE CRYSTALLOG DATA CTR,CAMBRIDGE CB2 1EZ,ENGLAND
CAMBRIDGE CRYSTALLOG DATA CTR,CAMBRIDGE CB2 1EZ,ENGLAND
Taylor, R
.
CHEMISTRY-A EUROPEAN JOURNAL,
1997,
3
(01)
:89
-98
[6]
Partially modified retro-inverso peptides: Development, synthesis, and conformational behavior
[J].
Fletcher, MD
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Bath, Sch Chem, Bath BA2 7AY, Avon, England
Univ Bath, Sch Chem, Bath BA2 7AY, Avon, England
Fletcher, MD
;
Campbell, MM
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Bath, Sch Chem, Bath BA2 7AY, Avon, England
Univ Bath, Sch Chem, Bath BA2 7AY, Avon, England
Campbell, MM
.
CHEMICAL REVIEWS,
1998,
98
(02)
:763
-795
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NEW THIOL INHIBITORS OF NEUTRAL ENDOPEPTIDASE EC-3.4.24.11 - SYNTHESIS AND ENZYME ACTIVE-SITE RECOGNITION
[J].
GOMEZMONTERREY, I
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0
引用数:
0
h-index:
0
机构:
UNIV PARIS 05,UFR SCI PHARMACEUT & BIOL,CNRS,URA D1500,INSERM,U266,UNITE PHARMACOCHIM MOLEC,F-75270 PARIS 06,FRANCE
GOMEZMONTERREY, I
;
BEAUMONT, A
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV PARIS 05,UFR SCI PHARMACEUT & BIOL,CNRS,URA D1500,INSERM,U266,UNITE PHARMACOCHIM MOLEC,F-75270 PARIS 06,FRANCE
BEAUMONT, A
;
NEMECEK, P
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0
引用数:
0
h-index:
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