Detalhe da pesquisa
1.
Discovery of 4-(3-aminopyrrolidinyl)-3-aryl-5-(benzimidazol-2-yl)-pyridines as potent and selective SST5 agonists for the treatment of congenital hyperinsulinism.
Bioorg Med Chem Lett
; 71: 128807, 2022 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35605837
2.
Three-Dimensional Mapping of Resistivity and Microstructure of Composite Electrodes for Lithium-Ion Batteries.
Nano Lett
; 20(11): 8081-8088, 2020 Nov 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33125240
3.
Discovery of nonpeptide 3,4-dihydroquinazoline-4-carboxamides as potent and selective sst2 agonists.
Bioorg Med Chem Lett
; 30(17): 127391, 2020 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32738999
4.
Embelin and its derivatives unravel the signaling, proinflammatory and antiatherogenic properties of GPR84 receptor.
Pharmacol Res
; 131: 185-198, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29471103
5.
Degradation Mechanisms of Magnesium Metal Anodes in Electrolytes Based on (CF3SO2)2N- at High Current Densities.
Langmuir
; 33(37): 9398-9406, 2017 09 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-28636826
6.
Design and synthesis of new tricyclic indoles as potent modulators of the S1P1 receptor.
Bioorg Med Chem Lett
; 25(3): 659-63, 2015 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25532755
7.
Discovery of a novel trans-1,4-dioxycyclohexane GPR119 agonist series.
Bioorg Med Chem Lett
; 25(15): 3034-8, 2015 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26048791
8.
Discovery of 1a,2,5,5a-tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalen-4-carboxamides as potent and selective CB2 receptor agonists.
Bioorg Med Chem Lett
; 25(2): 322-6, 2015 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25488844
9.
Discovery and optimization of 5-fluoro-4,6-dialkoxypyrimidine GPR119 agonists.
Bioorg Med Chem Lett
; 24(17): 4332-5, 2014 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25088191
10.
Discovery of CRN04894: A Novel Potent Selective MC2R Antagonist.
ACS Med Chem Lett
; 15(4): 478-485, 2024 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38628803
11.
Improvement of ß-cell function after achievement of optimal glycaemic control via long-term continuous subcutaneous insulin infusion therapy in non-newly diagnosed type 2 diabetic patients with suboptimal glycaemic control.
Diabetes Metab Res Rev
; 29(6): 473-82, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23592489
12.
A case of acute motor and sensory axonal neuropathy following hepatitis a infection.
J Korean Med Sci
; 28(12): 1839-41, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24339719
13.
Structure Dependent Electrochemical Behaviors of Hard Carbon Anode Materials Derived from Natural Polymer for Next-Generation Sodium Ion Battery.
Polymers (Basel)
; 15(22)2023 Nov 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-38006097
14.
Discovery of Paltusotine (CRN00808), a Potent, Selective, and Orally Bioavailable Non-peptide SST2 Agonist.
ACS Med Chem Lett
; 14(1): 66-74, 2023 Jan 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36655128
15.
Fused tricyclic indoles as S1P1 agonists with robust efficacy in animal models of autoimmune disease.
Bioorg Med Chem Lett
; 22(13): 4404-9, 2012 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22633692
16.
A case of cerebellar infarction presenting as thunderclap headache.
Neurol Sci
; 33(2): 321-3, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21720896
17.
Promising therapeutics with natural bioactive compounds for improving learning and memory--a review of randomized trials.
Molecules
; 17(9): 10503-39, 2012 Sep 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-22945029
18.
Electrochemical Sodiation Mechanism in Magnetite Nanoparticle-Based Anodes: Understanding of Nanoionics-Based Sodium Ion Storage Behavior of Fe3O4.
ACS Appl Mater Interfaces
; 14(45): 50773-50782, 2022 Nov 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36318084
19.
Discovery and characterization of potent and selective 4-oxo-4-(5-(5-phenyl-1,2,4-oxadiazol-3-yl)indolin-1-yl)butanoic acids as S1P1 agonists.
Bioorg Med Chem Lett
; 21(19): 6013-8, 2011 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21852130
20.
Anti-neuroinflammatory activity of Kamebakaurin from Isodon japonicus via inhibition of c-Jun NH2-terminal kinase and p38 mitogen-activated protein kinase pathway in activated microglial cells.
J Pharmacol Sci
; 116(3): 296-308, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21705843