Adrenergic blocking agents

The active enantiomer of propranolol, a &beta-adrenergic receptor antagonist with log Kd values of -8.16, -9.

The active enantiomer of propranolol, a &beta-adrenergic receptor antagonist with log Kd values of -8.16, -9.

The active enantiomer of propranolol, a &beta-adrenergic receptor antagonist with log Kd values of -8.16, -9.

Application ( S )-(&#8722:)-Propranolol hydrochloride has been used: as a non-selective &#946:-blocker propranolol to inhibit the actions of epinephrine in mice as a &#946:1- and &#946:2-aadrenergic receptor blocker in rat as a medium

Application ( S )-(&#8722:)-Propranolol hydrochloride has been used: as a non-selective &#946:-blocker propranolol to inhibit the actions of epinephrine in mice as a &#946:1- and &#946:2-aadrenergic receptor blocker in rat as a medium

ApplicationS)-3-Amino-2-piperidone hydrochloride can be used as a building block for the synthesis of 5-hydroxy-2-[(3S)-2-oxo-3-piperidinyl]-1H-isoindole-1,3(2H)-dione by reacting with 4-hydroxyphthalic anhydride.[1] It is also used to prepare

ApplicationS)-3-Amino-2-piperidone hydrochloride can be used as a building block for the synthesis of 5-hydroxy-2-[(3S)-2-oxo-3-piperidinyl]-1H-isoindole-1,3(2H)-dione by reacting with 4-hydroxyphthalic anhydride.[1] It is also used to prepare

ApplicationS)-3-Amino-2-piperidone hydrochloride can be used as a building block for the synthesis of 5-hydroxy-2-[(3S)-2-oxo-3-piperidinyl]-1H-isoindole-1,3(2H)-dione by reacting with 4-hydroxyphthalic anhydride.[1] It is also used to prepare

ApplicationS)-3-Amino-2-piperidone hydrochloride can be used as a building block for the synthesis of 5-hydroxy-2-[(3S)-2-oxo-3-piperidinyl]-1H-isoindole-1,3(2H)-dione by reacting with 4-hydroxyphthalic anhydride.[1] It is also used to prepare

(S)-4-(tert-Butyl)-2-(pyrazin-2-yl)-4,5-dihydrooxazole.

(S)-4-(tert-Butyl)-2-(quinolin-8-yl)-4,5-dihydrooxazole.

(S)-4-(tert-Butyl)-2-(quinolin-8-yl)-4,5-dihydrooxazole.