Abstract: This invention provides compounds of the formula:
wherein X is (CH2)n, O, S, SO, SO2 or CR1R2; n is 1 or 2; R1 and R2 are H, halogen, hydroxy, alkyl of 1 to 6 carbon atoms, alkoxy of 1 to 6 carbon atoms, or R1 and R2, taken together form cycloalkyl of 3 to 6 carbon atoms, an alkylidene of up to 6 carbon atoms or a carbonyl; R3, R4 and R5 are H or alkyl of 1 to 6 carbon atoms; Z is H, alkyl of 1 to 6 carbon atoms, alkanoyl of 1 to 6 carbon atoms or alkoxycarbonyl of 2 to 7 carbon atoms; or a pharmaceutically acceptable salt thereof, as well as pharmaceutical compositions and methods for their use in treating or preventing characterized by glutamate hypofunction, including schizophrenia, schizoaffective disorder and schizophreniform disorder, and for the treatment of cognitive deficits due to aging, stroke, Alzheimer's disease or other neurodegenerative diseases.
Type:
Grant
Filed:
June 27, 2002
Date of Patent:
June 15, 2004
Assignee:
Wyeth
Inventors:
Gary Paul Stack, John Dunlop, Alexander Alexei Greenfield, Jonathan Laird Gross
Abstract: The present invention relates to new 2-Phenyl-1-[4-(2-Aminoethoxy)-Benzyl]-Indole compounds which are useful as estrogenic agents, as well as pharmaceutical compositions and methods of treatment utilizing these compounds, which have the general structures below: 1
Type:
Application
Filed:
November 24, 2003
Publication date:
June 10, 2004
Applicant:
Wyeth
Inventors:
Chris P. Miller, Michael D. Collini, Bach D. Tran, Arthur A. Santilli
Abstract: Methods, systems and equipment for diagnosing renal cell carcinoma (RCC) and other solid tumors. This invention identifies numerous disease genes that are differentially expressed in the peripheral blood of patients having RCC or other solid tumors relative to disease-free humans. These disease genes can be used as surrogate markers for detecting the presence or absence of RCC or other solid tumors.
Type:
Application
Filed:
November 21, 2003
Publication date:
June 10, 2004
Applicant:
Wyeth
Inventors:
Natalie C. Twine, Michael E. Burczynski, William L. Trepicchio, Andrew J. Dorner, Jennifer A. Stover, Donna K. Slonim
Abstract: This invention provides compounds of formula 1, having the structure 1
Type:
Application
Filed:
July 10, 2003
Publication date:
June 10, 2004
Applicant:
WYETH
Inventors:
Dan M. Berger, Minu D. Dutia, Frenel F. DeMorin, Diane H. Boschelli, Dennis W. Powell, Hwei-Ru Tsou, Allan Wissner, Nan Zhang, Fei Ye, Biqi Wu
Abstract: This invention provides a method of treating obesity, generalized anxiety disorder, post-traumatic stress disorder, late luteal phase dysphoric disorder (premenstrual syndrome), attention deficit disorder, with and without hyperactivity, Gilles de la Tourette syndrome, bulimia nervosa or Shy Drager Syndrome in a mammal by administering to the mammal an effective amount of a hydroxycycloalkanephenethyl amine of the following structural formula: 1
Abstract: The present invention relates to new 2-Phenyl-1-[4-(2-Aminoethoxy)-Benzyl]-Indole compounds which are useful as estrogenic agents, as well as pharmaceutical compositions and methods of treatment utilizing these compounds, which have the general structures below: 1
Type:
Application
Filed:
July 10, 2003
Publication date:
June 10, 2004
Applicant:
Wyeth
Inventors:
Chris P. Miller, Michael D. Collini, Bach D. Tran, Arthur A. Santilli
Abstract: This invention provides compounds of formula VI
wherein
Y is hydrogen, methyl, methoxy, methylthio or trifluoromethyl;
R is hydrogen, C1-3alkyl or (CH2)nAr;
n is 0, 1 or 2; and
Ar is phenyl or methoxyphenyl,
or a pharmaceutically acceptable salt thereof. These compounds are selective dopamine autoreceptor agonists useful in treating disease states involving hyperactivity of dopamine systems. The invention also comprises intermediate compounds, compositions and methods related to the compounds of formula VI.
