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Isoforms Recommended: P/Q-type calcium channel
Results for "

CaV2.1

" in MedChemExpress (MCE) Product Catalog:

7

Inhibitors & Agonists

3

Peptides

3

Oligonucleotides

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-120751

    Calcium Channel Neurological Disease
    TROX-1 is a selective, orally active and brain-penetrant N-type calcium channel (Cav2.2) inhibitor with an IC50 value of 0.11 μM. TROX-1 exerts state-dependent and use-dependent inhibition, preferentially targets open/inactivated channels, blocks depolarization-associated calcium influx, and fully blocks calcium influx in rat dorsal root ganglion neurons. TROX-1 reverses inflammatory-induced hyperalgesia, nerve injury-induced allodynia. TROX-1 can be used for the research of pain .
    TROX-1
  • HY-P1080
    ω-Agatoxin IVA
    1 Publications Verification

    Calcium Channel Cardiovascular Disease Neurological Disease
    ω-Agatoxin IVA is a potent, selective P/Q type Ca 2+ (Cav2.1) channel blocker with IC50 values of 2 nM and 90 nM. ω-Agatoxin IVA inhibits glutamate exocytosis and calcium influx elicited by high potassium. ω-Agatoxin IVA inhibits Capsaicin (HY-10448)-induced CGRP release and vasodilation. ω-Agatoxin IVA can be used for the research of neurological and cardiovascular disease .
    ω-Agatoxin IVA
  • HY-P1080A
    ω-Agatoxin IVA TFA
    1 Publications Verification

    Calcium Channel Neurological Disease
    ω-Agatoxin IVA TFA is a potent, selective P/Q type Ca 2+ (Cav2.1) channel blocker with IC50 values of 2 nM and 90 nM. ω-Agatoxin IVA TFA inhibits glutamate exocytosis and calcium influx elicited by high potassium. ω-Agatoxin IVA TFA inhibits Capsaicin (HY-10448)-induced CGRP release and vasodilation. ω-Agatoxin IVA TFA can be used for the research of neurological and cardiovascular disease .
    ω-Agatoxin IVA TFA
  • HY-P3269

    Calcium Channel Cardiovascular Disease
    Calciseptine is a natural polypeptide toxin found in the venom of the black mamba snake (Dendroaspis p. polylepis). Calciseptine is a highly effective and selective blocker of the L-type channel of the Cav1.2 subtype, with an IC50 value of 92 nM. Calciseptine has no effect on Cav3.1, Cav2.2, Cav2.1, Cav1.1, voltage-sensitive sodium channels and potassium channels. Calciseptine exhibits negative inotropic and negative relaxant effects on mice, and does not affect heart rate or the action potential of sinoatrial node pacemaker cells. Calciseptine can be used for research on cardiovascular diseases[1].
    Calciseptine
  • HY-RS01791

    Small Interfering RNA (siRNA) Others

    CACNA1A Human Pre-designed siRNA Set A contains three designed siRNAs for CACNA1A gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    CACNA1A Human Pre-designed siRNA Set A
    CACNA1A Human Pre-designed siRNA Set A
  • HY-RS21232

    Small Interfering RNA (siRNA) Others

    Cacna1a Mouse Pre-designed siRNA Set A contains three designed siRNAs for Cacna1a gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

    Cacna1a Mouse Pre-designed siRNA Set A
    Cacna1a Mouse Pre-designed siRNA Set A
  • HY-RS27749

    Small Interfering RNA (siRNA) Others
    Cacna1a Rat Pre-designed siRNA Set A contains three designed siRNAs for Cacna1a gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
    Cacna1a Rat Pre-designed siRNA Set A
    Cacna1a Rat Pre-designed siRNA Set A

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