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Pentacyclic triterpenes
United States Patent: 6,433,010
Glinski ,   et al. August 13, 2002

Abstract
The present invention relates to fungicidally effective compositions containing at least one pentacyclic triterpene compound.


Pentacyclic triterpenes
United States Patent:  6,303,589
Glinski ,   et al.      October 16, 2001

Abstract
The present invention relates to fungicidally effective compositions containing at least one pentacyclic triterpene compound.


Subsituted Isocoumarins as Serine Protease Inhibitors and Anti-Inflammatory Agents
United States Patent    5,324,648
Glinski ,   et al.      Jun. 28, 1994

Abstract
Substituted isocoumarins, their use in inhibiting serine proteases with trypsin-like, chymotrypsin-like and elastase-like specificity and their roles as anti-inflammatory agents.


Quaternary Pyridinium Compounds and Uses Therefor
United States Patent    5,290,942
Glinski ,   et al.      Mar. 1, 1994

Abstract
Quaternary pyridinium compounds for use as acetylcholinesterase inhibitors of the following formulas:

Quarternary Pyridinium Compounds


METHOD OF TREATING CANCERS SENSITIVE TO TREATMENT WITH WATER SOLUBLE DERIVATIVES OF TAXOL

United States Patent    5,157,049
Date of Patent:     Oct. 20, 1992

Inventors
Rudiger D. Haugwitz, Bethesda, Md. Leon Zalkow, Atlanta, Ga.; Jan Glinski, Ridgefield CT, Mathew Suffness, Silver Spring, Md.; Howard M. Deutsch, Atlanta, Ga.; Venkatachala Narayanan

Abstract
The invention involves the treatment of cancer in humans by administering water soluble derivatives of taxol. The types of cancer so treatable are those sensitive to treatment with taxol.


QUATERNARY PYRIDINIUM COMPOUNDS
United States Patent    5,206,371
Date of Patent:     Apr. 27, 1993

Inventors
James C. Powers; Sheldon W. May, both of Atlanta; Maria A. Hernandez, Norcross, all of Ga.; Steve Thornton, Raleigh, N.C.; Jan Glinski, New Fairfield, CT

Abstract
Quaternary pryidinium compounds, their use in inhibiting acetylcholinesterase, their roles in the prophylaxis and treatment of organophosphate poisoning, their roles in anticholinesterase therapy and their roles as agents mimicking or opposing the actions of the natural neurotransmitter acytylcholine.


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