Name | (±)-Bufuralol hydrochloride |
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Synonyms | 1-(7-Ethyl-1-benzofuran-2-yl)-2-[(2-methyl-2-propanyl)amino]ethan ol hydrochloride (1:1) |
Description | Bufuralol hydrochloride (Ro 3-4787 hydrochloride) is a potent non-selective, orally active β-adrenoreceptor antagonist with partial agonist activity. Bufuralol hydrochloride is a CYP2D6 probe substrate[1][2]. |
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Related Catalog | |
In Vitro | Bufuralol is widely used in the characterization of CYP2D6 activity, and possesses aromatic rings and a basic nitrogen that are characteristic of CYP2D6 substrates[3]. |
In Vivo | Bufuralol metabolism mediated by NADPH exhibits biphasic kinetics and is less efficient than that observed in the presence of cumene hydroperoxide (CuOOH) in and monkey intestines, in agreement with the observations in the livers[4]. |
References |
Boiling Point | 393.2ºC at 760 mmHg |
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Melting Point | 143-146ºC |
Molecular Formula | C16H24ClNO2 |
Molecular Weight | 297.82000 |
Flash Point | 191.6ºC |
Exact Mass | 297.15000 |
PSA | 45.40000 |
LogP | 4.60960 |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xn |
Risk Phrases | 22 |
RIDADR | NONH for all modes of transport |
Precursor 6 | |
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DownStream 0 |