Abstract: Here we describe the molecular identification of a cDNA encoding a novel serine protease we have termed D-G. The deduced amino acid sequence, and it's alignment with other well characterized serine proteases clearly indicates that it is a member of the S1 serine protease family. We have found that the protease D-G mRNA is widely expressed in several tissues throughout the body including epidermis, fibroblasts, keratinocytes, colon, small intestine, stomach, lung, kidney, bone marrow, lymph node, thymus, ovary, prostate, uterus and spinal cord. Interestingly, this protease contains a hydrophobic stretch of amino acids which is a putative transmembrane near the NH2-terminus. Thus, this serine protease is thought to be synthesized as a type II integral protein.
Type:
Grant
Filed:
June 30, 2000
Date of Patent:
June 15, 2004
Assignee:
Ortho-McNeil Pharmaceutical, Inc.
Inventors:
Andrew L. Darrow, Jenson (Jian-Shen) Qi, Patricia Andrade-Gordon
Abstract: Anticonvulsant compounds of the general formula I:
where X, R1, R2, R3, R4, R5, and R6 are as herein defined; are useful in treating acute ischemia-induced neurodegeneration, such as occurs during and after stroke, head trauma, spinal injury, non-fatal cardiac arrest, or major surgical procedures. Furthermore, pharmaceutical compositions containing a compound of formula I as well as methods for their use are disclosed.
Type:
Grant
Filed:
July 20, 2000
Date of Patent:
December 17, 2002
Assignee:
Ortho McNeil-Pharmaceutical, Inc.
Inventors:
Michael J. Costanzo, Bruce E. Maryanoff, Richard P. Shank
Abstract: A regimen for the administration of tramadol for the treatment of analgesia is described. The regimen involves a slower initial titration rate of tramadol which results in a significantly lower percentage of discontinuations of therapy due to a lower incidence and severity of side effects.
Abstract: &bgr;-Aminotetralin derivatives of the formula:
which are ligands for the neuropeptide Y Y5 (NPY5) receptor, methods of preparation and pharmaceutical compositions containing a &bgr;-aminotetralin derivative as the active ingredient are described. The 62 -aminotetralins are useful in the treatment of disorders and diseases associated with NPY receptor subtype Y5.
Type:
Grant
Filed:
October 6, 1999
Date of Patent:
March 13, 2001
Assignee:
Ortho-McNeil Pharmaceutical, Inc.
Inventors:
Scott L. Dax, Timothy W. Lovenberg, Ellen W. Baxter, John R. Carson, Donald W. Ludovici, Mark A. Youngman
Abstract: A compound of the general formula I:
is disclosed as useful in treating disorders of the central nervous system. Pharmaceutical compositions, processes for preparing the compounds and methods of treatment are also disclosed.
Type:
Grant
Filed:
October 5, 1998
Date of Patent:
March 13, 2001
Assignee:
Ortho-McNeil Pharmaceutical, Inc.
Inventors:
Allen B. Reitz, James J. McNally, Pauline Sanfilippo
Abstract: .beta.-Aminotetralin derivatives of the formula: ##STR1## which are ligands for the neuropeptide Y Y5 (NPY5) receptor, methods of preparation and pharmaceutical compositions containing a .beta.-aminotetralin derivative as the active ingredient are described. The .beta.-aminotetralins are useful in the treatment of disorders and diseases associated with NPY receptor subtype Y5.
Type:
Grant
Filed:
April 12, 1999
Date of Patent:
October 31, 2000
Assignee:
Ortho-McNeil Pharmaceutical, Inc.
Inventors:
Scott L. Dax, Timothy W. Lovenberg, James McNally, Allen B. Reitz, Mark A. Youngman
Abstract: Carboxamide derivatives of pyrrolidine, piperidine, and hexahydroazepine of formula (I): ##STR1## are disclosed as useful in treating platelet-mediated thrombotic disorders.
Type:
Grant
Filed:
April 29, 1997
Date of Patent:
May 30, 2000
Assignee:
Ortho Pharmaceutical Corp.
Inventors:
Michael J. Costanzo, William J. Hoekstra, Bruce E. Maryanoff
Abstract: This invention relates to a series of substituted 3-oxo-pyrrolo[1,2-a]imidazopyridine derivatives of the formula 1 ##STR1## where X.sub.1 -X.sub.4, R.sub.1, R.sub.2 and Ar are defined herein. In addition the invention relates to pharmaceutical compositions containing them and intermediates used in their manufacture. The compounds of the invention are ligands for the benzodiazepine site on the GABA-A receptor and display anxiolytic and anticonvulsant activity in animal models.
Type:
Grant
Filed:
October 5, 1998
Date of Patent:
October 19, 1999
Assignee:
Ortho-McNeil Pharmaceutical, Inc.
Inventors:
Bruce E. Maryanoff, David McComsey, James J. McNally, Samuel O. Nortey, Allen B. Reitz
Abstract: A compound of the general formula 1; ##STR1## is disclosed as useful in treating disorders of the central nervous system. Pharmaceutical compositions and methods of treatment are also disclosed.
Type:
Grant
Filed:
October 3, 1997
Date of Patent:
October 6, 1998
Assignee:
Ortho Pharmaceutical Corporation
Inventors:
Allen B. Reitz, Alfonzo D. Jordan, Pauline J. Sanfilippo, Malcolm K. Scott, Anna Vavouyios-Smith