Abstract: The invention relates to 1-aminoethylquinoline derivatives, to pharmaceutical compositions containing them, to therapeutic methods of using them and to processes for preparing them.
Type:
Grant
Filed:
May 9, 2001
Date of Patent:
December 18, 2001
Assignee:
Sanofi-Synthelabo
Inventors:
Christophe Philippo, Patrick Mougenot, Gérard Defosse, Alain Braun, Philippe Bovy
Abstract: In accordance with the present invention there is provided a method of treating a mammal having a solid tumor, the method comprising:
a) administering to the mammal an effective amount of 3-ainino-1,2,4-benzotriazine 1,4-dioxide;
b) administering to the mammal an effective amount of paclitaxel; and
c) administering to the mammal an effective amount of a platinum complex. The method provides unexpected synergistic efficacy. The invention further provides a kit for treatment of a mammalian tumor comprising 3-amino-1,2,-benzotriazine 1,4-dioxide, paclitaxel and a platinum complex.
Type:
Grant
Filed:
February 16, 2000
Date of Patent:
November 20, 2001
Assignee:
Sanofi-Synthelabo Inc.
Inventors:
Daniel L. Dexter, Paul E. Juniewicz, James B. Rake, Daniel D. Von Hoff
Abstract: The invention relates to compounds of formula
in which R1 to R9, R16 and R17 are as defined in Claim 1.
These compounds are pharmacologically active.
Type:
Grant
Filed:
June 13, 2000
Date of Patent:
November 6, 2001
Assignee:
Sanofi-Synthelabo
Inventors:
Bernard Ferrari, Jean Gougat, Claude Muneaux, Yvette Muneaux, Pierre Perreaut, Claudine Planchenault
Abstract: This invention relates to a cosmetic composition containing at least one NPY-antagonist component mixed with an excipient for cosmetic preparations.
Type:
Grant
Filed:
February 9, 2000
Date of Patent:
November 6, 2001
Assignee:
Sanofi-Synthelabo
Inventors:
Elisabeth Blanc-Ferras, Francoise Bono-Colombie, Bernard Breda, Jean Courregelongue, Catherine Ducasse, Remy Mounier, Paul Raymond, Michel Sabadie, Claudine Serradeil-Le-Gal, Vilain Pol, Jean-Marie Pereillo
Abstract: The toothbrush includes a head which is placed at a front longitudinal end of a handle and which is equipped, on an upper face, with a bunch of parallel filaments and a series of rods made from elastomer material which each extend substantially parallel to the filaments and which are placed substantially in two longitudinal rows with one row on each side of the bunch of filaments. Each row of rods includes tall rods which are arranged longitudinally substantially in the center of the row and the length of which is longer than the length of the adjacent filaments and short rods which are arranged at the ends of the row and the length of which is shorter than the length of the adjacent filaments.
Abstract: The invention relates to the method of use of compounds with B3-agonist activity for inhibiting uterine contractions, preventing or slowing down premature labor, or for the treatment and/or prophylaxis of dysmenorrhea.
Abstract: The invention relates to pharmaceutically stable oxaliplatin solution formulations, to the method of use thereof in the treatment of cancer tumors, to processes for the preparation of such formulations, and to a method for stabilizing solutions of oxaliplatin.
Type:
Grant
Filed:
February 22, 1999
Date of Patent:
October 23, 2001
Assignee:
Sanofi-Synthelabo
Inventors:
Nicholas H. Anderson, Ross Blundell, Stephen Brown, David A. England, Martin R. Gray
Abstract: The pharmaceutical formulations according to the invention contain from 0.5 to 50% by weight of a cyclic quaternary ammonium compound and pharmaceutically appropriate excipients and are formulated by wet granulation, preferably with polysorbate 80.
