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Rilmenidine hemifumarate

Catalog No. T21911Cas No. 207572-68-7
Alias S-3341 hemifumarate, Rilmenidine (hemifumarate)

Rilmenidine hemifumarate (S-3341 hemifumarate) is a novel, orally active and selective I1 imidazoline receptor and α2-adrenoceptor agonist that induces autophagy, regulates the proliferation of leukaemia cells, stimulates the pro-apoptotic protein Bax, and induces autophagy in human leukaemia K5 cells. induces disruption of the mitochondrial pathway and apoptosis in human leukaemia K562 cells.

Rilmenidine hemifumarate

Rilmenidine hemifumarate

Purity: 98.14%
Catalog No. T21911Alias S-3341 hemifumarate, Rilmenidine (hemifumarate)Cas No. 207572-68-7
Rilmenidine hemifumarate (S-3341 hemifumarate) is a novel, orally active and selective I1 imidazoline receptor and α2-adrenoceptor agonist that induces autophagy, regulates the proliferation of leukaemia cells, stimulates the pro-apoptotic protein Bax, and induces autophagy in human leukaemia K5 cells. induces disruption of the mitochondrial pathway and apoptosis in human leukaemia K562 cells.
Pack SizePriceAvailabilityQuantity
5 mg$721-2 weeks
10 mg$981-2 weeks
25 mg$1681-2 weeks
50 mg$2471-2 weeks
100 mg$3651-2 weeks
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Purity:98.14%
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Product Introduction

Bioactivity
Description
Rilmenidine hemifumarate (S-3341 hemifumarate) is a novel, orally active and selective I1 imidazoline receptor and α2-adrenoceptor agonist that induces autophagy, regulates the proliferation of leukaemia cells, stimulates the pro-apoptotic protein Bax, and induces autophagy in human leukaemia K5 cells. induces disruption of the mitochondrial pathway and apoptosis in human leukaemia K562 cells.
In vitro
Rilmenidine offers antihypertensive efficacy comparable to diuretics, beta-blockers, calcium channel blockers, and angiotensin-converting enzyme (ACE) inhibitors. Rilmenidine (25-100 μM; 24 hours) also inhibits K562 cell proliferation[3].
In vivo
In Rilmenidine-treated N171-82Q mice (i.p.; 4-times a week), significant improvement in forelimb grip strength and all limbs grip strength is observed from 12 to 22 weeks of age. Rilmenidine also decreases levels of mutant huntingtin[2].
AliasS-3341 hemifumarate, Rilmenidine (hemifumarate)
Chemical Properties
Molecular Weight238.28
FormulaC10H16N2O.1/2C4H4O4
Cas No.207572-68-7
Storage & Solubility Information
Storagestore at low temperature,store under nitrogen | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: 30 mg/mL (125.90 mM)
DMSO: 5 mg/mL (125.90 mM), Sonication is recommended.
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM4.1967 mL20.9837 mL41.9674 mL209.8372 mL
5 mM0.8393 mL4.1967 mL8.3935 mL41.9674 mL
10 mM0.4197 mL2.0984 mL4.1967 mL20.9837 mL
20 mM0.2098 mL1.0492 mL2.0984 mL10.4919 mL
50 mM0.0839 mL0.4197 mL0.8393 mL4.1967 mL
100 mM0.0420 mL0.2098 mL0.4197 mL2.0984 mL

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