American Cyanamid Company

Raymond G Wilkinson

Andrew S Tomcufcik

Ralph G Child

Yang-I Lin

Thomas L Fields

Stanley A Lang, Jr

Soon M Kang

This invention concerns novel 3,6-bis(substituted) acridine N-oxides and N,N-dioxides which are active as modulators of the immune system in warm-blooded animals.

3,6-bis (substituted) acridine N-oxides and N,N-dioxides and methods of

This invention concerns novel substituted acridine compounds which are useful as modulators of the immune system in warm-blooded animals.

Substituted acridine derivatives useful as modulators of the immune

A method of modulating the immune response system in a warm-blooded animal by the administration of N-substituted-phenylthioanilines, N-substituted-phenylsulfinylanilines, and N-substituted-phenylsulfonylanilines, certain of which are new compounds.

2-Amino-4'(phenylsulfonyl) acetanilides

Novel 1-substituted-2-(substitutedimino)-1H-1,2-dihydrobenz[cd]indoles useful as inhibitors of platelet aggregation.

1-Substituted-2-(substituted-imino)-1H-1,2-dihydrobenz[cd]indoles

Novel 2-(substituted amino)benz[cd]indoles useful as inhibitors of platelet aggregation and the process for their preparation.

2-(Substituted amino)benz[cd]indoles

The preparation of 2-(1,3-diazacycloalkenyl)-2-hydrazones of 1-(substituted 2-benzofuranyl)-3-(substituted aryl)-2-propen-1-ones is described. These compounds are useful as anti-tubercular agents in warm blooded animals.

Substituted 2-benzofuranyl propenones as anti-tubercular agents

The preparation of 2-(1,3-Diazacycloalkenyl)-2-hydrazones of substituted chalcones is described. These compounds are useful as anti-tubercular agents in warm-blooded animals.

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Montvale, NJ, United States of America

Raymond G Wilkinson