skip to main content
Idioma:
Resultados 1 2 3 4 5 next page
Mostrar Somente
Refinado por: assunto: Female remover assunto: Pharmacology & Pharmacy remover Mice remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Design, Synthesis, and Evaluation of [18F]BIBD-300 as a Positron Emission Tomography Tracer for Poly(ADP-Ribose) Polymerase‑1
Design, Synthesis, and Evaluation of [18F]BIBD-300 as a Positron Emission Tomography Tracer for Poly(ADP-Ribose) Polymerase‑1
Material Type:
Artigo 		Adicionar ao Meu Espaço

Design, Synthesis, and Evaluation of [18F]BIBD-300 as a Positron Emission Tomography Tracer for Poly(ADP-Ribose) Polymerase‑1

Zheng, Wei ; Huang, Yong ; Xie, Yi ; Yang, Tingyu ; Cheng, Xuebo ; Chen, Hualong ; Li, Chengze ; Jiang, Zeng ; Yu, Ziyue ; Li, Zhongjing ; Zhang, Lu ; Yuan, Leilei ; Liu, Yajing ; Liang, Ying ; Wu, Zehui

Molecular pharmaceutics, 2024-05, Vol.21 (5), p.2606-2621 [Periódico revisado por pares]

United States: American Chemical Society

Texto completo disponível

Citações Citado por
2
Design, synthesis, in-vitro, in-vivo and in-silico studies of pyrrolidine-2,5-dione derivatives as multitarget anti-inflammatory agents
Design, synthesis, in-vitro, in-vivo and in-silico studies of pyrrolidine-2,5-dione derivatives as multitarget anti-inflammatory agents
Material Type:
Artigo 		Adicionar ao Meu Espaço

Design, synthesis, in-vitro, in-vivo and in-silico studies of pyrrolidine-2,5-dione derivatives as multitarget anti-inflammatory agents

Jan, Muhammad Saeed ; Ahmad, Sajjad ; Hussain, Fida ; Ahmad, Ashfaq ; Mahmood, Fawad ; Rashid, Umer ; Abid, Obaid-ur-Rahman ; Ullah, Farhat ; Ayaz, Muhammad ; Sadiq, Abdul

European journal of medicinal chemistry, 2020-01, Vol.186, p.111863, Article 111863 [Periódico revisado por pares]

France: Elsevier Masson SAS

Texto completo disponível

Citações Citado por
3
A Molecular Hybridization Approach for the Design of Potent, Highly Selective, and Brain-Penetrant N‑Myristoyltransferase Inhibitors
A Molecular Hybridization Approach for the Design of Potent, Highly Selective, and Brain-Penetrant N‑Myristoyltransferase Inhibitors
Material Type:
Artigo 		Adicionar ao Meu Espaço

A Molecular Hybridization Approach for the Design of Potent, Highly Selective, and Brain-Penetrant N‑Myristoyltransferase Inhibitors

Harrison, Justin R ; Brand, Stephen ; Smith, Victoria ; Robinson, David A ; Thompson, Stephen ; Smith, Alasdair ; Davies, Kenneth ; Mok, Ngai ; Torrie, Leah S ; Collie, Iain ; Hallyburton, Irene ; Norval, Suzanne ; Simeons, Frederick R. C ; Stojanovski, Laste ; Frearson, Julie A ; Brenk, Ruth ; Wyatt, Paul G ; Gilbert, Ian H ; Read, Kevin D

Journal of medicinal chemistry, 2018-09, Vol.61 (18), p.8374-8389 [Periódico revisado por pares]

United States: American Chemical Society

Texto completo disponível

Citações Citado por
4
Design, synthesis and biological evaluation of novel 4-alkapolyenylpyrrolo[1,2-a]quinoxalines as antileishmanial agents – Part III
Design, synthesis and biological evaluation of novel 4-alkapolyenylpyrrolo[1,2-a]quinoxalines as antileishmanial agents – Part III
Material Type:
Artigo 		Adicionar ao Meu Espaço

Design, synthesis and biological evaluation of novel 4-alkapolyenylpyrrolo[1,2-a]quinoxalines as antileishmanial agents – Part III

Ronga, Luisa ; Del Favero, Marco ; Cohen, Anita ; Soum, Claire ; Le Pape, Patrice ; Savrimoutou, Solène ; Pinaud, Noël ; Mullié, Catherine ; Daulouede, Sylvie ; Vincendeau, Philippe ; Farvacques, Natacha ; Agnamey, Patrice ; Pagniez, Fabrice ; Hutter, Sébastien ; Azas, Nadine ; Sonnet, Pascal ; Guillon, Jean

