Blockers

L-Type (CaV1) Channels

Blockers

L-type Ca2+ channels include four different isoforms of the α1 pore-forming subunit: CaV1.1, CaV1.2, CaV1.3 and CaV1.4. Their expression is detected in muscle, heart, retina and neurons where they play important roles in muscle contraction, hormone secretion, neuronal excitability and gene expression.

Displaying 21 to 27 (out of 27 products)
  • Nicardipine HCl

    A Potent Dihydropyridine Blocker of Ca2+ Channels

    Cat # N-125
    Source Synthetic
    MW 515.9
    Target L-type and T-type Ca2+ channels
  • Nifedipine

    A Blocker of L-Type CaV Channels

    Cat # N-120
    Source Synthetic
    MW 346.3
    Target L-type CaV channels
  • Nimodipine

    A Potent Blocker of L-Type CaV Channels

    Cat # N-150
    Source Synthetic
    MW 418.4
    Target L-type Ca2+ channels
  • Nisoldipine

    A Potent and Selective Blocker of L-type CaV Channels

    Cat # N-160
    Source Synthetic
    MW 388.4
    Target L-type Ca2+ channels
  • Nitrendipine

    A Potent and Selective Blocker of L-type CaV Channels

    Cat # N-155
    Source Synthetic
    MW 360.4
    Target L-type Ca2+ channels
  • SR 33805 oxalate

    A Specific Blocker of L-Type CaV Channels

    Cat # S-105
    Source Synthetic
    MW 654.77
    Target L-type Ca2+ channels
  • Verapamil HCl

    A Potent Phenylalkylamine Blocker of L-type Ca2+ Channels

    Cat # V-100
    Source Synthetic
    MW 491.1
    Target L-type Ca2+ channels

* See product page

Displaying 21 to 27 (out of 27 products)