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SZL 49

Known as: Piperazine, 1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-(bicyclo(2.2.2)octa-2,5-dien-2-ylcarbonyl)-, SZL-49 
National Institutes of Health

Papers overview

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2002
2002
The effects of irreversible α1‐adrenoceptor antagonists, SZL‐49 (an alkylating analogue of prazosin), dibenamine and benextramine… 
1996
1996
1. alpha 1-Adrenoceptor agonists, noradrenaline, phenylephrine, methoxamine, oxymetazoline and SDZ NVI 085 but not alpha 2… 
1996
1996
alpha 1-Adrenoceptor agonists ((-)-adrenaline = (-)-noradrenaline > > L-phenylephrine > methoxamine > (-)-(4a R, 10a R)-3,4,4a,5… 
1995
1995
Summary: The effects of the nonpeptide angiotensin II receptor antagonist losartan and the angiotensin-converting enzyme… 
1995
1995
We compared the inactivation of [3H]prazosin binding sites in membrane preparations of cell-lines expressing the cloned alpha 1b… 
1994
1994
A series of alpha 1-adrenoceptor agonists evoked concentration-dependent contraction of isolated guinea-pig spleen strips… 
1991
1991
A chemically reactive prazosin analog (SZL 49) has been suggested to be an alpha 1A-selective alkylating agent. We found SZL 49… 
1988
1988
In rat parotid acinar cells, maximal α1-adrenergic receptor stimulation (10−5 M epinephrine +10−5 M propranolol) leads to a rapid… 
1988
1988
In rat parotid acinar cells, maximal alpha 1-adrenergic receptor stimulation (10(-5) M epinephrine + 10(-5) M propranolol) leads…