Patents by Inventor Michael Dowle

Michael Dowle 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).

  • Publication number: 20080021058
    Abstract: The invention provides a compound of formula (I) or a salt thereof: wherein W is Ar, —CR4R5Ar or a group (y) or (y1), wherein Ar is (x) or (z): R1 is C1-4alkyl, C1-3fluoroalkyl or —CH2CH2OH. R2 is C2-6alkyl, C3-6cycloalkyl or —(CH2)n4-C3-6cycloalkyl; and R3 is optionally substituted C3-8cycloalkyl, optionally substituted mono-unsaturated-C5-7cycloalkenyl, an optionally substituted heterocyclic group (aa), (bb) or (cc) (in which Y is O, S, SO2, or NR10), or a bicyclic group (ee): These compounds are PDE4 inhibitors.
    Type: Application
    Filed: March 15, 2005
    Publication date: January 24, 2008
    Inventors: David Allen, Diane Coe, Caroline Cook, Michael Dowle, Christopher Edlin, Julie Hamblin, Martin Johnson, Paul Jones, Mika Lindvall, Charlotte Mitchell, Alison Redgrave, Naimisha Trivedi
  • Publication number: 20070293564
    Abstract: A method for the prevention of an orthomyxovirus or paramyxovirus infection comprising the step of administration to a subject in need thereof of an effective amount of a compound of formula (I)
    Type: Application
    Filed: December 4, 2006
    Publication date: December 20, 2007
    Inventors: Michael Dowle, Betty Jin, Simon MacDonald, Andrew Mason, Darryl McConnell, Van Nguyen, Stephen Shanahan, Wen-Yang Wu
  • Publication number: 20060089375
    Abstract: The invention relates to a compound of formula (I) or a salt thereof: wherein: R1 is C1-4alkyl, C1-3fluoroalkyl, —CH2CH2OH or —CH2CH2CO2C1-2alkyl; R2 is a hydrogen atom (H), methyl or C1fluoroalkyl; R3 is optionally substituted C3-8cycloalkyl or optionally substituted mono-unsaturated-C5-7cycloalkenyl or an optionally substituted heterocyclic group of sub-formula (aa), (bb) or (cc); in which n1 and n2 independently are 1 or 2; and in which Y is O, S, SO2, or NR10; or R3 is a bicyclic group (dd) or (ee): and wherein X is NR4R5 or OR5a. The compounds are phosphodiesterase (PDE) inhibitors, in particular PDE4 inhibitors. Also provided is the use of a compound of formula (I), or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for the treatment and/or prophylaxis of an inflammatory and/or allergic disease in a mammal such as a human, for example chronic obstructive pulmonary disease (COPD), asthma, or allergic rhinitis.
    Type: Application
    Filed: September 12, 2003
    Publication date: April 27, 2006
    Inventors: David Allen, Diane Coe, Caroline Cook, Michael Dowle, Christophen Edlin, Julie Hamblin, Martin Johnson, Paul Jones, Richard Knowles, Mika Lindvall, Charlotte Mitchell, Alison Redgrave, Peter Ward
  • Publication number: 20050038108
    Abstract: The invention relates to compounds of general formula (I); in which R is an amino or guanidino group; R2 is acetyl or trifluoroacetyl; X is CONH, SO2NH, NHCO or NHCONH; m is either 0 or 1; n is an integer from 2 to 6; q is an integer from 0 to 3; and Y is hydrogen or an aromatic substituent, or a pharmaceutically acceptable derivative thereof; methods for their preparation, pharmaceutical formulations containing them or their use in the prevention or treatment of a viral infection.
    Type: Application
    Filed: November 8, 2002
    Publication date: February 17, 2005
    Inventors: Michael Dowle, Betty Jin, Simon Macdonald, Andrew McM Mason, Darryl Mcconnell, Van Nguyen, Stepehn Shanahan, Wen-Yang Wu