Overview
Cat #:
G-140
Lyophilized Powder yes
Source Synthetic
MW: 374.2
Purity: >98%
Form Lyophilized powder.
Effective concentration 1-100 µM.
Structure
Chemical name (2R)-2-[(6-{[(5-Methylthiophen-2-yl)methyl]amino}-9-propyl-9H-purin-2-yl)amino]butan-1-ol.
Molecular formula C18H26N6OS.
CAS No.: 1402821-41-3
Activity GV-58 is an opener of N- and P/Q-type Ca2+ channels1.
References-Activity
- Tarr, T.B. et al. (2013) J. Neurosci. 33, 10559.
Shipping and storage Shipped at room temperature. Product as supplied can be stored intact at room temperature for several weeks. For longer periods, it should be stored at -20°C.
Solubility 100 mM in DMSO. Centrifuge all product preparations before use (10000 x g for 1 min).
Storage of solutions Up to four weeks at 4°C or three months at -20°C.
Our bioassay
- Alomone Labs GV-58 increases P/Q-type CaV channel tail currents expressed in Xenopus oocytes.A. Time course of CaV2.1 (co-expressed with α2δ1 and β1 auxiliary subunits) normalized tail current area (see tails in panel B, at the end of the ramp stimulation, back at -100 mV), elicited by 100 ms voltage ramp from holding potential of -100 mV to +50 mV (see panel B, top), delivered every 10 seconds. Application of 20 and 100 µM GV-58 (#G-140) increases the CaV2.1 tail current (periods of application are indicated by the horizontal bars) up to 18 fold, in a reversible manner. B. Representative current traces before and during application of 20 and 100 µM GV-58 as indicated. Note the lack of effect on CaV currents during the ramp stimulation.
References - Scientific background
- Tarr, T.B. et al. (2012) Ann. N. Y. Acad. Sci. 1275, 85.
- Liang, M. et al. (2012) ACS Med. Chem. Lett. 3, 985.
Scientific background
GV-58, a Ca2+ channel agonist, is selective for N- (CaV2.2) and P/Q-type (CaV2.1) channels. GV-58 was developed as a modification of (R)-roscovitine, which was previously shown to be a Ca2+ channel agonist. 100 μM GV-58 was originally tested on N-, P/Q-, or L-type channels expressed in tsA-201 cells. GV-58 was shown to be more potent on N- and P/Q Ca2+ channels with an EC50 = 6.8 and 9.9 μM, respectively over L-type calcium channels (EC50 > 100 μM)1. GV-58 slows the closing of the channel, resulting in a large increase in total Ca2+ entry during motor nerve action potential activity.
GV-58 is being tested for the treatment of neuromuscular weakness2.
Target CaV2.1, CaV2.2 Ca2+ channels
Lyophilized Powder
GV-58 (#G-140) is a highly pure, synthetic, and biologically active compound.
Image & Title
Alomone Labs GV-58 activates presynaptic Ca2+ influx in rat neuronal cells.Representative whole cell recordings of evoked neurotransmission in cultures treated with vehicle or GV-58 (#G-140).Adapted from Beske, P.H. et al. (2017) Sci. Rep. 7, 15862. with permission of SPRINGER NATURE.
Alomone Labs GV-58 activates presynaptic Ca2+ influx in rat neuronal cells.Representative whole cell recordings of evoked neurotransmission in cultures treated with vehicle or GV-58 (#G-140).Adapted from Beske, P.H. et al. (2017) Sci. Rep. 7, 15862. with permission of SPRINGER NATURE.
For research purposes only, not for human use
Last Update: 07/05/2024
Applications
Citations
Citations
Product citations
- Beske, P.H. et al. (2017) Sci. Rep. 7, 15862.
- Tedeschi, A. et al. (2016) Neuron 92, 419.