CNV1014802
CAS No. 934240-30-9
CNV1014802( GSK-1014802 | CNV-1014802 | Raxatrigine | Vixotrigine | BIIB074 )
Catalog No. M16676 CAS No. 934240-30-9
CNV1014802 (GSK-1014802, Raxatrigine, Vixotrigine, BIIB074) is a potent, selective Nav1.7 sodium channel blocker.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
2MG | 86 | In Stock |
|
5MG | 132 | In Stock |
|
10MG | 213 | In Stock |
|
25MG | 353 | In Stock |
|
50MG | 528 | In Stock |
|
100MG | 753 | In Stock |
|
200MG | Get Quote | In Stock |
|
500MG | Get Quote | In Stock |
|
1G | Get Quote | In Stock |
|
Biological Information
-
Product NameCNV1014802
-
NoteResearch use only, not for human use.
-
Brief DescriptionCNV1014802 (GSK-1014802, Raxatrigine, Vixotrigine, BIIB074) is a potent, selective Nav1.7 sodium channel blocker.
-
DescriptionCNV1014802 (GSK-1014802, Raxatrigine, Vixotrigine, BIIB074) is a potent, selective Nav1.7 sodium channel blocker, shows analgesic effects and potential in the treatment of cognitive symptoms of schizophrenia in vivo.Pain Phase 2 Clinical(In Vitro):Like lamotrigine, both GSK2 and GSK3 were able to prevent the deficit in reversal learning produced by PCP, thus confirming their potential in the treatment of cognitive symptoms of schizophrenia. However, higher doses than those required for anticonvulsant efficacy of the drugs were needed for activity in the reversal-learning model, suggesting a lower therapeutic window relative to mechanism-dependent central side effects for this indication. Raxatrigine (GSK-1014802) received orphan-drug designation from the US Food and Drug Administration in July 2013.
-
In VitroLike lamotrigine, both GSK2 and GSK3 were able to prevent the deficit in reversal learning produced by PCP, thus confirming their potential in the treatment of cognitive symptoms of schizophrenia. However, higher doses than those required for anticonvulsant efficacy of the drugs were needed for activity in the reversal-learning model, suggesting a lower therapeutic window relative to mechanism-dependent central side effects for this indication. Raxatrigine (GSK-1014802) received orphan-drug designation from the US Food and Drug Administration.
-
In Vivo——
-
SynonymsGSK-1014802 | CNV-1014802 | Raxatrigine | Vixotrigine | BIIB074
-
PathwayMembrane Transporter/Ion Channel
-
TargetSodium Channel
-
RecptorSodiumChannel
-
Research AreaNeurological Disease
-
IndicationPain
Chemical Information
-
CAS Number934240-30-9
-
Formula Weight314.3541
-
Molecular FormulaC18H19FN2O2
-
Purity>98% (HPLC)
-
Solubility10 mM in DMSO
-
SMILESC1CC(NC1C2=CC=C(C=C2)OCC3=CC=CC=C3F)C(=O)N
-
Chemical Name2-Pyrrolidinecarboxamide, 5-[4-[(2-fluorophenyl)methoxy]phenyl]-, (2S,5R)-
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Bagal SK, et al. Bioorg Med Chem Lett. 2014 Aug 15;24(16):3690-9.
2. Deuis JR, et al. Toxins (Basel). 2016 Mar 17;8(3). pii: E78.
3. Zakrzewska JM, et al. Lancet Neurol. 2017 Apr;16(4):291-300.
molnova catalog
related products
-
Rimeporide hydrochlo...
Rimeporide (EMD-87580) is a potent and selective Sodium hydrogen exchange 1 (NHE-1) inhibitor.
-
Bulleyaconi cine A
Bulleyaconitine A is an analgesic and antiinflammatory drug isolated from Aconitum plants; has several potential targets, including voltage-gated Na+ channels.
-
Tenapanor
Tenapanor (AZD-1722;RDX5791) is a potent, selective inhibitor of the Na+/H+ exchanger 3 (NHE3) with IC50 of 5 and 10 nM for human and rat NHE3, respectively.