Abstract: The present invention describes the use of fumitremorgin A, B and C and a series of diketopiperazines of Formula (I) to resensitize multidrug resistant (MDR) cancer cells to the cytotoxic effects of chemotherapeutic drugs.
Type:
Application
Filed:
February 28, 2002
Publication date:
May 1, 2003
Applicant:
American Cyanamid Company
Inventors:
Sridhar Krishna Rabindran, Haiyin He, Lee Martin Greenberger
Abstract: The invention relates to compounds of Formula (I), to processes for their preparation and pharmaceutical compositions thereof, that inhibit the Ras farnesyl-protein transferase enzyme (FPTase), and may be used as an alternative to, or in conjunction with, traditional cancer therapy for the treatment of ras oncogene-dependent tumors, such as cancers of the pancreas, colon, bladder, and thyroid.
Type:
Application
Filed:
August 23, 2002
Publication date:
May 1, 2003
Applicant:
American Cyanamid Company
Inventors:
Joseph William Epstein, Semiramis Ayral-Kaloustian
Abstract: The present invention relates to plant tissue culture methods, particularly for Beta vulgaris. Methods are provided for producing callus tissues, somatic embryos and plants. The methods find use in the field of agricultural biotechnology, particularly in the production of transgenic Beta vulgaris plants.
Abstract: Sustained-release compositions comprising a macrolide compound, a surfactant, a co-solvent, and a solvent. The sustained-release compositions of this invention may be parenterally administered to animals, and are useful for preventing or treating helminth, acarid or arthropod endo- or ectoparasitic infection or infestation in warm-blooded animals for prolonged periods of time.
Abstract: This invention provides compounds of formula I having the structure
Wherein substitutions at A″, Z, n, and X are set forth in the specification.
Type:
Grant
Filed:
December 21, 2001
Date of Patent:
April 15, 2003
Assignee:
American Cyanamid Company
Inventors:
Allan Wissner, Philip R. Hamann, Ayako Yamashita
Abstract: This invention provides, non-peptide inhibitors of matrix metalloproteinases (e.g. gelatinases, stromelysins and collagenases) and TNF-&agr; converting enzyme (TACE. tumor necrosis factor-&agr; converting enzyme) which arc useful for the treatment of diseases in which these enzymes are implicated.
Type:
Grant
Filed:
December 11, 2000
Date of Patent:
April 15, 2003
Assignee:
American Cyanamid Company
Inventors:
Jeremy I. Levin, Arie Zask, Yansong Gu, Jay D. Albright, Xuemei Du
Abstract: This invention provides methods of increasing urine flow in humans while minimizing the loss of electrolytes or ions, the methods comprising administering to a human in need thereof a combination of N-[4-(5H-pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)ylcarbonyl)-3-chlorophenyl]-5-fluoro-2-methylbenzamide (or a pharmaceutically acceptable salt thereof), also known as VPA-985, and one or more diuretic agents, as well as pharmaceutical compositions and kits or packages for such combinations.
Abstract: Compounds having the following formula:
are useful in treating disease conditions mediated by matrix metalloproteinases and TACE, such as tumor growth, osteoarthritis, rheumatoid arthritis and degenerative cartilage loss.
Type:
Grant
Filed:
January 27, 2000
Date of Patent:
April 8, 2003
Assignee:
American Cyanamid Company
Inventors:
Jay Donald Albright, Efren Guillermo Delos Santos, Jeremy Ian Levin, James Ming Chen
Abstract: The invention provides new substantially pure antibiotics designated AC-98-1, AC-98-2, AC-98-3, AC-98-4 and AC-98-5 derived from the microorganism Streptomyces hygroscopicus.
Abstract: This invention provides, non-peptide inhibitors of matrix metalloproteinases (e.g. gelatinases, stroinelysins and collagenases) and TNF-&agr; converting enzyme (TACE, tumor necrosis factor-&agr;converting enzyme) which are useful for the treatment of diseases in which these enzymes are implicated.
