skip to main content
Idioma:
Resultados 1 2 3 4 5 next page
Refinado por: Nome da Publicação: Bioorganic & Medicinal Chemistry Letters remover assunto: Medical Sciences remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Discovery of small molecule isozyme non-specific inhibitors of mammalian acetyl-CoA carboxylase 1 and 2
Discovery of small molecule isozyme non-specific inhibitors of mammalian acetyl-CoA carboxylase 1 and 2
Material Type:
Artigo 		Adicionar ao Meu Espaço

Discovery of small molecule isozyme non-specific inhibitors of mammalian acetyl-CoA carboxylase 1 and 2

Corbett, Jeffrey W. ; Freeman-Cook, Kevin D. ; Elliott, Richard ; Vajdos, Felix ; Rajamohan, Francis ; Kohls, Darcy ; Marr, Eric ; Zhang, Hailong ; Tong, Liang ; Tu, Meihua ; Murdande, Sharad ; Doran, Shawn D. ; Houser, Janet A. ; Song, Wei ; Jones, Christopher J. ; Coffey, Steven B. ; Buzon, Leanne ; Minich, Martha L. ; Dirico, Kenneth J. ; Tapley, Susan ; Kirk McPherson, R. ; Sugarman, Eliot ; James Harwood, H. ; Esler, William

Bioorganic & medicinal chemistry letters, 2010-04, Vol.20 (7), p.2383-2388 [Periódico revisado por pares]

Amsterdam: Elsevier Ltd

Texto completo disponível

Citações Citado por
2
Discovery and optimisation of potent, selective, ethanolamine inhibitors of bacterial phenylalanyl tRNA synthetase
Discovery and optimisation of potent, selective, ethanolamine inhibitors of bacterial phenylalanyl tRNA synthetase
Material Type:
Artigo 		Adicionar ao Meu Espaço

Discovery and optimisation of potent, selective, ethanolamine inhibitors of bacterial phenylalanyl tRNA synthetase

Jarvest, Richard L. ; Erskine, Symon G. ; Forrest, Andrew K. ; Fosberry, Andrew P. ; Hibbs, Martin J. ; Jones, Joanna J. ; O’Hanlon, Peter J. ; Sheppard, Robert J. ; Worby, Angela

Bioorganic & medicinal chemistry letters, 2005-05, Vol.15 (9), p.2305-2309 [Periódico revisado por pares]

Oxford: Elsevier Ltd

Texto completo disponível

Citações Citado por
3
1-Aryl-3,4-dihydroisoquinoline inhibitors of JNK3
1-Aryl-3,4-dihydroisoquinoline inhibitors of JNK3
Material Type:
Artigo 		Adicionar ao Meu Espaço

1-Aryl-3,4-dihydroisoquinoline inhibitors of JNK3

Christopher, John A. ; Atkinson, Francis L. ; Bax, Benjamin D. ; Brown, Murray J.B. ; Champigny, Aurélie C. ; Chuang, Tsu Tshen ; Jones, Emma J. ; Mosley, Julie E. ; Musgrave, James R.

Bioorganic & medicinal chemistry letters, 2009-04, Vol.19 (8), p.2230-2234 [Periódico revisado por pares]

Amsterdam: Elsevier Ltd

Texto completo disponível

Citações Citado por
4
Integration of optimized substituent patterns to produce highly potent 4-aryl-pyridine glucagon receptor antagonists
Integration of optimized substituent patterns to produce highly potent 4-aryl-pyridine glucagon receptor antagonists
Material Type:
Artigo 		Adicionar ao Meu Espaço

Integration of optimized substituent patterns to produce highly potent 4-aryl-pyridine glucagon receptor antagonists

Ladouceur, Gaetan H. ; Cook, James H. ; Hertzog, Donald L. ; Jones, J.Howard ; Hundertmark, Thomas ; Korpusik, Mary ; Lease, Timothy G. ; Livingston, James N. ; MacDougall, Margit L. ; Osterhout, Martin H. ; Phelan, Kathleen ; Romero, Romulo H. ; Schoen, William R. ; Shao, Chunning ; Smith, Roger A.

Bioorganic & medicinal chemistry letters, 2002-12, Vol.12 (23), p.3421-3424 [Periódico revisado por pares]

Oxford: Elsevier Ltd

Texto completo disponível

Citações Citado por
5
Optimization of the 4-aryl group of 4-aryl-pyridine glucagon antagonists: development of an efficient, alternative synthesis
Optimization of the 4-aryl group of 4-aryl-pyridine glucagon antagonists: development of an efficient, alternative synthesis
Material Type:
Artigo 		Adicionar ao Meu Espaço

Optimization of the 4-aryl group of 4-aryl-pyridine glucagon antagonists: development of an efficient, alternative synthesis

Smith, Roger A. ; Hertzog, Donald L. ; Osterhout, Martin H. ; Ladouceur, Gaetan H. ; Korpusik, Mary ; Bobko, Mark A. ; Jones, J.Howard ; Phelan, Kathleen ; Romero, Romulo H. ; Hundertmark, Thomas ; MacDougall, Margit L. ; Livingston, James N. ; Schoen, William R.

