Patents by Inventor Clyde R. Kinsolving

Clyde R. Kinsolving 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: 4845122
    Abstract: As an anti-allergic treatment for warm-blooded animals, therapeutic amounts of a compound having the formula I (including acid salts thereof) or II are administered: ##STR1## where; R is OR.sup.4 or NHR.sup.5 in which R.sup.4 is hydrogen or lower alkyl, R.sup.5 is selected from phenyl and phenyl monosubstituted with halogen, lower alkyl, lower alkoxy, R.sup.1 and R.sup.2 are independently hydrogen or lower alkyl, andR.sup.3 is selected from lower alkyl, arylcyclopropyl, naphthyl, phenyl, and phenyl monosubstituted with lower alkyl, lower alkoxy, trifluoromethyl, halogen, nitro, carboxyl, or ethyl carboxylate; ##STR2## R.sup.6 is lower alkyl, R.sup.7 is selected from phenyl and phenyl monosubstituted with lower alkyl, lower alkoxy, halogen or acetyl, and M is an alkali or alkaline earth metal.
    Type: Grant
    Filed: December 5, 1986
    Date of Patent: July 4, 1989
    Inventors: Vassil S. Georgiev, Clyde R. Kinsolving, Robert A. Mack
  • Patent number: 4730063
    Abstract: Alkali metal 2,5-dihydro-3-ethoxycarbonyl-2-[(substituted phenyl)amino]-4-furanyloxides are useful as anti-allergy agents.
    Type: Grant
    Filed: December 5, 1986
    Date of Patent: March 8, 1988
    Assignee: Pennwalt Corportion
    Inventors: Vassil S. Georgiev, Clyde R. Kinsolving, Robert A. Mack
  • Patent number: 4614810
    Abstract: 4,5-dihydro-4-oxo-2-[(2-trans-phenylcyclopropyl)amino]-3-furancarboxylic acids and derivatives are described.
    Type: Grant
    Filed: September 24, 1984
    Date of Patent: September 30, 1986
    Assignee: Pennwalt Corporation
    Inventors: Vassil S. Georgiev, Robert A. Mack, Clyde R. Kinsolving
  • Patent number: 4600782
    Abstract: Substituted spiro[oxazolidine-5,2'-adamantane] compounds are described.
    Type: Grant
    Filed: June 15, 1984
    Date of Patent: July 15, 1986
    Assignee: Pennwalt Corporation
    Inventors: Vassil S. Georgiev, Clyde R. Kinsolving
  • Patent number: 4557865
    Abstract: 5-Substituted and/or N-Substituted 4-azatricyclo [4.3.1.1.sup.3,8 ]undecane and 4-azatricyclo[4.3.1.1.sup.3,8 ]undecan-5-one compounds are prepared.
    Type: Grant
    Filed: May 7, 1984
    Date of Patent: December 10, 1985
    Assignee: Pennwalt Corporation
    Inventors: Vassil S. Georgiev, Clyde R. Kinsolving
  • Patent number: 4537908
    Abstract: Treatment of warm-blooded animals infected with the herpes II virus by concurrently orally administering an antiviral agent effective against said virus and suitable for oral administration while topically applying the same or a different such agent to lesions caused by the infection. Effective antivirals include .alpha.,.alpha.-dimethyl-beta-adamantylethylamine and N,N-dialkyl,.alpha.,.alpha.-dimethyl-beta-adamantylethylamine.
    Type: Grant
    Filed: September 27, 1982
    Date of Patent: August 27, 1985
    Assignee: Pennwalt Corporation
    Inventors: Ronald C. Griffith, Clyde R. Kinsolving
  • Patent number: 4386105
    Abstract: Warm-blooded animals are treated by administering to the animal a dosage, effective to alleviate the symptoms of measles, of a compound of the formula I or its acid salt: ##STR1## wherein R.sub.1 and R.sub.2 are selected from the class consisting of hydrogen and --CH.sub.3 and at least on pharmaceutically acceptable carrier, wherein the compound is 0.01 to 95% by weight of the composition.
    Type: Grant
    Filed: February 19, 1982
    Date of Patent: May 31, 1983
    Assignee: Pennwalt Corporation
    Inventors: Clyde R. Kinsolving, Ronald C. Griffith
  • Patent number: 4351847
    Abstract: Warm-blooded animals are treated by administering to the animal a dosage, effective to prevent or to alleviate the symptoms of herpes virus, type II, of a compound of the formula I or its acid salt: ##STR1## wherein R.sub.1 and R.sub.2 are selected from the class consisting of H and --CH.sub.3 ; and at least one pharmaceutically acceptable carrier, wherein the compound is 0.01 to 95% by weight of the composition.
    Type: Grant
    Filed: June 26, 1981
    Date of Patent: September 28, 1982
    Assignee: Pennwalt Corporation
    Inventors: Ronald C. Griffith, Clyde R. Kinsolving