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ChemicalBook--->CAS DataBase List--->123388-25-0

123388-25-0

123388-25-0 Structure

123388-25-0 Structure
IdentificationBack Directory
[Name]

Semotiadil (recemate fumarate)
[CAS]

123388-25-0
[Synonyms]

Semotiadil (recemate fumarate)
[Molecular Formula]

C33H36N2O10S
[MDL Number]

MFCD31382173
[MOL File]

123388-25-0.mol
[Molecular Weight]

652.711
Chemical PropertiesBack Directory
[Melting point ]

131-133 °C(Solv: ethanol (64-17-5))
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
Hazard InformationBack Directory
[Uses]

Semotiadil recemate fumarate is the recemate of Semotiadil fumarate. Semotiadil fumarate is a novel vasoselective Ca2+ channel antagonist.
[in vivo]

Semotiadil fumarate, a novel benzothiazine calcium antagonist, is given alone or in combination with either Enalapril or trichlormethiazide to conscious, spontaneously hypertensive, rats daily for 2 weeks. When given alone, the antihypertensive effects of Semotiadil (10 mg/kg, p.o.) and Enalapril (5 mg/kg, p.o.) first became apparent after the 3rd dose and thereafter the effects appeared to develop daily although this effect had waned by the time of the next dose. These results indicate that combined daily dosing of Semotiadil, especially with Enalapril, each at relatively low doses may be able to control hypertension in a continuous manner[3].

[References]

[1] Koidl B, et al. A novel benzothiazine Ca2+ channel antagonist, Semotiadil, inhibits cardiac L-type Ca2+ currents. Eur J Pharmacol. 1997 Mar 19;322(2-3):243-7. DOI:10.1016/s0014-2999(96)00995-8
[2] Teramoto N. Mechanisms of the inhibitory action of Semotiadil fumarate, a novel Ca antagonist, on the voltage-dependent Ca current in smooth muscle cells of the rabbit portal vein. Jpn J Pharmacol. 1993 Mar;61(3):183-95. DOI:10.1254/jjp.61.183
[3] Ichikawa M, et al. Antihypertensive effects of a novel calcium antagonist, Semotiadil fumarate (SD-3211), alone and in combination with Enalapril or trichlormethiazide in spontaneously hypertensive rats. Biol Pharm Bull. 1994 Nov;17(11):1513-5. DOI:10.1248/bpb.17.1513
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