Betaxolol hydrochloride
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Betaxolol hydrochloride
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CAS No:
63659-19-8
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Formula:
C18H29NO3.ClH
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Chemical Name:
Betaxolol hydrochloride
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Synonyms:
2-Propanol,1-[4-[2-(cyclopropylmethoxy)ethyl]phenoxy]-3-[(1-methylethyl)amino]-,hydrochloride (1:1);2-Propanol,1-[4-[2-(cyclopropylmethoxy)ethyl]phenoxy]-3-[(1-methylethyl)amino]-,hydrochloride;Betaxolol hydrochloride;Betoptic;SL 75212;Kerlone;SLD 212;Betoptima;Betapress;Optipress;Lusopress;72424-72-7
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CAS No:
Description
Betaxolol Hydrochloride is a selective beta1 adrenergic receptor blocker used in the treatment of hypertension and glaucoma.Target: Beta1 Adrenergic ReceptorBetaxolol is a cardioselective beta-adrenergic receptor blocking agent. Betaxolol (5 mg/kg via i.p. injection) was administered at 24 and then 44 h following the final chronic cocaine administration. Animals treated with betaxolol during cocaine withdrawal exhibited a significant attenuation of anxiety-like behavior characterized by
A cardioselective beta-1-adrenergic antagonist with no partial agonist activity.
Characteristics
50.7
3.58630
white solid
116 °C
448ºC at 760 mmHg
224.7ºC
H2O: 36 mg/mL, soluble
Store at RT
LD50 in mice (mg/kg): 944 orally; 37 i.v. (Manoury)
Safety Information
NONH for all modes of transport
3
22
UA9823000
Xn
P301 + P312 + P330
H302
|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P201, P202, P264, P270, P281, P301+P312, P308+P313, P330, P405, and P501|Aggregated GHS information provided by 49 companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Drug Information
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 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.)|Drugs that bind to and block the activation of ADRENERGIC BETA-1 RECEPTORS. (See all compounds classified as Adrenergic beta-1 Receptor Antagonists.)
Alcon, Betaxolol
Betaxolol hydrochloride Use and Manufacturing
antifungal
Human Drugs -> FDA Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) -> Active Ingredients
Computed Properties
Molecular Weight:343.9
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:11
Exact Mass:343.1914215
Monoisotopic Mass:343.1914215
Topological Polar Surface Area:50.7
Heavy Atom Count:23
Complexity:286
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
Drug Function and Efficacy
1. Betaxolol hydrochloride is a cardioselective β1-adrenergic receptor blocker; 2. It does not have a cell membrane stabilizing effect, so it does not affect the sensitivity of the cornea; 3. It does not have endogenous sympathomimetic activity; 4. It can reduce the intraocular pressure of patients with high intraocular pressure or glaucoma; 5. It exerts an intraocular pressure-lowering effect by reducing the production of aqueous humor; 6. It has minimal adverse reactions to the heart and lungs; 7. It does not inhibit the effect of isoproterenol; 8. It has little effect on blood pressure and heart rate; 9. It has no carcinogenic, mutagenic or teratogenic effects.
Registered Holders
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INDOCO REMEDIES LTD
Active
United States
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FINORGA S.A.S.
Active
Japan
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LUSOCHIMICA SPA
Active
Brazil
Recommended Suppliers of Betaxolol hydrochloride
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CN
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