Type:
Grant
Filed:
July 30, 1999
Date of Patent:
October 16, 2001
Assignee:
Sanofi-Synthelabo
Inventors:
Bernard Abramovici, Xavier Boulenc, Jean-Claude Gautier, Pol Vilain
Abstract: A method for treating diseases which involve interaction of neurokinin B with NK3 receptors in humans. The method comprises administering a therapeutically effective amount of a NK3 antagonist compound having the formula:
in which: R1 and R11 together represent a —(CH2)3-group.
Type:
Grant
Filed:
May 7, 1999
Date of Patent:
September 25, 2001
Assignee:
Sanofi-Synthelabo
Inventors:
Daniel Bichon, Patrick Gueule, Didier Van Broeck, Xavier Emonds-Alt, Vincenzo Proietto
Abstract: The subject of the invention is a freeze-dried formulation consisting of an amorphous phase and a crystalline phase, which is pharmaceutically acceptable, comprising at least one nonprotein active ingredient, characterized in that it contains mannitol and alanine in a ratio R of between 0.1 and 1, R representing the mass of mannitol to the mass of alanine.
Type:
Grant
Filed:
December 9, 1998
Date of Patent:
September 4, 2001
Assignee:
Sanofi-Synthelabo
Inventors:
Colette Bouloumie, Thierry Breul, Laurence Colliere, Philippe Faure
Abstract: This invention relates to a purified polypeptide which constitutes the type-2 neurotensin receptor (NT-R2), as well as the nucleotide sequence encoding this polypeptide.
Type:
Grant
Filed:
December 28, 1999
Date of Patent:
August 14, 2001
Assignee:
Sanofi-Synthelabo
Inventors:
Daniel Caput, Pascale Chalon, Pascual Ferrara, Natalio Vita
Abstract: The invention relates to azacycloalkane derivatives, to pharmaceutical compositions containing them, to processes for preparing them, and to methods for the treatment of hyperglycaemia, diabetes, obesity or inflammation utilizing them.
Type:
Grant
Filed:
November 27, 2000
Date of Patent:
July 17, 2001
Assignee:
Sanofi-Synthelabo
Inventors:
Manuel Bedoya-Zurita, Juan Antonio Diaz Martin, Marc Daumas
Abstract: Compounds of general formula (I)
in which X represents a hydrogen or halogen atom or a methyl, methoxy or phenylmethoxy group, Y represents a hydrogen atom, 1 or 2 halogen atoms or a hydroxyl, methoxy, nitro or methyl group, R1 represents a hydrogen atom or a (C1-C4)alkyl group, R2 and R3 each represent a hydrogen atom, a (C1-C4)alkyl group or a phenylmethyl group or else R2 and R3 form, with the nitrogen atom which carries them, an azetidinyl, pyrrolidinyl, 3-ethoxypyrrolidinyl, piperidinyl, morpholinyl, 4-methylpiperazinyl or 1,3-thiazolidinyl group. Application in therapeutics.
Type:
Grant
Filed:
April 13, 2000
Date of Patent:
July 17, 2001
Assignee:
Sanofi-Synthelabo
Inventors:
Yannick Evanno, Laurent Dubois, Mireille Sevrin, Frank Marguet, Jacques Froissant, Régine Bartsch, Catherine Gille
Abstract:
A process for the preparation of 2-[(2-thienyl)-ethylamino]-(2-halogenophenyl)-acetamides of general formula (VII) starting from the nitriles of general formula (I). Compounds of general formula (VII) are valuable intermediates.
