GS967
CAS No. 1262618-39-2
GS967 ( GS967; GS-967; GS 967; GS458967 )
Catalog No. M11095 CAS No. 1262618-39-2
GS967 is a novel, potent, and selective inhibitor of cardiac late sodium current(late INa).
Purity : >98%(HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
2MG | 27 | In Stock |
|
5MG | 43 | In Stock |
|
10MG | 65 | In Stock |
|
25MG | 146 | In Stock |
|
50MG | 268 | In Stock |
|
100MG | 470 | In Stock |
|
200MG | 680 | In Stock |
|
500MG | 1053 | In Stock |
|
1G | Get Quote | In Stock |
|
Biological Information
-
Product NameGS967
-
NoteResearch use only, not for human use.
-
Brief DescriptionGS967 is a novel, potent, and selective inhibitor of cardiac late sodium current(late INa).
-
DescriptionGS967 is a novel, potent, and selective inhibitor of cardiac late sodium current(late INa); inhibits ATX-II-induced late I(Na) in ventricular myocytes and isolated hearts with IC(50) values of 0.13 and 0.21 μM, respectively.
-
SynonymsGS967; GS-967; GS 967; GS458967
-
PathwayMembrane Transporter/Ion Channel
-
TargetSodium Channel
-
RecptorlateINa,isolated hearts; lateINa,ventricular myocytes
-
Research AreaCardiovascular Disease
-
Indication——
Chemical Information
-
CAS Number1262618-39-2
-
Formula Weight347.22
-
Molecular FormulaC14H7F6N3O
-
Purity>98%(HPLC)
-
SolubilityDMSO: 10 mM
-
SMILESFC(C1=NN=C2C=CC(C3=CC=C(OC(F)(F)F)C=C3)=CN21)(F)F
-
Chemical Name6-(4-(trifluoromethoxy)phenyl)-3-(trifluoromethyl)(1,2,4)triazolo(4,3-a)pyridine
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Belardinelli L, et al. J Pharmacol Exp Ther. 2013 Jan;344(1):23-32.
molnova catalog
related products
-
APETx2
Acid-sensing ion channel 3 (ASIC3) channel blocker (IC50 values are 63 and 175 nM for homomeric rat and human ASIC3 channels). Also inhibits NaV1.8 and NaV1.2 channels (IC50 values are 55 and 114 nM respectively). Demonstrates analgesic properties against acid-induced and inflammatory pain.
-
Benzocaine
Benzocaine is a local anesthetic; inhibits voltage-dependent sodium channels (VDSCs) on the neuron membrane, stopping the propagation of the action potential.
-
Proparacaine hydroch...
An irreversible local anesthetic; inhibits pain sensations that is believed to act as an antagonist on voltage-gated sodium channels.