For research use only. Not for therapeutic Use.
Maprotiline Hydrochloride is the hydrochloride salt form of maprotiline, a tetracyclic antidepressant closely related to the tricyclic antidepressants with adrenergic activity and sedative properties. Maprotiline hydrochloride exerts its effect by blocking the re-uptake of norepinephrine, thereby increasing the synaptic concentration of norepinephrine in the central nervous system and subsequently prolonging the action of norepinephrine on central receptors.
Catalog Number | A000741 |
CAS Number | 10347-81-6 |
Synonyms | 10347-81-6; Maprotiline Hcl; Ludiomil; Psymion; Maprotilline HCl |
Molecular Formula | C20H24ClN |
Purity | ≥95% |
Target | Autophagy |
Solubility | Soluble in DMSO > 10 mM |
Storage | -20°C |
InChI | 1S/C20H23N.ClH/c1-21-14-6-12-20-13-11-15(16-7-2-4-9-18(16)20)17-8-3-5-10-19(17)20;/h2-5,7-10,15,21H,6,11-14H2,1H3;1H |
InChIKey | NZDMFGKECODQRY-UHFFFAOYSA-N |
SMILES | CNCCCC12CCC(C3=CC=CC=C31)C4=CC=CC=C24.Cl |
Reference | 1: Ozkul A, Oztunç A. Determination of maprotiline hydrochloride in tablets by <br> 3: Celentano AM, González Cappa SM. [Chagas/’ disease and blood transfusion: 4: Atri PB, Julius DA. Maprotiline hydrochloride associated with a clinical state 5: Multicenter evaluation of maprotiline hydrochloride for treatment of 6: North DS, Retzinger T, Thompson JD. Seizures and delirium associated with 7: Treatment of depression with maprotiline hydrochloride: multicenter evaluation 8: Schwartz L, Swaminathan S. Maprotiline hydrochloride and convulsions: a case 9: Wells BG, Gelenberg AJ. Chemistry, pharmacology, pharmacokinetics, adverse 10: Marks P, Anderson J, Vincent R, Hutchinson JT, Rees HM. Epileptiform seizures |