Type:
Grant
Filed:
November 12, 1999
Date of Patent:
July 10, 2001
Assignee:
Sanofi-Synthelabo
Inventors:
Mária Bakonyi, Marianna Csatári née Nagy, Erzsébet Molnár née Bakó, Zoltán Makovi, Piroska Jobb, Edit Bai née Tállai
Abstract: Compound of general formula (I)
in which R1 represents an alkyl or cycloalkylmethyl group, X1 represents a hydrogen or halogen atom or an alkoxy group, or alternatively OR1 and X1 together represent an —OCH2O—, —O(CH2)2—, —O(CH2)3—, —O(CH2)2O— or —(CH2)3O— group, X2 represents a hydrogen atom or an amino group, X3 represents a hydrogen or halogen atom, and R2 represents a hydrogen atom, an optionally substituted alkyl group, an optionally substituted phenylalkyl group or a group —(CH2)nCO—Z in which n represents a number from 1 to 6 and Z represents a 1-piperidyl group. Therapeutic application.
Abstract: The invention concerns compounds of formula (I)
in which: R is —NO2 or —NHR3, R3 being hydrogen, —COR4 (R4 selected among (C1-C4) alkyl, aryl and aryl (C1-C4) alkyl, —COOR5 (R5 selected among (C1-C4) alkyl and aryl (C1-C4) alkyl), —CONHR6 or SO2R6 (R6 selected among (C1-C5) alkyl, aryl and aryl(C1-C4) alkyl), —SO2NR7R8 (R7 and R8 independently of each other represent hydrogen or (C1-C4) alkyl or form with the nitrogen atom a morpholine group), aryl (C1-C4) alkyl, R1 is a (C1-C4) alkyl group linear or branched, cyclo (C3-C8) alkyl, aryl optionally substituted, aryl (C1-C4) alkyl optionally substituted, heteroaryl, R2 is a hydrogen atom, a (C1-C4) alkyl or arylmethyl group, X is an oxygen or sulphur atom, a —CH2—, —SO2 or —NR1— group and Y is a hydrogen atom or (C1-C6) alkyl. The invention is applicable to synthesis intermediates.
Type:
Grant
Filed:
July 14, 1999
Date of Patent:
June 26, 2001
Assignee:
Sanofi-Synthelabo
Inventors:
Gilbert Lassalle, Patrice Bellevergue, Jean-Claude Bourbier, Daniel Galtier, Valérie Martin
Abstract: Compounds corresponding to the general formula (I)
in which R1 represents hydrogen or an alkyl or cycloalkylmethyl group, X1 represents hydrogen or a halogen or an alkoxy group, or alternatively OR1 and X1 together represent a group of formula —OCH2O—, —O(CH2)2—, —O(CH2)3—, —O(CH2)2O— or —O(CH2)3O—, X2 represents hydrogen, an amino group or a group of general formula —NHCO2R in which R represents an alkyl or phenylalkyl group, X3 represents hydrogen or a halogen, and R2 represents hydrogen or an alkyl, phenylalkyl or [(4-dimethylamino)piperid-1-ylcarbonyl]alkyl group. Therapeutic application.
Type:
Grant
Filed:
November 4, 1999
Date of Patent:
June 19, 2001
Assignee:
Sanofi-Synthelabo
Inventors:
Alistair Lochead, Samir Jegham, Jean Jeunesse
Abstract: Descriptive summary: use of a compound with the formula (I)
where
R1 is a hydrogen atom, a C1-2 alkyl group, a C1-2 fluoroalkyl group or a C1-2 perfluoroalkyl group and R2, R3 and R4, which may be the same or different, all represent a hydrogen atom, a straight- or branched-chain C1-4 alkyl group or a C3-4 cycloalkyl group, and
R5 is a hydrogen atom, a halogen such as fluorine or chlorine, a C1-4 alkyl group or a straight- or branched-chain C1-4 alkoxy group to manufacture a medicinal agent which can be used to treat ejaculation problems such as retrograde ejaculation or aspermia.
Abstract: A method is provided for preventing a cerebral infarction by administering to a patient a combination of an ADP-receptor blocking antiplatelet drug, such as clopidogrel, in combination with an antihypertensive agent such as an angiotensin AII antagonist (for example, irbesartan), an ACE inhibitor (for example, fosinopril) or a NEP/ACE inhibitor such as omapatrilat.