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EFONIDIPINE

EFONIDIPINE Structure
CAS No.
111011-76-8
Chemical Name:
EFONIDIPINE
Synonyms
nz-105;nz105ethanolate;Hydrochloride ethanol;EFONIDIPINE USP/EP/BP;r,p-oxide,monohydrochloride;efonidipinehydrochlorideethanolate;NZ-105 HYDROCHLORIDE MONOETHANOLATE;2-(phenyl(phenylmethyl)amino)ethyleste;Efonidipine hydrochloride monoethanolate;Efonidipine Hydrochloride ethanol (1:1:1)
CBNumber:
CB9317820
Molecular Formula:
C34H38N3O7P
Molecular Weight:
631.66
MOL File:
111011-76-8.mol
Modify Date:
2024/7/2 8:55:41

EFONIDIPINE Properties

Melting point 151° (dec)
storage temp. Inert atmosphere,2-8°C
solubility DMSO : 25 mg/mL (35.01 mM; Need ultrasonic)H2O : < 0.1 mg/mL (insoluble)
form Powder
color Light yellow to yellow

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS08
Signal word  Warning
Hazard statements  H361
Precautionary statements  P201-P202-P281-P308+P313-P405-P501

EFONIDIPINE price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) E0159 Efonidipine hydrochloride monoethanolate ≥98% (HPLC) 111011-76-8 5MG ₹9255.38 2022-06-14 Buy
Sigma-Aldrich(India) E0159 Efonidipine hydrochloride monoethanolate ≥98% (HPLC) 111011-76-8 25MG ₹36415.3 2022-06-14 Buy
Product number Packaging Price Buy
E0159 5MG ₹9255.38 Buy
E0159 25MG ₹36415.3 Buy

EFONIDIPINE Chemical Properties,Uses,Production

Description

Efonidipine hydrochloride ethanol was first launched in Japan for the treatment of essential severe and renal hypertension. As the fourteenth dihydropyridine (DHP) calcium channel blocker to reach the market, it functions by binding to the DHP receptors on voltage-dependent calcium channels to cause diuretic and natriuretic actions in patients with essential hypertension. Its vasodilating and calcium antagonist effects are very slow in onset and long-lasting in all types of experimentally hypertensive models and the agent is reported to exhibit an improved side effect profile compared with other drugs of the same class. This may be explained by the slow and long-lasting inhibition of transmembrane Ca+2 uptake, which is accompanied by its very slow binding to and dissociation from the DHP receptors. A recent study in cholesterol-fed rabbits suggested that efonidipine may suppress the development of atherosclerosis without affecting the plasma lipids. Clinical trials for angina, peetoris, and for cerebrovasodilatory disorders have been reported.

Uses

Efonidipine Hydrochloride Monoethanolate is a potent inhibitor of the L-type calcium channel.

Biological Activity

Selective blocker of L-type and T-type Ca 2+ channels. Displays minimal inhibition of N- and P/Q-type channels and no inhibition of R-type channels. R (-) and S (+)-enantiomers displays different channel selectivity; S (+)-Efonidipine blocks L-type and T-type channels whereas R (-)-Efonidipine displays selectivity for T-type channels. Exhibits antihypertensive activity.

EFONIDIPINE Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 87)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
Angle Biopharma 08046067501 Ahmedabad, India 142 58 Inquiry
Pharma Affiliates 172-5066494 Haryana, India 6761 58 Inquiry
Henan Tianfu Chemical Co.,Ltd. +86-0371-55170693 +86-19937530512 China 21675 55 Inquiry
Shaanxi Dideu Medichem Co. Ltd +86-029-89586680 +86-18192503167 China 9030 58 Inquiry
Dideu Industries Group Limited +86-29-89586680 +86-15129568250 China 26165 58 Inquiry
Wuhan Fortuna Chemical Co., Ltd +86-027-59207850 China 5999 58 Inquiry
Nantong HI-FUTURE Biology Co., Ltd. +undefined18051384581 China 3136 58 Inquiry

EFONIDIPINE Spectrum

111011-76-8(EFONIDIPINE)Related Search:

Efonidipine hydrochloride monoethanolate Efonidipine Hydrochloride ethanol (1:1:1) 2-(phenyl(phenylmethyl)amino)ethyleste 3-pyridinecarboxylicacid,1,4-dihydro-2,6-dimethyl-5-(5,5-dimethyl-1,3,2-dioxa efonidipinehydrochlorideethanolate nz-105 nz105ethanolate r,p-oxide,monohydrochloride 5-(5,5-Dimethyl-2-oxido-1,3,2-dioxaphosphorinan-2-yl)-1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3-pyridinecarboxylicacid2-[phenyl(phenylmethyl)amino]ethylesterhydrochloridemonoethanolate Hydrochloride ethanol NZ-105 HYDROCHLORIDE MONOETHANOLATE EFONIDIPINE USP/EP/BP Ethanol, compd. with 2-(phenyl(phenylmethyl)amino)ethyl 5-(5,5-dimethyl-1,3,2-dioxaphosphorinan-2-yl)-1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3-pyridinecarboxylate P-oxide monohydrochloride (1:1) 2-(Benzyl(phenyl)amino)ethyl 5-(5,5-dimethyl-2-oxido-1,3,2-dioxaphosphinan-2-yl)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate compound with ethanol (1:1) hydrochloride 2-(Benzyl(phenyl)amino)ethyl 5-(5,5-dimethyl-2-oxido-1,3,2-dioxaphosphinan-2-yl)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate ethanol hydrochloride inhibit,Efonidipine hydrochloride monoethanolate,Ca channels,Ca2+ channels,Calcium Channel,Inhibitor 111011-76-8 C34H38N3O7P C34H38N3O7PHClC2H5OH