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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 1 to 20 (out of 27 products)
  • (R)(+)-Bay K8644

    A Blocker of L-Type CaChannels

    Cat # B-352
    Source Synthetic
    MW 356.3
    Target L-type Ca2+ channels
    • Bioassay Tested
  • Benidipine hydrochloride

    A Dihydropyridine Blocker of Voltage-Gated Ca2+ Channels

    Cat # B-120
    Source Synthetic
    MW 542
    Target CaV1, CaV3 Ca2+ channels
    • Bioassay Tested
  • Calcicludine

    A Blocker of Neuronal L-Type CaV Channels

    Cat # SPC-650
    MW 6979 Da.
    Target L-type Ca2+ channels
    • Bioassay Tested
  • Calciseptine

    A Specific Blocker of L-Type CaV Channels

    Cat # SPC-500
    MW 7036 Da.
    Target L-type Ca2+ channels
    • Bioassay Tested
  • Cilnidipine

    A Blocker of L- and N-Type CaV Channels 

    Cat # C-135
    Source Synthetic
    MW 492.5
    Target L- and N-type Ca2+ channels
    • Bioassay Tested
  • FS-2

    A Blocker of L-Type CaV Channels

    Cat # F-700
    MW 7026 Da.
    Target L-type Ca2+ channels
    • Bioassay Tested
  • L-651,582

    An Effective Blocker of L-Type CaV Channels

    Cat # L-110
    Source Synthetic
    MW 424.7
    Target L-type Ca2+ channels
    • Bioassay Tested
  • Lomerizine dihydrochloride

    A Blocker of L-Type Voltage-Gated Ca2+ Channels

    Cat # L-125
    Source Synthetic
    MW 541.5
    Target L-type Ca2+ channels
    • Bioassay Tested

* See product page

Displaying 1 to 20 (out of 27 products)