Synthesis and vasorelaxant properties of hybrid molecules out of NO-donors and the β-receptor blocking drug propranolol

Bioorganic and Medicinal Chemistry Letters

Volumn 14, Issue 19, 2004, Pages 4995-4997

  Decker, Michael ^a   König, Andreas ^a   Glusa, Erika ^a   Lehmann, Jochen ^a  

^a FRIEDRICH SCHILLER UNIVERSITY JENA   (Germany)

Author keywords

Hybrids; NO donors; Propranolol; Vasorelaxation

Indexed keywords

3 NITROOXYPIVALOYL ACID; 3 NITROOXYPIVALOYLPROPRANOLOL; AMIDE; BETA ADRENERGIC RECEPTOR BLOCKING AGENT; ESTER DERIVATIVE; N ACETYL S NITROSOPENICILLAMINE; N ACETYL S NITROSOPENICILLAMINE PROPRANOLOL; NITRIC OXIDE DONOR; PROPRANOLOL; PROPRANOLOL DERIVATIVE; UNCLASSIFIED DRUG; VASODILATOR AGENT;

ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DRUG EFFECT; DRUG POTENCY; DRUG SYNTHESIS; HYBRID; IN VITRO STUDY; MOLECULE; NONHUMAN; PULMONARY ARTERY; SWINE; VASODILATATION;

ANIMALS; NITRIC OXIDE DONORS; PRODRUGS; PROPRANOLOL; SWINE; VASODILATOR AGENTS;

SUIDAE;

EID: 4444316090     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2004.07.014     Document Type: Article

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