CAS 148849-67-6|Ivabradine hydrochloride

Introduction:Basic information about CAS 148849-67-6|Ivabradine hydrochloride, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameIvabradine hydrochloride
CAS Number148849-67-6Molecular Weight505.046
Density/Boiling Point626.9ºC at 760mmHg
Molecular FormulaC27H37ClN2O5Melting Point193-196?C
MSDSChineseUSAFlash Point332.9ºC
Symbol
GHS09
Signal WordWarning

Names

Nameivabradine hydrochloride
SynonymMore Synonyms

Ivabradine hydrochloride BiologicalActivity

DescriptionIvabradine (hydrochloride) is a new If inhibitor with IC50 of 2.9 μM, and used as a pure heart rate lowering agent.
Related CatalogSignaling Pathways >>GPCR/G Protein >>Adrenergic ReceptorResearch Areas >>Cardiovascular Disease
In VivoIvabradine treatment (10 mg/kg/d) induces long-term HRR, and that improves diastolic LV function probably involving attenuated hypoxia, reduced remodeling, and/or preserved nitric oxide bioavailability, resulting from processes triggered early after HRR initiation: angiogenesis and/or preservation of endothelial nitric oxide synthase expression[1]. Ivabradine leads to a sustained 15-20% heart rate reduction, but has no effect on blood pressure. While ivabradine has no effect on endothelial function and vascular reactive oxygen species production in angiotensin II-treated rats, it improves both parameters in ApoE knockout mice. Ivabradine treatment leads to an attenuation of angiotensin II signaling and increased the expression of telomere-stabilizing proteins in ApoE knockout mice, which may explain its beneficial effects on the vasculature. The absence of these protective ivabradine effects in angiotensin II-infused rats may relate to the treatment duration or the presence of arterial hypertension[2].
References

[1]. Fang, Y., et al. Heart rate reduction induced by the if current inhibitor ivabradine improves diastolic function and attenuates cardiac tissue hypoxia. J Cardiovasc Pharmacol, 2012. 59(3): p. 260-7.

[2]. Kroller-Schon, S., et al. Differential effects of heart rate reduction with ivabradine in two models of endothelial dysfunction and oxidative stress. Basic Res Cardiol, 2011. 106(6): p. 1147-58.

Chemical & Physical Properties

Boiling Point626.9ºC at 760mmHg
Melting Point193-196?C
Molecular FormulaC27H37ClN2O5
Molecular Weight505.046
Flash Point332.9ºC
Exact Mass504.239105
PSA60.47000
LogP4.04990
Vapour Pressure1.24E-15mmHg at 25°C
InChIKeyHLUKNZUABFFNQS-ZMBIFBSDSA-N
SMILESCOc1cc2c(cc1OC)CC(=O)N(CCCN(C)CC1Cc3cc(OC)c(OC)cc31)CC2.Cl
Storage condition-20°C Freezer

Safety Information

Symbol
GHS09
Signal WordWarning
Hazard StatementsH400
Precautionary StatementsP273
Hazard CodesN
Risk Phrases50/53
Safety Phrases60-61
RIDADRUN 3077 9 / PGIII

Articles1

More Articles
Beat Rate Variability in Murine Embryonic Stem Cell-Derived Cardiomyocytes: Effect of Antiarrhythmic Drugs.

Cell Physiol. Biochem. 38 , 646-58, (2016)

Heart rate variability (HRV) refers to the fluctuation of the time interval between consecutive heartbeats in humans. It has recently been discovered that cardiomyocytes derived from human embryonic a...

Synonyms

Ivabradine hydrochloride
AMG 998
Coralan
Procoralan
Corlentor
3-[3-[[(7S)-3,4-dimethoxy-7-bicyclo[4.2.0]octa-1,3,5-trienyl]methyl-methylamino]propyl]-7,8-dimethoxy-2,5-dihydro-1H-3-benzazepin-4-one,hydrochloride
ivabradine monohydrochloride
2H-3-Benzazepin-2-one, 3-(3-((((7S)-3,4-dimethoxybicyclo(4.2.0)octa-1,3,5-trien-7-yl)methyl)methylamino)propyl)-1,3,4,5-tetrahydro-7,8-dimethoxy-, monohydrochloride
Ivabradine hcl
2H-3-Benzazepin-2-one, 3-[3-[[[(7S)-3,4-dimethoxybicyclo[4.2.0]octa-1,3,5-trien-7-yl]methyl]methylamino]propyl]-1,3,4,5-tetrahydro-7,8-dimethoxy-, hydrochloride (1:1)
MFCD00929899
3-{3-[{[(7S)-3,4-Dimethoxybicyclo[4.2.0]octa-1,3,5-trien-7-yl]methyl}(methyl)amino]propyl}-7,8-dimethoxy-1,3,4,5-tetrahydro-2H-3-benzazepin-2-one hydrochloride (1:1)
UNII-TP19837BZK
Corlanor
CAS 63309-34-2|6-(3-Chloro-2-methylpropoxy)-3,4-dihydro-2(1h)-quinolinone
CAS 6526-93-8|2,7-Dimethoxy-9-phenoxyacridine
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