Detalhe da pesquisa
1.
Naphthylisoquinoline alkaloids, a new structural template inhibitor of Nav1.7 sodium channel.
Acta Pharmacol Sin
; 44(9): 1768-1776, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37142682
2.
Diversity-oriented synthesis of marine polybrominated diphenyl ethers as potential KCNQ potassium channel activators.
Bioorg Chem
; 126: 105909, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35661526
3.
SCN8A epileptic encephalopathy mutations display a gain-of-function phenotype and divergent sensitivity to antiepileptic drugs.
Acta Pharmacol Sin
; 43(12): 3139-3148, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-35902765
4.
(-)-Naringenin 4',7-dimethyl Ether Isolated from Nardostachys jatamansi Relieves Pain through Inhibition of Multiple Channels.
Molecules
; 27(5)2022 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35268839
5.
Discovery of aryl sulfonamide-selective Nav1.7 inhibitors with a highly hydrophobic ethanoanthracene core.
Acta Pharmacol Sin
; 41(3): 293-302, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31316182
6.
Antiepileptic geissoschizine methyl ether is an inhibitor of multiple neuronal channels.
Acta Pharmacol Sin
; 41(5): 629-637, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-31911638
7.
Inhibitory effects of lappaconitine on the neuronal isoforms of voltage-gated sodium channels.
Acta Pharmacol Sin
; 40(4): 451-459, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29991710
8.
Enhancing inactivation rather than reducing activation of Nav1.7 channels by a clinically effective analgesic CNV1014802.
Acta Pharmacol Sin
; 39(4): 587-596, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29094728
9.
Development of Novel Alkoxyisoxazoles as Sigma-1 Receptor Antagonists with Antinociceptive Efficacy.
J Med Chem
; 59(13): 6329-43, 2016 07 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-27309376