ChemicalBook--->CAS DataBase List--->130636-43-0

130636-43-0

130636-43-0 Structure

130636-43-0 Structure
IdentificationMore
[Name]

Nifekalant
[CAS]

130636-43-0
[Synonyms]

1,3-dimethyl-6-[2-(n-(2-hydroxyethyl)-3-(4-nitrophenyl)propylamino)ethylamino]-2,4(1h,3h)-pyrimidinedione hydrochloride
6-[2-[2-hydroxyethyl-[3-(4-nitrophenyl)propyl]amino]ethylamino]-1,3-dimethyl-pyrimidine-2,4-dione
6-((2-((2-hydroxyethyl)(3-(p-nitrophenyl)propyl)amino)ethyl)amino)-1,3-dimethyl-uracil
NIFEKALANT
NIFEKALANT HCL
NIFEKALANT HYDROCHLORIDE
NIFEKALANT [6-((2-((2-HYDROXYETHYL)(3-(P-NITROPHENYL)PROPYL)AMINO)ETHYL)AMINO)-1,3-DIMETHYL-URACIL]
[Molecular Formula]

C19H27N5O5
[MDL Number]

MFCD00892243
[Molecular Weight]

405.45
[MOL File]

130636-43-0.mol
Chemical PropertiesBack Directory
[Melting point ]

117.5-118.5°; mp 125-126° (Katakami, 1992)
[Boiling point ]

597.9±60.0 °C(Predicted)
[density ]

1.32±0.1 g/cm3(Predicted)
[pka]

14.74±0.10(Predicted)
[CAS DataBase Reference]

130636-43-0(CAS DataBase Reference)
Hazard InformationBack Directory
[Uses]

Nifekalant (MS-551), a class III antiarrhythmic agent, is a IKr potassium channel blocker with an IC50 of 10 μM. Nifekalant can be used for refractory ventricular tachyarrhythmias research[1][2].
[Definition]

ChEBI: Nifekalant is an amine.
[in vivo]

In rats (a species deficient in functional cardiac IK), before coronary ligation, 3 mg/kg and 10 mg/kg MS-551 decreased the heart rate by 6% and 12%, and increased mean arterial pressure (MAP) by 14% and 33%, respectively. MS-551 prolongs the QT interval and reduced the incidence of sustained ventricular fibrillation (VF) after reperfusion[3].

[References]

[1] Lü-Pei Du, et al. The pharmacophore hypotheses of I(Kr) potassium channel blockers: novel class III antiarrhythmic agents. Bioorg Med Chem Lett. 2004 Sep 20;14(18):4771-7. DOI:10.1016/j.bmcl.2004.06.070
[2] Ioannis N Pantazopoulos, et al. Nifekalant in the treatment of life-threatening ventricular tachyarrhythmias. World J Cardiol. 2011 Jun 26;3(6):169-76. DOI:10.4330/wjc.v3.i6.169
[3] J Chen, et al. IK independent class III actions of MS-551 compared with sematilide and dofetilide during reperfusion in anaesthetized rats. Br J Pharmacol. 1996 Nov;119(5):937-42. DOI:10.1111/j.1476-5381.1996.tb15762.x
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