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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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2018
2018
Highlights • X-ray CT was effectively used to quantify soil seal/crust thickness.• Different micro-morphological zones within… Expand
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2002
2002
The effects of irreversible α1‐adrenoceptor antagonists, SZL‐49 (an alkylating analogue of prazosin), dibenamine and benextramine… Expand
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1996
1996
  • M. Eltze
  • European journal of pharmacology
  • 1996
  • Corpus ID: 4543117
alpha 1-Adrenoceptor agonists ((-)-adrenaline = (-)-noradrenaline > > L-phenylephrine > methoxamine > (-)-(4a R, 10a R)-3,4,4a,5… Expand
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1995
1995
Summary: The effects of the nonpeptide angiotensin II receptor antagonist losartan and the angiotensin-converting enzyme… Expand
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Highly Cited
1994
Highly Cited
1994
Three alpha 1-adrenergic receptors (ARs) have been cloned, i.e., the alpha 1B-, alpha 1C-, and alpha 1D-ARs. Compared with the… Expand
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1994
1994
1 It is known that activation of α1‐adrenoceptors causes renal vasoconstriction and increased tubular Na+ and water reabsorption… Expand
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1994
1994
The ability of putative selective irreversible ligands SZL-49 (1-(4-amino-6,7-dimethoxy-2,5-diene-2-carbonyl)) and CEC… Expand
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1992
1992
Separate genes for alpha-1A and alpha-1B adrenoceptors have now been identified. Whereas alpha-1 adrenoceptors are known to… Expand
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1990
1990
The peripheral hemodynamic effects of SZL-49, a prazosin analog capable of selectively inactivating the alpha 1a-adrenoceptor… Expand
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1990
1990
The interaction of agonists with alpha-1 receptor subtypes sensitive and resistant to alkylation by a prazosin analog [1-(4-amino… Expand
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