serw-MX  [xml]  
 


    
 DeCS Categories

D12 Amino Acids, Peptides, and Proteins .
D12.776 Proteins .
D12.776.157 Carrier Proteins .
D12.776.157.530 Membrane Transport Proteins .
D12.776.157.530.400 Ion Channels .
D12.776.157.530.400.150 Calcium Channels .
D12.776.543 Membrane Proteins .
D12.776.543.550 Membrane Glycoproteins .
D12.776.543.550.450 Ion Channels .
D12.776.543.550.450.150 Calcium Channels .
D12.776.543.585 Membrane Transport Proteins .
D12.776.543.585.400 Ion Channels .
D12.776.543.585.400.150 Calcium Channels .
D27 Chemical Actions and Uses .
D27.505 Pharmacologic Actions .
D27.505.519 Molecular Mechanisms of Pharmacological Action .
D27.505.519.562 Membrane Transport Modulators .
D27.505.519.562.249 Calcium Channel Blockers .
D27.505.954 Therapeutic Uses .
D27.505.954.411 Cardiovascular Agents .
D27.505.954.411.192 Calcium Channel Blockers .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Calcium Channel Blockers .
Calcium Channel Antagonists .
Calcium Channel Blocking Drugs .
Exogenous Calcium Antagonists .
Exogenous Calcium Blockaders .
Exogenous Calcium Inhibitors .
Antagonists, Calcium Channel .
Antagonists, Exogenous Calcium .
Blockers, Calcium Channel .
Calcium Antagonists, Exogenous .
Calcium Blockaders, Exogenous .
Calcium Inhibitors, Exogenous .
Channel Blockers, Calcium .
A class of drugs that act by selective inhibition of calcium influx through cellular membranes. .
1.00
40035410
 
Calcium Channels .
Calcium Channel .
Calcium Channel Antagonist Receptor .
Calcium Channel Antagonist Receptors .
Calcium Channel Blocker Receptor .
Calcium Channel Blocker Receptors .
Ion Channel, Calcium .
Receptors, Calcium Channel Antagonist .
VDCC 13164 .
Voltage-Dependent Calcium Channels .
Calcium Channels, Voltage-Dependent .
Calcium Ion Channel .
Calcium Ion Channels .
Channels, Voltage-Dependent Calcium .
Voltage Dependent Calcium Channels .
Ion Channels, Calcium .
Receptors, Calcium Channel Blocker .
Voltage-dependent cell membrane glycoproteins selectively permeable to calcium ions. They are categorized as L-, T-, N-, P-, Q-, and R-types based on the activation and inactivation kinetics, ion specificity, and sensitivity to drugs and toxins. The L- and T-types are present throughout the cardiovascular and central nervous systems and the N-, P-, Q-, & R-types are located in neuronal tissue. .
0.84
11724724