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Lifarizine FA

Catalog No. T27830L
Synonyms: Lifarizine FA(119514-66-8 Free base)

Lifarizine FA is a sodium channel blocker used in the treatment of neurological disorders and cardiovascular diseases, study of stroke.

All products from TargetMol are for Research Use Only. Not for Human or Veterinary or Therapeutic Use.
Lifarizine FA Chemical Structure
Lifarizine FA, CAS N/A
Pack Size Availability Price/USD Quantity
1 mg In stock $ 195.00
5 mg In stock $ 430.00
10 mg In stock $ 636.00
25 mg In stock $ 987.00
50 mg In stock $ 1,360.00
100 mg In stock $ 1,830.00
500 mg In stock $ 3,680.00
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Purity: 99.87%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Lifarizine FA is a sodium channel blocker used in the treatment of neurological disorders and cardiovascular diseases, study of stroke.
In vivo Following the global ischaemic insult the rats were allowed to recover for 72 h before assessment of the damage, during which time one group of rats (n = 11) received 100 micrograms kg-1 lifarizine i.a. 5 min post-occlusion, 500 micrograms kg-1 lifarizine i.p. 15 min post-occlusion, and 500 micrograms kg-1 lifarizine i.p. twice daily for 72 h. A second group of rats (n = 12) was treated with appropriate volumes of vehicle (0.4 ml kg-1 i.a. and 2 ml kg-1 i.p.) at identical time points. The dosing regimen of lifarizine gave reduced damage in the hippocampal CA1 sub-field (4.1 +/- 0.3 to 2.8 +/- 0.6) and striatum (1.7 +/- 0.3 to 1.2 +/- 0.3) and significant neuroprotection in the anterior cortex (2.0 +/- 0.2 to 1.2 +/- 0.2; p < 0.05), thalamus (1.5 +/- 0.2 to 0.8 +/- 0.2; p < 0.01), posterior cortex (1.5 +/- 0.2 to 1.0 +/- 0.2; p < 0.05) and cerebellar brain stem (0.9 +/- 0.2 to 0.4 +/- 0.1; p < 0.01). The overall mean brain score was significantly reduced (from 1.5 +/- 0.1 to 0.9 +/- 0.2). These data show that the newly modified 2-vessel occlusion model produced a quantifiable level of ischaemic damage and that the novel agent lifarizine is neuroprotective in the model.[4]
Synonyms Lifarizine FA(119514-66-8 Free base)
Molecular Weight 482.62
Formula C30H34N4O2

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

TargetMolReferences and Literature

1. McGivern JG, et al. Actions of the novel neuroprotective agent, lifarizine (RS-87476), on voltage-dependent sodium currents in the neuroblastoma cell line, N1E-115. Br J Pharmacol. 1995;114(8):1738-1744. 2. Brown NA, et al. Block of human voltage-sensitive Na+ currents in differentiated SH-SY5Y cells by lifarizine. Br J Pharmacol. 1994;113(2):600-606. 3. Budd DC, et al. Inhibition by lifarizine of intracellular Ca2+ rises and glutamate exocytosis in depolarized rat cerebrocortical synaptosomes and cultured neurones. Br J Pharmacol. 1996;118(1):162-166. 4. McBean DE, et al. Neuroprotective efficacy of lifarizine (RS-87476) in a simplified rat survival model of 2 vessel occlusion. Br J Pharmacol. 1995;116(8):3093-3098.

Related compound libraries

This product is contained In the following compound libraries:
Bioactive Compound Library Bioactive Compounds Library Max Anti-Cancer Compound Library

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Keywords

Lifarizine FA Membrane transporter/Ion channel Sodium Channel Lifarizine FA(119514-66-8 Free base) inhibitor inhibit

 

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