Detalhe da pesquisa
1.
KATP Channel Prodrugs Reduce Inflammatory and Neuropathic Hypersensitivity, Morphine-Induced Hypersensitivity, and Precipitated Withdrawal in Mice.
J Pharmacol Exp Ther
; 387(1): 18-26, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36931644
2.
The anthelmintic drug praziquantel activates a schistosome transient receptor potential channel.
J Biol Chem
; 294(49): 18873-18880, 2019 12 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31653697
3.
Differential Evolution for the Optimization of DMSO-Free Cryoprotectants: Influence of Control Parameters.
J Biomech Eng
; 142(7)2020 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31891381
4.
Characterizing modes of action and interaction for multicomponent osmolyte solutions on Jurkat cells.
Biotechnol Bioeng
; 116(3): 631-643, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30475391
5.
ATP sensitive potassium channel openers: A new class of ocular hypotensive agents.
Exp Eye Res
; 158: 85-93, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27130546
6.
Ursodeoxycholic Acid Inhibits Clostridium difficile Spore Germination and Vegetative Growth, and Prevents the Recurrence of Ileal Pouchitis Associated With the Infection.
J Clin Gastroenterol
; 50(8): 624-30, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-26485102
7.
ATP sensitive potassium channel openers: A new class of ocular hypotensive agents.
Exp Eye Res
; 178: 225, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27353766
8.
Effects of cabergoline and dimethylcabergoline on the sexual behavior of male rats.
Psychopharmacology (Berl)
; 241(4): 717-726, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-37968530
9.
Preclinical Pharmacokinetic Profile of Topical Ophthalmic and Intravenous Delivery of QLS-101, a Novel ATP-Sensitive Potassium Channel Opening Ocular Hypotensive Agent.
J Ocul Pharmacol Ther
; 39(5): 332-346, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37200453
10.
Effect of ATP-sensitive Potassium Channel Openers on Intraocular Pressure in Ocular Hypertensive Animal Models.
Invest Ophthalmol Vis Sci
; 63(2): 15, 2022 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35129587
11.
Ocular Hypotensive Properties and Biochemical Profile of QLS-101, a Novel ATP-Sensitive Potassium (KATP) Channel Opening Prodrug.
Invest Ophthalmol Vis Sci
; 63(4): 26, 2022 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35486069
12.
Structural modifications that increase gut restriction of bile acid derivatives.
RSC Med Chem
; 12(3): 394-405, 2021 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34046622
13.
Pharmacological Profile and Ocular Hypotensive Effects of Cromakalim Prodrug 1, a Novel ATP-Sensitive Potassium Channel Opener, in Normotensive Dogs and Nonhuman Primates.
J Ocul Pharmacol Ther
; 37(5): 251-260, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33784195
14.
Convenient Protocol for Production and Purification of Clostridioides difficile Spores for Germination Studies.
STAR Protoc
; 1(2): 100071, 2020 09 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-33111107
15.
Pharmacological and pharmacokinetic profile of the novel ocular hypotensive prodrug CKLP1 in Dutch-belted pigmented rabbits.
PLoS One
; 15(4): e0231841, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32298376
16.
Flash-vacuum-pyrolytic reorganization of angular [4]phenylene.
Chem Commun (Camb)
; (15): 1967-9, 2009 Apr 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-19333459
17.
Solubilized phenyl-pyrazole ureas as potent, selective 5-HT(2A) inverse-agonists and their application as antiplatelet agents.
Bioorg Med Chem Lett
; 19(18): 5486-9, 2009 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19665894
18.
7-Methylation of Chenodeoxycholic Acid Derivatives Yields a Substantial Increase in TGR5 Receptor Potency.
J Med Chem
; 62(14): 6824-6830, 2019 07 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-31268316
19.
Discovery and structure-activity relationship of (1R)-8-chloro-2,3,4,5-tetrahydro-1-methyl-1H-3-benzazepine (Lorcaserin), a selective serotonin 5-HT2C receptor agonist for the treatment of obesity.
J Med Chem
; 51(2): 305-13, 2008 Jan 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-18095642
20.
Activation of host transient receptor potential (TRP) channels by praziquantel stereoisomers.
PLoS Negl Trop Dis
; 12(4): e0006420, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29668703