Abstract: The inventive micromixer for mixing liquid, viscous or gaseous phases has a housing bottom part (2) and a housing top part (3) which lie closely against each other via connecting surfaces (6, 7). Two delivery channels (1a, 1b) and an outlet channel (5) open out into the dividing surface between the two connecting surface (6, 7). Channel grooves (9, 10) which cross each other several times are formed in one connecting surfaces (6) and provide a mixing section for the phases being mixed.
Type:
Grant
Filed:
April 24, 2000
Date of Patent:
October 1, 2002
Assignee:
Merck Patent Gesellschaft mit
Inventors:
Ulrich Koop, Michael Schmelz, Andreas Beirau
Abstract: A micro mixer for liquid, viscous or gaseous phases with two adjacent housing parts (1,2) disposed on a parting plane (3). Capillary tubes (7) forming line connections are inserted into cross holes (6) in the top part of the housing (1) by welding, for instance, and run into the parting plane (3). The other free ends of the capillary tubes (7) are bent apart and respectively bear a screw connection.
Type:
Grant
Filed:
May 26, 2000
Date of Patent:
October 1, 2002
Assignee:
Merck Patent Gesellschaft mit
Inventors:
Andreas Beirau, Michael Schmelz, Frank Schwarz, Jöran Stoldt
Abstract: The present invention relates to compounds of the formula (I):
wherein R1, R2, R3, R4, R5, R6, R7, R8, R9, R10 and n are defined herein. The compounds are of particular use in the treatment or prevention of depression, anxiety, pain, inflammation, migraine, emesis and postherpetic neuralgia.
Type:
Grant
Filed:
September 10, 2001
Date of Patent:
October 1, 2002
Assignee:
Merck Sharp & Dohme Ltd.
Inventors:
Simon Neil Owen, Eileen Mary Seward, Christopher John Swain, Brian John Williams
Abstract: The present invention is directed toward radiolabeled farnesyl-protein transferase inhibitor compounds which are useful to label FPTase in assays, whether cell-based, tissue-based or in whole animal. The tracers can also be used in competitive binding assays to obtain information on the interaction of unlabeled FTIs with FPTase.
Type:
Grant
Filed:
June 12, 2000
Date of Patent:
October 1, 2002
Assignee:
Merck & Co., Inc.
Inventors:
H. Donald Burns, Terence G. Hamill, Raymond E. Gibson
Abstract: Certain novel substituted piperidine compounds are agonists of the human melanocortin receptor(s) and, in particular, are selective agonists of the human melanocortin-4 receptor (MC-4R). They are therefore useful for the treatment and control of obesity, diabetes, and sexual dysfunction, including erectile dysfunction and female sexual dysfunction.
Type:
Grant
Filed:
March 20, 2001
Date of Patent:
October 1, 2002
Assignee:
Merck & Co., Inc.
Inventors:
Brenda L. Palucki, Khaled J. Barakat, Liangqin Guo, Yingjie Lai, Ravi P. Nargund, Min K. Park, Patrick G. Pollard, Iyassu K. Sebhat, Zhixiong Ye
Abstract: Pharmaceutical compositions of bisphosphonic acids, and salts thereof, are prepared by wet granulation tablet formulation. These pharmaceutical compositions are useful in the treatment of disturbances involving calcium or phosphate metabolism, in particular, the treatment and prevention of diseases involving bone resorption, especially osteoporosis, Paget's disease, malignant hypercalcemia, and metastatic bone disease. These compositions are prepared without the addition of binder; instead, the drug itself acts as a binder.
Abstract: The present invention provides mice that have had their PTP-1B genes disrupted by targeted homologous recombination. The mice have no detectable PTP-1B protein, yet appear to be physiologically normal. However, in the fed state on a normal diet, the mice have half the level of circulating insulin as their wild-type littermates. In glucose and insulin tolerance tests, the mice show an increased insulin sensitivity. When fed a high fat, high carbohydrate diet, the mice show a resistance to weight gain as compared to their wild-type littermates.
Type:
Application
Filed:
July 30, 2001
Publication date:
September 26, 2002
Applicant:
Merck & Co., Inc.
Inventors:
Brian Kennedy, Paul Payette, Michael Gresser, Chidambaram Ramachandran, Michel Tremblay, Mounib Elchebly
Abstract: The present invention is related to a drug delivery device, that is pH insensitive, for the sustained in situ production and release of a dispersion, in an environment of use, which comprises
Type:
Application
Filed:
March 12, 2002
Publication date:
September 26, 2002
Applicant:
Merck & Co., Inc.
Inventors:
Michael W. McGlynn, Mandana Asgharnejad
Abstract: Certain novel substituted piperidine compounds are agonists of the human melanocortin receptor(s) and, in particular, are selective agonists of the human melanocortin-4 receptor (MC-4R). They are therefore useful for the treatment, control, or prevention of diseases and disorders responsive to the activation of MC-4R, such as obesity, diabetes, sexual dysfunction, including erectile dysfunction and female sexual dysfunction. Also provided are methods of treating sexual dysfunction with a compound that is a selective agonist of MC-4R over any other human melanocortin receptor.
Type:
Application
Filed:
November 21, 2001
Publication date:
September 26, 2002
Applicant:
Merck & Co., Inc.
Inventors:
Raman K. Bakshi, Khaled J. Barakat, Ravi P. Nargund, Brenda L. Palucki, Arthur A. Patchett, Iyassu Sebhat, Zhixiong Ye, Leonardus H.T. Van Der Ploeg
Abstract: A combination of a muscarinic agonist and an inverse agonist of the GABAA &agr;5 receptor subtype useful in treating neurodegenerative conditions such as Alzheimer's Disease is disclosed.
