formaldehyde has been researched along with cilnidipine in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hagiwara, K; Iijima, T; Miyoshi, I; Mobarakeh, II; Mori, T; Murakami, M; Murata, A; Nakagawasai, O; Sakurada, Y; Tadano, T; Tan-No, K; Yamadera, F; Yanai, K | 1 |
| Fujita, S; Iwata, S; Kito, M; Koganei, H; Matsueda, H; Niwa, S; Ohno, S; Onishi, T; Ono, Y; Saitou, Y; Shoji, M; Takahara, A; Takeda, T; Uneyama, H; Yamamoto, T | 1 |
| Iwata, S; Koganei, H; Shoji, M | 1 |
3 other study(ies) available for formaldehyde and cilnidipine
| Article | Year |
|---|---|
Inhibitory effect of pranidipine on N-type voltage-dependent Ca2+ channels in mice.
Topics: Animals; Animals, Newborn; Behavior, Animal; Calcium; Calcium Channel Blockers; Calcium Channels, N-Type; Cells, Cultured; Dicarbethoxydihydrocollidine; Dihydropyridines; Dose-Response Relationship, Drug; Formaldehyde; Ganglia, Spinal; Membrane Potentials; Mice; Neurons; Pain; Pain Measurement; Patch-Clamp Techniques; Potassium Chloride; Time Factors | 2004 |
Structure-activity relationship study of 1,4-dihydropyridine derivatives blocking N-type calcium channels.
Topics: Animals; Calcium Channel Blockers; Calcium Channels, N-Type; Dihydropyridines; Formaldehyde; Molecular Structure; Pain; Pain Measurement; Rats; Structure-Activity Relationship | 2006 |
Suppression of formalin-induced nociception by cilnidipine, a voltage-dependent calcium channel blocker.
Topics: Administration, Oral; Amines; Analgesics; Animals; Calcium Channel Blockers; Calcium Channels, N-Type; Cyclohexanecarboxylic Acids; Dihydropyridines; Formaldehyde; Gabapentin; gamma-Aminobutyric Acid; Male; Models, Animal; Nifedipine; omega-Conotoxins; Pain; Rats; Rats, Sprague-Dawley; Spinal Cord | 2009 |