The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
28131713 |
75 |
Discovery of MK-1832, a Kv1.5 inhibitor with improved selectivity and pharmacokinetics. |
Merck Research Laboratories |
25987375 |
20 |
Discovery of a novel Kv7 channel opener as a treatment for epilepsy. |
Pfizer |
25286150 |
75 |
Circumventing seizure activity in a series of G protein coupled receptor 119 (GPR119) agonists. |
Astrazeneca |
25087753 |
240 |
Prediction of Thorough QT study results using action potential simulations based on ion channel screens. |
University of Oxford |
24937104 |
30 |
GPR103 antagonists demonstrating anorexigenic activity in vivo: design and development of pyrrolo[2,3-c]pyridines that mimic the C-terminal Arg-Phe motif of QRFP26. |
Astrazeneca |
22793372 |
66 |
Discovery of a series of 2-phenyl-N-(2-(pyrrolidin-1-yl)phenyl)acetamides as novel molecular switches that modulate modes of K(v)7.2 (KCNQ2) channel pharmacology: identification of (S)-2-phenyl-N-(2-(pyrrolidin-1-yl)phenyl)butanamide (ML252) as a potent, brain penetrant K(v)7.2 channel inhibitor. |
Vanderbilt University Medical Center |
24900334 |
89 |
N-Pyridyl and Pyrimidine Benzamides as KCNQ2/Q3 Potassium Channel Openers for the Treatment of Epilepsy. |
TBA |
22607672 |
28 |
MK-8825: a potent and selective CGRP receptor antagonist with good oral activity in rats. |
Merck Research Laboratories |
11356099 |
20 |
Recent developments in the biology and medicinal chemistry of potassium channel modulators: update from a decade of progress. |
Abbott Laboratories |
21942426 |
113 |
Discovery of 1-amino-5H-pyrido[4,3-b]indol-4-carboxamide inhibitors of Janus kinase 2 (JAK2) for the treatment of myeloproliferative disorders. |
Merck |
21493064 |
69 |
Discovery of pyrimidine carboxamides as potent and selective CCK1 receptor agonists. |
Merck |
11689069 |
18 |
Synthesis and activity of novel and selective I(Ks)-channel blockers. |
Aventis Pharma Deutschland |
31566384 |
134 |
Development of Chemical Entities Endowed with Potent Fast-Killing Properties against |
Glaxosmithkline |
30869888 |
61 |
Discovery and Early Clinical Development of an Inhibitor of 5-Lipoxygenase Activating Protein (AZD5718) for Treatment of Coronary Artery Disease. |
TBA |
30879840 |
36 |
Potassium channel blocking 1,2-bis(aryl)ethane-1,2-diamines active as antiarrhythmic agents. |
Astrazeneca |
30429949 |
59 |
Discovery and Pharmacology of a Novel Somatostatin Subtype 5 (SSTR5) Antagonist: Synergy with DPP-4 Inhibition. |
Merck |
28753313 |
45 |
Neuroactive Steroids. 2. 3?-Hydroxy-3?-methyl-21-(4-cyano-1H-pyrazol-1'-yl)-19-nor-5?-pregnan-20-one (SAGE-217): A Clinical Next Generation Neuroactive Steroid Positive Allosteric Modulator of the (?-Aminobutyric Acid) |
Sage Therapeutics |
29172502 |
96 |
Discovery and Optimization of Pyrrolopyrimidine Inhibitors of Interleukin-1 Receptor Associated Kinase 4 (IRAK4) for the Treatment of Mutant MYD88 |
Astrazeneca |