US20070066575A1 - Methods and compositions for mitigating pain - Google Patents

Methods and compositions for mitigating pain Download PDF

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US20070066575A1
US20070066575A1 US11/507,995 US50799506A US2007066575A1 US 20070066575 A1 US20070066575 A1 US 20070066575A1 US 50799506 A US50799506 A US 50799506A US 2007066575 A1 US2007066575 A1 US 2007066575A1
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nitrate
cdcl
pain
compound
subject
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US11/507,995
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Gregory Thatcher
Brian Bennett
James Reynolds
Khem Jhamandas
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Queens University at Kingston
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Queens University at Kingston
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    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
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    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
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    • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04—Ortho-condensed systems
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    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/28—Phosphorus compounds with one or more P—C bonds
    • C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
    • C07F9/3804—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
    • C07F9/3808—Acyclic saturated acids which can have further substituents on alkyl
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    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/28—Phosphorus compounds with one or more P—C bonds
    • C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
    • C07F9/40—Esters thereof
    • C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
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    • C07J41/0055—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005 the 17-beta position being substituted by an uninterrupted chain of at least three carbon atoms which may or may not be branched, e.g. cholane or cholestane derivatives, optionally cyclised, e.g. 17-beta-phenyl or 17-beta-furyl derivatives
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    • C07J—STEROIDS
    • C07J41/00—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring
    • C07J41/0033—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005
    • C07J41/0055—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005 the 17-beta position being substituted by an uninterrupted chain of at least three carbon atoms which may or may not be branched, e.g. cholane or cholestane derivatives, optionally cyclised, e.g. 17-beta-phenyl or 17-beta-furyl derivatives
    • C07J41/0061—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005 the 17-beta position being substituted by an uninterrupted chain of at least three carbon atoms which may or may not be branched, e.g. cholane or cholestane derivatives, optionally cyclised, e.g. 17-beta-phenyl or 17-beta-furyl derivatives one of the carbon atoms being part of an amide group

Definitions

  • This invention relates to nitrate esters and use thereof in mitigating pain and effecting analgesia. More particularly this invention relates to organic nitrates which have therapeutic utility as analgesics, anti-inflammatory agents and sedatives.
  • nitrate ester glyceryl trinitrate (GTN), or nitroglycerin
  • GTN glyceryl trinitrate
  • NO nitric oxide
  • nitrate esters organic nitrates
  • NO itself has been identified as Endothelium Derived Relaxing Factor (EDRF) and several classes of compounds, for example nitrosothiols, in addition to organic nitrates, have been proposed as NO donors or NO prodrugs.
  • EDRF Endothelium Derived Relaxing Factor
  • organic nitrates themselves as analgesic agents, that is, organic nitrates that do not rely on an ASA or NSAID moiety, nor an opiate, for analgesic properties.
  • synthetic organic nitrates as new and useful therapeutic agents for treatment and mitigation of pain associated with disease states and chemotherapy of those disease states.
  • the present invention is based, at least in part, on the recognition that, although the potent vasodilatatory effects of organic nitrates may be either (a) deleterious to or, alternatively, (b) synergis tic with their analgesic effects, regulation of these two effects is required for the development of therapeutic agents useful in treatment and mitigation of pain. Pain may be treated or mitigated by, for example, an analgesic, anti-inflammatory and/or sedative agent.
  • Possible deleterious effects of organic nitrates may arise, for example, through an NO-donor potentiating hyperalgesia via a cyclic guanosine-3,5-monophosphate (cGMP)-independent mechanism.
  • cGMP cyclic guanosine-3,5-monophosphate
  • synergistic effects of organic nitrates may arise, for example, through the ability of an NO-donor to induce analgesia by activation of soluble guanylyl cyclase (GCase) and elevation of cGMP levels.
  • the present invention relates to methods for treating or mitigating pain through use of an organic nitrate, wherein regulation of these two effects is achieved.
  • selection of an appropriate organic nitrate provides modulation and balance between the ability of the organic nitrate to release NO and its potency for GCase activation.
  • gastrointestinal toxicity is known to be a deleterious side effect of some analgesic drugs and that NO donor molecules are gastro-protective
  • therapeutic analgesia can be achieved through utilization of an appropriate organic nitrate. This statement is based, at least in part, on bioassay data on such compounds.
  • This invention provides methods and compositions which are useful in treating pain, inhibiting inflammation, and/or providing analgesia.
  • Methods of the invention involve administering to a subject a therapeutic compound (nitrate ester) which provides analgesia.
  • the methods and compositions of the invention are useful for the treatment and mitigation of pain associated with disorders and disease states and chemotherapy of those disease states.
  • the methods and compositions of the invention can be used therapeutically to treat acute, chronic and/or inflammatory pain in conditions such as, but not limited to, nerve injury, post-herpetic neuralgia, arthritis, diabetic neuropathy, dysmenorrhea, endometriosis, phantom limb pain, pain associated with cancer and post-operative pain, or can be used prophylactically in a subject susceptible or predisposed to these conditions.
  • a therapeutic compound used in the method of the invention interacts with guanylyl cyclase, effecting analgesia.
  • a therapeutic compound used in the method of the invention modulates levels of the cyclic nucleotides cyclic guanosine-3′,5′- monophosphate (cGMP) and cyclic adenosine-3′,5′-monophosphate (cAMP).
  • cGMP cyclic guanosine-3′,5′- monophosphate
  • cAMP cyclic adenosine-3′,5′-monophosphate
  • the invention provides a method for treating pain, treating or inhibiting inflammation, providing analgesia, providing sedation, mitigating anxiety and/or providing anaesthesia in a subject, comprising administering to a subject in need thereof an effective amount of a therapeutic compound, wherein the therapeutic compound is of the formula (Ia): in which E, F 1 , F 2 , G 1 , and G 2 are the same or different organic radicals which may be joined in cyclic ring systems, and which may contain inorganic counterions;
  • R N is any aryl or heteroaryl group and Z N is (CO) mm -X N nn -Y N oo ;
  • mm, nn, oo are 0 or 1 and X N ,Y N are NH, NR NN , O or CH 2 ;
  • R NN is a short chain alkyl group (C 1 -C 12 ).
  • F 2 is a nitrate group and E, F 1 , G 1 , G 2 are the same or different organic radicals which may be joined in cyclic ring systems, and which may contain inorganic counterions;
  • R N is any aryl or heteroaryl group and Z N is (CO) mm -X N nn -Y N oo ;
  • mm, nn, oo are 0 or 1 and X N ,Y N are NH, NR NN , O or CH 2 ;
  • R NN is a short chain alkyl group (C 1 - C 12 )
  • the invention provides a method for treating pain, treating or inhibiting inflammation, providing analgesia, providing sedation, mitigating anxiety and/or providing anaesthesia in a subject, comprising administering to a subject in need thereof an effective amount of a therapeutic compound, wherein the therapeutic compound is of the formula (Ib): in which F 2 is an organic radical which may be joined in a cyclic ring system with G 2 , and which may contain inorganic counterions; E and G 1 are both methylene groups; F 1 is H; and G 2 is R N -Z N -;
  • R N is an organic radical possessing a heteroaryl group containing P or S atoms where said P or S are positioned ⁇ , ⁇ , or ⁇ to a nitrate group as identified in formula I; and ZN is W N mm -X N nn -Y N oo ;
  • mm, nn and oo are 0 or 1; and W N , X N , Y N are NH, NR NN , CO, O or CH 2 ;
  • R NN is a short chain alkyl group (C 1 -C 12 ).
  • F 2 is a nitrate group
  • E and G 1 are methylene groups
  • F 1 is H
  • G 2 is R N -Z N -;
  • R N is an organic radical possessing an heteroaryl group containing P or S atoms where said P or S are positioned ⁇ , ⁇ , or ⁇ to a nitrate group as identified in formula I; and Z N is W N mm -X N nn -Y N oo ;
  • mm, nn, oo are 0 or 1 and W N , X N , Y N are NH, NR NN , CO, O or CH 2 ;
  • R NN is a short chain alkyl group (C 1 -C 12 ).
  • the invention provides a method for treating pain, treating or inhibiting inflammation, providing analgesia, providing sedation, mitigating anxiety and/or providing anaesthesia in a subject, comprising administering to a subject in need thereof an effective amount of a therapeutic compound, wherein the therapeutic compound is of the formula (1c):
  • E is (R 1 R 2 C) m and G 2 -G 1 -CF 1 F 2 - is R 19 -(R 3 R 4 C) p -(R 17 R 18 C) n -;
  • A is selected from a substituted or unsubstituted aliphatic group (preferably a branched or straight-chain aliphatic moiety having from 1 to 24 carbon atoms in the chain, which optionally may contain O, S, NR 6 and unsaturations in the chain, optionally bearing from 1 to 4 hydroxy, nitrate, amino, aryl, or heterocyclic groups; an unsubstituted or substituted cyclic aliphatic moiety having from 3 to 7 carbon atoms in the aliphatic ring, which optionally may contain O, S, NR 6 and unsaturations in the ring, optionally bearing from 1 to 4 hydroxy, nitrate, amino, aryl, or heterocyclic groups; an unsubstituted or substituted aliphatic moiety constituting a linkage of from 0 to 5 carbons, between R 1 and R 3 and/or between R 17 and R 4 , which optionally may contain O, S, NR 6 and unsaturations in the linkage, and optionally
  • X is F, Br, Cl, NO 2 , CH 2 , CF 2 , O, NH, NMe, CN, NHOH, N 2 H 3 , N 2 H 2 R 13 , N 2 HR 13 R 14 , N 3 , S, SCN, SCN 2 H 2 (R 15 ) 2 , SCN 2 H 3 (R 15 ), SC(O)N(R 15 ) 2 , SC(O)NHR 15 , SO 3 M, SH, SR 7 , SO 2 M, S(O)R 8 , S(O)-R9, S(O)OR 8 , S(O) 2 O R 9 , PO 2 HM, PO 3 HM, PO 3 M 2 , P(O)(OR 15 )(OR 16 ), P(O)(OR 16 )(OM), P(O)(R 15 )(OR8), P(O)(OM)R 15 , CO 2 M, CO 2 H, CO 2 R 11 , C(O), C(O)RI 2
  • R 2 , R 5 , R 18 , R 19 are optionally hydrogen, A or X-Y;
  • R 6 , R 7 , R 8 , R 9 , R 11 , R 12 , R 13 , R 14 , R 15 , R 16 are the same or different alkyl or acyl groups containing 1-24 carbon atoms which may contain 1-4 ON0 2 substituents; or Cl - C 6 connections to R 1 - R 4 in cyclic derivatives; or are each independently hydrogen a nitrate group or A;
  • M is H, Na+, K+, NH 4 +, N+H k R 11 (4-k) where k is 0-3; or other pharmaceutically acceptable counterion;
  • R 19 is X-Y.
