Patents by Inventor Marc Gaston Venet

Marc Gaston Venet has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Patent number: 7067531
    Abstract: This invention comprises the novel compounds of formula (I) wherein r, t, Y1—Y2, R1, R2, R3, R4, R5, R6 and R7 have defined meanings, having farnesyl transferase inhibiting activity; their preparation, compositions containing them and their use as a medicine.
    Type: Grant
    Filed: September 18, 2001
    Date of Patent: June 27, 2006
    Inventors: Patrick René Angibaud, Marc Gaston Venet, Laurence Anne Mevellec
  • Patent number: 7053105
    Abstract: This invention comprises the novel compounds of formula (I) wherein r, s, t, Y1—Y2, R1, R2, R3, R4, R5 and R7 have defined meanings, having farnesyl transferase inhibiting activity; their preparation, compositions containing them and their use as a medicine.
    Type: Grant
    Filed: September 18, 2001
    Date of Patent: May 30, 2006
    Assignee: Janssen Pharmaceutica, N.V.
    Inventors: Patrick René Angibaud, Marc Gaston Venet, Isabelle Noëlle Constance Pilatte
  • Patent number: 6936626
    Abstract: The present invention is concerned with compounds of formula the N-oxides, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein X represents O, S or NR3; R1 represents hydrogen, hydroxy, C1-6alkyl or aryl; R2 represents hydrogen; optionally substituted C1-12alkyl; C3-7cycloalkyl; C2-8alkenyl; aryl; Het1; or R1 and R2 taken together may form a bivalent radical of formula —(CH2)n— wherein n is 2, 3, 4, 5 or 6; R3 represents hydrogen, optionally substituted C1-6alkyl, aryl, Het1; R4 represents hydrogen; hydroxy; mercapto; C1-6alkyloxy; C1-6alkylthio; aryloxy; arylthio; Het1-oxy; Het1-thio; optionally substituted C1-12alkyl; optionally substituted C2-8alkenyl; optionally substituted C2-8alkynyl; optionally substituted C3-7cycloalkyl; optionally substituted C5-7cycloalkenyl; aryl; Het1; or -Alk—NR3R5 (i) or —NR3R5 (ii) wherein Alk represents C1-6alkanediyl; and R5 represents hydrogen, C1-6alkyl, aryl, Het1, (aryl or Het1)C1-6alkyl, (aryl or Het1)carbonyl or (a
    Type: Grant
    Filed: September 25, 2001
    Date of Patent: August 30, 2005
    Assignee: Janssen Pharmaceutica N.V.
    Inventors: Dominique Mabire, Christophe Denis Adelinet, Imré Christian Csoka, Marc Gaston Venet
  • Publication number: 20050171111
    Abstract: This invention comprises the novel compounds of formula (I) wherein r, t, Y1, Y2, R1, R2, R3, R5, R6and R7 have defined meanings, having farnesyl transferase inhibiting activity; their preparation, compositions containing them and their use as a medicine.
    Type: Application
    Filed: March 18, 2003
    Publication date: August 4, 2005
    Inventors: Patrick Angibaud, Marc, Gaston Venet, Christophe Meyer, Henry Breslin
  • Patent number: 6914066
    Abstract: This invention concerns compounds of formula the pharmaceutically acceptable acid addition salts and the stereochemically isomeric forms thereof, wherein ?X1—X2—X3— is a trivalent radical,; >Y1—Y2— is a trivalent radical; r and s are each independently 0, 1, 2, 3, 4 or 5; t is 0, 1, 2 or 3; each R1 and R2 are independently hydroxy, halo, cyano, C1-6alkyl, trihalomethyl, trihalomethoxy, C2-6alkenyl, C1-6alkyloxy, hydroxyC1-6alkyloxy, C1-6alkylthio, C1-6alkyloxyC1-6alkyloxy, C1-6alkyloxycarbonyl, aminoC1-6alkyloxy, mono- or di(C1-6alkyl)amino, mono- or di(C1-6alkylaminoC1-6alkyloxy, aryl, arylC1-6alkyl, aryloxy or arylC1-6alkyloxy, hydroxycarbonyl, C1-6alkyloxycarbonyl; or two R1 or R2 on adjacent positions form together a bivalent radical; R3 is hydrogen, halo, C1-6alkyl, cyano, haloC1-6alkyl, hydroxyC1-6alkyl, cyanoC1-6alkyl, aminoC1-6alkyl, C1-6alkyloxyC1-6alkyl, C1-6alkylthio-C1-6alkyl, aminocarbonylC1-6alkyl, hydroxycarbonyl, hydroxycarbonylC1-6alkyl, C1-6alkyoxycarbonylC1-6alkyl, C1-6alkylcarbonylC
    Type: Grant
    Filed: June 24, 2002
    Date of Patent: July 5, 2005
    Assignee: Janssen Pharmaceutica N.V.
