Abstract: Kalahide F. of formula I below, may be isolated from a secoglossan. The compound may be used in the manufacture of pharmaceutical compositions or in the treatment of tumors or viral conditions.
Type:
Grant
Filed:
September 25, 1997
Date of Patent:
January 4, 2000
Assignee:
Pharma Mar, s.a.
Inventors:
Paul J Scheuer, Mark T Hamann, Dolores G. Gravalos
Abstract: Dehydrodidemnin B with useful biological activity has formula (1). It can be isolated from natural sources or synthesized, and it forms active derivatives.
Type:
Grant
Filed:
July 25, 1994
Date of Patent:
November 10, 1998
Assignee:
Pharma Mar, S.A.
Inventors:
Kenneth L. Rinehart, Anna M. Lithgow-Bertelloni
Abstract: The invention provides a pharmaceutical composition containing a somatostatin analogue, and its use in the treatment of breast cancer. The pharmaceutical composition preferably contains lactic acid in addition to the somatostatin analogue and is better tolerated when administered by injection.
Abstract: Analogs of porcine Vasoactive Intestinal Peptide are disclosed. The analogs have been cyclized by the covalent attachment, via an amide bond, of the side-chain carboxy terminus of one amino acid in the peptide chain to the side-chain amino terminus of another amino acid in the peptide chain. The claimed compounds are useful for the treatment of asthma.
Abstract: Compounds represented by the formula (Seq ID Nos. 1-6) ##STR1## wherein all substituents are fully defined, are disclosed. These compounds exhibit utilities as antibiotic and antifungal agents and for the treatment and prevention of Pneumocystis infections.
Type:
Grant
Filed:
March 12, 1996
Date of Patent:
September 16, 1997
Assignee:
Merck & Co., Inc.
Inventors:
James M. Balkovec, Frances A. Bouffard, Milton L. Hammond
Abstract: An improved process for the preparation of side chain derivatives of cyclohexapeptidyl lipopeptides represented by the formula ##STR1## wherein R.sup.1 is fully defined, is disclosed.
Type:
Grant
Filed:
May 16, 1996
Date of Patent:
July 8, 1997
Inventors:
James M. Balkovec, Frances A. Bouffard, James F. Dropinski, Akinlolu A. Adefarati, Jan S. Tkacz
Abstract: The present invention is directed to novel aza cyclohexapeptide compounds of the formula ##STR1## where all substituents are defined herein, which are useful as antifungal agents and for the treatment of Pneumocystis carinii infections. Compositions containing the compounds of the invention are also disclosed.
Type:
Grant
Filed:
October 31, 1994
Date of Patent:
May 14, 1996
Assignee:
Merck & Co., Inc.
Inventors:
James M. Balkovec, Frances A. Bouffard, James F. Dropinski
Abstract: There are disclosed novel semi-synthetic lipopeptides of the formula (Seq. ID Nos. 1-6) ##STR1## wherein the substituents are defined herein, which show utility as antifungal and anti-Pneumocystis agents. Pharmaceutical compositions containing said compounds are also disclosed.
Abstract: Ceretain aza cyclohexapeptide compounds have been found to have superior antibiotic properties. Novel processes for their preparation are also described.
Type:
Grant
Filed:
August 29, 1994
Date of Patent:
May 7, 1996
Assignee:
Merck & Co., Inc.
Inventors:
James M. Balkovec, Regina M. Black, Frances A. Bouffard
Abstract: The present invention relates to aza cyclohexapeptide compounds of the formula (Seq ID Nos. 1-10) ##STR1## which may be useful as antibiotics, antifungal agents and for the treatment of Pneumocystis carinii infections.
Type:
Grant
Filed:
September 16, 1994
Date of Patent:
May 7, 1996
Assignee:
Merck & Co., Inc.
Inventors:
James M. Balkovec, Frances A. Bouffard, James F. Dropinski
Abstract: Certain aminoalkyl substituted amides which have a cyclohexapeptidyl group and which are found to have antibiotic activity with physical properties suitable for use in therapeutic compositions are described.
Abstract: Aza cyclohexapeptide compounds are disclosed with a nitrogen attached to the cyclohexapeptide ring at the 5-carbon of the 4-hydroxyornithine component. Such compounds are represented by the formula: ##STR1## The compounds are disclosed as having antifungal, antiprotozoal and anti-Pneumocystis carinii activity.
Type:
Grant
Filed:
March 16, 1993
Date of Patent:
January 3, 1995
Assignee:
Merck & Co., Inc.
Inventors:
James M. Balkovec, Regina M. Black, Frances A. Bouffard
Abstract: This invention relates to personal care compositions, and, more specifically, to a composition comprising a pyrithione salt or acid, a basic lipopeptide, and a suitable carrier. The pyrithione plus the lipopeptide provide antimicrobial efficacy to the personal care composition. The personal care composition is useful in a variety of dermatological items, such as soaps, shampoos, and skin care medicaments.
Abstract: Certain propionitrile compounds which have a cyclohexapeptidyl nucleus and which are found to have antibiotic activity with physical properties suitable for use in therapeutic compositions are described. A novel process for their preparation is also described.
Abstract: A new and demonstratably active cyclo-octapeptide is isolated from the South Pacific Ocean Hymeniacidon sp. and structurally elucidated. The substance, herein denominated Hymenistatin 1, demonstrated utility by inhibiting tumor growth when measured by the National Cancer Institute P388 leukemia cell line (ED.sub.50 =3.5 .mu.g/mL).
Type:
Grant
Filed:
November 30, 1989
Date of Patent:
July 14, 1992
Assignee:
Arizona Board of Regents, a body corporate of Arizona State University