The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
2391701 |
26 |
Dihydropyrimidine calcium channel blockers. 2. 3-substituted-4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridines. |
Squibb Institute For Medical Research |
2840498 |
10 |
Dimeric 1,4-dihydropyridines as calcium channel antagonists. |
State University of New York |
3339603 |
9 |
Crystal structures and pharmacologic activities of 1,4-dihydropyridine calcium channel antagonists of the isobutyl methyl 2,6-dimethyl-4-(substituted phenyl)-1,4-dihydropyridine-3,5-dicarboxylate (nisoldipine) series. |
University of Oslo |
26101566 |
14 |
Optimization of ADME Properties for Sulfonamides Leading to the Discovery of a T-Type Calcium Channel Blocker, ABT-639. |
Abbvie |
21300721 |
90 |
Simulation of multiple ion channel block provides improved early prediction of compounds' clinical torsadogenic risk. |
University of Oxford |
11585444 |
295 |
From hit to lead. Analyzing structure-profile relationships. |
Universities of Lille |
| 15 |
Phenyl-glycinol based NK1 receptor antagonists — towards the minimum pharmacophore |
TBA |
31724859 |
23 |
New Dual Small Molecules for Alzheimer's Disease Therapy Combining Histamine H |
Universit£ |
30538065 |
48 |
The discovery and optimization of benzimidazoles as selective Na |
Pfizer |
23812503 |
55 |
MICE models: superior to the HERG model in predicting Torsade de Pointes. |
Chantest |
8377012 |
2 |
Polycyclic guanidine alkaloids from the marine sponge Crambe crambe and Ca++ channel blocker activity of crambescidin 816. |
University of Brussels |
30052039 |
172 |
Design, Synthesis, and Pharmacological Evaluation of Second-Generation Tetrahydroisoquinoline-Based CXCR4 Antagonists with Favorable ADME Properties. |
Emory University |
2142737 |
14 |
4-Isoxazolyl-1,4-dihydropyridines: biological, theoretical, and structural studies. |
State University of New York |