  • R 1 and R 3 are the same or different and selected from H and Cl-C 4 , alkyl chains, which chains may include one 0 linking R 1 and R 3 to form pentosyl, hexosyl, cyclopentyl, or cyclohexyl rings, which rings may optionally bear hydroxyl substituents;
  • R 2 and R 4 are the same or different and selected from H, a nitrate group, Cl-C 4 alkyl chains optionally bearing 1-3 nitrate groups, and acyl groups (-C(O)R 5 );
  • R 7 , R 11 are the same or different Cl - C 8 alkyl or acyl;
  • R 5 , R 6 , R 8 , R 9 , R 12 , R 13 , R 14 , R 15 , R 16 are the same or different and are alkyl groups containing 1-12 carbon atoms which may contain 1-4 ONO 2 substituents; or C 1 or C 2 connections to R 1 - R 3 in cyclic derivatives; and
  • M is H, Na + , K + , NH 4 + or N + H k R 11 (4-k),where k is 0-3.
  • X is CH 2 , O, NH, NMe, CN, NHOH, N 2 H 3 , N 2 H 2 R 13 , N 2 HR 13 R 14 , N 3 , S, SCN, SCN 2 H 2 (RI 5 ) 2 , SCN 2 H 3 (R 5 ), SC(O)N(R 15 ) 2 , SC(O)NHR 15 , SO 3 M, SH, SR 7 , SO 2 M, S(O)R 8 , S(O) 2 R 9 , S(O)OR 8 , S(O) 2 OR 9 , PO 3 HM, PO 3 M 2 , P(O)(OR 15 )(OR 16 ), P(O)(OR 16 )(OM), P(O)(R15)(OR 8 ), P(O)(OM)R 15 , CO 2 M, CO 2 H, CO 2 R 11 , C(O), C(O)R 12 , C(O)(OR 13 ), PO 2 M, P(
  • Y is CN, N 2 H 2 R 13 , N 2 HR 13 R 14 , N 3 , SCN, SCN 2 H 2 (R 15 ) 2 , SC(O)N(R 15 ) 2 , SC(O)NHR 15 , SO 3 M, SR 4 , SO 2 M, PO 3 HM, PO 3 M 2 , P(O)(OR 15 )(OR 16 ), P(O)(OR 16 )(OM), P(O)(R 15 )(OR 8 ), P(O)(OM)R 15 , CO 2 M, CO 2 H, CO 2 R 11 , C(O)R 12 , C(O)(SR 13 ), SR 5 , or SSR 5 , or does not exist.
  • R 5 , R 6 , R 8 , R 9 , R 12 , R 13 , R 14 , R 15 , R 16 are the same or different and are alki4s containing 1-12 carbon atoms; or Cl or C2 connections to R 1 or R 3 in cyclic derivatives;
  • X is CH 2 , O, NH, NMe, S, SO 3 M, SH, SR 7 , SO 2 M, S(O)R 8 , S(O) 2 R 9 , S(O)OR 8 , S(O) 2 O R 9 , PO 3 M 2 , P(O)(OR1 5 )(OR 16 ), P(O)(OR 16 )(OM), P(O)(R 15 )(OR8), PO 3 HM or P(O)(OM)R 15 ; and
  • Y is SOM, SO 3 M, PO 3 HM, PO 3 M 2 , P(O)(OR 15 )(OR 16 ), P(O)(OR 16 )(OM), SR 5 , SR 4 or SSR 5 , or does not exist.
  • therapeutic compounds of the invention act as analgesic, sedative and/or anti-inflammatory agents.
  • Preferred therapeutic compounds for use in the invention include compounds having the formula (Formula II):
  • n and p are integers from 0 to 10;
  • R 3,17 are each independently hydrogen; a nitrate group; or A;
  • R 1,4 are each independently hydrogen; or A;
  • A is selected from: a substituted or unsubstituted aliphatic group (preferably a branched, or straight-chain aliphatic moiety having from 1 to 24 carbon atoms in the chain, which optionally may contain 0, S, NR 6 and unsaturations in the chain, optionally bearing from 1 to 4 hydroxy, or nitrate, or amino or aryl, or heterocyclic groups; an unsubstituted or substituted cyclic aliphatic moiety having from 3 to 7 carbon atoms in the aliphatic ring, which optionally may contain O, S, NR 6 and unsaturations in the ring, optionally bearing from 1 to 4 hydroxy, or nitrate, or amino 8 or aryl, or heterocyclic groups; an unsubstituted or substituted aliphatic moiety constituting a linkage of from 0 to 5 carbons, between RI and R 3 and/or between R 17 and R 4 , which optionally may contain 0, S, NR 6 and unsaturations in the link
  • R 2 , R 5 , R 18 , R 19 are optionally hydrogen; or A; or X-Y.
  • X is F, Br, Cl, NO 2 , CH 2 , CF 2 , O, NH, NMe, CN, NHOH, N 2 H 3 , N 2 H 2 R 13 , N 2 HR 13 R 14 , N 3 , S, SCN, SCN 2 H 2 (R 15 ) 2 , SCN2H3(RI 5 ), SC(O)N(R 15 ) 2 , SC(O)NHR 15 , SO 3 M, SH, SR 7 , SO 2 M, S(O)R 8 , S(O) 2 R 9 , S(O)OR 8 , S(O) 2 O R 9 , PO 2 HM, PO 3 HM, PO 3 M 2 , P(O)(OR 15 )(OR1 6 ), P(O)(OR 16 )(OM), P(O)(R 15 )(OR 8 ), P(O
  • R 6 , R 7 , R 8 , R 9 , R 10 , R 1 l, R1 2 , R 13 , R 14 , R 15 , R 16 are the same or different alkyl or acyl groups containing 1-24 carbon atoms which may contain 1-4 ON0 2 substituents; or C 1 - C 6 connections to R 1 - R 4 in cyclic derivatives; or are each independently hydrogen; a nitrate group; or W.
  • therapeutic compounds of the invention are analgesic, sedative and/or anti-inflammatory agents.
  • Preferred therapeutic compounds for use in the invention include compounds in which R 19 is X-Y.
  • R 19 is X-Y and R 5 , R 6 , R 8 , R 9 , R 10 , R 12 , R 13 , R 14 , R 15 , R 16 are the same or different alkyl groups containing 1-24 carbon atoms which may contain 1-4 ON0 2 substituents, or Cl or C2 connections to R 1 -R 3 in cyclic derivatives;
  • R 1 and R 3 are the same or different and selected from H, Cl-C 4 , alkyl chains, which may inlude one O, linking R 1 and R 3 to form pentosyl, hexosyl, cyclopentyl, or cycohexyl rings, which rings may optionally bear hydroxyl substituents;
  • R 2 and R 4 are the same or different and selected from H,
  • Rig is X-Y
  • m is selected from CH 2 , O, NH, NMe, CN, NHOH, N 2 H 3 , N 2 H 2 R 13 , N 2 HR 13 R 14 , N 3 , S, SCN, SCN 2 H 2 (R 15 ) 2 , SCN 2 H 3 (R 15 ), SC(O)N(R 15 ) 2 , SC(O)NHR 15 , SO 3 M, SH, SR 7 , SO,M, S(O)R 8 , S(O) 2 R 9 , S(O)OR 8 , S(O) 2 OR 9 , PO 3 HM, PO 3 M 2 , P(O)(OR 15 )(OR 16 ), P(O)(OR 16 )(OM), P(O)(R 15 )(OR 8 ), P(O)(OM)R 15 , CO 2
  • Y is selected from CN, N 2 H 2 R 13 , N 2 HR 13 R 14 , N 3 , SCN, SCN 2 H 2 (R 15 ) 2 , SC(O)N(R 15 ) 2 , SC(O)NHR 15 , SO 3 M, SR 4 , SO 2 M, PO 3 HM, PO 3 M 2 , P(O)(OR 15 )(OR 16 ), P(O)(OR 16 )(OM), P(O)(R 15 )(OR 8 ), P(O)(OM)R 15 , CO 2 M, CO 2 H, CO?R 1 , C(O)R 12 , C(O)(SR 13 ), SR 5 , SSR 5 , or does not exist.
  • X and/or Y contain a sulfur-containing functional group.
  • the compound of the invention comprises a heterocyclic functionality, more preferably, a nucleoside or nucleobase.
  • the compound of the invention comprises a carbocyclic functionality, more preferably, a steroidal or carbohydrate moiety.
  • a therapeutic compound of the invention is represented by the formula (Formula III):
  • R 6 - R 16 are the same or different alkyl or acyl groups contaiunig 1-24 carbon atoms which may contain 1-4 ON0 2 substituents, or Cl - C6 connections to R 1 -R 4 in cyclic derivatives.
  • a therapeutic compound of the invention is represented by the formula (Formula IV):
  • R 3 , R 1 ⁇ H; n, R 2 R4- 18 , X, and Y have the meaning as defined above.
