123388-25-0
123388-25-0 structure
- Name: Semotiadil (recemate fumarate)
- Chemical Name: 3,4-dihydro-2-<5-methoxy-2<3-ethyl>amino>propoxy>phenyl>-4-methyl-3-oxo-2H-1,4-benzothiazine hydrogen fumarate
- CAS Number: 123388-25-0
- Molecular Formula: C33H36N2O10S
- Molecular Weight: 652.71100
- Catalog: Signaling Pathways Membrane Transporter/Ion Channel Calcium Channel
- Create Date: 2018-02-11 13:05:45
- Modify Date: 2024-01-06 20:17:36
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Semotiadil recemate fumarate is the recemate of Semotiadil fumarate. Semotiadil fumarate is a novel vasoselective Ca2+ channel antagonist.
| Name | 3,4-dihydro-2-<5-methoxy-2<3-ethyl>amino>propoxy>phenyl>-4-methyl-3-oxo-2H-1,4-benzothiazine hydrogen fumarate |
|---|---|
| Synonyms |
3,4-dihydro-2-[5-methoxy-2-[3-[N-methyl-N-[2-[(3,4-methylenedioxy)phenoxy]ethyl]amino]propoxy]phenyl]-4-methyl-3-oxo-2H-1,4-benzothiazine fumarate
3,4-dihydro-2-{5-methoxy-2[3-(N-methyl-N-{2-[3,4-(methylenedioxy)phenoxy]ethyl}amino)propoxy]phenyl}-4-methyl-3-oxo-2H-1,4-benzothiazine hydrogen fumarate 2-[2-(3-{[2-(Benzo[1,3]dioxol-5-yloxy)-ethyl]-methyl-amino}-propoxy)-5-methoxy-phenyl]-4-methyl-4H-benzo[1,4]thiazin-3-one compound with (E)-but-2-enedioic acid Semotiadil (recemate fumarate) |
| Description | Semotiadil recemate fumarate is the recemate of Semotiadil fumarate. Semotiadil fumarate is a novel vasoselective Ca2+ channel antagonist. |
|---|---|
| Related Catalog | |
| Target |
Ca2+ channel[1] |
| In Vitro | Semotiadil in a concentration of 1 μM produces an inhibition of 12.4±9.7% and in a concentration of 10 μM an inhibition of 25±11.0%[1]. Effects of Semotiadil on the voltage-dependent Ca current (ICa) are investigated in dispersed smooth muscle cells of the rabbit portal vein. At a holding potential of -100 mV, Semotiadil (> or =0.1 μM; dissolved in DMSO) inhibits the ICa in a concentration-dependent manner (IC50=2.0 μM). At a holding potential of -80 mV or -60 mV, the concentration-inhibition curve observed in the presence of Semotiadil is shifted to the left compared with that observed at -100 mV; and Semotiadil shifts the voltage-dependent inactivation curve to the left. The curve for the decay of ICa is fitted with two time constants. Semotiadil (<1 μM) reduces the slow but not the fast time constant. The curve for the recovery from ICa inactivation also consisted of two time constants, and Semotiadil (1 microM) prolongs the slow recovery. Semotiadil dissolved in deionized water more potently inhibits ICa than Semotiadil dissolved in DMSO[2]. |
| 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]. |
| Kinase Assay | Semotiadil is dissolved in DMSO. Appropriate dilutions are made freshly for each experiment[1]. The experiments are performed in an experimental bathing chamber (volume 1 ml) mounted on the stage of an inverted microscope. The cells are superfused with warm (37°C) extracellular solution at the rate of 3 mL/min. The solution could be exchanged for an identical solution containing the substance under study without any significant alteration either in the flow rate or in the temperature of the superfusing fluid. A complete exchange of the bath solution was achieved within 1 min[1]. |
| Animal Admin | Rats[3] Semotiadil fumarate is given alone or in combination with either Enalapril or trichlormethiazide to conscious, spontaneously hypertensive, rats daily for 2 weeks. Systolic blood pressure and heart rate are recorded 24 h before the start of the regimen and then every 2 and 24 h after the 1st, 3rd, 7th, 10th and 14th doses. 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. |
| References |
| Molecular Formula | C33H36N2O10S |
|---|---|
| Molecular Weight | 652.71100 |
| Exact Mass | 652.20900 |
| PSA | 169.60000 |
| LogP | 4.79020 |