2-Methoxy-5-methyL-N,N-bis(1-methyLethyL)-γ-phenyLbenzenepropanamine fumarate

CAS: 124935-88-2

Ref. 3D-FM39718

Produktinformation

• Name: 2-Methoxy-5-methyL-N,N-bis(1-methyLethyL)-γ-phenyLbenzenepropanamine fumarate
• Synonyme: Tolterodine impurity C, 2-Methoxy-5-Methyl-N,N-Bis(1-Methylethyl)-Gamma-Phenylbenzene Propanamine Fumara, 2-Methoxy-5-Methyl-N,N-Bis(1-Methylethyl)-Y-Phenylbenzenepropanamine Fumarate, 2-Methoxy-5-Methyl-N,N-Bis(1-Methylethyl)-Gamma-Phenyl., N,N-Diisopropyl-3-(2-Methoxyl-5-Methylphenyl)-3-PhenylPropylAmine(ForTolterodine-L-Tartrate), 2-Methoxy-5-methyl-N,N-bis(1-methylethyl)--phenylbenzenepropanaminefurmarate, 2-[3-[Bis(1-Methylethyl)Amino]-1-Phenyl-Propyl]-4-Methyl-Methoxybenzene, 3-(2-methoxy-5-methylphenyl)-3-phenyl-N,N-di(propan-2-yl)propan-1-amine (2E)-but-2-enedioate (1:1)

Beschreibung

2-Methoxy-5-methyL-N,N-bis(1-methyLethyl)-gamma-phenyLbenzenepropanamine fumarate (DMXBPC) is an analgesic that has been shown to be a potent inhibitor of the cytosolic phospholipase A2 and is also cytotoxic. DMXBPC has significant cholinergic activity and can inhibit the synthesis of prostaglandins in the prostate gland. DMXBPC binds to the pyridine ring of DOPA and inhibits its conversion to dopamine. The enantiomers of DMXBPC have different effects on inhibition of phospholipase A2, with the (+) form being more potent than the (-) form. This is due to the fact that (+)DMXBPC binds more tightly to the enzyme than (-)DMXBPC does.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 339.51 g/mol
• Formel: C₂₃H₃₃NO
• Reinheit: Min. 95%