  • X is CH 2 or does not exist
  • Y is selected from, F, Br, Cl, CH 3 , CF 2 H, CF 3 , OH, NH 2 , NHR6, NR6R 7 , CN, NHOH, N2H 3 , N 2 H 2 R 13 , N 2 HR 13 R 14 , N 3 , S, SCN, SCN 2 H 2 (R 15 ) 2 , SCN 2 H 3 (R 15 ), SC(O)N(R 15 ) 2 , SC(O)NHR 15 , SO 3 M, SH, SR 7 , SO 2 M, S(O)R8, S(O) 2 R 9 , S(O)OR8, S(O) 2 O R 9 , PO 2 HM, PO 3 M 2 , P(O)(OR 15 )(OR 16 ), P(O)
  • a compound of the invention is represented by the formula (Formula V):
  • the invention includes novel compounds useful for treating pain, mitigating inflammation, effecting analgesia and/or providing sedation.
  • the compounds of the invention can be represented by the structures shown hereinbelow, for example, the structures of Formula III, IV and V.
  • Novel compounds of the invention include nitrates IlIr - IIIaj, Vn - Ivt, and Vd-Vag, whose syntheses are described in the following examples.
  • the invention also provides methods for treating a disease state associated with inflammation, comprising administering to a subject an effective amount of a therapeutic compound having a formula set forth above, such that a disease state associated with inflammation is treated.
  • the invention further provides methods for treating a disease state or disorder in which a level of sedation is desired, comprising administering to a subject an effective amount of a sedative therapeutic compound having a formula set forth above, such that a disease state or disorder is treated.
  • the invention provides methods for effecting analgesia comprising administering to a subject an effective amount of a therapeutic compound having a formula set forth above, such that analgesia is effected.
  • the invention father provides novel pharmaceutical compositions for treating pain, mitigating inflammation, effecting analgesia and/or effecting sedation.
  • a said pharmaceutical composition comprises a therapeutic compound of the invention in an effective amount for the particular indication and a pharmaceutically acceptable vehicle.
  • the invention also provides packaged pharmaceutical compositions for treating pain, mitigating inflammation, effecting analgesia and/or effecting sedation.
  • the packaged pharmaceutical compositions include a therapeutic compound of the invention and instructions for using the pharmaceutical composition for treatment of inflammation and/or pain.
  • FIG. 1 is a graph showing the effect of IVd neat (diamonds); with added L-cysteine (2mM, triangles); with added dithiothreitol (2 mM, DTr, squares); on soluble GCase activity in rat aorta homogenate normalized to the maximal GTN response. Bars represent the mean ⁇ standard errors calculated separately for each point.
  • FIG. 2 ( a - b ) is a graph showing the comparison of GTN (squares), IlIm (circles) and IVh (triangles) with added L-cysteine (1 mM) on soluble GCase activity in rat aorta homogenate (a), and rat hippocampus homogenate (b). Data points represent the mean of duplicate determinations carried out in identical GCase preparations.
  • FIG. 11 is a graph showing the plasma levels (uM) of Vb (circles) and its mononitrate metabolite Vc (open squares) after subcutaneous administration of 200 ⁇ mol/kg Vb in conscious unrestrained rats. Data points represent the mean of two experiments.
  • FIG. 13 is a graph showing the effect of Vm and Va in the mouse writhing test.
  • GT Vm produced a dose-dependent analgesic effect (A).
  • Va also produced analgesia in the mouse writhing test (B).
  • FIG. 14 is a graph showing the effect of Vm on paw flinches in rats after injection of formnalin into the footpad.
  • A the initial pain response to formalin injection
  • B a cumulative score (total number of flinches over 60 minutes) was calculated (B).
  • FIG. 15 (A-B) is a graph showing (A) the effects of chlormethiazole (CHLOR) and WVk (200 ⁇ M of each) on the membrane current induced by 10 jiM GABA in a Xenopus oocyte expressing the ⁇ 1 ⁇ 1 ⁇ 2L isoform of human recombinant GABAA receptors, and (B) the effect of IVk on loss of the righting reflex in mice after intraperitoneal injection of 100 mg/kg and 200 mg/kg.
  • Data in part B are mean +standard error for three animals at each dose.
  • Methods of the invention involve administering to a subject an effective amount of a therapeutic compound which provides analgesia, mitigates inflammation and/or provides sedation.
  • the invention provides prophylactic methods for avoiding or pre-empting pain, inflammation and the like in a subject.
  • the subject may be susceptible or predisposed to these conditions, e.g., arthritic.
  • the subject may be undergoing a course of treatment, e.g. cancer chemotherapy, which produces pain, inflammation or the like as a side effect.
  • Methods of the invention may be practiced prior to, concurrently with, or after such a course of treatment.
  • analgesic, anti-inflammatory and/or sedative activity can be effected by modulating an interaction with guanylyl cyclase (GCase; the enzyme responsible for cGMP production in various areas of the body), and/or by modulating levels of cGMP and cAMP messenger molecules.
  • GCase guanylyl cyclase
  • treating pain encompasses preventing, ameliorating, mitigating and/or managing pain and/or conditions that may cause pain, such as inflammation.
  • inhibiting pain or inflammation encompasses preventing, reducing and halting progression of same.
  • organic nitrate and “nitrate ester” are used interchangeably herein, with no distinction drawn between them.
  • a method for treating pain in a subject comprising administering to the subject an effective amount of a compound (nitrate ester) which effects analgesia in the subject.
  • analgesia is effected by stimulating GCase.
  • GCase activation is effected by nitric oxide (NO), the proximal activator of GCase, which is generated endogenously by enzyme action on arginine in response to many biological triggers (J. R. Stone and M. A. Marletta, Biochemistry (1996) 35, 1093).
  • NO nitric oxide
  • One of the major targets for organic nitrates is GCase activation, resulting in the production of cGMP.
  • organic nitrates act as NO-surrogates.
  • organic nitrates may act also as NO-donors, but these two properties should be differentiated and can be modulated by choice of the appropriate organic nitrate.
  • peripheral analgesic effects of morphine were attributed to elevations of cGMP levels in sensory nerve fibres (Ferreira et al., 1991; Granados-Soto et al., 1997) in both the rat paw pressure and formalin tests, since inhibition of GCase activity attenuated the analgesic effects of locally applied morphine.
  • Activation of the NO-cGMP system by NO donors such as SNP has also been reported to potentiate beta-endorphin-induced analgesia in thermal tail-flick test in mice (Xu et al., 1995), an effect that was potentiated by a selective inhibitor (zaprinast) of a cGMP-specific phosphodiesterase.
  • Sensitization of sensory nerve fibres leading to hyperalgesia is assumed to involve increased concentrations of cAMP and calcium ions in sensory neurons, a process that may be attenuated or counteracted by activation of the NO-cGMP pathway (Ferreira, 1993; Cunha et al., 1999).
  • administering effects analgesia in the subject by modulating levels of cAMP and/or cGMP.
  • levels of cAMP and/or cGMP For example, it has been shown that NO-donors modulate hyperalgesia via modulation of levels of cAMP, separately from and in addition to modulation of cGMP levels, in rat models of pain and nociceptor sensitization (Aley et al. 1998).
  • modulation of cAMP/cGMP levels is expected to be effective in inducing analgesia and in pain management in individuals suffering injury, disease or aging.
  • a method for treating or hibitng imflammation in a subject comprising administering to the subject an effective amount of a compound which mitigates inflammation in the subject.
  • inflammation is mitigated by modulation of levels of cGMP/cAMP.
  • Inflammatory hyperalgesia has been shown to be linked directly to the NO-cGMP pathway (Ferreira, 1993).
  • the invention relates to a method for providing sedation and/or anaesthesia in a subject, comprising administering to the subject an effective amount of a compound (organic nitrate) which effects sedation or anaesthesia in the subject.
  • a compound organic nitrate
  • the invention provides methods and compositions useful for reducing anxiety, and/or aiding or inducing sleep.
  • GABA ⁇ -Aminobutyric acid
  • GABA ⁇ -Aminobutyric acid
  • GABA acts on three major classes of neurotransmitter receptor, designated type A (GABA A ), type B (GABA B ) and type C (GABA C ).
  • GABA A receptors play an important role in regulating many behavioural and physiological functions.
  • drugs that modulate GABA A receptor function are among the most widely used in clinical medicine.
  • drugs that selectively potentiate GABAA receptor function are extensively used to relieve anxiety, produce sedation and induce sleep.
  • nitrate esters are useful as sedative agents. Such agents are useful as therapeutics for treating conditions such as, for example, anxiety and pain associated with disease states; and as hypnotic agents. According to the invention, nitrate esters may also be employed prophylactically, to prevent or reduce anxiety, or to aid sleep.
  • Therapeutic compounds of the invention comprise at least one nitrate group.
  • the nitrate groups(s) can optionally be covalendy bound to a carrier (e.g., an aromatic group, an aliphatic group, peptide, steroid, nucleobase, nucleoside, peptidomimetic, steroidomimetic, or nucleoside analogue, or the like).
  • a carrier e.g., an aromatic group, an aliphatic group, peptide, steroid, nucleobase, nucleoside, peptidomimetic, steroidomimetic, or nucleoside analogue, or the like.
  • the carrier molecule can enable the compound to traverse biological membranes and to be biodistributed preferentially, without excessive or premature metabolism.
  • the carrier molecule can enable the compound to exert amplified analgesic, sedative, or anti-inflammatory effects through synergism with the nitrate functionality.
  • the invention provides a method comprising administering to a subject an effective amount of a therapeutic compound which has at least one nitrate group and is capable of effecting analgesia.
  • the therapeutic compound is capable of mitigating inflammation.
  • the therapeutic compound is capable of effecting sedation.
  • the therapeutic compound has the formula (Formula I):
  • E, F 1 , F 2 , G 1 , G 2 are the same or different organic radicals which may be joined in cyclic ring systems, and which may contain inorganic counterions.
