Patents by Inventor Edward S. Neiss

Edward S. Neiss 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: 5276060
    Abstract: The invention relates to methods useful in the treatment of benign, premalignant and malignant solid tumors, especially those of the skin comprising methods for the administration of pharmacologically active compositions containing catecholic butanes. The invention also relates to methods of preventing the occurrence of tumors, and the use of catecholic butanes as a sunscreening agent. The preferred catecholic butane is nordihydroguaiaretic acid. The preferred methods of application of the compositions containing catecholic butanes are by topical application and intratumor injection.
    Type: Grant
    Filed: April 15, 1991
    Date of Patent: January 4, 1994
    Assignee: Block/Chemex, G.P.
    Inventors: Edward S. Neiss, Larry M. Allen, Russell T. Jordan
  • Patent number: 5008294
    Abstract: The invention relates to methods useful in the treatment of benign, premalignant and malignant solid tumors, especially those of the skin comprising methods for the administration of pharmacologically active compositions containing catecholic butanes. The invention also relates to methods of preventing the occurence of tumors, and the use of catecholic butanes as a sunscreening agent. The preferred catecholic butane is nordihydroguaiaretic acid. The preferred methods of application of the compositions containing catecholic butanes are by topical application and intratumor injection.
    Type: Grant
    Filed: June 3, 1987
    Date of Patent: April 16, 1991
    Assignee: Chemex Pharmaceuticals, Inc.
    Inventors: Edward S. Neiss, Larry M. Allen
  • Patent number: 4804742
    Abstract: New peptides are disclosed which have biological activity of the same type as known calcitonins and which are amide analogs of natural calcitonins.
    Type: Grant
    Filed: December 5, 1986
    Date of Patent: February 14, 1989
    Assignee: Rorer Pharmaceutical Corporation
    Inventors: Edward S. Neiss, David Stevenson, Laurence L. Ho, Robert C. Liu, John T. Suh
  • Patent number: 4749698
    Abstract: Compounds having the general structure ##STR1## and their pharmaceutically acceptable salts, wherein the substituents are defined herein, which exhibit antihypertensive activity.
    Type: Grant
    Filed: July 8, 1985
    Date of Patent: June 7, 1988
    Assignee: Rorer Pharmaceutical Corporation
    Inventors: Edward S. Neiss, John T. Suh, John R. Regan, Jerry W. Skiles, Jeffrey N. Barton, James J. Mencel, Paul Menard
  • Patent number: 4746676
    Abstract: Compounds having the general structure ##STR1## and their pharmaceutically acceptable salts, wherein the substituents are defined herein, which exhibit antihypertensive activity.
    Type: Grant
    Filed: September 12, 1984
    Date of Patent: May 24, 1988
    Assignee: Rorer Pharmaceutical Corporation
    Inventors: Edward S. Neiss, John T. Suh, John R. Regan, Jerry W. Skiles, Jeffrey N. Barton, Paul Menard
  • Patent number: 4696939
    Abstract: Compounds of the formula ##STR1## and their pharmaceutically acceptable salts, wherein the substituents are as defined herein, having antihypertensive activity.
    Type: Grant
    Filed: November 29, 1985
    Date of Patent: September 29, 1987
    Assignee: USV Pharmaceutical Corporation
    Inventors: John T. Suh, John J. Piwinski, Howard Jones, Edward S. Neiss
  • Patent number: 4666906
    Abstract: Compounds of the formula ##STR1## and their pharmaceutically acceptable salts, wherein the substituents are as defined herein, having antihypertensive activity.
    Type: Grant
    Filed: July 19, 1985
    Date of Patent: May 19, 1987
    Assignee: USV Pharmaceutical Corporation
    Inventors: John J. Piwinski, John T. Suh, Paul Menard, Howard Jones, Edward S. Neiss, John R. Regan
  • Patent number: 4661515
    Abstract: Novel compounds possessing both angiotensin enzyme inhibitory activity and diuretic activity are disclosed. The compounds are represented by the general formula ##STR1## in which X is ##STR2## in which R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5 and R.sub.6 are hydrogen, alkyl, alkenyl, alkynyl, phenyl-alkyl, and cycloalkyl, and may be the same or different; n is an integer from 0 to 4 inclusive; M is alkenyl, alkynyl, cycloalkyl, cycloalkyl-alkyl, polycycloalkyl, polycycloalkyl-alkyl, aryl, aralkyl, heteroaryl, heteroaryl-alkyl, hetero-cyloalkyl, hetero-cycloalkyl-alkyl, fused aryl-cycloalkyl, fused aryl-cycloalkyl-alkyl, fused heteroaryl-cycloalkyl, fused heteroaryl-cycloalkyl-alkyl, alkoxyalkyl, alkylthioalkyl, alkylamino-alkyl, or dialkylaminoalkyl, or M and R.sub.6 taken together with the nitrogen to which M is bonded and the carbon to which R.sub.