Bioorganic & medicinal chemistry letters, 2002-05, Vol.12 (9), p.1303-1306 [Periódico revisado por pares]

Oxford: Elsevier Ltd

Texto completo disponível

Citações Citado por
6
Inhibition of the RTEM-1 β-lactamase by boronic acids
Inhibition of the RTEM-1 β-lactamase by boronic acids
Material Type:
Artigo 		Adicionar ao Meu Espaço

Inhibition of the RTEM-1 β-lactamase by boronic acids

Martin, Richard ; Gold, Marvin ; Jones, J.Bryan

Bioorganic & medicinal chemistry letters, 1994-05, Vol.4 (10), p.1229-1234 [Periódico revisado por pares]

Oxford: Elsevier Ltd

Texto completo disponível

Citações Citado por
7
1-[2-[(Heteroarylmethoxy)aryl]carbamoyl]indolines are selective and orally active 5-HT2C receptor inverse agonists
1-[2-[(Heteroarylmethoxy)aryl]carbamoyl]indolines are selective and orally active 5-HT2C receptor inverse agonists
Material Type:
Artigo 		Adicionar ao Meu Espaço

1-[2-[(Heteroarylmethoxy)aryl]carbamoyl]indolines are selective and orally active 5-HT2C receptor inverse agonists

BROMIDGE, S. M ; DAVIES, S ; LIGHTOWLER, S ; MIDDLEMISS, D. N ; RILEY, G. J ; TRAIL, B ; WOOD, M. D ; DUCKWORTH, D. M ; FORBES, I. T ; JONES, G. E ; JONES, J ; KING, F. D ; BLACKBURN, T. P ; HOLLAND, V ; KENNETT, G. A

Bioorganic & medicinal chemistry letters, 2000-08, Vol.10 (16), p.1867-1870 [Periódico revisado por pares]

Oxford: Elsevier

Texto completo disponível

Citações Citado por
8
1-[2-[(Heteroaryloxy)heteroaryl]carbamoyl]indolines : Novel and selective 5-HT2C receptor inverse agonists with potential as antidepressant/anxiolytic agents
1-[2-[(Heteroaryloxy)heteroaryl]carbamoyl]indolines : Novel and selective 5-HT2C receptor inverse agonists with potential as antidepressant/anxiolytic agents
Material Type:
Artigo 		Adicionar ao Meu Espaço

1-[2-[(Heteroaryloxy)heteroaryl]carbamoyl]indolines : Novel and selective 5-HT2C receptor inverse agonists with potential as antidepressant/anxiolytic agents

BROMIDGE, S. M ; DABBS, S ; HOLLAND, V ; KENNETT, G. A ; LIGHTOWLER, S ; MIDDLEMISS, D. N ; RILEY, G. J ; TRAIL, B ; WOOD, M. D ; DAVIES, S ; DUCKWORTH, D. M ; FORBES, I. T ; JONES, G. E ; JONES, J ; KING, F. D ; SAUNDERS, D. V ; BLACKBURN, T. P

Bioorganic & medicinal chemistry letters, 2000-08, Vol.10 (16), p.1863-1866 [Periódico revisado por pares]

Oxford: Elsevier

Texto completo disponível

Citações Citado por
9
Allosteric Akt (PKB) inhibitors: discovery and SAR of isozyme selective inhibitors
Allosteric Akt (PKB) inhibitors: discovery and SAR of isozyme selective inhibitors
Material Type:
Artigo 		Adicionar ao Meu Espaço

Allosteric Akt (PKB) inhibitors: discovery and SAR of isozyme selective inhibitors

Lindsley, Craig W. ; Zhao, Zhijian ; Leister, William H. ; Robinson, Ronald G. ; Barnett, Stanley F. ; Defeo-Jones, Deborah ; Jones, Raymond E. ; Hartman, George D. ; Huff, Joel R. ; Huber, Hans E. ; Duggan, Mark E.

Bioorganic & medicinal chemistry letters, 2005-02, Vol.15 (3), p.761-764 [Periódico revisado por pares]

Oxford: Elsevier Ltd

Texto completo disponível

Citações Citado por
10
Oligodeoxynucleotides containing 5-(1-propynyl)-2'-deoxyuridine formacetal and thioformacetal dimer synthons: Modified oligonucleotides
Oligodeoxynucleotides containing 5-(1-propynyl)-2'-deoxyuridine formacetal and thioformacetal dimer synthons: Modified oligonucleotides
Material Type:
Artigo 		Adicionar ao Meu Espaço

Oligodeoxynucleotides containing 5-(1-propynyl)-2'-deoxyuridine formacetal and thioformacetal dimer synthons: Modified oligonucleotides

KUEI-YING LIN ; PUDLO, J. S ; JONES, R. J ; BUSCHOFBERGER, N ; MATTEUCCI, M. D ; FROEHLER, B. C

Bioorganic & medicinal chemistry letters, 1994, Vol.4 (8) [Periódico revisado por pares]

Oxford: Elsevier

Texto completo disponível

Citações Citado por
Resultados 1 2 3 4 5 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.