  • therapeutic compounds of the invention effect analgesia, effect sedation and/or mitigate inflammation in a subject to which the therapeutic compound is administered, and have the formula (Formula II).
  • A is selected from: a substituted or unsubstituted aliphatic group (preferably a branched, or straight-chain aliphatic moiety having from 1 to 24 carbon atoms in the chain, which optionally may contain O, S, NR 6 and unsaturations in the chain, optionally bearing from 1 to 4 hydroxy, or nitrate, or amino or aryl, or heterocyclic groups; an unsubstituted or substituted cyclic aliphatic moiety having from 3 to 7 carbon atoms in the aliphatic ring, which optionally may contain O, S, NR 6 and unsaturations in the ring, optionally bearing from 1 to 4 hydroxy, or nitrate, or ammno or aryl, or heterocyclic groups; an unsubstituted or substituted aliphatic group (preferably a branched, or straight-chain aliphatic moiety having from 1 to 24 carbon atoms in the chain, which optionally may contain O, S, NR 6 and unsaturations in
  • R 19 is X-Y.
  • R 19 is X-Y and R 5 , R 6 , R 8 , R 9 , R 10 , R 12 , R 13 , R 14 , R 15 , 19 R 16 are the same or different alkyl groups containing 1-24 carbon atoms which may contain 1-4 ON02 substituents, or Cl or C2 connections to R 1 -R 3 in cyclic derivatives;
  • R 1 and R 3 are the same or different and selected from H, Cl-C 4 , alkyl chains, which may inlude one 0, linking R 1 and R 3 to form pentosyl, hexosyl, cyclopentyl, or cycohexyl rings, which rings may optionally bear hydroxyl substituents;
  • R 2 and R 4 are the same or different and selected from H, a nitrate group, Cl-C 4 alkyl optionally bearing 1-3 nitrate group, and acyl
  • Rig is X-Y
  • m is selected from CH 2 , O, NH, NMe, CN, NHOH, N 2 H 3 , N 2 H 2 R 13 , N 2 HR 13 R 14 , N 3 , S, SCN, SCN 2 H 2 (R 5 ) 2 , SCN 2 H 3 (R 15 ), SC(O)N(RI 5 ) 2 , SC(O)NHR 15 , SO 3 M, SH, SR 7 , SO?M, S(O)R 8 , S(O) 2 R 9 , S(O)OR 8 , S(O) 2 O R 9 , PO 3 HM, PO 3 M 2 , P(O)(OR 15 )(OR 16 ), P(O)(OR 16 )(OM), P(O)(R 15 )(ORB), P(O)(OM)R 15 , CO 2
  • Y is selected from CN, N 2 H 2 R 13 , N 2 HR1 3 R 14 , N 3 , SCN, SCN2H2(R 15 )2, SC(O)N(R 15 )2, SC(O)NHR 15 , SO 3 M, SR 4 , SO?M, PO 3 HM, PO 3 M 2 , P(O)(OR 15 )(OR 16 ), P(O)(OR 16 )(OM), P(O)(R 15 )(OR8), P(O)(OM)R 15 , CO 2 M, CO 2 H, CO 2 R 1 l, C(O)R 12 , C(O)(SR 13 ), SR 5 , SSR 5 , or does not exist.
  • X and/or Y contain a sulfur-containing functional group.
  • the compound of the invention comprises a heterocyclic functionality, more preferably, a nucleoside or nucleobase.
  • the compound of the invention comprises a carbocyclic functionality, more preferably, a steroidal or carbohydrate moiety.
  • a therapeutic compound of the invention is represented by the formula (Formula III):
  • R 6 - R 16 are the same or different alkyl or acyl groups containing 1-24 carbon atoms which may contain 1-4 ON0 2 substituents, or C 1 -C 6 connections to R 1 -R 4 in cyclic derivatives.
  • therapeutic compounds of the invention have a formula selected from (Formulae IIIa-IIIam):
  • a therapeutic compound of the invention is represented by the formula (Formula IV):
  • R 2 , R 4 , R 5 , R6, R 7 , Rg, Rg, Rio, Ril, R 12 , R 13 , R 14 , R 15 , and R 16 are as defined above.
  • R 2 and R 4 are optionally H, a nitrate group or a connection to R 5 -R 16 in cyclic derivatives.
  • a compounds of the invention is represented by the formula (Formulae IVa-IVt):
  • R 2 is optionally H or a connection to R 5 in cyclic derivatives
  • R 4 is H or a nitrate group
  • R 5 is as described above.
  • compounds of the invention are represented by the formula (Formulae Va-Vag):
  • the invention provides novel compounds which can be represented by structures of Formula III, Formula IV, and Formula V.
  • Table 1 lists data associated with these compounds using art-recognized characterization techniques.
  • the invention provides novel pharmaceutical compositions comprising a therapeutic compound (nitrate ester) of the invention and a pharmaceutically acceptable vehicle.
  • Vj (CDCl 3 ): ⁇ 7.55-7.62(d, arom 2H, J 7.16), (CDCl 3 ): ⁇ 36.97, 69.88, 77.61, 7.29-7.44(m, arom 3H), 5.46-5.58(m, 1H), 4.82-4.92(dd, 128.60, 129.50, 129.85, 136.02 1H, J 12.85, 2.79), 4.57-4.67(dd, 1H, J 12.86, 5.67), 3.01-3.13(dd, 1H, J 14.51, 6.24), 2.92-3.02(dd, 1H, J 14.52, 7.4)
  • Vk (CDCl3, 300MHz): 8.09(1H, dd, J 8.12, 0.36), (CDCl3, 75.48MHz): 166.21, 8.02(1H, dd, J 7.8, 1.15), 7.51-7.59(1H, m, J 7.24, 1.44), 140.41,
  • the structure of some of the compounds of this invention include asymmetric carbon atoms. It is to be understood accordingly that the isomers (e.g., enantiomers, diastereomers) arising from such asymmetry are included within the scope of this invention. Such isomers can be obtained in substantially pure form by classical separation techniques and by asymmetric synthesis (for example, see below in Example 21). Unless expressly noted to the contrary, compounds referred to herein shall be construed to include both the R and S stereolsomers at each stereogenic centre.
  • a therapeutic compound of the invention comprises a cation (i.e., in certain embodiments, one of X or Y includes a cation, e.g., in the compound of formula IVd). If the cationic group is a proton, then the compound is considered an acid. If the proton is replaced by a metal ion or its equivalent, the compound is a salt. Pharmaceutically acceptable salts of the therapeutic compound are within the scope of the invention.
  • M can be a pharmaceutically acceptable alkali metal (e.g., Li, Na, K), ammonium, alkaline earth metal (e.g., Ca, Ba, Mg), higher valency cation, or polycationic counter ion (e.g., polyammonium cation) (see e.g., Berge et al. (1977)).
  • alkali metal e.g., Li, Na, K
  • ammonium e.g., alkaline earth metal
  • alkaline earth metal e.g., Ca, Ba, Mg
  • polycationic counter ion e.g., polyammonium cation
  • Preferred pharmaceutically acceptable salts include a sodium, potassium, or calcium salt, but other salts are also contemplated within their pharmaceutically acceptable range.
  • Therapeutic compounds of the invention can be administered in a pharmaceutically acceptable vehicle.
  • pharmaceutically acceptable vehicle includes any and all solvents, excipients, dispersion media, coatings, antibacterial and antifuangal agents, isotonic and absorption delaying agents, and the like which are compatible with the activity of the compound and are physiologically acceptable to the subject.
  • An example of a pharmaceutically acceptable vehicle is buffered normal saline (0.15 M NaCi).
  • the use of such media and agents for pharmaceutically active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the therapeutic compound, use thereof in the compositions suitable for pharmaceutical administration is contemplated. Supplementary active compounds can also be incorporated into the compositions.
  • Carrier or substituent moieties useful in the present invention may also include moieties which allow a therapeutic compound to be selectively delivered to a target organ.
  • delivery of a therapeutic compound to the brain may be enhanced by a carrier moiety using either active or passive transport (a “targeting moiety”).
  • the carrier molecule may be a redox moiety, as described in, for example, U.S. Pat. Nos. 4,540,654 and 5,389,623, both to Bodor.
  • These patents disclose drugs linked to dihydropyridine moieties which can enter the brain, where they are oxidized to a charged pyridinium species which is trapped in the brain. Thus drugs accumulate in 45 the brain.
  • carrier moieties include compounds, such as amino acids or thyroxine, which can be passively or actively transported in vivo. Such a carrier moiety can be metabolically removed in vivo, or can remain intact as part of an active compound. Structural mimics of amino acids (and other actively transported moieties) including peptidomimetics, are also useful in the invention.
  • peptidomimetic is intended to include peptide analogs which serve as appropriate substitutes for peptides in interactions with e.g., receptors and enzymes. The peptidomimetic must possess not only affinity, but also efficacy and substrate function.
  • a peptidomimetic exhibits functions of a peptide, without restriction of structure to amino acid constituents.
  • Peptidomimetics, methods for their preparation and use are described in Morgan et al., (1989) “Approaches to the discovery of non-peptide ligands for peptide receptors and peptidases”. In Annual sorts in Medicinal Chemistg (Vinick, FJ., ed.) pp. 243-252, Academic Press, San Diego, Calif.
  • Many targeting moieties are known, and include, for example, asialoglycoproteins (see e.g., Wu, U.S. Pat. No. 5,166,320) and other ligands which are transported into cells via receptor-mediated endocytosis (see below for further examples of targeting moieties which may be covalendy or non-covalently bound to a target molecule).
  • pain and/or inflammation in a subject is mitigated by administering an analgesic, sedative or anti-inflammatory therapeutic compound of the invention to the subject.
  • subject is intended to include living organisms in which pain can occur. Examples of subjects include humans, apes, monkeys, cows, sheep, goats, dogs, cats, mice, rats, and transgenic species thereof.