Type:
Grant
Filed:
May 3, 2002
Date of Patent:
June 1, 2004
Assignee:
Wyeth
Inventors:
Lynne P. Greenblatt, Ivo Jirkovsky, Richard E. Mewshaw
Abstract: This invention provides compounds of Formula I having the structure
wherein R1, R2, R3, R4, W, X, and Y are as defined hereinbefore or a pharmaceutically acceptable salt thereof, which are useful in treating metabolic disorders related to insulin resistance or hyperglycemia.
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:
Grant
Filed:
August 23, 2002
Date of Patent:
May 25, 2004
Assignee:
Wyeth Holdings Corporation
Inventors:
Joseph William Epstein, Semiramis Ayral-Kaloustian
Abstract: This invention provides compositions, organisms and methodologies employing a novel human protein kinase, NRHK1. The novel protein kinase is encoded by a human gene comprising 21 exons. The human gene is localized in or near the 9q34 locus of human chromosome 9. The sequence similarity between the novel human protein and the consensus sequence of NIMA-related kinase indicates that the novel human protein may function as an NIMA-related kinase.
Abstract: This invention provides a method of treating or inhibiting cardiovascular, cerebral vascular, or peripheral vascular disease in a mammal in need thereof, which comprises providing said mammal with an effective amount of a rapamycin.
Type:
Application
Filed:
October 29, 2003
Publication date:
May 20, 2004
Applicant:
Wyeth
Inventors:
Neal I. Azrolan, Surendra N. Sehgal, Uma Sehgal, Steven J. Adelman
Abstract: This invention provides compositions, organisms and methodologies employing a novel human protein kinase, HPK3P23. The novel human kinase has sequence homology to the catalytic domains of several protein kinases. The gene encoding this novel protein kinase is localized in or near the 3p23 locus of the human chromosome 3. The sequence similarity between the novel human protein and the catalytic domain of protein kinases indicates that the novel human protein may function as a protein kinase.
Abstract: The present invention provides a compound of formula I and the use thereof for the therapeutic treatment of disorders relating to or affected by the 5-HT6 receptor.
Abstract: This invention provides compositions, organisms and methodologies employing a novel human gene encoding a protein that has sequence homology to a consensus sequence of calcineurin-like phosphoesterase family are disclosed. The novel protein is encoded by a human gene comprising 4 exons. The human gene is localized in the 10p15 locus of human chromosome 10. The sequence similarities between the novel human protein and the consensus sequence of calcineurin-like phosphoesterases indicate that the novel human protein may function as a calcineurin-like protein phosphatase.
Type:
Application
Filed:
October 24, 2003
Publication date:
May 13, 2004
Applicant:
Wyeth
Inventors:
Wei Liu, Leeying Wu, Roger Ford, Xiaobing Be
Abstract: The present invention provides a compound of formula I and the use thereof in the therapeutic treatment of disorders related to or affected by the 5-HT6 receptor.
Type:
Application
Filed:
October 23, 2003
Publication date:
May 13, 2004
Applicant:
Wyeth
Inventors:
Ping Zhou, Derek Cecil Cole, Michael Gerard Kelly, William Joseph Lennox
Abstract: This invention provides methods of using a pharmacological combination of a biguanide agents, such as metformin, and one or more PTPase inhibiting agents and, optionally, one or more sulfonlylurea agents, including glyburide, glyburide, glipizide, glimepiride, chlorpropamide, tolbutamide, or tolazamide, for treatment in a mammal of Syndrome X, type II diabetes or metabolic disorders mediated by insulin resistance or hyperglycemia. Further included in this invention is a method of modulating blood glucose levels in a mammal utilizing the combination of one or more PTPase inhibiting agents and one or more sulfonlylurea agents.
Type:
Grant
Filed:
June 6, 2002
Date of Patent:
May 11, 2004
Assignee:
Wyeth
Inventors:
Bruce Paul Randazzo, Philippe John Robert Vitou, John Thomas Gwynne
Abstract: The present invention relates to processes for the preparation of tablets which dissolve rapidly in the mouth and provide an excellent mouthfeel. The tablets of the invention comprise a compound which melts at about 37° C. or lower, have a low hardness, high stability and generally comprise few insoluble disintegrants which may cause a gritty or chalky sensation in the mouth. Convenient and economically feasible processes by which the tablets of the invention may be produced are also provided.
Type:
Grant
Filed:
December 6, 2000
Date of Patent:
May 11, 2004
Assignee:
Wyeth
Inventors:
Khawla A. Abu-Izza, Vincent H. Li, Jee L. Look, Graham D. Parr, Matthew K. Schineller