Cart
sales@molnova.com
Metaflumizone
CAS No. 139968-49-3
Metaflumizone( BAS-320I )
Catalog No. M20643 CAS No. 139968-49-3
Metaflumizone is a sodium channel blocker insecticide.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 30 | In Stock |
|
| 100MG | 28 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 84 | In Stock |
|
| 1G | 123 | In Stock |
|
Biological Information
-
Product NameMetaflumizone
-
NoteResearch use only, not for human use.
-
Brief DescriptionMetaflumizone is a sodium channel blocker insecticide.
-
DescriptionMetaflumizone is a sodium channel blocker insecticide.
-
In VitroMetaflumizone (10 μM) completely inhibits the Para/TipE sodium currents in Xenopus oocytes.
-
In Vivo——
-
SynonymsBAS-320I
-
PathwayMembrane Transporter/Ion Channel
-
TargetSodium Channel
-
RecptorSodium Channel
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number139968-49-3
-
Formula Weight506.4
-
Molecular FormulaC24H16F6N4O2
-
Purity>98% (HPLC)
-
SolubilityDMSO:300 mg/mL (592.42 mM)
-
SMILESFC(F)(F)Oc1ccc(NC(=O)NN=C(Cc2ccc(cc2)C#N)c2cccc(c2)C(F)(F)F)cc1
-
Chemical Name2-(2-(4-cyanophenyl)-1-(3-(trifluoromethyl)phenyl)ethylidene)-N-(4-(trifluoromethoxy)phenyl)hydrazinecarboxamide
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Gosselin-Badaroudine P Charnet P Collet C et al. Metaflumizone inhibits the honeybee Na\r V\r 1 channel by targeting recovery from slow inactivation[J]. FEBS Letters 2017.
molnova catalog
related products
-
Huwentoxin IV
Selective NaV1.7 channel blocker. Preferentially inhibits neuronal NaV1.7, 1.2 and 1.3 (IC50 values are 26, 150 and 338 nM respectively), compared to muscle subtypes NaV1.4 and 1.5 (IC50 = >10 μM). Inhibits the channel by binding at the neurotoxin receptor site 4 in the S3-S4 linker of domain II, trapping the voltage sensor in the inward, closed configuration.
-
AZ194
CRMP2-Ubc9-NaV1.7 inhibitor 194, is a CRMP2-Ubc9-NaV1.7 inhibitor.
-
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.
