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105737-62-0

105737-62-0 Structure

105737-62-0 Structure
IdentificationBack Directory
[Name]

1-[2-((3-CARBAMOYL-4-HYDROXY)PHENOXY)ETHYLAMINO]-3-[4-(1-METHYL-4-TRIFLUOROMETHYL-2-IMIDAZOLYL)PHENOXY]-2-PROPANOL DIHYDROCHLORIDE
[CAS]

105737-62-0
[Synonyms]

CGP207122HCl
CGP 20712 mesylate
CGP 20712 DIHYDROCHLORIDE
CGP-20712A methanesulfonate salt
CGP 20712A METHANESULFONATE SELECTIVE B1 ADRENOCE
CGP-20712A methanesulfonate salt solid, >=98% (HPLC)
1-(2-((3-Carbamoyl-4-hydroxy)phenoxy)ethylamino)-3-(4-(1-methyl-4-trifluoromethyl-2-imidazolyl)phenoxy)-2-propanoldihyd
1-[2-((3-Carbamoyl-4-hydroxy)phenoxy)ethylamino]-3-[4-(1-methyl-4-trifluoromethyl-2-imidazoyl)phenoxy]-2-propanol mesylate
1-[2-((3-CARBAMOYL-4-HYDROXY)PHENOXY)ETHYLAMINO]-3-[4-(1-METHYL-4-TRIFLUOROMETHYL-2-IMIDAZOLYL)PHENOXY]-2-PROPANOL DIHYDROCHLORIDE
(+/-)-1-(2-(3-carbamoyl-4-hydroxyphenoxy)ethylamino)-3-(4-(1-methyl-4-trifluoromethyl-2-imidazolyl)-phenoxy)-2-propanol methane sulfonate
(±)-2-Hydroxy-5-[2-[[2-hydroxy-3-[4-[1-methyl-4-(trifluoromethyl)-1H-imidazol-2-yl]phenoxy]propyl] amino]ethoxy]-benzamide methanesulfonate salt
[Molecular Formula]

C23H25F3N4O5.CH4O3S
[MDL Number]

MFCD06798358
[MOL File]

105737-62-0.mol
[Molecular Weight]

590.57
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

H2O: 10 mg/mL
[form ]

solid
[color ]

white
[Water Solubility ]

H2O: >10mg/mL
DMSO: 100mg/mL
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

CGP-20712A methanesulfonate salt has been used as a β1-adrenergic receptor antagonist in adult rat ventricular myocytes (ARVM) and rat cardiac fibroblasts. It may also be used as an antagonist for the β1-adrenergic receptor in rat bladder smooth muscles.
[Biological Activity]

Highly selective and potent β 1 -adrenoceptor antagonist (IC 50 = 0.7 nM). Displays 10,000-fold selectivity over β 2 -adrenoceptors. Also available as part of the β -Adrenoceptor Antagonist Tocriset™ .
[Biochem/physiol Actions]

CGP-20712A methanesulfonate salt is a selective β1-adrenoceptor antagonist.
[in vitro]

In myocytes, the activation of adenylate cyclase causes by β2-adrenoceptors is not detected in the presence of 10 nM, 100 nM or 1000 nM CGP 20712 A (CGP 20712 mesylate), which selectively antagonized beta1-adrenoceptors.
[in vivo]

Pretreatment of 8-day-old rats with 5 mg/kg CGP 20712 A do not change the plasma ACTH response to insulin injection.
[IC 50]

β adrenergic receptor
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