Metoprolol tartrate
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Metoprolol tartrate
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CAS No:
56392-17-7
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Formula:
C15H25NO3.1/2C4H6O6
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Chemical Name:
Metoprolol tartrate
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Synonyms:
2-Propanol,1-[4-(2-methoxyethyl)phenoxy]-3-[(1-methylethyl)amino]-,(2R,3R)-2,3-dihydroxybutanedioate (2:1);2-Propanol,1-[4-(2-methoxyethyl)phenoxy]-3-[(1-methylethyl)amino]-,(±)-,[R-(R*,R*)]-2,3-dihydroxybutanedioate (2:1) (salt);2-Propanol,1-[4-(2-methoxyethyl)phenoxy]-3-[(1-methylethyl)amino]-,(2R,3R)-2,3-dihydroxybutanedioate (2:1) (salt);Metoprolol tartrate;Lopresor;Seloken;Betaloc;Slow Lopresor;H 93/26;Metoprolol tartrate (2:1);(±)-Metoprolol tartrate;Beloc;(±)-Metoprolol bitartrate;1-(Isopropylamino)-3-[4-(2-methoxyethyl)phenoxy]-2-propanol tartrate;Vasocardin;(±)-1-(Isopropylamino)-3-[4-(2-methoxyethyl)phenoxy]-2-propanol tartrate;2-Propanol,1-[4-(2-methoxyethyl)phenoxy]-3-[(1-methylethyl)amino]-,[R-(R*,R*)]-2,3-dihydroxybutanedioate (2:1) (salt);Selopral;CGP 2175E;Prelis;HCTCGP 2175E;Metoprolol (+)-tartrate;Metapro;Metolar;(±)Metoprolol-(+)-tartarate salt;MetoHEXAL;RS-metoprolol tartrate;129947-83-7;54112-93-5;55250-54-9;60168-92-5;71307-49-8;74220-04-5
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CAS No:
Description
Metoprolol is a cardioselective β1-adrenergic blocking agent.Target: β1- adrenergic ReceptorPatients took 50 mg metoprolol twice daily with weekly titration to response or 200 mg twice daily. beta(1)-adrenergic receptor polymorphisms are important determinants of antihypertensive response to metoprolol. In the future, codon 49 and 389 genotypes or beta(1)-adrenergic receptor haplotypes might be used to predict the diastolic blood pressure response to metoprolol in patients with hypertens
Metoprolol tartrate is a member of phenols and an alcohol.|A selective adrenergic beta-1 blocking agent that is commonly used to treat ANGINA PECTORIS; HYPERTENSION; and CARDIAC ARRHYTHMIAS.
Characteristics
216.50000
1.88560
white to off-white
1.1946 (rough estimate)
120-123 °C
398.6ºC at 760 mmHg
9℃
soluble in water (>1000 mg/ml), methanol (>500 mg/ml), chloroform (496 mg/ml), ethanol (31 mg/ml at 25°C), and DMSO (100 mg/ml at 25°C).
Desiccate at RT
Oral-Rat LD50: 5500 mg/kg; Oral-Mouse LD50: 1500 mg/kg
Combustible; Fire site decomposes toxic nitrogen oxide gas
Safety Information
UN1230 - class 3 - PG 2 - Methanol, solution
3
11-23/24/25-39/23/24/25
7-16-36/37-45-24/25
UB7450100
F,T
Warehouse low temperature, ventilated, dry
Stable. Incompatible with strong oxidizing agents.
P210-P260-P280-P301 + P310-P311
H225-H301 + H311 + H331-H370
|Warning|H302 (11.39%): Harmful if swallowed [Warning Acute toxicity, oral]|P201, P202, P264, P270, P273, P280, P281, P301+P312, P302+P352, P305+P351+P338, P308+P313, P321, P330, P332+P313, P337+P313, P362, P405, and P501|Aggregated GHS information provided by 80 companies from 21 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Drug Information
Agents used for the treatment or prevention of cardiac arrhythmias. They may affect the polarization-repolarization phase of the action potential, its excitability or refractoriness, or impulse conduction or membrane responsiveness within cardiac fibers. Anti-arrhythmia agents are often classed into four main groups according to their mechanism of action: sodium channel blockade, beta-adrenergic blockade, repolarization prolongation, or calcium channel blockade. (See all compounds classified as Anti-Arrhythmia Agents.)|Drugs used in the treatment of acute or chronic vascular HYPERTENSION regardless of pharmacological mechanism. Among the antihypertensive agents are DIURETICS; (especially DIURETICS, THIAZIDE); ADRENERGIC BETA-ANTAGONISTS; ADRENERGIC ALPHA-ANTAGONISTS; ANGIOTENSIN-CONVERTING ENZYME INHIBITORS; CALCIUM CHANNEL BLOCKERS; GANGLIONIC BLOCKERS; and VASODILATOR AGENTS. (See all compounds classified as Antihypertensive Agents.)|Drugs that bind to and block the activation of ADRENERGIC BETA-1 RECEPTORS. (See all compounds classified as Adrenergic beta-1 Receptor Antagonists.)|Drugs that inhibit the actions of the sympathetic nervous system by any mechanism. The most common of these are the ADRENERGIC ANTAGONISTS and drugs that deplete norepinephrine or reduce the release of transmitters from adrenergic postganglionic terminals (see ADRENERGIC AGENTS). Drugs that act in the central nervous system to reduce sympathetic activity (e.g., centrally acting alpha-2 adrenergic agonists, see ADRENERGIC ALPHA-AGONISTS) are included here. (See all compounds classified as Sympatholytics.)
Beloc Duriles
Metoprolol tartrate Use and Manufacturing
A b1-Adrenergic blocker
Human Drugs -> FDA Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) -> Active Ingredients
Computed Properties
Molecular Weight:684.8
Hydrogen Bond Donor Count:8
Hydrogen Bond Acceptor Count:14
Rotatable Bond Count:21
Exact Mass:684.38332523
Monoisotopic Mass:684.38332523
Topological Polar Surface Area:217
Heavy Atom Count:48
Complexity:349
Defined Atom Stereocenter Count:2
Undefined Atom Stereocenter Count:2
Covalently-Bonded Unit Count:3
Compound Is Canonicalized:Yes
Drug Function and Efficacy
This drug belongs to Class 2A, i.e., a β1-receptor blocker without partial agonist activity (cardioselective β-receptor blocker). It has a selective blocking effect on β1-receptors, no PAA (partial agonist activity), and no membrane stabilizing effect. Its effect on blocking β-receptors is approximately equal to that of propranolol (PP), and its selectivity for β1-receptors is slightly inferior to that of atenolol. Metoprolol's effects on the heart, such as slowing heart rate, inhibiting cardiac contractility, reducing automaticity, and delaying atrioventricular conduction time, are similar to those of propranolol and atenolol (AT). Its effect on reducing elevated blood pressure and heart rate during exercise testing is also similar to that of PP and AT. Its contraction effect on vascular and bronchial smooth muscle is weaker than that of PP, so its effect on the respiratory tract is also smaller, but still stronger than that of AT. Metoprolol can also reduce plasma renin activity.
Registered Holders
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KOPRAN RESEARCH LABORATORIES LTD
Active
United States
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MSN LIFE SCIENCES PRIVATE LTD
Active
United States
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CTX LIFE SCIENCES PVT LTD
Active
United States
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