Type:
Grant
Filed:
December 11, 2000
Date of Patent:
March 18, 2003
Assignee:
American Cyanamid Company
Inventors:
Jeremy I. Levin, Arie Zask, Yansong Gu, Jay D. Albright, Xuemei Du
Abstract: There are provided non-aqueous pour-on, water-fast formulations effective for the control of internal and external parasitic infections and infestations of homothermic animals such as mammalian quadrupeds. The pour-on formulations of the present invention contain as the active ingredient, a compound selected from the group consisting of LL-F28249&agr;-&lgr;, 23-oxo (keto) and 23-imino derivatives of the compounds collectively defined as LL-F28249, and milbemycin and avermectin molecules.
Abstract: N-methyl-N-(3-{3-[2-thienylcarbonyl]-pyrazol-[1,5-&agr;]-pyrimidin-7-yl}phenyl)acetamide, and use of the same as a sedative-hypnotic, anxiolytic, anticonvulsant, and skeletal muscle relaxant agent. Compositions containing N-methyl-N-(3-{3-[2-thienylcarbonyl]-pyrazol-[1,5-&agr;]-pyrimidin-7-yl}phenyl)acetamide, as well as pharmaceutically acceptable salts thereof, are also disclosed.
Type:
Application
Filed:
December 21, 2001
Publication date:
December 26, 2002
Applicant:
American Cyanamid Company
Inventors:
John P. Dusza, Andrew S. Tomcufcik, Jay D. Albright, Bernard Beer
Abstract: This invention provides low molecular weight, non-peptide inhibitors of matrix metalloproteinases and TNF-&agr; converting enzyme (TACE, tumor necrosis factor-&agr; converting enzyme) of formula (B) as shown herein or a pharmaceutically acceptable salt thereof.
Type:
Grant
Filed:
December 11, 2000
Date of Patent:
December 24, 2002
Assignee:
American Cyanamid Company
Inventors:
Jeremy I. Levin, Arie Zask, Yansong Gu, Jay D. Albright, Xuemei Du
Abstract: Matrix metalloproteinases (MMPs) are a group of enzymes that have been implicated in the pathological destruction of connective tissue and basement membranes. These zinc containing endopeptidases consist of several subsets of enzymes including collagenases, stromelysins and gelatinases. TNF-&agr; converting enzyme (TACE), a pro-inflammatory cytokine, catalyzes the formation of TNF-&agr; from membrane bound TNF-&agr; precursor protein. It is expected that small molecule inhibitors of MMPs and TACE therefore have the potential for treating a variety of disease states.
Abstract: The 6-(spirocyclopropyl)-penicillanic acid 4,4-dioxides of the general Formula (I):
as defined herein above which exhibit beta-lactamase inhibiting activity, use of such compounds in combination with beta-lactam antibiotics for inhibiting beta-lactamases, pharmaceutical compositions and processes for preparing such compounds.
Type:
Grant
Filed:
January 26, 2001
Date of Patent:
December 3, 2002
Assignee:
American Cyanamid Company
Inventors:
Vincent P. Sandanayaka, Amarnauth S. Prashad
Abstract: The present invention provides methods for synergistic control of ectoparasitic arthropods with a synergistically effective amount of a combination of the macrocyclic lactone moxidectin and an arylpyrrole compound. Also provided are methods of protecting animals from infestation and attack by ectoparasites with said combination. The present invention also provides synergistic insecticidal compositions comprising as essential active ingredients the macrocyclic lactone moxidectin and an arylpyrrole compound.
Type:
Grant
Filed:
November 21, 2001
Date of Patent:
November 12, 2002
Assignee:
American Cyanamid Company
Inventors:
Kathleen Heaney, Mary E. Doscher, Douglas Rugg
Abstract: The present invention describes the use of fumitremorgin A, B and C and a series of diketopiperazines of Formula (I) to resensitize multidrug resistant (MDR) cancer cells to the cytotoxic effects of chemotherapeutic drugs.
Type:
Application
Filed:
February 28, 2002
Publication date:
October 24, 2002
Applicant:
American Cyanamid Company
Inventors:
Sridhar Krishna Rabindran, Haiyin He, Maya Prakash Singh, Lee Martin Greenberger