Journal of Medicinal Chemistry 1980-11-01

Optically active derivatives of imidazolines. alpha-Adrenergic blocking properties.

F L Hsu, A Hamada, M E Booher, H Fuder, P N Patil, D D Miller

Index: J. Med. Chem. 23 , 1232, (1980)

Full Text: HTML

Abstract

The synthesis and alpha-adrenergic blocking activity of a series of optically active 2,4-disubstituted imidazolines are presented. The substituted analogues of naphazoline, tolazoline, and clonidine possess moderate alpha-adrenergic blocking activity with -log KB values in the range from 4.77 to 6.57. The differences between the alpha-adrenergic blocking activity of the stereoisomers of the 2,4-disubstituted imidazolines were small or insignificant in the rabbit aortic tissue preparations.


Related Compounds

Related Articles:

Capillary gas chromatographic determination of methylglyoxal from serum of diabetic patients by precolumn derivatization with 1,2-diamonopropane.

2008-09-15

[J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 873(1) , 15-9, (2008)]

Stereochemical studies of adrenergic drugs. Optically active derivatives of imidazolines.

1976-12-01

[J. Med. Chem. 19 , 1382, (1976)]

Chiral cyanide-bridged Mn(II)Mn(III) ferrimagnets, [Mn(II)(HL)(H2O)][Mn(III)(CN)6].2H2O (L = S- or R-1,2-diaminopropane): syntheses, structures, and magnetic behaviors.

2007-01-17

[J. Am. Chem. Soc. 129(2) , 248-9, (2007)]

Distribution of diaminopropane, putrescine and cadaverine in Haemophilus and Actinobacillus.

2000-01-01

[Microbios 103(404) , 43-51, (2000)]

Activation and cross-reactivity pattern of a new allergen in adhesive plaster.

2000-01-01

[Contact Dermatitis 42(1) , 11-7, (2000)]

More Articles...