  • Administration of the compositions of the present invention to a subject to be treated can be carried out using known procedures, at dosages and for periods of time effective to alleviate pain in the subject.
  • an effective amount of the therapeutic compound necessary to achieve a therapeutic effect may vary according to factors such as the subject, the age, sex, and weight of the subject, and the ability of the therapeutic compound to mitigate pain and inflammation in the subject. Dosage regimens can be adjusted to provide the optimum therapeutic response. For example, several divided doses may be administered daily or the dose may be proportionally reduced as indicated by the exigencies of the therapeutic situation.
  • a non-limiting example of an effective dose range for a therapeutic compound of the invention e.g., Va
  • preferred concentrations for the active compound i.e., the therapeutic compound that can mitigate pain
  • therapeutic compounds are administered to a subject by a route which is effective for mitigating inflammation, effecting analgesia and/or effecting sedation.
  • routes of administration include but are not limited to sublingual, oral, buccal, transdermal, nasal, subcutaneous, intraocular, intravenous, intramuscular and intraperitoneal (e.g., by injection).
  • Preferred routes of administration are oral and transdermal.
  • the therapeutic compounds can be administered with a pharmaceutically acceptable vehicle.
  • the active compound may be coated in a material to protect the compound from the action of acids, enzymes and other natural conditions which may inactivate the compound.
  • Therapeutic compounds of the invention can be formulated to ensure proper distribution in tivo.
  • the blood-brain barrier excludes many highly hydrophilic compounds.
  • they can be formulated, for example, in liposomes.
  • liposomes For methods of manufacturing liposomes, see, e.g., U.S. Patents 4,522,811; 5,374,548; and 5,399,331.
  • the liposomes may comprise one or more moieties which are selectively transported into specific cells or organs (“targeting moieties”), thus providing targeted drug delivery (see, e.g., Ranade et al., 1989).
  • targeting moieties include folate or biotin (see, e.g., U.S. Patent 5,416,016 to Low et al.); mannosides (Umezawa et al., 1988); antibodies (Bloeman et al., 1995; Owais et al., 1995); surfactant protein A receptor (Briscoe et al., 1995).
  • therapeutic compounds of the invention are formulated in liposomes; in a more preferred embodiment, the liposomes include a targeting moiety.
  • anionic groups such as phosphonate or carboxylate can be esterified to provide compounds with desirable pharmocokinetic, pharmacodynamic, biodistributive, or other properties.
  • Exemplary compounds include Mi and pharmaceutically acceptable salts or esters thereof
  • a therapeutic compound may be administered to a subject in an appropriate carrier, for example, liposomes, or a diluent.
  • Pharmaceutically acceptable diluents include saline and aqueous buffer solutions.
  • Liposomes include water-in-oil-in-water CGF emulsions as well as conventional liposomes (Strejan et al, J. Neuroimmunol. (1984) 7, 27). 47
  • a therapeutic compound may also be administered parenterally (e.g., intramuscularly, intravenously, intraperitoneally, intraspinally, or intracerebrally).
  • Dispersions can be prepared in glycerol, liquid polyethylene glycols, lactose, dextrose and mixtures thereof and in oils. Under ordinary conditions of storage and use, these preparations may contain a preservative to prevent the growth of microorganisms.
  • Pharmaceutical compositions suitable for injectable use include sterile aqueous solutions (where water soluble) or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersion. In all cases, the composition must be sterile and must be fluid to the extent that easy syringability exists.
  • the vehicle can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (for example, glycerol, propylene glycol, dextrose, and liquid polyethylene glycol, and the like), suitable mixtures thereof, and vegetable oils.
  • the proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants.
  • Prevention of the action of microorganisms can be achieved by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, ascorbic acid, thimerosal, and the like.
  • isotonic agents for example, sugars, sodium chloride, or polyalcohols such as mannitol and sorbitol, in the composition.
  • Prolonged absorption of the injectable compositions can be brought about by including in the composition an agent which delays absorption, for example, aluminum monostearate or gelatin.
  • Sterile injectable solutions can be prepared by incorporating a therapeutic compound in the required amount in an appropriate solvent with one or a combination of ingredients enumerated above, as required, followed by filter sterilization.
  • dispersions are prepared by incorporating the therapeutic compound into a sterile vehicle which contains a basic dispersion medium and the required other ingredients from those enumerated above.
  • the preferred methods of preparation are vacuum drying and freeze-drying which yields a powder of the active ingredient (i.e., the therapeutic compound) plus any additional desired ingredient from a previously sterile-filtered solution thereof.
  • a therapeutic compound can be orally administered, for example, with an inert diluent or an assimilable edible carrier.
  • a therapeutic compound and other ingredients may also be enclosed in a hard or soft shell gelatin capsule, compressed into tablets, or incorporated directly into the subject's diet.
  • a therapeutic compound may be incorporated with 48 excipients and used in the form of ingestible tablets, buccal tablets, troches, capsules, elixirs, suspensions, syrups, wafers, and the like.
  • the percentage of therapeutic compound in the compositions and preparations may, of course, be varied. The amount of therapeutic compound in such therapeutically useful compositions is such that a suitable dosage will be obtained.
  • Dosage unit form refers to physically discrete units suited as unitary dosages for the subjects to be treated; each unit containing a predetermined quantity of therapeutic compound calculated to produce the desired therapeutic effect in association with the required pharmaceutical vehicle.
  • the specification for the dosage unit forms of the invention are dictated by and directly dependent on (a) the unique characteristics of the therapeutic compound and the particular therapeutic effect to be achieved, and (b) the limitations inherent in the art of compounding such a therapeutic compound for the treatment of pain and inflammation in subjects, or effecting sedation.
  • a therapeutic composition can be administered in time-release or depot form, to obtain sustained release of a therapeutic compound over time.
  • a therapeutic compound of the invention can also be administered transdermally (e.g., by providing a therapeutic compound, with a suitable carrier, in patch form, or in an unguent or cream).
  • Active compounds are administered at a therapeutically effective dosage sufficient to mitigate pain and/or inflammation in a subject.
  • the ability of a compound to mitigate pain or inflammation can be evaluated in model systems that may be predictive of analgesia and anti-inflammation in human diseases, such as animal model systems known in the art (including, e.g., the preclinical acute pain writhing model in the mouse; and the formalin-sensitization model of tissue injury pain in the rat) or by in mitro methods, (including, e.g., the assays described above and below, tide infra).
  • model systems that may be predictive of sedation of use in treatment of human diseases, such as animal model systems known in the art (including, e.g., the loss of the righting reflex in the mouse as described, tide infra) or by in vitro methods, (including, e.g., modulation of the activity of GABAA receptors as described above and below, tide infra).
  • the ability of a compound of the invention to mitigate pain and/or inflammation in certain embodiments, be evaluated by observation of one or more symptoms or signs associated with pain and inflammation in vivo.
  • the ability of a compound to alleviate pain may be associated with an observable improvement in a clinical manifestation of the 49 underlying pain or inflammation related disease state or condition, or a slowing or delay in progression of symptoms of the condition.
  • monitoring of clinical manifestations of disease can be usefuil in evaluating the analgesic, sedative and anti-inflammatory efficacy of a compound of the invention.
  • Treating or mitigating pain may involve effecting analgesia, effecting sedation, inhibiting or preventing inflammation, and/or ameliorating the manifestations or impact of pain inducing stimuli.
  • Modulating a biological process such as the biological levels of cGMP or cAMP, or activity of soluble GCase, includes regulating increases and decreases in such activity, and inhibition, potentiation, agomism, or antagonism of the biological process.
  • pain and inflammation can be associated with, but not limited to, tissue injury, post-operative tissue injury, nerve injury, post-herpetic neuralgia, phantom limb pain, diabetic neuropathy, arthritis, dysmenorthea, endometriosis, cancer, chemotherapy, myocardial infarction, cerebral vascular occlusion, or result from surgical procedures.
  • nitrate esters can be prepared from the corresponding alcohol, oxirane or alkene by standard methods that include: nitration of alcohols and oxiranes, mixed aqueous/organic solvents using mixtures of nitric and sulfuric acid and/or their salts, with temperature control (see Yang et al., 1996); nitration of alcohols and oxiranes in acetic anhydride using nitric acid or its salts with or without added acid catalyst, with temperature control (see, e.g., Louw, et al., 1976); nitration of an alcohol with a nitronium salt, e.g., a tetrafluoroborate; nitration of an alkene with thallium nitrate in an appropriate solvent (Ouellette et al., 1976).
  • Compounds of the present invention also can be prepared as described below.
  • GCase soluble guanylyl cyclase
  • the GCase assay data show that WVd activates GCase, with a submiulimolar EC-50 (effective concentration for 50% of the subjects) in the absence of any added thiol, in contrast to GTN, which requires added cysteine.
  • Compounds WVd also activates GCase in the presence of DTT, in contrast to GTN, which, emgmatically, does not. Relative to GTN itself, a wide range of potency was observed for these novel nitrate esters. No activation of GCase by glycerol mononitrates was observed in this assay at the concentrations of nitrate employed.
  • Activation of GCase, in titrv, by some of these organic nitrates is via release of NO, since in the presence of cysteine, substantial NO is released at rates which are measurable amperometrically, using the method described by Artz and Thatcher (1998).
  • nitroglycerin which is currently understood by others skilled in the art to act only as an NO-donor therapeutic agent, does not release NO at a rate measurable amperometrically, in the absence nor the presence of cysteine.
  • Relative rates for NO release, at 37° C, pH 7.4, in the presence of cysteine (2mM) from nitrates Vj, Vu, Vi, Vh, Vg, Vf, and Ve, (lmM) were 1.0, 1.0, 1.8, 0, 1.2, 0.5, 1.8, respectively.
