Niguldipine (hydrochloride)

Niguldipine (hydrochloride) Suppliers list
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
Tel: 021-65675885 18964387627
Email: info@efebio.com
Company Name: BOC Sciences  
Tel: 16314854226; +8616314854226
Email: inquiry@bocsci.com
Company Name: ChemeGen(Shanghai) Biotechnology Co.,Ltd.  
Tel: 18818260767
Email: sales@chemegen.com
Niguldipine (hydrochloride) Basic information
Product Name:Niguldipine (hydrochloride)
Synonyms:Niguldipine Hydrochloride DISCONTINUED PLEASE SEE N598530;Niguldipine HCl;(±)-Niguldipine hydrochloride
CAS:119934-51-9
MF:C36H40ClN3O6
MW:646.18
EINECS:
Product Categories:
Mol File:119934-51-9.mol
Niguldipine (hydrochloride) Structure
Niguldipine (hydrochloride) Chemical Properties
storage temp. RT
solubility Soluble in DMSO (up to 25 mg/ml) or in Methanol (up to 25 mg/ml).
form Yellow crystalline solid.
color White
Stability:Stable for 1 year from date of purchase as supplied. Solutions in DMSO or methanol may be stored at -20°C for up to 3 months.
Safety Information
MSDS Information
Niguldipine (hydrochloride) Usage And Synthesis
DescriptionNiguldipine HCl (119934-51-9) is an L-type calcium channel blocker (IC50 = 75 nM), which can also inhibit T-type calcium channels at higher concentrations (IC50 = 244 nM). Novel inhibitor of drug transport by p-glycoprotein.
UsesNiguldipine Hydrochloride is a selective α 1-adrenoceptor antagonist. Also, it is a new calcium antagonist.
in vitroniguldipine significantly increased the rate of long-lived protein degradation in human glioblastoma h4 cell, which indicated that niguldipine triggered autophagic degradation without inducing obvious cellular damage. also, niguldipine blocked intracellular ca2+ currents [1].
in vivofemale albino swiss mice were administered intraperitoneally in a volume of 10 ml/kg niguldipine for 30 min. niguldipine did not affect the electroconvulsive threshold in mice. compared to the anticonvulsive activity of niguldipine against electroconvulsions, niguldipine remarkably impaired the protective action of both phenobarbital and carbamazepine [2].
IC 50s = 0.4 μm: inhibits l-type ca2+ channels
References[1] WOLFGANG STENGEL  Klaus A  Monika Jainz. Different potencies of dihydropyridine derivatives in blocking T-type but not L-type Ca2+ channels in neuroblastoma-glioma hybrid cells[J]. European journal of pharmacology, 1998, 342 2: Pages 339-345. DOI:10.1016/s0014-2999(97)01495-7
[2] VOLKER HÖLL . Stereoisomers of calcium antagonists which differ markedly in their potencies as calcium blockers are equally effective in modulating drug transport by P-glycoprotein[J]. Biochemical pharmacology, 1992, 43 12: Pages 2601-2608. DOI:10.1016/0006-2952(92)90149-d
Niguldipine (hydrochloride) Preparation Products And Raw materials
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