Phenamil methanesulfonate salt
SIGMA/P203 - solid
Synonym: 3,5-
CAS Number: 1161-94-0
Empirical Formula (Hill Notation): C12H12ClN7O · CH4O3S
Molecular Weight: 401.83
MDL Number: MFCD00274070
Linear Formula: C12H12ClN7O · CH3SO3H
Product Type: Chemical
| color | yellow |
| form | solid |
| InChI | 1S/C12H12ClN7O.CH4O3S/c13 |
| InChI key | MHPIZTURFVSLTJ-UHFFFAOYSA |
| Quality Level | 100 ![]() |
| SMILES string | CS(O)(=O)=O.Nc1nc(N)c(nc1 |
| solubility | 0.1 M HCl: insoluble |
| 45% (w/v) aq 2-hydroxypropyl-β-cyclode |
|
| DMSO: ≥5 mg/mL (with warming) | |
| H2O: insoluble | |
| storage temp. | 2-8°C |
| Application: | Phenamil methanesulfonate salt has been used: • to stimulate adipocyte differentiation in 3T3 cells • to test its effect on lateral flagella expression in Vibrio shilonii • in nanoparticle preparation to test its effect on osteo/odontoblastic differentiation |
| Biochem/physiol Actions: | Phenamil is an inducer of peroxisome proliferator-activated receptor γ (PPARγ) and inhibits diamine oxidase. By favoring tribbles homolog 3 (Trb3) expression, phenamil holds therapeutic potential to treat pulmonary artery hypertension (PAH) and idiopathic PAH. It is also a bone morphogenetic protein (BMP) activator, which favors osteogenesis and odontogenesis of stem cells. |
| General description: | Phenamil, a derivative of amiloride is an inhibitor of sodium channels including acid sensing ion channel (ASIC) and epithelial sodium channels (ENaC). |
| Packaging: | 5, 25 mg in glass bottle |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 3 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Storage Temp. | 2-8°C |
| UNSPSC | 12352200 |

