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  • Calcium Channel
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Results for "

α2δ calcium channels

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    10
    TargetMol | Inhibitors_Agonists
  • Natural Products
    1
    TargetMol | Natural_Products
Atagabalin HCl
PD-0200390 HCl, Atagabalin HCl(223445-75-8 Free base)
T30188L223445-67-8In house
Atagabalin HCl is a novel voltage-dependent calcium channel (VDCC) α2δ subunit (1 and 2) ligand that affects slow-wave sleep and can be used to treat insomnia.
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L-Phenylalanine
phenylalanine, 3-Phenyl-L-alanine, (S)-2-Amino-3-phenylpropionic acid
T337763-91-2
L-Phenylalanine (3-Phenyl-L-alanine) is an essential amino acid and the precursor of the amino acid tyrosine, acts as an antagonist at α2δ calcium channels.
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Gabapentin hydrochloride
Neurontin HCl, Gabapentin HCl
T650760142-95-2
Gabapentin hydrochloride (Neurontin HCl) is a GABA analogue, used to treat seizures and neuropathic pain.
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Atagabalin
PD 0200390,PD-0200390,PD0200390
T30188223445-75-8In house
Atagabalin, also known as PD 0200390, is a gabamimetic agent under development for the treatment for insomnia. Atagabalin is related to gabapentin, which similarly binds to the α2δ calcium channels (1 and 2). It was discontinued following unsatisfactory t
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Mirogabalin
DS5565
T72161138245-13-2
Mirogabalin (DS5565) is a calcium channel blocker with analgesic effects.
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1-(aminomethyl)cyclopropanecarboxylic acid hydrochloride
T776421421601-23-1
1-(aminomethyl)cyclopropanecarboxylic acid hydrochloride inhibits L amino acid transporter proteins and the α2δ subunit of voltage-gated calcium channels.1-(aminomethyl)cyclopropanecarboxylic acid hydrochloride can be used as a biological module for the synthesis of active biochemical reagents.
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(rel)-Mirogabalin
(rel)-DS5565
T2005061138244-97-9
(rel)-Mirogabalin ((rel)-DS5565) is an inhibitor of voltage-dependent calcium channels, specifically targeting the α2δ-1 subunit.
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3-6 months
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Mirogabalin besylate
T614341138245-21-2
Mirogabalin besylate is a potent and orally active ligand that selectively targets the α2δ subunit of voltage-gated calcium channels. It displays high affinity (K d ) values, namely 13.5 nM, 22.7 nM, 27 nM, and 47.6 nM, for human α2δ-1, human α2δ-2, rat α2δ-1, and rat α2δ-2, respectively.
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1-2 weeks
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Cavα2δ1&NET-IN-3
T727012143584-82-9
Cavα2δ1&NET-IN-3 (example 216) is an inhibitor targeting both the α2δ subunit of voltage-gated calcium channels (VGCC) and the noradrenaline transporter (NET), exhibiting inhibitory constants (Ki) ranging from 100 to 500 nM for the human α2δ-1 subunit of the Cav2.2 calcium channel and NET, respectively.
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8-10 weeks
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Phenibut (hydrochloride)
3-Amino-4-phenylbutyric acid hydrochloride
T86393060-41-1
Phenibut hydrochloride (3-Amino-4-phenylbutyric acid hydrochloride) is a GABA mimetic that acts as an agonist at GABAB receptors, blocks α2δ subunit-containing voltage-gated calcium channels, stimulates dopamine receptors, and inhibits the actions of β-phenethylamine
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