Phenamil methanesulfonate salt
WebPhenamil Methanesulfonate Salt induced differentiation and peroxisome proliferator-activator receptor γ expression through ETS variant 4 in mouse preadipocyte. General Description. Phenamil, a derivative of amiloride is an inhibitor of sodium channels including acid sensing ion channel (ASIC) and epithelial sodium channels (ENaC). ... WebPhenamil, a derivative of amiloride is an inhibitor of sodium channels including acid sensing ion channel (ASIC) and epithelial sodium channels (ENaC). Application Phenamil …
Phenamil methanesulfonate salt
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WebPhenamil methanesulfonate (free base) is an amiloride analog. Irreversibly blocks ENaC (amiloride-sensitive Na + channels). References. Phenamil: an irreversible inhibitor of … WebPhenamil (methanesulfonate) is soluble in organic solvents such as DMSO and dimethyl formamide, which should be purged with an inert gas. The solubility of phenamil (methanesulfonate) in these solvents is approximately 1 and 0.1 mg/ml, respectively. Phenamil (methanesulfonate) is sparingly soluble in aqueous buffers. For maximum …
http://www.cnreagent.com/s/sv80891.html WebProduct Name: Phenamil methanesulfonate salt Test CAS Number: 2038-35-9 Molecular Formula: C12H12ClN7O•CH3SO3H Molecular Weight: 401.8 Lot Number: sc-202480 CERTIFICATE OF ANALYSIS Specification Result Native Source: Sample Appearance Yellow powder Light yellow powder Identification Complies Purity (HPLC) ≥ 98.0% 98.1% …
WebPhenamil, a derivative of amiloride is an inhibitor of sodium channels including acid sensing ion channel (ASIC) and epithelial sodium channels (ENaC). Application Phenamil … WebPhenamil methanesulfonate is also a competive inhibitor of TRPP3 and inhibits TRPP3-mediated Ca 2+ transport with an IC50 of 140 nM in a Ca 2+ uptake assay. Phenamil …
WebJul 3, 2024 · Each 99 µL of cell suspension was mixed with 1 µL of CCCP, EIPA or phenamil methanesulfonate salt (Sigma-Aldrich, MO, USA) dissolved in DMSO at the final concentrations of 50 µM.
cxr of chfWebThe biosurfactant production in minimal medium was carried out at different temperatures and salt concentrations, where it produced an efficient biosurfactant at 30-45°C and in … cxr of pneumoniaWebAlfa Chemistry offers Phenamil for experimental / research use. View information & documentation regarding Phenamil, including CAS, structure & more. cheap hotels at seasideWebPhenamil methanesulfonate is an intriguing small molecule to promote bone repair by strongly activating BMP signaling pathway. Phenamil methanesulfonate is used for the … cxr opacityWebAug 1, 2024 · 1-Aminooctadecane (SA, 99.0%), 3β-hydroxy-5-cholestene (Chol, >99%), phenamil methanesulfonate salt (Phe), benzene (high purity), methanol (spectrograde), dimethyl sulfoxide (DMSO, >99%), tris (hydroxymethyl)-aminomethane (TRIS, 99%), NaCl (>99%), β-glycerophosphate, l-ascorbic acid, dexamethasone, nitro blue tetrazolium (NBT), … cheap hotels at shantinikWebPhenamil Methanesulfonate Salt induced differentiation and peroxisome proliferator-activator receptor ╬│ expression through ETS variant 4 in mouse preadipocyte: References: Park, K. W., et. al.: J. Lipid Res., 51, 2775 (2010) Related Products. 7-Diethylamino-3-[N-(3-maleimidopropyl)carbamoyl]coumarin; cheap hotels at spiWebPhenamil is an inhibitor of transient receptor potential polycystin-L (TRPP3; IC 50 = 140 nM) and a derivative of amiloride (Item No. 14409 ). 1 It also inhibits the epithelial sodium channel (ENaC; IC 50 = 400 nM). 2 Phenamil decreases basal short-circuit currents in human and ovine bronchial epithelial cells with IC 50 values of 75 and 116 nM, … cheap hotels at singapore