Product overview

Name GV-58
Purity >97%
Description Selective N- and P/Q-type Ca2+-channel agonist
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Biological Data

Biological description Selective N- and P/Q-type Ca2+-channel agonist. These Ca2+-channels regulate transmitter release in synapses. Potential lead compound for a variety of disorders that result in neuromuscular weakness.

Solubility & Handling

Storage instructions +4°C
Storage of solutions Prepare and use solutions on the same day if possible. Store solutions at -20°C for up to one month if storage is required. Equilibrate to RT and ensure the solution is precipitate free before use.
Shipping Conditions Stable for ambient temperature shipping. Follow storage instructions on receipt.
Important This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.

Calculators

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Dilution

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Chemical Data

Purity >97%
Chemical name (2R)-2-[[6-[[(5-Methyl-2-thienyl)methyl]amino]-9-propyl-9H-purin-2-yl]amino]-1-butanol
Molecular Weight 374.5
Chemical structure GV-58 Chemical Structure
Molecular Formula C18H26N6OS
CAS Number 1402821-41-3
InChiKey DPTXJOUVBMUSGY-CYBMUJFWSA-N
Appearance White to off-white solid

References for GV-58

References are publications that support the biological activity of the product
  • Potentiation of neuromuscular transmission by a small molecule calcium channel gating modifier improves motor function in a severe spinal muscular atrophy mouse model.

    Ojala KS et al (2023) Human molecular genetics 32 : 1901-1911
  • Activation of Voltage-Gated Na(+) Current by GV-58, a Known Activator of Ca(V) Channels.

    Cho HY et al (2022) Biomedicines 10 :
  • Evaluation of a novel calcium channel agonist for therapeutic potential in Lambert-Eaton myasthenic syndrome.

    Tarr TB et al (2013) The Journal of neuroscience : the official journal of the Society for Neuroscience 33 : 10559-67

3 Item(s)