Bepridil hydrochloride structure, CAS 74764-40-2

Bepridil hydrochloride

CAS Number74764-40-2

Synonyms3-isobutoxy-2-pyrrolidino-n-phenyl-n-benzylpropylaminehydrochloridehydrate; MFCD00065498; l)-,monohydrochloride,monohydrate; angopril; Bepridil hydrochloride,N-Benzyl-N-(3-isobutoxy-2-pyrrolidin-1-yl-propyl)anilinehydrochloride

Molecular FormulaC24H37ClN2O2

Molecular Weight403.00

Purity98.00%

Density

Boiling Point

Melting Point91 ±2°

Flash Point

Appearancepowder

EINECS

MSDSChineseEnglish

Symboltransportation

Signal WordWarning

Cat. No.: 2A-9047788 Purity: 98.00%
Change View

Please Login or Create an Account to: See VlP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

Quality Control of [ 74764-40-2 ] Purity: 98.00% SDS Specification MoL

Chemical & Physical Properties
CAS Number74764-40-2
Catalog No.2A-9047788
Chinese Name盐酸苄普地尔
Synonyms3-isobutoxy-2-pyrrolidino-n-phenyl-n-benzylpropylaminehydrochloridehydrate; MFCD00065498; l)-,monohydrochloride,monohydrate; angopril; Bepridil hydrochloride,N-Benzyl-N-(3-isobutoxy-2-pyrrolidin-1-yl-propyl)anilinehydrochloride
Molecular FormulaC24H37ClN2O2
Molecular Weight403.00
Purity98.00
Melting Point91 ±2°
Appearancepowder
Storage ConditionDesiccate at RT
ApplicationBepridil hydrochloride hydrate ((±)-Bepridil hydrochloride hydrate) is a non-selective, long-acting calcium channel (Ca+ channel) antagonist, sodium ion, potassium ion channel (Na+, K+ channel) inhibi
PubChem ID24277824
MDL NumberMFCD00065498
SMILESCl.CC(C)COCC(CN(Cc1ccccc1)c2ccccc2)N3CCCC3
InChI1S/C24H34N2O.ClH/c1-21(2)19-27-20-24(25-15-9-10-16-25)18-26(23-13-7-4-8-14-23)17-22-11-5-3-6-12-22;/h3-8,11-14,21,24H,9-10,15-20H2,1-2H3;1H
InChI KeyJXBBWYGMTNAYNM-UHFFFAOYSA-N
NACRES CodeNA.77
UNSPSC12352202
Hazard Symbolstransportation
MSDSmsds/47788_1_74764_40_2.pdf
BioactivityBepridil hydrochloride hydrate ((±)-Bepridil hydrochloride hydrate) is a non-selective, long-acting Ca+ channel antagonist and Na+, K+ channel inhibitor, with antianginal and type I antiarrhythmic effects. Bepridil hydrochloride hydrate also acts as a cardiac Na+/Ca2+ exchange (NCX1) inhibitor. Bepridil hydrochloride hydrate can be used for the research of cardiovascular disorders[1][2][3][4][5]. Related Catalog Signaling Pathways >> Membrane Transporter/Ion Channel >> Calcium Channel Research Areas >> Cardiovascular Disease Target Ca2+ In Vitro Bepridil hydrochloride hydrate blockades of Ca2+-dependent action potentials in vascular smooth muscle of dog coronary artery[2]. Bepridil hydrochloride hydrate blocks Ca currents and Na currents with IC50s of 0.5 μM and 30 μM, respectively in cultured ventricular cells[4]. Bepridil hydrochloride hydrate decreases IKs under blockade of IKr with E4031 (5 μM), in a concentration-dependent manner[5]. In Vivo Bepridil hydrochloride hydrate exhibits a half-life of averages 33±15 hours after single-dose administration[6]. References [1]. A Gill, et al. Pharmacology of Bepridil. Am J Cardiol. 1992 Apr 9;69(11):11D-16D. [2]. D R Harder, et al. Bepridil Blockade of Ca2+-dependent Action Potentials in Vascular Smooth Muscle of Dog Coronary Artery. J Cardiovasc Pharmacol. Jul-Aug 1981;3(4):906-14. [3]. Yasuhide Watanabe. Cardiac Na +/Ca 2+ Exchange Stimulators Among Cardioprotective Drugs. J Physiol Sci. 2019 Nov;69(6):837-849. [4]. A Yatani, et al. Bepridil Block of Cardiac Calcium and Sodium Channels. J Pharmacol Exp Ther. 1986 Apr;237(1):9-17. [5]. J C Wang, et al. Bepridil Differentially Inhibits Two Delayed Rectifier K(+) Currents, I(Kr) and I(Ks), in Guinea-Pig Ventricular Myocytes. Br J Pharmacol. 1999 Dec;128(8):1733-8. [6]. L Z Benet, et al. Pharmacokinetics and Metabolism of Bepridil. Am J Cardiol. 1985 Mar 15;55(7):8C-13C. Chemical & Physical Properties Melting Point 91 ±2° Molecular Formula C24H37ClN2O2 Molecular Weight 421.01600 Exact Mass 420.25400 PSA 24.94000 LogP 5.50580 Appearance of Characters powder | white InChIKey UEECHQPWQHYEDE-UHFFFAOYSA-N SMILES CC(C)COCC(CN(Cc1ccccc1)c1ccccc1)N1CCCC1.Cl.O Storage condition Desiccate at RT