  • cysteine (2mM) from nitrates Vj, Vu, Vi, Vh, Vg, Vf, and Ve, (lmM) were 1.0, 1.0, 1.8, 0, 1.2, 0.5, 1.8, respectively.
  • Va was found to have greater efficacy, but equal potency, to GTN in rat aorta ( FIG. 3a ). In contrast, Va had greater efficacy and greater potency to stimulate GCase in rat hippocampus ( FIG. 3b ).
  • nitrates have differential effects on GCase activation that are dependent on both structure of the compound and the tissue assayed for GCase activity, supporting the notion that effects of nitrates elicited through GCase activation, such as analgesia and vasodilation, are separable and may be regulated in a tissue-specific and/or activity-specific manner, by appropriate choice of organic nitrate.
  • FIGS. 4 , 5 the effects of nitrates Va, IlIm, Vb, Vc, and WVk on cyclic GMP accumulation in intact isolated rat aorta were examined ( FIGS. 4 , 5).
  • Thoracic aortic strips were prepared from male Sprague-Dawley rats (Charles-River, Canada) as described in McGuire et al. (1994) and Stewart et al. (1989). Tissues were contracted submaximally with phenylephrine (0.1CtM) and exposed to various concentrations of drug for 1 min. Cyclic GMP accumulation was determined using the radioitnmunoassay method described by Bennett et al. (1992).
  • FIGS. 5 At concentrations of 1 liM and 10 AM, GTN and WVk significantly increased cGMP accumulation ( FIGS. 5 ). At a concentration of 1 AM, Va, IIlm, Vb, and Vc did not significantly increase cyclic GMP accumulation ( FIGS. 4a , 5a). At a concentration of 10 [tM, Va, Vb, and WVk significantly increased cyclic GMP accumulation whereas IIIm and Vc did not ( FIGS. 4b , 5b).
  • FIG. 6 shows that Va causes a concentration-dependent increase in the tissue levels of cGMP in rat hippocampal brain slices in vitro, and that at high concentration (100 lM) Va is more effective than GTN in elevating cGMP levels in hippocampal brain slices in vitm.
  • the EC-50 values for relaxation were 0.61 nM, 3.19 nM, 8.40 nM, 0.153 ⁇ M, 0.437 ⁇ M and 6.89 lM for GTN, WVk, Vb, IIIm, Vc, and IVh, respectively ( FIG. 7,8 ).
  • Compounds WVd and WVc were tested for their ability to cause vascular relaxation in tissues that had been made tolerant to the relaxant effect of GTN.
  • GTN tolerance was induced by incubating tissues with high concentrations of GTN (0.5 mM GTN for 30 min). Under these conditions, the maximal relaxant effects of WVd ( FIG. 12 a ) and WVc ( FIG. 12 b ) were not significantly different to that of untreated tissue.
  • the EC-50 for relaxation was imcreased approximately threefold, but the difference was not statistically significant.
  • Va and GTN were injected into rats in which the abdominal aorta was cannulated for blood pressure recording.
  • Va and GTN were injected subcutaneously at a dose of 400 lmol/kg body weight into conscious, freely moving animals. GTN caused a small and transient decrease in blood pressure in these animals, whereas Va had no discernable effect on arterial blood pressure ( FIG. 9 ).
  • Va and GTN were subsequently tested in anesthetized rats in which the abdominal vena cava was also cannulated to allow for bolus intravenous injection of drugs. In this preparation, GTN caused a substantial and dose-dependent decrease in arterial blood pressure.
  • Va at equal doses had very modest effects on blood pressure at doses lower than 2 lmol/kg body weight ( FIG. 10 ).
  • Vb and Vc the denitrated metabolite of Vb
  • Cannulas were placed in the abdominal aorta for blood sampling. After a two-day recovery period, a single subcutaneous dose of Vb (200 lmol/kg) was administered and blood samples collected over a period of six hours. Samples were centrifuged, the plasma collected, and the concentration of Vb and Vc determined by gas-liquid chromatography by the method of McDonald and Bennett (1990). The data obtained for Vb and Vc indicate that nitrates achieve maximal plasma levels within 30 minutes after subcutaneous injection, and therafter decline at a steady rate ( FIG. 11 ). These data suggest that nitrates have excellent bioavailability after subcutaneous injection.
  • Vm induced a significant, dose-dependent analgesic effect, manifested as a decrease in the number of writhes per 10 minute period after intraperitoneal injection of dilute acetic acid ( FIG. 13 a ).
  • Va was also able to act as an analgesic (decreased writhing) in this experimental model when administered at a dose of 500 mg/kg subcutaneously ( FIG. 13b ).
  • the delayed pain response is considered to be a hyperalgesia/allodynia caused by a combination of sensitization of peripheral sensory afferents and sensitization of synaptic connections in the spinal cord.
  • the formalin test in the rat is considered to be an appropriate model for tissue injury pain occurring in humans (Tjolsen et al., Pain (1992) 51, 5-17; Yaksh, 77PS (1999) 20, 329-337).
  • Vm 500 mg/kg significantly reduced both phases of the pain response to formalin injection ( FIG. 14a ,b).
  • Nitrate IIIi was obtained by two routes. Route I proceeded from the elimination reaction of IIIm in basic solution. Route II proceeded from nitration of trans-3-bromo-4-hydroxytetrahydrothiophene-1,1-dioxide, yielding nitrate Illn, followed by reaction with a weak base, e.g., sodium thiocyanate in 2-butanone. Purification may be achieved with silica flash column chromatography using 1:1 hexane:ethyl acetate as eluant.
  • Nitrate HIIj 1,4-Dibromo-2,3-butanediol may be nitrated: (a) using a nitration mixture prepared from HNO 3 and H 2 SO 4 over 2 days; or (b) using acetyl nitrate reacting for 2 hours. Work-up requires quenching of the reaction mixture in ice-water for an hour, extraction, drying, and evaporation. Successful purification of the title compound by silica gel column chromatography is achieved on a 25 g scale using a mixture of 70% hexane and 30% CH 2 CI 2 as eluent.
  • the solution of diazonium salt was added over 1.5 h to a solution of ethyl xanthate (24 g, 0.149 mole) in water (30 niL) at 45-500C. The mixture was kept at this temperature, under strring, for a further 1 h.
  • the xanthate ester was separated as a maroon oil, washed with 50 mL 10% NaOH and with water to neutral pH and dried over MgSO 4 ( 20 g of crude product).
  • the crude xanthate was dissolved in 60 mL absolute ethanol and to this solution 20 g KOH (pellets) were added in portions.
  • the reaction mixture was refluxed under stiring and Ar for 8 h, then concentrated under vacuum.
  • the concentrate was taken up in 50 niL H 2 0 and extracted with 3x100 mL diethyl ether.
  • the aqueous layer was acidified with a 6N H2SO4 solution and extracted with 3x100 mL CH 2 Cl 2 .
  • Nitrate IIIm 3,4-Epoxytetrahydrothiophene-1,1-dioxide 250 mg,1.9 nmnol was refluxed for 24 h in 10 miL of water and 25mg of toluenesulfonic acid. After the first 6 h, another 25 mg of the acid was added. The reaction was monitored by thin layer chromatography (LLC) (5% methanol in dichloromethane). Purification was by Si flash column chromatography using 5% methanol/CH2Ck2 as eluent to afford 200 mg of diol. The diol was nitrated in a cooled solution of conc.
  • IVd ( 0.43 g, 1.37 mmol) was dissolved in 10 mL of distilled water and the emulsion of 0.23 g (1.28 mmol) of the ethyl ester of thiosalycilic acid in 1.3 niL of 1 M NaOH was added. The resulting solution immediately became turbid and was stirred for 3 min, then extracted with ethyl acetate (4x15 iL). The resulting extracts were washed with H 2 O, dried (MgSO4), and concentrated by evaporation.
  • a catalyst AD-mix-B, Aldrich: K.B.Sharpless, W.Amberg, Y.L.Bennani, G.A.Crispino, J.Hartung, K.-S.Jeong, H.-L.Kwong, K.Morikawa, Z.-M
  • the tide compound was synthesised by the reaction of IVd (0.345 g, 1.15 mmoles) with captopril methyl ester (0.2 g, 0.865 mmoles) in the presence of 1 mL of 1M NaOH.
  • the crude product was purified by column chromatography (Silicagel, ethyl acetate) to afford 0.1 g (18.03%) of unsymmetrical disulphide.
  • the tide compound was synthesised by the reaction of Bunte salt (2.4 g, 8 mtnoles) with 4,4′-thiobisbenzenetliol (0.5 g, 2 mmoles) in the presence of 4.4 mL of 1M NaOH.
  • the crude product was purified by column chromatography (silica gel, hexanes/CH 2 CI2: 3/7) to afford 0.28 g (21.82%) disulphide.
  • the title compound was synthesised by the reaction of IVd (0.5 g, 1.58 mmoles) with ethyl 2-mercapto-3-(3′,4′-methylenedioxy-phenyl) propenoate (0.2 g, 0.8 rmmoles).
  • the crude product was purified by column chromatography (Silicagel, hexanes/CH 2 Cl 2 : 3/7) to give Vr (0.1 g, 28.09%).
  • Diethyl 1-chloro-2-tnmethylsiloxypropylphosphonate was obtained by adaptation of literature methods (T.Azuhata, Y.Okamoto, Synthesis (1983) 916-917). This phosphonate was quantitatively converted to diethyl 1-chloro-2-hydroxypropylphosphonate using CH 3 0H. After stirring for 15 min the resulting reaction mixture was evaporated to a minimum and subjected to nitration with a mixture of HNO 3 and H 2 SO4 Work-up and flash column chromatography on silica (ethyl acetate eluant) yielded pure product in 25% yield. 31P (CDCl 3 , 162 MHz): 24.60.
  • the effect of a drug that induces brief periods of sedation/hypnosis in animals is characterized by loss of the righting reflex (loss of the ability of the animal to right its posture when placed on its back).
