Lidoflazine

Modify Date: 2024-01-11 19:58:42

Lidoflazine structure	Common Name	Lidoflazine
	CAS Number	3416-26-0	Molecular Weight	491.61500
	Density	1.161g/cm3	Boiling Point	632.6ºC at 760mmHg
	Molecular Formula	C₃₀H₃₅F₂N₃O	Melting Point	158-162ºC
	MSDS	Chinese USA	Flash Point	336.4ºC

Use of Lidoflazine

Lidoflazine is a high affinity blocker of the HERG (human ether-a-go-go-related gene) K+ channel. Lidoflazine is an antianginal calcium channel blocker that carries a significant risk of QT interval prolongation and ventricular arrhythmia[1].

Name	Lidoflazine
Synonym	More Synonyms

Description	Lidoflazine is a high affinity blocker of the HERG (human ether-a-go-go-related gene) K+ channel. Lidoflazine is an antianginal calcium channel blocker that carries a significant risk of QT interval prolongation and ventricular arrhythmia[1].
Target	Ca2+
In Vitro	Lidoflazine inhibits potently HERG current (IHERG) recorded from HEK 293 cells stably expressing wild-type HERG (IC50 of ~16 nM).
References	[1]. https://www.ncbi.nlm.nih.gov/pubmed/15135665

Density	1.161g/cm3
Boiling Point	632.6ºC at 760mmHg
Melting Point	158-162ºC
Molecular Formula	C₃₀H₃₅F₂N₃O
Molecular Weight	491.61500
Flash Point	336.4ºC
Exact Mass	491.27500
PSA	35.58000
LogP	5.69880
Appearance of Characters	white
Index of Refraction	1.581
Storage condition	2-8°C
Water Solubility	DMSO: ≥10mg/mL

Lidoflazine MSDS(Chinese)

CHEMICAL IDENTIFICATION

RTECS NUMBER :: TK7910000

CHEMICAL NAME :: 1-Piperazineaceto-2',6'-xylidide, 4-(4,4-bis(p-fluorophenyl)butyl)-

CAS REGISTRY NUMBER :: 3416-26-0

BEILSTEIN REFERENCE NO. :: 0904339

LAST UPDATED :: 199612

DATA ITEMS CITED :: 5

MOLECULAR FORMULA :: C30-H35-F2-N3-O

MOLECULAR WEIGHT :: 491.68

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :: TDLo - Lowest published toxic dose

ROUTE OF EXPOSURE :: Oral

SPECIES OBSERVED :: Human

DOSE/DURATION :: 20570 ug/kg/8D-I

TOXIC EFFECTS :: Cardiac - arrhythmias (including changes in conduction)

REFERENCE :: ARZNAD Arzneimittel-Forschung. Drug Research. (Editio Cantor Verlag, Postfach 1255, W-7960 Aulendorf, Fed. Rep. Ger.) V.1- 1951- Volume(issue)/page/year: 22,923,1972

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Oral

SPECIES OBSERVED :: Rodent - rat

DOSE/DURATION :: >3200 mg/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

REFERENCE :: FRPSAX Farmaco, Edizione Scientifica. (Casella Postale 227, 27100 Pavia, Italy) V.8-43 1953-88 For publisher information, see FRMCE8 Volume(issue)/page/year: 32,461,1977

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Intraperitoneal

SPECIES OBSERVED :: Rodent - rat

DOSE/DURATION :: >3200 mg/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

REFERENCE :: FRPSAX Farmaco, Edizione Scientifica. (Casella Postale 227, 27100 Pavia, Italy) V.8-43 1953-88 For publisher information, see FRMCE8 Volume(issue)/page/year: 32,461,1977

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Oral

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: >2 gm/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

REFERENCE :: ARPMAS Archiv der Pharmazie (Weinheim, Germany) (VCH Pub., Inc., 303 NW 12th Ave., Deerfield Beach, FL 33441) V.51-261, 1835-1923; V.305- 1972- Volume(issue)/page/year: 322,359,1989

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Intravenous

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 40 mg/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

REFERENCE :: FRXXBL French Demande Patent Document. (U.S. Patent and Trademark Office, Foreign Patents, Washington, DC 20231) Volume(issue)/page/year: #2279383

Personal Protective Equipment	dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes	Xn: Harmful;
Risk Phrases	R22
Safety Phrases	36
RIDADR	NONH for all modes of transport
RTECS	TK7910000

Protective effects of the lazaroid U74500A and lidoflazine on liver preservation with UW solution.

Transpl. Int. 6(5) , 281-4, (1993)

The effect of adding a 21-aminosteroid, U74500A, and a Ca2+ antagonist, lidoflazine, alone and together to UW solution was assessed in a rat liver preservation model. Following preservation, the liver...

Simpson's paradox and clinical trials: what you find is not necessarily what you prove.

Ann. Emerg. Med. 21(12) , 1480-2, (1992)

Expensive clinical trials have become the gold standard for evaluating the efficacy of promising new therapeutic agents. Full exploration of the collected data is routine to maximize the yield of the ...

1,4-Dihydropyridines bearing a pharmacophoric fragment of lidoflazine.

Bioorg. Med. Chem. 4(10) , 1629-35, (1996)

A series of 1,4-dihydropyridines bearing a pharmacophoric fragment of lidoflazine was synthesized. The compounds were evaluated for inotropic, chronotropic, and calcium antagonist activities. All comp...

4-[4,4-Bis(4-fluorophenyl)butyl]-N-(2,6-dimethylphenyl)-1-piperazineacetamide

2-[4-[4,4-bis(4-fluorophenyl)butyl]piperazin-1-yl]-N-(2,6-dimethylphenyl)acetamide

Shanghai Nianxing Industrial Co., Ltd
China
Product Name: Lidoflazine
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DC Chemicals Limited
China
Product Name: Lidoflazine
Price: $Inquiry/100mg $Inquiry/250mg $Inquiry/500mg
Purity: 98.0%
Delivery: 3 Day
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Lidoflazine

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