Open main menu
Home
Random
Recent changes
Special pages
Community portal
Preferences
About Wikipedia
Disclaimers
Incubator escapee wiki
Search
User menu
Talk
Dark mode
Contributions
Create account
Log in
Editing
Calcium channel blocker
(section)
Warning:
You are not logged in. Your IP address will be publicly visible if you make any edits. If you
log in
or
create an account
, your edits will be attributed to your username, along with other benefits.
Anti-spam check. Do
not
fill this in!
==== Phenylalkylamine ==== [[Image:Verapamil skeletal.svg|thumb|class=skin-invert-image|[[Skeletal formula]] of [[verapamil]]]] Phenylalkylamine calcium channel blockers are relatively selective for myocardium, reduce myocardial oxygen demand and reverse coronary vasospasm, and are often used to treat angina. They have minimal vasodilatory effects compared with dihydropyridines and therefore cause less reflex tachycardia, making it appealing for treatment of angina, where tachycardia can be the most significant contributor to the heart's need for oxygen. Therefore, as vasodilation is minimal with the phenylalkylamines, the major mechanism of action is causing negative inotropy. Phenylalkylamines are thought to access calcium channels from the intracellular side, although the evidence is somewhat mixed.<ref>{{Cite journal |last=Hockerman, G.H. |last2=Peterson, B.Z. |last3=Johnson, B.D. |last4=Catterall, W.A. |year=1997 |title=Molecular Determinants of Drug Binding and Action on L-Type Calcium Channels |journal=Annual Review of Pharmacology and Toxicology |volume=37 |pages=361β96 |doi=10.1146/annurev.pharmtox.37.1.361 |pmid=9131258 |s2cid=16275155}}</ref> * [[Fendiline]] * [[Gallopamil]] * [[Verapamil]] (Calan, Isoptin)
Edit summary
(Briefly describe your changes)
By publishing changes, you agree to the
Terms of Use
, and you irrevocably agree to release your contribution under the
CC BY-SA 4.0 License
and the
GFDL
. You agree that a hyperlink or URL is sufficient attribution under the Creative Commons license.
Cancel
Editing help
(opens in new window)