Use ofBepridil hydrochloride hydrate ((±)-Bepridil hydrochloride hydrate) is a non-selective, long-acting Ca+ channel antagonist and Na+, K+ channel inhibitor, with antianginal and type I antiarrhythmic effects. Bepridil hydrochloride hydrate also acts as a cardiac Na+/Ca2+ exchange (NCX1) inhibitor. Bepridil hydrochloride hydrate can be used for the research of cardiovascular disorders[1][2][3][4][5]. Properties Articles34 Name bepridil hydrochloride monohydrate Synonym More Synonyms Bepridil hydrochloride Biological Activity Description Bepridil hydrochloride hydrate ((±)-Bepridil hydrochloride hydrate) is a non-selective, long-acting Ca+ channel antagonist and Na+, K+ channel inhibitor, with antianginal and type I antiarrhythmic effects. Bepridil hydrochloride hydrate also acts as a cardiac Na+/Ca2+ exchange (NCX1) inhibitor. Bepridil hydrochloride hydrate can be used for the research of cardiovascular disorders[1][2][3][4][5]. Related Catalog Signaling Pathways >> Membrane Transporter/Ion Channel >> Calcium Channel Research Areas >> Cardiovascular Disease In Vitro Bepridil hydrochloride hydrate blockades of Ca2+-dependent action potentials in vascular smooth muscle of dog coronary artery[2]. Bepridil hydrochloride hydrate blocks Ca currents and Na currents with IC50s of 0.5 μM and 30 μM, respectively in cultured ventricular cells[4]. Bepridil hydrochloride hydrate decreases IKs under blockade of IKr with E4031 (5 μM), in a concentration-dependent manner[5]. References [1]. A Gill, et al. Pharmacology of Bepridil. Am J Cardiol. 1992 Apr 9;69(11):11D-16D. [2]. D R Harder, et al. Bepridil Blockade of Ca2+-dependent Action Potentials in Vascular Smooth Muscle of Dog Coronary Artery. J Cardiovasc Pharmacol. Jul-Aug 1981;3(4):906-14. [3]. Yasuhide Watanabe. Cardiac Na +/Ca 2+ Exchange Stimulators Among Cardioprotective Drugs. J Physiol Sci. 2019 Nov;69(6):837-849. [4]. A Yatani, et al. Bepridil Block of Cardiac Calcium and Sodium Channels. J Pharmacol Exp Ther. 1986 Apr;237(1):9-17. [5]. J C Wang, et al. Bepridil Differentially Inhibits Two Delayed Rectifier K(+) Currents, I(Kr) and I(Ks), in Guinea-Pig Ventricular Myocytes. Br J Pharmacol. 1999 Dec;128(8):1733-8. Chemical & Physical Properties Exact Mass 420.25400 PSA 24.94000 LogP 5.50580 Appearance of Characters powder | white InChIKey UEECHQPWQHYEDE-UHFFFAOYSA-N Storage condition Desiccate at RT
Transport InfoShipping Name: UN
MSDS Transport InfoModule 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 United Nations shipping name European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Danger Regulations: No International Maritime Danger Regulations International Air Transport Danger Regulations: No Marine pollutants (yes/no): No 14.6 Special reminder to users No data available
Related Products in Specialty Chemicals
Methacryloxymethyltris(trimethylsiloxy)silane74681-63-32A-9047780
Ticarcillin sodium74682-62-52A-9047781
1-(3-Bromophenyl)-1-methylethylamine74702-93-52A-9047782
4-Amino-L-phenyl-N-phthalylalanine ethyl ester74743-23-02A-9047785
Methylthiomethyl hexanoate74758-91-12A-9047786
2,6-Dimethylbenzylamine74788-82-22A-9047791
Cefpiramide sodium74849-93-72A-9047794
4-(2-Methyl-1H-imidazol-1-yl)phenylamine74852-81-62A-9047797
4-Amino-3,5-dimethylbenzonitrile74896-24-52A-9047808
Methyl 3,5-dibromo-4-methylbenzoate74896-66-52A-9047809
Browse all Specialty Chemicals products »
Contact Us

Phone:

630-322-8886

630-322-8887

Email:

[email protected]

Office Locations:

Chicago, IL, USA

San Francisco, CA, USA