    Inventors: Patrick René Angibaud, Marc Gaston Venet, Xavier Marc Bourdrez
  • Patent number: 6894046
    Abstract: The present invention is concerned with the compounds of formula the N-oxides, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein p is 0 to 4; X is O, S, NR5 or a direct bond; Y is O, S, NR5 or S(O)2; R1 independently is C1-6alkyl, halo, polyhaloC1-6alkyl, hydroxy, mercapto, C1-6alkyloxy, C1-6alkylthio, C1-6alkylcarbonyloxy, aryl, cyano, nitro, Het3, R6, NR7R8 or substituted C1-4alkyl; R2 is Het1, C3-7cycloalkyl or optionally substituted C1-6alkyl and if X is O, S or NR5, then R2 may also represent aminocarbonyl, aminothiocarbonyl, C1-4alkylcarbonyl, C1-4alkylthiocarbonyl, arylcarbonyl, arylthiocarbonyl, Het1carbonyl or Het1thiocarbonyl; R3 and R4 independently are hydrogen, C1-6alkyl or C3-7cycloalkyl; R3 and R4 form a C2-6alkanediyl; R5 is hydrogen or C1-4alkyl; R6 is a sulfonyl or sulfinyl derivative; R7 and R8 are independently hydrogen, optionally substituted C1-4alkyl, aryl, a carbonyl containing moiety, C3-7cycloalkyl, —Y—C1-4alkanediyl-C(?O)—O—R
    Type: Grant
    Filed: March 19, 2001
    Date of Patent: May 17, 2005
    Assignee: Janssen Pharmaceutica N.V.
    Inventors: Eddy Jean Edgard Freyne, Jean Fernand Armand Lacrampe, Frederik Dirk Deroose, Marc Gaston Venet
  • Patent number: 6867207
    Abstract: The present invention is concerned with the compounds of formula the N-oxides, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, p and q are 0, 1, 2, 3 or 4 and q is also 5; X is O, S, NR3 or a direct bond; R1 is hydrogen, hydroxy, halo, optionally substituted amino, optionally substituted C1-6alkyl, C1-6alkyloxy, C3-7cycloalkyl or aryl; R2 is aryl, Het1, C3-7cycloalkyl, optionally substituted C1-6alkyl; and if X is O, S or NR3, then R2 may also be a carbonyl or thiocarbonyl linked substituent; R3 is hydrogen or C1-4alkyl; R4 and R5 independently are optionally substituted C1-6alkyl, halo, hydroxy, mercapto, C1-6alkyloxy, C1-6akylthio, C1-6alkylcarbonyloxy, aryl, cyano, nitro, Het3, R6 or NR7R8; R6 is substituted sulfonyl or sulfinyl; R7 and R8 are hydrogen, optionally substituted C1-4alkyl, aryl, a carbonyl or thiocarbonyl linked substituent, C3-7cycloalkyl, Het3 and R6; R9 and R10 are each independently selected from hydrogen, optionally substituted C1-4alky
    Type: Grant
    Filed: June 26, 2001
    Date of Patent: March 15, 2005
    Assignee: Janssen Pharmaceutica N.V.
    Inventors: Jean Fernand Armand Lacrampe, Eddy Jean Edgard Freyne, Marc Gaston Venet, Gustaaf Maria Boeckx
  • Patent number: 6833375
    Abstract: The present invention is concerned with compounds of formula the N-oxides, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein R1 is hydrogen, hydroxy, C1-6alkyl or aryl; R2 is hydrogen; optionally substituted C1-12alkyl; C3-7cycloalkyl; C2-8alkenyl, optionally substituted pyrrolidinyl or aryl; R3 is hydrogen, optionally substituted C1-6alkyl or aryl; Het is an optionally substituted unsaturated heterocycle selected from imidazolyl, triazolyl, tetrazolyl and pyridinyl; is an optionally substituted unsaturated mono- or bicyclic heterocycle; and aryl is optionally substituted phenyl. The present invention also relates to processes for their preparation and compositions comprising said new compounds, as well as their use as a medicine.
    Type: Grant
    Filed: September 10, 2002
    Date of Patent: December 21, 2004
    Assignee: Janssen Pharmaceutica, N.V.
