Detalhe da pesquisa
1.
Inhibition of AAK1 Kinase as a Novel Therapeutic Approach to Treat Neuropathic Pain.
J Pharmacol Exp Ther;
358(3): 371-86, 2016 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27411717
2.
The discovery of potent agonists for GPR88, an orphan GPCR, for the potential treatment of CNS disorders.
Bioorg Med Chem Lett;
25(7): 1443-7, 2015 Apr 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25754495
3.
Design, synthesis, and evaluation of phenylglycinols and phenyl amines as agonists of GPR88.
Bioorg Med Chem Lett;
25(7): 1448-52, 2015 Apr 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25690789
4.
Checkpoint inhibition through small molecule-induced internalization of programmed death-ligand 1.
Nat Commun;
12(1): 1222, 2021 02 22.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33619272
5.
Multifunctional magnetic MgMn-oxide composite for efficient purification of Cd2+ and paracetamol pollution: Synergetic effect and stability.
J Hazard Mater;
388: 122078, 2020 04 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31962212
6.
Pharmacological and x-ray structural characterization of a novel selective androgen receptor modulator: potent hyperanabolic stimulation of skeletal muscle with hypostimulation of prostate in rats.
Endocrinology;
148(1): 4-12, 2007 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17008401
7.
Synthesis and SAR of tetrahydropyrrolo[1,2-b][1,2,5]thiadiazol-2(3H)-one 1,1-dioxide analogues as highly potent selective androgen receptor modulators.
Bioorg Med Chem Lett;
17(16): 4487-90, 2007 Aug 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17574413
8.
Tandem optimization of target activity and elimination of mutagenic potential in a potent series of N-aryl bicyclic hydantoin-based selective androgen receptor modulators.
Bioorg Med Chem Lett;
17(7): 1860-4, 2007 Apr 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17292608
9.
Quinolines as extremely potent and selective PDE5 inhibitors as potential agents for treatment of erectile dysfunction.
Bioorg Med Chem Lett;
14(6): 1577-80, 2004 Mar 22.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15006407