    Type: Grant
    Filed: January 17, 1986
    Date of Patent: April 28, 1987
    Assignee: USV Pharmaceutical Corporation
    Inventors: Edward S. Neiss, John T. Suh, John J. Piwinski
  • Patent number: 4650854
    Abstract: New peptides are disclosed which have biological activity of the same type as known calcitonins and which are amide analogs of natural calcitonins.
    Type: Grant
    Filed: June 6, 1985
    Date of Patent: March 17, 1987
    Assignee: USV Pharmaceutical Corporation
    Inventors: Edward S. Neiss, David Stevenson, Laurence L. Ho, Robert C. Liu, John T. Suh
  • Patent number: 4625034
    Abstract: This invention relates to novel lipoxygenase inhibitors possessing anti-inflammatory and anti-allergic activities. The present new compounds are di- and tetra-hydroquinoline or di- and tetra-hydronapthalene derivatives, more particularly, 1,2-, 1,4-, 5,6-, or 7,8-dihydro; 1,2,3,4-tetrahydro-; 5,8-dihydro-; or 5,6,7,8-tetrahydroquinoline or napthalene derivatives of a compound of the formula: ##STR1## and oxides, quaternary ammonium salts and acid salts thereof; wherein A is CH or N;Z is an alkylene chain containing up to 10 carbon atoms in the principal chain and a total of up to 12 carbon atoms and the said alkylene chain may be attached to the phenyl group through an oxygen atom;R is the substituent OR.sub.6 attached to one of the carbon atoms of Z in which R.sub.6 is H, lower alkyl or phenyl;X is --O(CHR.sub.5).sub.m --, alkylene of up to 2 carbon atoms in the principal chain and up to a total of 4 carbon atoms or ##STR2## wherein R.sub.5 is H or CH.sub.3 ;R.sub.1, R.sub.2, R.sub.3 and R.sub.
    Type: Grant
    Filed: February 4, 1985
    Date of Patent: November 25, 1986
    Assignee: USV Pharmaceutical Corp.
    Inventors: Edward S. Neiss, Rohit M. Desai, Raymond D. Youssefyeh
  • Patent number: 4596791
    Abstract: Compounds of the formula ##STR1## and their pharmaceutically acceptable salts, wherein the substituents are as defined herein, having antihypertensive activity.
    Type: Grant
    Filed: January 10, 1985
    Date of Patent: June 24, 1986
    Assignee: USV Pharmaceutical Corp.
    Inventors: John J. Piwinski, John T. Suh, Paul Menard, Howard Jones, Edward S. Neiss
  • Patent number: 4576941
    Abstract: Compounds of the formula ##STR1## and their pharmaceutically acceptable salts, wherein the substituents are as defined herein, having antihypertensive activity.
    Type: Grant
    Filed: February 29, 1984
    Date of Patent: March 18, 1986
    Assignee: USV Pharmaceutical Corp.
    Inventors: John T. Suh, John J. Piwinski, Howard Jones, Edward S. Neiss
  • Patent number: 4364940
    Abstract: A composition for the treatment of acne in the form of a solution, lotion or cream containing from about 1 to 10% by weight of a compound of the formula ##STR1## wherein R is an alkyl having up to 6 carbon atoms or aryl having up to 10 carbon atoms and R.sub.1 and R.sub.2 are independently hydrogen, lower alkyl having up to 6 carbon atoms, phenyl, phenyl-lower alkyl, lower alkylphenyl, halogen, halophenyl, trifluoromethyl, trifluoromethylphenyl, lower alkoxy, methylenedioxy, and lower alkoxyphenyl.
    Type: Grant
    Filed: February 23, 1981
    Date of Patent: December 21, 1982
    Assignee: USV Pharmaceutical Corporation
    Inventors: Edward S. Neiss, Bernard Loev