Patents by Inventor Edward Lunt

Edward Lunt 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: 5260291
    Abstract: [ 3H]-Imidazo[ 5,1-d] -1,2,3,5-tetrazin-4-one derivatives of the formula: ##STR1## wherein R.sup.1 represents hydrogen, or an alkyl, alkenyl or alkynyl group containing up to 6 carbon atoms, each such group being unsubstituted or substituted by from one to three substituents selected from halogen atoms, alkoxy, alkylthio, alkylsulphinyl and alkylsulphonyl groups containing up to 4 carbon atoms, and optionally substituted phenyl groups, or R.sup.1 represents a cycloalkyl group containing from 3 to 8 carbon atoms, and R.sup.2 represents a carbamoyl group optionally N-substituted by one or two groups selected ftom alkyl and alkenyl groups containing up to 4 carbon atoms, and cycloalkyl groups containing 3 to 8 carbon atoms, are new therapeutically useful compounds possessing antineoplastic and immunomodulatory activity.
    Type: Grant
    Filed: October 18, 1991
    Date of Patent: November 9, 1993
    Assignee: Cancer Research Campaign Technology Limited
    Inventors: Edward Lunt, Malcolm F. G. Stevens, Robert Stone, Kenneth R. H. Wooldridge, Edward S. Newlands
  • Patent number: 4659727
    Abstract: Ethene derivatives of the formula:[R.sup.5 (R.sup.1 CR.sup.4 .dbd.CR.sup.2 R.sup.3).sub.m ].sub.n Iwherein R.sup.5 represents optionally substituted heterocyclyl or a group --CR.sup.4 .dbd.CR.sup.2 R.sup.3, or optionally substituted aryl, heterocyclylalkyl or arylalkyl and R.sup.1 represents --NR.sup.6 -- wherein R.sup.6 represents hydrogen or optionally substituted alkyl or aryl, or R.sup.5 represents a quinonoidal group, and R.sup.1 represents .dbd.N--, R.sup.4 represents hydrogen, alkoxy, alkylthio, trifluoromethyl or optionally substituted alkyl or aryl, R.sup.2 represents cyano, formyl, alkoxycarbonyl, alkylsulphonyl, dialkylcarbamoyl, dialkylthiocarbamoyl, aryloxycarbonyl, arylsulphinyl or arylsulphonyl, R.sup.3 represents a group R.sup.2 or hydrogen, nitro or optionally substituted aryl or aroyl or alkanoyl, and m and n are 1 or 2, and pharmaceutically acceptable salts thereof, with the exclusion of certain compounds in which R.sup.
    Type: Grant
    Filed: September 10, 1985
    Date of Patent: April 21, 1987
    Assignee: May & Baker Limited
    Inventors: Adnan H. Al-Shaar, Barbara J. Broughton, Robert K. Chambers, David W. Gilmour, Diane M. Kelsey, Peter Lowden, Edward Lunt, David J. Lythgoe, Ian McClenaghan, Duncan C. McDougall, Libert C. Saunders, Keith A. J. Stuttle, Peter J. Warne
  • Patent number: 4442115
    Abstract: New tetrazole derivatives of the general formula: ##STR1## [wherein R.sup.1 represents a halogen atom, a straight- or branched-chain alkyl, alkoxy, alkylthio, alkylsulphinyl, alkylsulphonyl or alkylsulphamoyl group, each such group containing from 1 to 6 carbon atoms, a dialkylsulphamoyl, dialkylamino, or dialkylcarbamoyl group (wherein the two alkyl groups may be the same or different and each contains from 1 to 4 carbon atoms), a straight- or branched-chain alkanoyl, alkoxycarbonyl, alkoxycarbonylamino, alkylcarbamoyl or alkanoylamino group containing from 2 to 6 carbon atoms, a cycloalkylcarbonyl group containing from 3 to 8 carbon atoms in the cycloalkyl moiety, or a hydroxy, formyl, nitro, trifluoromethyl, trifluoroacetyl, aryl, benzyloxycarbonylamino, amino, sulphamoyl, cyano, tetrazol-5-yl, carboxy, carbamoyl, benzyloxy, aralkanoyl or aroyl group, or a group of the formula:--CR.sup.2 .dbd.NOR.sup.3 II(wherein R.sup.
    Type: Grant
    Filed: June 1, 1979
    Date of Patent: April 10, 1984
    Assignee: May & Baker Limited
    Inventors: Christopher A. Ramsden, Philip Knowles, Edward J. Lewis, Edward Lunt, Derek E. Wright
  • Patent number: 4167568
    Abstract: 8-Azapurin-6-one derivatives of the formula: ##STR1## wherein R.sup.8 represents alkoxy of from 1 to 6 carbon atoms, and R.sup.9 represents cyano, or a group of the formula V, VI, VII, VIII or IX indicated below: ##STR2## wherein R.sup.10, R.sub.13 and R.sup.14 each represents cyano, or alkanoyl or alkoxycarbonyl of from 2 to 6 carbon atoms, R.sup.11 represents hydrogen, cyano, or alkanoyl or alkoxycarbonyl of from 2 to 6 carbon atoms, R.sup.12 represents hydrogen or, when R.sup.11 represents hydrogen, R.sup.12 represents alkyl of from 1 to 6 carbon atoms or alkoxycarbonyl of from 2 to 6 carbon atoms, or the pair of symbols R.sup.11 and R.sup.12 form together an alkylene chain of the formula --(C.sub.q H.sub.2q)-- wherein q is an integer from 3 to 6, R.sup.15 and R.sup.16 each represents hydrogen or alkyl of from 1 to 6 carbon atoms, and Y.sup.
    Type: Grant
    Filed: October 20, 1977
    Date of Patent: September 11, 1979
    Assignee: May & Baker Limited
    Inventors: Philip Knowles, Edward Lunt, Stuart M. Marshall, Roger E. Ford
  • Patent number: 4146631
    Abstract: Benzamide derivatives of the formula:- ##STR1## wherein R.sup.1 represents a fluorine, chlorine or bromine atom, or an alkyl, alkoxy, alkylthio, alkylsulphonyl, alkanoylamino, alkylamino or alkylsulphamoyl group, each such group containing from 1 to 6 carbon atoms, a dialkylsulphamoyl, dialkylamino or dialkylcarbamoyl group (wherein the two alkyl groups may be the same or different and each contains from 1 to 4 carbon atoms), an alkanoyl, alkoxycarbonyl, alkoxycarbonylamino or alkylcarbamoyl group containing from 2 to 6 carbon atoms, or a hydroxy, formyl, nitro, trifluoromethyl, aryl, benzyloxycarbonylamino, amino, sulphamoyl, cyano, tetrazol-5-yl, carboxy, carbamoyl or aroyl group, and n represents an integer 1, 2 or 3, are new compounds possessing pharmacological properties, in particular properties of value in the treatment of respiratory disorders manifested by the interaction of tissue-fixed antibodies with specific antigens.
    Type: Grant
    Filed: November 3, 1977
    Date of Patent: March 27, 1979
    Assignee: May & Baker Limited
    Inventors: Roger E. Ford, Philip Knowles, Edward Lunt, Stuart M. Marshall, Anthony J. H. Summers