European journal of medicinal chemistry, 2014-06, Vol.81, p.378-393 [Periódico revisado por pares]

France: Elsevier Masson SAS

Texto completo disponível

Citações Citado por
5
Design and Synthesis of Pyridone-Containing 3,4-Dihydroisoquinoline-1(2H)‑ones as a Novel Class of Enhancer of Zeste Homolog 2 (EZH2) Inhibitors
Design and Synthesis of Pyridone-Containing 3,4-Dihydroisoquinoline-1(2H)‑ones as a Novel Class of Enhancer of Zeste Homolog 2 (EZH2) Inhibitors
Material Type:
Artigo 		Adicionar ao Meu Espaço

Design and Synthesis of Pyridone-Containing 3,4-Dihydroisoquinoline-1(2H)‑ones as a Novel Class of Enhancer of Zeste Homolog 2 (EZH2) Inhibitors

Kung, Pei-Pei ; Rui, Eugene ; Bergqvist, Simon ; Bingham, Patrick ; Braganza, John ; Collins, Michael ; Cui, Mei ; Diehl, Wade ; Dinh, Dac ; Fan, Connie ; Fantin, Valeria R ; Gukasyan, Hovhannes J ; Hu, Wenyue ; Huang, Buwen ; Kephart, Susan ; Krivacic, Cody ; Kumpf, Robert A ; Li, Gary ; Maegley, Karen A ; McAlpine, Indrawan ; Nguyen, Lisa ; Ninkovic, Sacha ; Ornelas, Martha ; Ryskin, Michael ; Scales, Stephanie ; Sutton, Scott ; Tatlock, John ; Verhelle, Dominique ; Wang, Fen ; Wells, Peter ; Wythes, Martin ; Yamazaki, Shinji ; Yip, Brian ; Yu, Xiu ; Zehnder, Luke ; Zhang, Wei-Guo ; Rollins, Robert A ; Edwards, Martin

Journal of medicinal chemistry, 2016-09, Vol.59 (18), p.8306-8325 [Periódico revisado por pares]

United States: American Chemical Society

Texto completo disponível

Citações Citado por
6
Immunity by formulation design: Induction of high CD8 + T-cell responses by poly(I:C) incorporated into the CAF01 adjuvant via a double emulsion method
Immunity by formulation design: Induction of high CD8 + T-cell responses by poly(I:C) incorporated into the CAF01 adjuvant via a double emulsion method
Material Type:
Artigo 		Adicionar ao Meu Espaço

Immunity by formulation design: Induction of high CD8 + T-cell responses by poly(I:C) incorporated into the CAF01 adjuvant via a double emulsion method

Nordly, Pernille ; Rose, Fabrice ; Christensen, Dennis ; Nielsen, Hanne Mørck ; Andersen, Peter ; Agger, Else Marie ; Foged, Camilla

Journal of controlled release, 2011-03, Vol.150 (3), p.307-317 [Periódico revisado por pares]

Kidlington: Elsevier B.V

Texto completo disponível

Citações Citado por
7
Design, Synthesis, and Mechanism Study of Benzenesulfonamide-Containing Phenylalanine Derivatives as Novel HIV‑1 Capsid Inhibitors with Improved Antiviral Activities
Design, Synthesis, and Mechanism Study of Benzenesulfonamide-Containing Phenylalanine Derivatives as Novel HIV‑1 Capsid Inhibitors with Improved Antiviral Activities
Material Type:
Artigo 		Adicionar ao Meu Espaço

Design, Synthesis, and Mechanism Study of Benzenesulfonamide-Containing Phenylalanine Derivatives as Novel HIV‑1 Capsid Inhibitors with Improved Antiviral Activities

Sun, Lin ; Dick, Alexej ; Meuser, Megan E ; Huang, Tianguang ; Zalloum, Waleed A ; Chen, Chin-Ho ; Cherukupalli, Srinivasulu ; Xu, Shujing ; Ding, Xiao ; Gao, Ping ; Kang, Dongwei ; De Clercq, Erik ; Pannecouque, Christophe ; Cocklin, Simon ; Lee, Kuo-Hsiung ; Liu, Xinyong ; Zhan, Peng

