Effect of CI-922, a potential new antiallergy agent, on arachidonic acid metabolism in vitro

Author:

Boctor Amal M.,Pugsley Thomas A.

Publisher

Springer Science and Business Media LLC

Subject

Immunology,Immunology and Allergy

Reference16 articles.

1. Robichaud, L. J., andR. L. Adolphson. 1984. A new mediator release inhibitor: The in vitro pharmacology of CI-922, (4H-furo[3,2-b]indole-2-carboxamide,3,7-dimethoxy-4-phenyl-N-1H-tetrazol-5-yl).J. Allergy Clin. Immunol. 73(1, part II):184.

2. Adolphson, R. L., andL. J. Robichaud. 1984. In vivo antiallergic activity of CI-922 (4H-furo[3,2-b]indole-2-carboxamide,3,7-dimethoxy-4-phenyl-N-1H-tetrazol-5-yl).J. Allergy Clin. Immunol. 73(1, part II): 128.

3. Hope, W. C., A. F. Welton, C. Fiedler-Nagy, C. Batula-Bernardo, andJ. W. Coffey. 1983. In vitro inhibition of the biosynthesis of slow-reacting substance of anaphlaxis (SRS-A) and lipoxygenase activity by quercetin.Biochem. Pharmacol. 32:367?371.

4. Sun, F. F., andJ. C. McGuire. 1984. Inhibition of human neutrophil arachidonate 5-lipoxygenase by 6,9-deepoxy-6,9-(phenylimino)-?6,8-prostaglandin I1 (U-60257).Prostaglandins 26:211?221.

5. Dawson, W., andW. J. F. Sweatman. 1980. The pharmacology of isamoxole [2-methyl-N-butyl-N(4-methyloxazole-2-yl) propanamide] LRCL 3950, a new antiallergic compound.Br. J. Pharmacol. 71:387?398.

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