GV-58
CAS No. 1402821-41-3
GV-58( GV58 )
Catalog No. M11683 CAS No. 1402821-41-3
GV-58 is a potent, selective N-Type and P/Q-type Ca2+ Channel agonist with EC50 of 7.2 and 8.8 uM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 154 | In Stock |
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| 5MG | 140 | In Stock |
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| 10MG | 217 | In Stock |
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| 25MG | 432 | In Stock |
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| 50MG | 611 | In Stock |
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| 100MG | 854 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | 1702 | In Stock |
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| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameGV-58
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NoteResearch use only, not for human use.
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Brief DescriptionGV-58 is a potent, selective N-Type and P/Q-type Ca2+ Channel agonist with EC50 of 7.2 and 8.8 uM.
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DescriptionGV-58 is a potent, selective N-Type and P/Q-type Ca2+ Channel agonist with EC50 of 7.2 and 8.8 uM, shows no acitivity for L-type calcium channels (EC50>100 uM); has 20-fold less potent cyclin-dependent kinase antagonist effect; slows deactivation (closing) of the channel, resulting in a large increase in total calcium entry during motor nerve action potential activity; weakens Lambert-Eaton myasthenic syndrome-model neuromuscular synapses in a passive transfer mouse model of Lambert-Eaton myasthenic syndrome.
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In VitroGV-58 (50 μM; 30 min) restores function in LEMS passive transfer neuromuscular junction. Cell Viability Assay Cell Line:Upper arm muscle isolated from LEMS mice Concentration:50 μM Incubation Time:30 min Result:Increased the mEPP frequency from 3.27 s?1 in vehicle controls to 10.45 s?1. Showed a slight facilitation followed by depression to ~94% at the final EPP in the train.
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In Vivo——
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SynonymsGV58
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PathwayGPCR/G Protein
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TargetCalcium Channel
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RecptorCalcium Channel
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Research AreaNeurological Disease
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Indication——
Chemical Information
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CAS Number1402821-41-3
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Formula Weight374.5036
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Molecular FormulaC18H26N6OS
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESCCCN1C=NC2=C(N=C(N=C21)NC(CC)CO)NCC3=CC=C(S3)C
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Chemical Name1-Butanol, 2-[[6-[[(5-methyl-2-thienyl)methyl]amino]-9-propyl-9H-purin-2-yl]amino]-, (2R)-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Azumolene
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Ziconotide Acetate ...
Ziconotide is an analgesic agent and has been used to treat neuropathic and non-neuropathic pain. Ziconotide acts by binding to N-type calcium channels situated on the terminal part of primary afferent neurons of the nociceptive pathway therefore reducing synaptic transmission with potent antinociceptive effects.
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