343 related articles for article (PubMed ID: 29884692)
1. Identification of WB4101, an
Li M; Wu Y; Zou B; Wang X; Li M; Yu H
Mol Pharmacol; 2018 Aug; 94(2):896-906. PubMed ID: 29884692
[TBL] [Abstract][Full Text] [Related]
2. Modulation of peripheral Na(+) channels and neuronal firing by n-butyl-p-aminobenzoate.
Thériault O; Poulin H; Sculptoreanu A; de Groat WC; O'Leary ME; Chahine M
Eur J Pharmacol; 2014 Mar; 727():158-66. PubMed ID: 24486399
[TBL] [Abstract][Full Text] [Related]
3. Unique electrophysiological property of a novel Nav1.7, Nav1.8, and Nav1.9 sodium channel blocker, ANP-230.
Kamei T; Kudo T; Yamane H; Ishibashi F; Takada Y; Honda S; Maezawa Y; Ikeda K; Oyamada Y
Biochem Biophys Res Commun; 2024 Aug; 721():150126. PubMed ID: 38776832
[TBL] [Abstract][Full Text] [Related]
4. A novel isoquinoline alkaloid HJ-69 isolated from Zanthoxylum bungeanum attenuates inflammatory pain by inhibiting voltage-gated sodium and potassium channels.
Wang L; Hao H; Meng X; Zhang W; Zhang Y; Chai T; Wang X; Gao Z; Zheng Y; Yang J
J Ethnopharmacol; 2024 Aug; 330():118218. PubMed ID: 38677570
[TBL] [Abstract][Full Text] [Related]
5. The endocannabinoid anandamide inhibits voltage-gated sodium channels Nav1.2, Nav1.6, Nav1.7, and Nav1.8 in Xenopus oocytes.
Okura D; Horishita T; Ueno S; Yanagihara N; Sudo Y; Uezono Y; Sata T
Anesth Analg; 2014 Mar; 118(3):554-62. PubMed ID: 24557103
[TBL] [Abstract][Full Text] [Related]
6. Enhancing inactivation rather than reducing activation of Nav1.7 channels by a clinically effective analgesic CNV1014802.
Zheng YM; Wang WF; Li YF; Yu Y; Gao ZB
Acta Pharmacol Sin; 2018 Apr; 39(4):587-596. PubMed ID: 29094728
[TBL] [Abstract][Full Text] [Related]
7. Antidepressants inhibit Na
Horishita T; Yanagihara N; Ueno S; Okura D; Horishita R; Minami T; Ogata Y; Sudo Y; Uezono Y; Sata T; Kawasaki T
Naunyn Schmiedebergs Arch Pharmacol; 2017 Dec; 390(12):1255-1270. PubMed ID: 28905186
[TBL] [Abstract][Full Text] [Related]
8. Oxidation differentially modulates the recombinant voltage-gated Na(+) channel α-subunits Nav1.7 and Nav1.8.
Schlüter F; Leffler A
Brain Res; 2016 Oct; 1648(Pt A):127-135. PubMed ID: 27450927
[TBL] [Abstract][Full Text] [Related]
9. Recombinant PaurTx-3, a spider toxin, inhibits sodium channels and decreases membrane excitability in DRG neurons.
Chen M; Peng S; Wang L; Yang L; Si Y; Zhou X; Zhang Y; Liu Z
Biochem Biophys Res Commun; 2020 Dec; 533(4):958-964. PubMed ID: 33004176
[TBL] [Abstract][Full Text] [Related]
10. Cannabidiol Inhibition of Murine Primary Nociceptors: Tight Binding to Slow Inactivated States of Na
Zhang HB; Bean BP
J Neurosci; 2021 Jul; 41(30):6371-6387. PubMed ID: 34131037
[TBL] [Abstract][Full Text] [Related]
11. NAN-190, a 5-HT
Li S; Jin Y; Li M; Yu H
Life Sci; 2023 Apr; 319():121520. PubMed ID: 36828129
[TBL] [Abstract][Full Text] [Related]
12. Loperamide inhibits sodium channels to alleviate inflammatory hyperalgesia.
Wu Y; Zou B; Liang L; Li M; Tao YX; Yu H; Wang X; Li M
Neuropharmacology; 2017 May; 117():282-291. PubMed ID: 28216001
[TBL] [Abstract][Full Text] [Related]
13. Selective Closed-State Nav1.7 Blocker JZTX-34 Exhibits Analgesic Effects against Pain.
Zeng X; Li P; Chen B; Huang J; Lai R; Liu J; Rong M
Toxins (Basel); 2018 Feb; 10(2):. PubMed ID: 29393892
[TBL] [Abstract][Full Text] [Related]
14. Analgesic Effects of Topical Amitriptyline in Patients With Chemotherapy-Induced Peripheral Neuropathy: Mechanistic Insights From Studies in Mice.
Genevois AL; Ruel J; Penalba V; Hatton S; Petitfils C; Ducrocq M; Principe P; Dietrich G; Greco C; Delmas P
J Pain; 2021 Apr; 22(4):440-453. PubMed ID: 33227509
[TBL] [Abstract][Full Text] [Related]
15. 3'-O-Methylorobol Inhibits the Voltage-Gated Sodium Channel Nav1.7 with Anti-Itch Efficacy in A Histamine-Dependent Itch Mouse Model.
Zhang F; Wu Y; Xue S; Wang S; Zhang C; Cao Z
Int J Mol Sci; 2019 Dec; 20(23):. PubMed ID: 31805638
[TBL] [Abstract][Full Text] [Related]
16. Additive antinociceptive effects of the selective Nav1.8 blocker A-803467 and selective TRPV1 antagonists in rat inflammatory and neuropathic pain models.
Joshi SK; Honore P; Hernandez G; Schmidt R; Gomtsyan A; Scanio M; Kort M; Jarvis MF
J Pain; 2009 Mar; 10(3):306-15. PubMed ID: 19070548
[TBL] [Abstract][Full Text] [Related]
17. The small molecule compound C65780 alleviates pain by stabilizing voltage-gated sodium channels in the inactivated and slowly-recovering state.
Kong X; Li Y; Perez-Miller S; Luo G; Liao Q; Wu X; Liang S; Tang C; Khanna R; Liu Z
Neuropharmacology; 2022 Jul; 212():109057. PubMed ID: 35413303
[TBL] [Abstract][Full Text] [Related]
18. Distinct repriming and closed-state inactivation kinetics of Nav1.6 and Nav1.7 sodium channels in mouse spinal sensory neurons.
Herzog RI; Cummins TR; Ghassemi F; Dib-Hajj SD; Waxman SG
J Physiol; 2003 Sep; 551(Pt 3):741-50. PubMed ID: 12843211
[TBL] [Abstract][Full Text] [Related]
19. Bulleyaconitine A attenuates hyperexcitability of dorsal root ganglion neurons induced by spared nerve injury: The role of preferably blocking Nav1.7 and Nav1.3 channels.
Xie MX; Yang J; Pang RP; Zeng WA; Ouyang HD; Liu YQ; Liu XG
Mol Pain; 2018; 14():1744806918778491. PubMed ID: 29783906
[TBL] [Abstract][Full Text] [Related]
20. Inhibition of Nav1.7 channel by a novel blocker QLS-81 for alleviation of neuropathic pain.
Niu HL; Liu YN; Xue DQ; Dong LY; Liu HJ; Wang J; Zheng YL; Zou AR; Shao LM; Wang K
Acta Pharmacol Sin; 2021 Aug; 42(8):1235-1247. PubMed ID: 34103689
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
