The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
28233679 |
2 |
Synthesis and biological evaluation of novel N3-substituted dihydropyrimidine derivatives as T-type calcium channel blockers and their efficacy as analgesics in mouse models of inflammatory pain. |
South Dakota State University |
27517811 |
12 |
Synthesis and T-type calcium channel-blocking effects of aryl(1,5-disubstituted-pyrazol-3-yl)methyl sulfonamides for neuropathic pain treatment. |
Korea Institute of Science & Technology (Kist) |
27933950 |
304 |
Structure-Activity Relationship, Drug Metabolism and Pharmacokinetics Properties Optimization, and in Vivo Studies of New Brain Penetrant Triple T-Type Calcium Channel Blockers. |
Actelion Pharmaceuticals |
27579577 |
91 |
Preparation, Antiepileptic Activity, and Cardiovascular Safety of Dihydropyrazoles as Brain-Penetrant T-Type Calcium Channel Blockers. |
Actelion Pharmaceuticals |
26231163 |
50 |
Discovery of novel bridged tetrahydronaphthalene derivatives as potent T/L-type calcium channel blockers. |
Actelion Pharmaceuticals |
26101566 |
14 |
Optimization of ADME Properties for Sulfonamides Leading to the Discovery of a T-Type Calcium Channel Blocker, ABT-639. |
Abbvie |
25155913 |
32 |
Optimization of physicochemical properties and safety profile of novel bacterial topoisomerase type II inhibitors (NBTIs) with activity against Pseudomonas aeruginosa. |
Astrazeneca |
23200256 |
54 |
Discovery of N-[[1-[2-(tert-butylcarbamoylamino)ethyl]-4-(hydroxymethyl)-4-piperidyl]methyl]-3,5-dichloro-benzamide as a selective T-type calcium channel (Cav3.2) inhibitor. |
Astrazeneca |
18160281 |
10 |
Design and SAR of selective T-type calcium channel antagonists containing a biaryl sulfonamide core. |
Bristol-Myers Squibb R & D |
21316226 |
12 |
Pyridyl amides as potent inhibitors of T-type calcium channels. |
Merck Research Laboratories |
20934333 |
2 |
Design, syntheses, and SAR of 2,8-diazaspiro[4.5]decanones as T-type calcium channel antagonists. |
Icagen |
20659804 |
19 |
Synthesis and T-type calcium channel blocking activity of novel diphenylpiperazine compounds, and evaluation of in vivo analgesic activity. |
Ewha Womans University |
20580233 |
82 |
T-type calcium channel blockers: spiro-piperidine azetidines and azetidinones-optimization, design and synthesis. |
Merck Research Laboratory |
32327350 |
38 |
Synthesis and cytotoxic effects of 2-thio-3,4-dihydroquinazoline derivatives as novel T-type calcium channel blockers. |
Kyung Hee University |
27774123 |
37 |
Discovery of AZD2716: A Novel Secreted Phospholipase A |
Astrazeneca |
27591007 |
16 |
Synthesis and evaluation of 6-pyrazoylamido-3N-substituted azabicyclo[3,1,0]hexane derivatives as T-type calcium channel inhibitors for treatment of neuropathic pain. |
Korea Institute of Science & Technology (Kist) |
30869888 |
61 |
Discovery and Early Clinical Development of an Inhibitor of 5-Lipoxygenase Activating Protein (AZD5718) for Treatment of Coronary Artery Disease. |
TBA |
30928197 |
13 |
Structural hybridization of pyrrolidine-based T-type calcium channel inhibitors and exploration of their analgesic effects in a neuropathic pain model. |
Korea Institute of Science and Technology |
30031654 |
14 |
Design and synthesis of novel anti-hyperalgesic agents based on 6-prenylnaringenin as the T-type calcium channel blockers. |
University of Toyama |
29622412 |
64 |
Synthesis and evaluation of aminobenzothiazoles as blockers of N- and T-type calcium channels. |
Iitb-Monash Research Academy |
30034586 |
90 |
Design of Selective sPLA |
Astrazeneca |
29116786 |
265 |
Discovery of a Potent, Selective T-type Calcium Channel Blocker as a Drug Candidate for the Treatment of Generalized Epilepsies. |
Idorsia Pharmaceuticals |
29074257 |
115 |
Discovery and evaluation of Ca |
Idorsia Pharmaceuticals |
29066309 |
87 |
Discovery and evaluation of Ca |
Idorsia Pharmaceuticals |
28720324 |
7 |
Synthesis and diabetic neuropathic pain-alleviating effects of 2N-(pyrazol-3-yl)methylbenzo[d]isothiazole-1,1-dioxide derivatives. |
Korea University of Science and Technology (Ust) |
28720332 |
3 |
Synthesis and biological evaluation of fluoro-substituted 3,4-dihydroquinazoline derivatives for cytotoxic and analgesic effects. |
Kyung Hee University |
28530802 |
121 |
Discovery of N-(5-Fluoropyridin-2-yl)-6-methyl-4-(pyrimidin-5-yloxy)picolinamide (VU0424238): A Novel Negative Allosteric Modulator of Metabotropic Glutamate Receptor Subtype 5 Selected for Clinical Evaluation. |
Vanderbilt University Institute of Imaging Science |
15831442 |
46 |
Beneficial effects of a new 20-hydroxyeicosatetraenoic acid synthesis inhibitor, TS-011 [N-(3-chloro-4-morpholin-4-yl) phenyl-N'-hydroxyimido formamide], on hemorrhagic and ischemic stroke. |
Taisho Pharmaceutical |
8887981 |
72 |
A-85380 [3-(2(S)-azetidinylmethoxy) pyridine]: in vitro pharmacological properties of a novel, high affinity alpha 4 beta 2 nicotinic acetylcholine receptor ligand. |
Abbott Laboratories |
7518514 |
46 |
(S)-3-methyl-5-(1-methyl-2-pyrrolidinyl) isoxazole (ABT 418): a novel cholinergic ligand with cognition-enhancing and anxiolytic activities: I. In vitro characterization. |
Abbott Laboratories |