  • the “loss of the righting reflex” response is a commonly used test for sedative-hypnotic agents.
  • Wk produced a dose-dependent and reversible loss of the righting reflex in mice when given by intraperitoneal injection at doses of 100 and 200 mg/kg ( FIG. 15b ).
  • the organic nitrate WVk exhibits the activity of a sedative/hypnotic, and represents a novel class of compounds that may have utility as new anti-anxiety, sedative and/or hypnotic agents.

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Abstract

Methods and therapeutic compounds for treating pain, mitigating inflammation, effecting analgesia and/or effecting sedation in a subject are described. A subject is administered an effective amount of a therapeutic compound which is a nitrate ester. Novel pharmaceutical compositions are also described.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • The application is a continuation of U.S. Ser. No. 09/473,713, filed Dec. 29, 1999, which is incorporated herein by reference.
    • FIELD OF THE INVENTION
  • This invention relates to nitrate esters and use thereof in mitigating pain and effecting analgesia. More particularly this invention relates to organic nitrates which have therapeutic utility as analgesics, anti-inflammatory agents and sedatives.
    • BACKGROUND OF THE INVENTION
  • The nitrate ester, glyceryl trinitrate (GTN), or nitroglycerin, has been used as a vasodilator in the treatment of angina pectoris for over a hundred years, and the dominant, contemporary belief is that GTN exerts its therapeutic effect through in tivo release of nitric oxide (NO). Other organic nitrates (nitrate esters), such as isosorbide dinitrate, have also been identified as effective and clinically important vasodilators. NO itself has been identified as Endothelium Derived Relaxing Factor (EDRF) and several classes of compounds, for example nitrosothiols, in addition to organic nitrates, have been proposed as NO donors or NO prodrugs.
  • Several organic nitrates, in which an alkyl mononitrate is appended to a moiety with analgesic properties, such as aspirin (ASA) or a Non-Steroidal Anti-Inflammatory Drug (NSAID) have been reported as analgesics which possess reduced gastro-intestinal irritation and ulceration properties, purportedly through release of NO. The combination of the vasodilator nitroglycerin with opioid analgesics such as morphine, has been suggested to be effective in the management of both surgical and cancer pain. However, no attempt has been made to develop organic nitrates themselves as analgesic agents, that is, organic nitrates that do not rely on an ASA or NSAID moiety, nor an opiate, for analgesic properties. Thus, there is a need for synthetic organic nitrates as new and useful therapeutic agents for treatment and mitigation of pain associated with disease states and chemotherapy of those disease states.
    • OBJECT OF THE INVENTION
  • It is an object of the present invention to provide methods and compositions for use in treating pain and/or conditions associated with pain. Another object of the present invention is to provide methods and compositions for providing analgesia and/or sedation.
    • BRIEF DESCRIPTION OF THE INVENTION
  • The present invention is based, at least in part, on the recognition that, although the potent vasodilatatory effects of organic nitrates may be either (a) deleterious to or, alternatively, (b) synergis tic with their analgesic effects, regulation of these two effects is required for the development of therapeutic agents useful in treatment and mitigation of pain. Pain may be treated or mitigated by, for example, an analgesic, anti-inflammatory and/or sedative agent.
  • Possible deleterious effects of organic nitrates may arise, for example, through an NO-donor potentiating hyperalgesia via a cyclic guanosine-3,5-monophosphate (cGMP)-independent mechanism. Alternatively, synergistic effects of organic nitrates may arise, for example, through the ability of an NO-donor to induce analgesia by activation of soluble guanylyl cyclase (GCase) and elevation of cGMP levels. The present invention relates to methods for treating or mitigating pain through use of an organic nitrate, wherein regulation of these two effects is achieved. According to the invention, selection of an appropriate organic nitrate provides modulation and balance between the ability of the organic nitrate to release NO and its potency for GCase activation. Inasmuch as gastrointestinal toxicity is known to be a deleterious side effect of some analgesic drugs and that NO donor molecules are gastro-protective, it is set forth herein that therapeutic analgesia can be achieved through utilization of an appropriate organic nitrate. This statement is based, at least in part, on bioassay data on such compounds.
  • This invention provides methods and compositions which are useful in treating pain, inhibiting inflammation, and/or providing analgesia. Methods of the invention involve administering to a subject a therapeutic compound (nitrate ester) which provides analgesia. The methods and compositions of the invention are useful for the treatment and mitigation of pain associated with disorders and disease states and chemotherapy of those disease states. The methods and compositions of the invention can be used therapeutically to treat acute, chronic and/or inflammatory pain in conditions such as, but not limited to, nerve injury, post-herpetic neuralgia, arthritis, diabetic neuropathy, dysmenorrhea, endometriosis, phantom limb pain, pain associated with cancer and post-operative pain, or can be used prophylactically in a subject susceptible or predisposed to these conditions. In certain preferred embodiments, a therapeutic compound used in the method of the invention interacts with guanylyl cyclase, effecting analgesia. In other preferred embodiments, a therapeutic compound used in the method of the invention modulates levels of the cyclic nucleotides cyclic guanosine-3′,5′- monophosphate (cGMP) and cyclic adenosine-3′,5′-monophosphate (cAMP).
  • In one aspect, the invention provides a method for treating pain, treating or inhibiting inflammation, providing analgesia, providing sedation, mitigating anxiety and/or providing anaesthesia in a subject, comprising administering to a subject in need thereof an effective amount of a therapeutic compound, wherein the therapeutic compound is of the formula (Ia):
    Figure US20070066575A1-20070322-C00001
    in which E, F1, F2, G1, and G2 are the same or different organic radicals which may be joined in cyclic ring systems, and which may contain inorganic counterions;
  • with the proviso that when E and G1 are methylene groups and F1 is H, G2 is not a nitrate group, nor RN-ZN-;
  • wherein RN is any aryl or heteroaryl group and ZN is (CO)mm-XN nn-YN oo;
  • wherein mm, nn, oo are 0 or 1 and XN,YN are NH, NRNN, O or CH2;
  • wherein RNN is a short chain alkyl group (C1-C12).
  • In a preferred embodiment, F2 is a nitrate group and E, F1, G1, G2 are the same or different organic radicals which may be joined in cyclic ring systems, and which may contain inorganic counterions;
  • with the proviso that when E and G1 are methylene groups and F1 is H, G2 is not a nitrate group, nor RN-ZN-;
  • wherein RN is any aryl or heteroaryl group and ZN is (CO)mm-XN nn-YN oo;
  • wherein mm, nn, oo are 0 or 1 and XN,YN are NH, NRNN, O or CH2;
  • wherein RNN is a short chain alkyl group (C1- C12)
  • In another aspect, the invention provides a method for treating pain, treating or inhibiting inflammation, providing analgesia, providing sedation, mitigating anxiety and/or providing anaesthesia in a subject, comprising administering to a subject in need thereof an effective amount of a therapeutic compound, wherein the therapeutic compound is of the formula (Ib):
    Figure US20070066575A1-20070322-C00002
    in which F2 is an organic radical which may be joined in a cyclic ring system with G2, and which may contain inorganic counterions; E and G1 are both methylene groups; F1 is H; and G2 is RN-ZN-;
  • wherein RN is an organic radical possessing a heteroaryl group containing P or S atoms where said P or S are positioned β, γ, or δ to a nitrate group as identified in formula I; and ZN is WN mm-XN nn-YN oo;
  • wherein mm, nn and oo are 0 or 1; and WN, XN, YN are NH, NRNN, CO, O or CH2;
  • wherein RNN is a short chain alkyl group (C1-C12).
  • In a preferred embodiment, F2 is a nitrate group; E and G1 are methylene groups; F1 is H; and G2 is RN-ZN-;
  • wherein RN is an organic radical possessing an heteroaryl group containing P or S atoms where said P or S are positioned β, γ, or δ to a nitrate group as identified in formula I; and ZN is WN mm-XN nn-YN oo;
  • wherein mm, nn, oo are 0 or 1 and WN, XN, YN are NH, NRNN, CO, O or CH2;
  • wherein RNN is a short chain alkyl group (C1-C12).