Abstract: The present invention provides nucleotide sequences encoding the &agr;4 and &dgr; subunits of the human GABAA receptor, preparations of &agr;4 and &dgr; receptor subunit proteins, preparations of receptors including &agr;4 or &dgr; polypeptides, expression vectors including the nucleotide sequences, stably co-transfected eukaryotic cells and methods of their preparation and methods of screening for and designing medicaments which act upon the GABAA receptor.
Type:
Grant
Filed:
June 19, 1997
Date of Patent:
September 24, 2002
Assignee:
Merck Sharp & Dohme Ltd.
Inventors:
Beatrice Le Bourdelles, Paul John Whiting
Abstract: The present invention is directed to pyrrolidine compounds of the formula I:
(wherein R1, R2, R3, R4c, R4d, and R4f are defined herein) which are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of the chemokine receptors CCR-3 and/or CCR-5.
Type:
Grant
Filed:
February 27, 2001
Date of Patent:
September 24, 2002
Assignee:
Merck & Co., Inc.
Inventors:
Jennifer Chee, Jill N. Johanson, Frank Kayser, William H. Parsons, Kathleen M. Rupprecht
Abstract: Compounds of the invention are useful in inhibiting thrombin and associated thrombotic occlusions having the following structure:
A is
wherein Y1 and Y2 are independently
hydrogen,
C1-4 alkyl,
C1-4 alkoxy,
FuHvC(CH2)0-1 O—, wherein u and v are either 1 or 2, provided that when u is 1, v is 2, and when u is 2, v is 1,
C3-7 cycloalkyl,
thio C1-4 alkyl,
C1-4 sulfinylalkyl,
C1-4 sulfonylalkyl,
halogen
cyano, or
trifluoromethyl, and
wherein b is 0 or 1.
Type:
Grant
Filed:
June 1, 2000
Date of Patent:
September 24, 2002
Assignee:
Merck & Co., Inc.
Inventors:
Christopher S. Burgey, Kyle A. Robinson, Peter D. Williams, Craig Coburn, Terry A. Lyle, Philip E. Sanderson
Abstract: Compounds of the formula I
in which R1, R2 and R3 have the stated meanings, and their physiologically acceptable salts, inhibit the binding of fibrinogen to the corresponding receptor and can be used for the treatment of thromboses, osteoporoses, oncoses, stroke, myocardial infarct, ischemias, inflammations, arteriosclerosis and osteolytic disorders.
Type:
Grant
Filed:
May 3, 1996
Date of Patent:
September 24, 2002
Assignee:
Merck Patent Gesellschaft mit beschraenkter Haftung
Inventors:
Joachim Gante, Hörst Juraszyk, Peter Raddatz, Hanns Wurziger, Sabine Bernotat-Danielowski, Guido Melzer
Abstract: The thienopyrimidines of the formula (I) and their physiologically compatible salts display a phosphodiesterase V inhibiting activity and can be used for treating diseases of the cardiovascular system and for treatment and/or therapy of erectile dysfunction.
Type:
Application
Filed:
May 16, 2002
Publication date:
September 19, 2002
Applicant:
Merck Patent GmbH
Inventors:
Rochus Jonas, Pierre Schelling, Franz-Werner Kluxen, Maria Christadler
Abstract: The invention describes polyesters containing (meth)acrylate end groups, of the general formula (I) CH2═CRCOO—PE—OCOCR═CH2 where R=CH3 or H, where PE=[—A—OCO—B—COO—]m—A—, [—CHR′—COO—]n—A—[—OCOCHR′—]n, or combinations thereof, in which A is an alkylidene radical having 2-20 carbon atoms or an alkoxylidene radical having 2-1000, preferably 2-500, alkoxylidene units, B is a saturated alkylidene radical having 2-10 carbon atoms, R′ is H or CH3, m is 1-100, n is 1-100, and, if both m and n are present, the sum m+n is 2-200, where the polyesters containing (meth)acrylate end groups are characterised in that a) the content of short-chain di(meth)acrylates (II) CH2═CRCOO—A—OCOCR═CH2 is <5% by weight, b) the content of hydroxyl groups is <0.25 mol/mol of (meth)acrylate, and c) the APHA color number is <200.
Abstract: An apparatus suitable for securely gripping and holding a microplate or other containers during robotic de-lidding operations. A microplate placed on the apparatus is held by a vacuum drawn through the base thereof, allowing the lid of the microplate to be removed without movement of the plate. Afterwards, the vacuum can be discontinued and the plate removed from the apparatus.
Type:
Grant
Filed:
October 10, 2000
Date of Patent:
September 17, 2002
Assignee:
Merck & Co., Inc
Inventors:
Glenn A. Clarke, Marc N. Feiglin, Gary S. Kath, Gregory W. King
Abstract: The present invention relates to a transgenic non-human animal embryo lacking native presenilin 1 and a transgenic non-human animal having only a non-native presenilin 1. The transgenic animals and cells derived therefrom can be used in the study of the expression pattern, activity and modulators of presenilin 1, in the study of the role of presenilin 1 in Alzheimer's Disease and in the study of disorders of the central nervous system.
Type:
Grant
Filed:
May 14, 1998
Date of Patent:
September 17, 2002
Assignees:
Merck & Co., Inc., Johns Hopkins University
Inventors:
Hui Zheng, Ping Jiang, Su Qian, Leonardus H. T. Van Der Ploeg, Philip Chun-Ying Wong, Sangram S. Sisodia