Name | 5-[2-[3-(tert-butylamino)-2-hydroxypropyl]sulfanyl-1,3-thiazol-4-yl]thiophene-2-carboxamide |
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Synonyms |
Arotinolo
5-(2-{[3-(tert-Butylamino)-2-hydroxypropyl]sulfanyl}-1,3-thiazol-4-yl)thiophene-2-carboxamide 5-[2-({2-Hydroxy-3-[(2-methyl-2-propanyl)amino]propyl}sulfanyl)-1,3-thiazol-4-yl]-2-thiophenecarboxamide Arottnolol Arotinolol UNII:394E3P3B99 2-Thiophenecarboxamide, 5-[2-[[3-[(1,1-dimethylethyl)amino]-2-hydroxypropyl]thio]-4-thiazolyl]- (±)-5-[2-[[3-[(1,1-Dimethylethyl)amino]-2-hydroxypropyl]thio]-4-thiazolyl]-2-thiophenecarboxamide ARL 2-(3'-tert-Butylamino-2'-hydroxypropylthio)-4-(5'-carbamoyl-2'-thienyl)thiazole 5-[2-({3-[(1,1-dimethylethyl)amino]-2-hydroxypropyl}thio)-1,3-thiazol-4-yl]thiophene-2-carboxamide |
Description | Arotinolol is a nonselective α/β-adrenergic receptor blocker and a vasodilating β-blocker. Arotinolol is an antihypertensive agent for the treatment of a variety of cardiovascular pathologies as well as non-cardiovascular diseases[1]. |
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Related Catalog | |
Target |
IC50: α/β-adrenergic receptor |
In Vivo | Arotinolol (oral gavage; 200 mg/kg; 8 weeks) can significantly decrease central arterial pressure (CAP) and pulse wave velocity (PWV), in addition, it reduces aortic collagen depositions and finally improves arterial stiffness in SHR mouse[1]. Animal Model: SHR mice[1] Dosage: 200 mg/kg Administration: Orally gavage; 200 mg/kg; once daily; 8 weeks Result: Improved arterial stiffness in SHR. |
References |
Density | 1.4±0.1 g/cm3 |
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Boiling Point | 599.8±60.0 °C at 760 mmHg |
Melting Point | 148-149ºC |
Molecular Formula | C15H21N3O2S3 |
Molecular Weight | 371.541 |
Flash Point | 316.6±32.9 °C |
Exact Mass | 371.079590 |
PSA | 170.02000 |
LogP | 2.67 |
Vapour Pressure | 0.0±1.8 mmHg at 25°C |
Index of Refraction | 1.646 |
Storage condition | 2-8°C |
Hazard Codes | Xi |
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~% 68377-92-4 |
Literature: US3932400 A1, ; US 3932400 A |
Precursor 1 | |
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DownStream 0 |