    Inventors: Marc Gaston Venet, Dominique Jean-Pierre Mabire, Jean Fernand Armand Lacrampe, Gerard Charles Sanz
  • Publication number: 20040167333
    Abstract: The present invention is concerned with the compounds of formula 1
    Type: Application
    Filed: February 19, 2004
    Publication date: August 26, 2004
    Inventors: Jean Fernand Armand Lacrampe, Eddy Jean Edgard Freyne, Marc Gaston Venet, Gustaaf Maria Boeckx
  • Publication number: 20040082592
    Abstract: The present invention concerns compounds of formula. In a preferable embodiment, X represents O; R1 represents C1-6alkyl; cycloC3-12alkyl or (cycloC3-12alkyl)C1-6alkyl, wherein one or more hydrogen atoms in a C1-6alkyl-moiety or in a cycloC3-12alkyl-moiety optionally may be replaced by C1-6alkyloxy, aryl, halo or thienyl; R2 represents hydrogen; halo; C1-6alkyl or amino; R3 and R4 each independently represent hydrogen or C1-6alkyl; or R2 and R3 may be taken together to form —R2-R3-, which represents a bivalent radical of formula -Z4-CH2-CH2-CH2- or -Z4-CH2-CH2- with Z4 being O or NR11 wherein R11 is C1-6alkyl; and wherein each bivalent radical is optionally substituted with C1-6alkyl; or R3 and R4 may be taken together to form a bivalent radical of formula —CH2-CH2-CH2-CH2-; R5 represents hydrogen; Y represents O; and aryl represents phenyl optionally substituted with halo.
    Type: Application
    Filed: August 14, 2003
    Publication date: April 29, 2004
    Inventors: Dominique Jean-Pierre Mabire, Marc Gaston Venet, Sophie Coupa, Alain Philippe Poncelet, Anne Simone Josephine Lesage
  • Publication number: 20040067968
    Abstract: This invention comprises the novel compounds of formula (I): 1
    Type: Application
    Filed: June 26, 2003
    Publication date: April 8, 2004
    Inventors: Patrick Rene Angibaud, Marc Gaston Venet, Virginie Sophie Poncelet
  • Publication number: 20040063944
    Abstract: This invention comprises the novel compounds of formula (I) 1
    Type: Application
    Filed: June 26, 2003
    Publication date: April 1, 2004
    Inventors: Patrick Rene Angibaud, Marc Gaston Venet
  • Publication number: 20040048882
    Abstract: This invention comprises the novel compounds of formula (I) wherein r, s, t, Y1—Y2, R1, R2, R3, R4, R5, R6 and R7 have defined meanings, having farnesyl transferase inhibiting activity; their preparation, compositions containing them and their use as a medicine.
    Type: Application
    Filed: March 24, 2003
    Publication date: March 11, 2004
    Inventors: Patrick Rene Angibaud, Marc Gaston Venet, Ashis Kumar Saha, Laurence Anne Mevellec
  • Publication number: 20040034218
    Abstract: This invention comprises the novel compounds of formula (I) 1
    Type: Application
    Filed: May 19, 2003
    Publication date: February 19, 2004
    Inventors: Patrick Rene Angibaud, Marc Gaston Venet, Virginie Sophie Poncelet
  • Publication number: 20030207887
    Abstract: This invention comprises the novel compounds of formula (I) 1
    Type: Application
    Filed: March 24, 2003
    Publication date: November 6, 2003
    Inventors: Patrick Rene Angibaud, Marc Gaston Venet, Laurence Anne Mevellec
  • Publication number: 20030203904
    Abstract: This invention comprises the novel compounds of formula (I)wherein r, s, t, Y1-Y2, R1, R2, R3, R4, R5 and R7 have defined meanings, having farnesyl transferase inhibiting activity; their preparation, compositions containing them and their use as a medicine.
    Type: Application
    Filed: March 24, 2003
    Publication date: October 30, 2003
    Inventors: Patrick Rene Angibaud, Marc Gaston Venet, Isabelle Boelle Constance Pilatte
  • Publication number: 20030199547
    Abstract: This invention comprises the novel compounds of formula (I) 1
    Type: Application
    Filed: March 24, 2003
    Publication date: October 23, 2003
    Inventors: Patrick Rene Angibaud, Marc Gaston Venet, Laurence Anne Mevellec
  • Publication number: 20030176419
    Abstract: The present invention is concerned with compounds of formula 1
    Type: Application
    Filed: September 10, 2002
    Publication date: September 18, 2003
    Inventors: Marc Gaston Venet, Dominique Jean-Pierre Mabire, Jean Fernand Armand Lacrampe, Gerard Charles Sanz
  • Publication number: 20030119843
    Abstract: This invention concerns compounds of formula 1
    Type: Application
    Filed: June 24, 2002
    Publication date: June 26, 2003
    Applicant: Janssen Pharmaceutica, N.V.
    Inventors: Patrick Rene Angibaud, Marc Gaston Venet, Xavier Marc Bourdrez
  • Publication number: 20030114471
    Abstract: (−)-5-(3-Chlorophenyl)-&agr;-(4-chlorophenyl)-&agr;-(1-methyl-1H-imidazol-5-yl)tetrazolo-[1,5-a]quinazoline-7-methanamine and its pharmaceutically acceptable acid addition salts, and the use of such compounds in medicine especially for the treatment of cancer
    Type: Application
    Filed: December 20, 2002
    Publication date: June 19, 2003
    Inventors: Marc Gaston Venet, Patrick Rene Angibaud, David William End