Patents by Inventor James J. Korst

James J. Korst has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Patent number: 4491583
    Abstract: A process for inducing the production of endogenous interferon in a vertebrate animal which comprises parenterally, intranasally or topically adminstering to the animal an interferon-inducing effective amount of composition containing as the essential active ingredient a compound of the formula ##STR1## or a non-toxic acid addition salt thereof wherein R.sub.7 and R.sub.8 are each alkyl of from 12 to 30 carbon atoms and Z is selected from the group consisting of N-(lower alkyl)-piperazino and N-(W-hydroxy-lower alkyl)-piperazino, said lower alkyl groups having from 1 to 4 carbon atoms.
    Type: Grant
    Filed: July 18, 1983
    Date of Patent: January 1, 1985
    Assignee: Pfizer Inc.
    Inventors: Timothy H. Cronin, Hermann Faubl, William W. Hoffman, James J. Korst
  • Patent number: 4258061
    Abstract: Combating viral infections in vertebrate animals by administering to the animals a monoamine, a diamine or a triamine.
    Type: Grant
    Filed: February 13, 1978
    Date of Patent: March 24, 1981
    Assignee: Pfizer Inc.
    Inventors: Timothy H. Cronin, Hermann Faubl, William W. Hoffman, James J. Korst
  • Patent number: 4087552
    Abstract: Combating viral infections in vertebrate animals by administering to the animals an amine selected from those having the formulae: ##STR1## and the non-toxic acid addition salts thereof wherein R.sub.1 is selected from the group consisting of alkyl of from 1 to 20 carbon atoms, aralkyl, aryloxyalkyl, hydroxyalkyl of from 2 to 8 carbon atoms and ##STR2## R.sub.2 is selected from the group consisting of alkyl of from 12 to 20 carbon atoms, aralkyl and aryloxyalkyl of from 12 to 24 carbon atoms and ##STR3## R.sup.o is alkoxy of from 1 to 18 carbon atoms; EACH OF R' and R" is selected from the group consisting of hydrogen, alkyl, alkoxy of from 1 to 18 carbon atoms; R' and R" when taken together are methylenedioxy;Provided that the total number of carbon atoms in R.sup.o, R' and R" is from 5 to 48;R.sub.3 is selected from the group consisting of hydrogen, alkyl of from 1 to 20 carbon atoms, hydroxyalkyl of from 2 to 8 carbon atoms, phenylcarbamoyloxy(lower alkyl), .omega.
    Type: Grant
    Filed: May 18, 1976
    Date of Patent: May 2, 1978
    Assignee: Pfizer Inc.
    Inventors: Timothy H. Cronin, Hermann Faubl, William W. Hoffman, James J. Korst
  • Patent number: 4034040
    Abstract: Compounds of the formula ##STR1## or a non-toxic acid addition salt thereof wherein R.sub.1 is alkyl of from 1 to 20 carbon atoms;R.sub.2 is alkyl of from 12 to 20 carbon atoms;R.sub.3 is selected from the group consisting of hydrogen and hydroxyalkyl of from 2 to 8 carbon atoms; andR.sub.4 is selected from the group consisting of hydrogen, alkyl of from 1 to 8 carbon atoms and hydroxyalkyl of from 2 to 8 carbon atoms, said compounds are useful for combating viral infections in vertebrate animals.
    Type: Grant
    Filed: March 14, 1975
    Date of Patent: July 5, 1977
    Assignee: Pfizer Inc.
    Inventors: Timothy H. Cronin, Hermann Faubl, William W. Hoffman, James J. Korst