Journal of medicinal chemistry, 2020-05, Vol.63 (9), p.4790-4810 [Periódico revisado por pares]

United States: American Chemical Society

Texto completo disponível

Citações Citado por
8
Design and Validation of Liposomal ApoE2 Gene Delivery System to Evade Blood–Brain Barrier for Effective Treatment of Alzheimer’s Disease
Design and Validation of Liposomal ApoE2 Gene Delivery System to Evade Blood–Brain Barrier for Effective Treatment of Alzheimer’s Disease
Material Type:
Artigo 		Adicionar ao Meu Espaço

Design and Validation of Liposomal ApoE2 Gene Delivery System to Evade Blood–Brain Barrier for Effective Treatment of Alzheimer’s Disease

Arora, Sanjay ; Layek, Buddhadev ; Singh, Jagdish

Molecular pharmaceutics, 2021-02, Vol.18 (2), p.714-725 [Periódico revisado por pares]

United States: American Chemical Society

Texto completo disponível

Citações Citado por
9
Design, Synthesis, and Pharmacological Evaluation of N‑Acylhydrazones and Novel Conformationally Constrained Compounds as Selective and Potent Orally Active Phosphodiesterase‑4 Inhibitors
Design, Synthesis, and Pharmacological Evaluation of N‑Acylhydrazones and Novel Conformationally Constrained Compounds as Selective and Potent Orally Active Phosphodiesterase‑4 Inhibitors
Material Type:
Artigo 		Adicionar ao Meu Espaço

Design, Synthesis, and Pharmacological Evaluation of N‑Acylhydrazones and Novel Conformationally Constrained Compounds as Selective and Potent Orally Active Phosphodiesterase‑4 Inhibitors

Kümmerle, Arthur E ; Schmitt, Martine ; Cardozo, Suzana V. S ; Lugnier, Claire ; Villa, Pascal ; Lopes, Alexandra B ; Romeiro, Nelilma C ; Justiniano, Hélène ; Martins, Marco A ; Fraga, Carlos A. M ; Bourguignon, Jean-Jacques ; Barreiro, Eliezer J

Journal of medicinal chemistry, 2012-09, Vol.55 (17), p.7525-7545 [Periódico revisado por pares]

United States: American Chemical Society

Texto completo disponível

Citações Citado por
10
Design, Synthesis, Mechanisms of Action, and Toxicity of Novel 20(S)‑Sulfonylamidine Derivatives of Camptothecin as Potent Antitumor Agents
Design, Synthesis, Mechanisms of Action, and Toxicity of Novel 20(S)‑Sulfonylamidine Derivatives of Camptothecin as Potent Antitumor Agents
Material Type:
Artigo 		Adicionar ao Meu Espaço

Design, Synthesis, Mechanisms of Action, and Toxicity of Novel 20(S)‑Sulfonylamidine Derivatives of Camptothecin as Potent Antitumor Agents

Wang, Mei-Juan ; Liu, Ying-Qian ; Chang, Ling-Chu ; Wang, Chih-Ya ; Zhao, Yong-Long ; Zhao, Xiao-Bo ; Qian, Keduo ; Nan, Xiang ; Yang, Liu ; Yang, Xiao-Ming ; Hung, Hsin-Yi ; Yang, Jai-Sing ; Kuo, Daih-Huang ; Goto, Masuo ; Morris-Natschke, Susan L ; Pan, Shiow-Lin ; Teng, Che-Ming ; Kuo, Sheng-Chu ; Wu, Tian-Shung ; Wu, Yang-Chang ; Lee, Kuo-Hsiung

Journal of medicinal chemistry, 2014-07, Vol.57 (14), p.6008-6018 [Periódico revisado por pares]

United States: American Chemical Society

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.   

Mostrar Somente

  1. Revistas revisadas por pares (1.789)

Data de Publicação 

De até
Refinar
  1. Antes de1988  (18)
  2. 1988Até1996  (50)
  3. 1997Até2005  (166)
  4. 2006Até2015  (803)
  5. Após 2015  (773)
  6. Mais opções open sub menu

Idioma 

  1. Inglês  (1.807)
  2. Japonês  (255)
  3. Alemão  (11)
  4. Russo  (2)
  5. Chinês  (2)
  6. Português  (1)
  7. Norueguês  (1)
  8. Mais opções open sub menu

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

Buscando em bases de dados remotas. Favor aguardar.