Carteolol hydrochloride

Carteolol hydrochloride Basic information
Product Name:Carteolol hydrochloride
Synonyms:CARTEOLOL (HYDROCHLORIDE);NSC 300906;OPC 1085;5-[3-[(1,1-Dimethylethyl)amino]-2-hydroxypropoxy]-3,4-dihydro-2(1H)-quinolinone Hydrochloride;5-[3-[(tert-butyl)amino]-2-hydroxypropoxy]-3,4-dihydro-2-quinolone monohydrochloride;Arteoptic;Caltidren;Carteol;Cartrol;dl-Carteolol hydrochloride
CAS:51781-21-6
MF:C16H25ClN2O3
MW:328.83
EINECS:257-415-7
Product Categories:API;CARTROL;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:51781-21-6.mol
Carteolol hydrochloride Structure
Carteolol hydrochloride Chemical Properties
Melting point 278°C
storage temp. Refrigerator
solubility Soluble in water, sparingly soluble in methanol, slightly soluble in ethanol 96 per cent, practically insoluble in methylene chloride.
form neat
color White to Off-White
Merck 14,1866
Safety Information
RTECS VC8282000
HS Code 2933790002
ToxicityLD50 in male mice, rats (mg/kg): 810, 1380 orally; 54.5, 158 i.v.; 380, 400 i.p. (Lang)
MSDS Information
Carteolol hydrochloride Usage And Synthesis
Chemical PropertiesCrystalline Solid
Usesβ-Adrenergic blocker. Antihypertensive; antianginal; antiarrhythmic; antiglaucoma.
Usesbeta-adrenergic blocker
Brand nameCartrol (Abbott); Ocupress (Novartis).
Biological Activitybeta-adrenergic antagonist are an important class of drugs for the treatment of various heart diseases, such as high blood pressure, insufficiency of blood flow to the heart muscle, irregular heart beat, thickened heart muscle, and decreased ability of the heart to empty or fill normally. β-blockers can also be used to treat migraine headache and increased eye pressure (glaucoma). carteolol is a nonselective beta-adrenoceptor antagonist.
in vitroprevious findings demonstrate that carteolol, unlike xamoterol, is a nonconventional partial agonist, which causes agonistic effects via interaction with the low-affinity propranolol-resistant site of β1-adrenoceptors and antagonistic actions by the high-affinity site of the same receptors [1].
in vivoboth 8-oh carteolol and carteolol suppressed the water-load induced intraocular pressure (iop) rise in rabbits. 8-oh carteolol was more effective in suppressing water-load induced iop rise in rabbits compared with carteolol on equimolar basis. both 8-oh carteololand carteolol caused a significant decrease in iop in monkeys. 8-oh carteolol was estimated to be more potent than carteolol in lowering iop on equimolar basis in monkeys [2].
references[1] maura floreani, guglielmina froldi, luigi quintieri, katia varani, pier andrea borea, maria teresa dorigo and paola dorigo. in vitro evidence that carteolol is a nonconventional partial agonist of guinea pig cardiac β1-adrenoceptors: a comparison with xamoterol. jpet 315:1386–1395, 2005
[2] sugiyama k, enya t, kitazawa y. ocular hypotensive effect of 8-hydroxycarteolol, a metabolite of carteolol. int ophthalmol. 1989 jan;13(1-2):85-9.
[3] trinquand c, romanet jp, nordmann jp, allaire c; groupe d'étude. efficacy and safety of long-acting carteolol 1% once daily. a double-masked, randomized study. j fr ophtalmol. 2003 feb;26(2):131-6.
Carteolol hydrochloride Preparation Products And Raw materials
Preparation Products8-hydroxycarteolol
D-Timolol maleate Betaxolol hydrochloride Timolol Brinzolamide Clenbuterol hydrochloride Tobramycin 5-METHOXY-3,4-DIHYDRO-1H-QUINOLIN-2-ONE Carteolol 2'-Methyl-3'-methoxyacetanilide Dihydroalprenolol 2-Methyl-3-methoxyaniline hydrochloride N1-[3-(3-AMINOPROPOXY)PHENYL]ACETAMIDE 5-HYDROXY-3,4-DIHYDRO-1H-QUINOLIN-2-ONE 2(1H)-Quinolinone, 5-[3-[(1,1-dimethylethyl)amino]-2-hydroxypropoxy]-3,4-dihydro-, monohydrochloride, (R)- Carteolol hydrochloride 2(1H)-Quinolinone, 5-[3-[(1,1-dimethylethyl)amino]-2-hydroxypropoxy]-3,4-dihydro-, monohydrochloride, (S)- 5-METHOXY-1,2,3,4-TETRAHYDRO-QUINOLINE HYDROCHLORIDE 4-PROPOXYACETANILINE

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