Name | 1-(isopropylamino)-3-[4-[2-(cyclopropylmethoxy)ethyl]phenoxy]propan-2-ol hydrochloride |
Synonyms | SL 75212 BETAXOLOL HCL BETAXOLOL CHLOROHYDRATE Betaxolol Hydrochloride BETAXOLOL HYDROCHLORIDE BETAXOLOL HYDROCHLORIDE MONOHYDRATE (+-)-1-(4-(2-(cyclopropylmethoxy)ethyl)phenoxy)-3-(isopropylamino)-2-propano 1-(4-(2-(cyclopropylmethoxy)ethyl)phenoxy)-3-isopropylaminopropan-2-olhydroc 1-[4-[2-(CYCLOPROPYLMETHOXY)ETHYL]PHENOXY]-3-ISOPROPYLAMINO-2-PROPANOL HYDROCHLORIDE 1-(isopropylamino)-3-[4-[2-(cyclopropylmethoxy)ethyl]phenoxy]propan-2-ol hydrochloride |
CAS | 63659-19-8 |
EINECS | 264-384-3 |
InChI | InChI=1/C18H29NO3.ClH/c1-14(2)19-11-17(20)13-22-18-7-5-15(6-8-18)9-10-21-12-16-3-4-16;/h5-8,14,16-17,19-20H,3-4,9-13H2,1-2H3;1H |
Molecular Formula | C18H30ClNO3 |
Molar Mass | 343.89 |
Melting Point | 116° |
Boling Point | 448°C at 760 mmHg |
Flash Point | 224.7°C |
Solubility | H2O: 36mg/mL, soluble |
Vapor Presure | 8.26E-09mmHg at 25°C |
Appearance | solid |
Color | white |
Merck | 14,1182 |
Storage Condition | 2-8°C |
In vitro study | Betaxolol protects retinal neurons. Betaxolol attenuates NMDA induction when β-adrenoceptor agonists are ineffective. Glutamate-induced LDH release was essentially completely blocked by the addition of Betaxolol (10 μm). Betaxolol (100 μm) is effective in preventing the release of LDH in cortical tissue caused by hypoxia. |
In vivo study | Changes in calreticulin and ChAT immunoreactivity were reduced and the B- wave was prevented by intraperitoneal injection of Betaxolol before regional anemia and reperfusion injury in rats. The inclusion of Betaxolol can partially block the changes caused by NMDA and hypoxia/glucose. |
Hazard Symbols | Xn - Harmful |
Risk Codes | 22 - Harmful if swallowed |
WGK Germany | 3 |
RTECS | UA9823000 |
HS Code | 2922504500 |
Toxicity | LD50 in mice (mg/kg): 944 orally; 37 i.v. (Manoury) |
Update Date: | 2022/11/12 10:05:38 |
biological activity | Betaxolol (SL 75212) is a beta 1 adrenergic receptor blocker with an IC50 of 6 m. |
Target | Value |
β1-adrenergic receptor | 6 μM |