Patents Represented by Attorney Hesna Pfeiffer
  • Patent number: 4874745
    Abstract: A phenyl derivative of pepstatin A, which is much more potent than pepstatin in inhibiting renin enzyme activity and has significantly greater selectivity for renin over pepsin inhibition than does pepstatin, which is useful in treating hypertension and congestive heart failure.
    Type: Grant
    Filed: October 1, 1987
    Date of Patent: October 17, 1989
    Assignee: Merck & Co., Inc.
    Inventors: Leeyuan Huang, Lawrence Koupal, Joseph Dunn, Jr., Jerrold M. Liesch, Otto Hensens, H. Boyd Woodruff
  • Patent number: 4780311
    Abstract: The compounds of the following general structural formula (I) ##STR1## wherein R is hydrogen or a pharmaceutically acceptable salt thereof, are .beta.-ketoacyl-coenzyme A thiolase inhibitors and are useful as antihypercholesterolemic agents for the treatment of disease in which the inhibition of cholesterol biosynthesis would be useful, such as arteriosclerosis, hyperlipidemia and familial hypercholesterolemia.
    Type: Grant
    Filed: May 26, 1987
    Date of Patent: October 25, 1988
    Assignee: Merck & Co., Inc.
    Inventors: Janet Onishi, Michael Greenspan
  • Patent number: 4324554
    Abstract: TKP is used for the control of migration during pad dyeing of fabrics.
    Type: Grant
    Filed: November 9, 1978
    Date of Patent: April 13, 1982
    Assignee: Merck & Co., Inc.
    Inventor: Joseph S. Racciato
  • Patent number: 4317811
    Abstract: A herpes simplex type 1 subunit vaccine is prepared from infected chick embryo cells by urea-extraction of the virus while the infected cells are still attached to the growth surface.
    Type: Grant
    Filed: September 11, 1980
    Date of Patent: March 2, 1982
    Assignee: Merck & Co., Inc.
    Inventors: Alexander U. Bertland, George P. Lampson
  • Patent number: 4071529
    Abstract: Novel 6-methoxy and 6-thioalkyl-6-acylamidopenicillanic acids and their non-toxic pharmaceutically-acceptable salts, esters and amides which are useful as antibiotics. The products are prepared by treating an ester of 6-substituted-6-aminopenicillanic acid with an acylating agent followed by removal of the ester group. Also disclosed are novel intermediates.
    Type: Grant
    Filed: August 5, 1974
    Date of Patent: January 31, 1978
    Assignee: Merck & Co., Inc.
    Inventors: Burton G. Christensen, Lovji D. Cama