  • In another aspect, the invention provides a method for treating pain, treating or inhibiting inflammation, providing analgesia, providing sedation, mitigating anxiety and/or providing anaesthesia in a subject, comprising administering to a subject in need thereof an effective amount of a therapeutic compound, wherein the therapeutic compound is of the formula (1c):
    Figure US20070066575A1-20070322-C00003
  • in which E is (R1R2C)m and G2-G1-CF1F2- is R19-(R3R4C)p-(R17R18C)n-;
      • wherein: m, n, p are integers from 0 to 10;
      • R3,17 are each independently hydrogen, a nitrate group, or A; and
      • R1,4 are each independently hydrogen, or A;
  • where A is selected from a substituted or unsubstituted aliphatic group (preferably a branched or straight-chain aliphatic moiety having from 1 to 24 carbon atoms in the chain, which optionally may contain O, S, NR6 and unsaturations in the chain, optionally bearing from 1 to 4 hydroxy, nitrate, amino, aryl, or heterocyclic groups; an unsubstituted or substituted cyclic aliphatic moiety having from 3 to 7 carbon atoms in the aliphatic ring, which optionally may contain O, S, NR6 and unsaturations in the ring, optionally bearing from 1 to 4 hydroxy, nitrate, amino, aryl, or heterocyclic groups; an unsubstituted or substituted aliphatic moiety constituting a linkage of from 0 to 5 carbons, between R1 and R3 and/or between R17 and R4, which optionally may contain O, S, NR6 and unsaturations in the linkage, and optionally bearing from 1 to 4 hydroxy, nitrate, amino, aryl, or heterocyclic groups); a substituted or unsubstituted aliphatic group (preferably a branched, cyclic or straight-chain aliphatic moiety having from 1 to 24 carbon atoms in the chain) containing carbonyl linkages (e.g., C═O, C═S, C═NOH), which optionally may contain O, S, NR6 and unsaturations in the chain, optionally bearing from 1 to 4 hydroxy, nitrate, amino, aryl, or heterocyclic groups; a substituted or unsubstituted aryl group; a heterocyclic group; amino (including alkylamino, dialkylamino (including cyclic amino, diamino and triamino moieties), arylamino, diarylamino, and alkylarylamino); hydroxy; alkoxy; a substituted or unsubstituted aryloxy;
  • wherein X is F, Br, Cl, NO2, CH2, CF2, O, NH, NMe, CN, NHOH, N2H3, N2H2R13, N2HR13R14, N3, S, SCN, SCN2H2(R15)2, SCN2H3(R15), SC(O)N(R15)2, SC(O)NHR15, SO3M, SH, SR7, SO2M, S(O)R8, S(O)-R9, S(O)OR8, S(O)2O R9, PO2HM, PO3HM, PO3M2, P(O)(OR15)(OR16), P(O)(OR16)(OM), P(O)(R15)(OR8), P(O)(OM)R15, CO2M, CO2H, CO2R11, C(O), C(O)RI2, C(O)(OR13), PO2H, PO2M,P(O)(OR14), P(O)(R13), SO, SO2, C(O)(SR13), SR5, SSR7 or SSR5; Y is F, Br, Cl, CH3, CF2H, CF3, OH, NH2, NHR6, NR6R7, CN, NHOH, N,H3, N2H2RI3, N2HR13R14, N3, S, SCN, SCN2H2(RI5)2, SCN2H3(R15), SC(O)N(R15)2, SC(O)NHR15, SO3M, SH, SR7, SOSM, S(O)R8, S(O)2R9, S(O)OR8, S(O)2O R9, PO2HM, PO3M2, P(O)(OR15)(OR16), P(O)(OR16)(OM), P(O)(R15)(OR8), P(O)(OM)R15, CO2M, CO2H, CO2R11, C(O)R12, C(O)(OR13), C(O)(SR13), SR5, SSR7 or SSR5, or does not exist;
  • R2, R5, R18, R19 are optionally hydrogen, A or X-Y;
  • R6, R7, R8, R9, R11, R12, R13, R14, R15, R16 are the same or different alkyl or acyl groups containing 1-24 carbon atoms which may contain 1-4 ON02 substituents; or Cl - C6 connections to R1- R4 in cyclic derivatives; or are each independently hydrogen a nitrate group or A;
  • M is H, Na+, K+, NH4+, N+HkR11(4-k) where k is 0-3; or other pharmaceutically acceptable counterion;
  • and with the proviso that when m=n p=1 and R19, R2, R18, R1=H and R17, R3 are nitrate groups, R4 is not H.
  • In a preferred embodiment, R19 is X-Y.
  • In other embodiments, R1 and R3 are the same or different and selected from H and Cl-C4, alkyl chains, which chains may include one 0 linking R1 and R3 to form pentosyl, hexosyl, cyclopentyl, or cyclohexyl rings, which rings may optionally bear hydroxyl substituents;
  • R2 and R4 are the same or different and selected from H, a nitrate group, Cl-C4 alkyl chains optionally bearing 1-3 nitrate groups, and acyl groups (-C(O)R5);
  • R7, R11 are the same or different Cl - C8 alkyl or acyl;
  • R5, R6, R8, R9, R12, R13, R14, R15, R16 are the same or different and are alkyl groups containing 1-12 carbon atoms which may contain 1-4 ONO2 substituents; or C1 or C2 connections to R1- R3in cyclic derivatives; and
  • M is H, Na+, K+, NH4 + or N+HkR11(4-k),where k is 0-3.
  • In other embodiments, m=1, n=0, p=1.
  • In further embodiments, X is CH2, O, NH, NMe, CN, NHOH, N2H3, N2H2R13, N2HR13R14, N3, S, SCN, SCN2H2(RI5)2, SCN2H3(R5), SC(O)N(R15)2, SC(O)NHR15, SO3M, SH, SR7, SO2M, S(O)R8, S(O)2R9, S(O)OR8, S(O)2OR9, PO3HM, PO3M2, P(O)(OR15)(OR16), P(O)(OR16)(OM), P(O)(R15)(OR8), P(O)(OM)R15, CO2M, CO2H, CO2R11, C(O), C(O)R12, C(O)(OR13), PO2M, P(O)(OR14), P(O)(R13), SO, SO2, C(O)(SR13), or SSR4; and
    Figure US20070066575A1-20070322-C00004
  • Y is CN, N2H2R13, N2HR13R14, N3, SCN, SCN2H2(R15)2, SC(O)N(R15)2, SC(O)NHR15, SO3M, SR4, SO2M, PO3HM, PO3M2, P(O)(OR15)(OR16), P(O)(OR16)(OM), P(O)(R15)(OR8), P(O)(OM)R15, CO2M, CO2H, CO2R11, C(O)R12, C(O)(SR13), SR5, or SSR5, or does not exist.
  • In yet further embodiments, R5, R6, R8, R9, R12, R13, R14, R15, R16 are the same or different and are alki4s containing 1-12 carbon atoms; or Cl or C2 connections to R1 or R3 in cyclic derivatives;
  • X is CH2, O, NH, NMe, S, SO3M, SH, SR7, SO2M, S(O)R8, S(O)2R9, S(O)OR8, S(O)2O R9, PO3M2, P(O)(OR15)(OR16), P(O)(OR16)(OM), P(O)(R15)(OR8), PO3HM or P(O)(OM)R15; and
  • Y is SOM, SO3M, PO3HM, PO3M2, P(O)(OR15)(OR16), P(O)(OR16)(OM), SR5, SR4 or SSR5, or does not exist.
  • In preferred embodiments, therapeutic compounds of the invention act as analgesic, sedative and/or anti-inflammatory agents. Preferred therapeutic compounds for use in the invention include compounds having the formula (Formula II):
  • (Formula II)
  • in which: m and n and p are integers from 0 to 10;
  • R3,17 are each independently hydrogen; a nitrate group; or A;
  • R1,4 are each independently hydrogen; or A;
  • where A is selected from: a substituted or unsubstituted aliphatic group (preferably a branched, or straight-chain aliphatic moiety having from 1 to 24 carbon atoms in the chain, which optionally may contain 0, S, NR6 and unsaturations in the chain, optionally bearing from 1 to 4 hydroxy, or nitrate, or amino or aryl, or heterocyclic groups; an unsubstituted or substituted cyclic aliphatic moiety having from 3 to 7 carbon atoms in the aliphatic ring, which optionally may contain O, S, NR6 and unsaturations in the ring, optionally bearing from 1 to 4 hydroxy, or nitrate, or amino 8 or aryl, or heterocyclic groups; an unsubstituted or substituted aliphatic moiety constituting a linkage of from 0 to 5 carbons, between RI and R3 and/or between R17 and R4, which optionally may contain 0, S, NR6 and unsaturations in the linkage, and optionally beating from 1 to 4 hydroxy, or nitrate, or amino or aryl, or heterocyclic groups); a substituted or unsubstituted aliphatic group (preferably a branched, cyclic or straight-chain aliphatic moiety having from 1 to 24 carbon atoms in the chain), containing carbonyl linkages (e.g., C=O, C=S, C=NOH), which optionally may contain 0, S, NR6 and unsaturations in the chain, optionally bearing from 1 to 4 hydroxy, or nitrate, or amino or aryl, or heterocyclic groups; a substituted or unsubstituted aryl group; a heterocyclic group; ammno (including alkylamino, dialkylamino, such as cyclic amino, diamino and triamino moieties), arylamnino, diarylanino, and alkylarylamino); hydroxy; alkoxy; a substituted or unsubstituted aryloxy.
  • R2, R5, R18, R19 are optionally hydrogen; or A; or X-Y. where X is F, Br, Cl, NO2, CH2, CF2, O, NH, NMe, CN, NHOH, N2H3, N2H2R13, N2HR13R14, N3, S, SCN, SCN2H2(R15)2, SCN2H3(RI5), SC(O)N(R15)2, SC(O)NHR15, SO3M, SH, SR7, SO2M, S(O)R8, S(O)2R9, S(O)OR8, S(O)2O R9, PO2HM, PO3HM, PO3M2, P(O)(OR15)(OR16), P(O)(OR16)(OM), P(O)(R15)(OR8), P(O)(OM)RI5, CO2M, CO2H, CO2R11, C(O), C(O)R12, C(O)(OR13), PO2H, PO2M,P(O)(OR14), P(O)(R13), SO, SO2, C(O)(SR13), SR5, SSR7 or SSR5, Y is F, Br, Cl, CH3, CF2H, CF3, OH, NH2, NHR6, NR6R7, CN, NHOH, N2H3, N2H2R13, N2HR13R14, N3, S, SCN, SCN2H2(RI5)2, SCN2H3(R15), SC(O)N(R5)2, SC(O)NHR15, SO3M, SH, SR7, SO-M, S(O)R8, S(O)2R9, S(O)OR8, S(O)2O R9, PO2HM, PO3M2, P(O)(OR15)(OR16), P(O)(OR16)(OM), P(O)(R15)(OR8), P(O)(OM)R15, CO2M, CO2H, CO2R11, C(O)R12, C(O)(OR13), C(O)(SR13), SR5, SSR7 or SSR5, or does not exist;
  • R6, R7, R8, R9, R10, R1l, R12, R13, R14, R15, R16 are the same or different alkyl or acyl groups containing 1-24 carbon atoms which may contain 1-4 ON02 substituents; or C1 - C6 connections to R1 - R4 in cyclic derivatives; or are each independently hydrogen; a nitrate group; or W.
  • M is H, Na+, K+, NH4 +, N+HkR11(4-k) where k is 0-3, or other pharmaceutically acceptable counterion; and with the proviso that, when m=n=p=1; R19, R2, R18, R1=H; R17, R3 are nitrate groups; that R4 is not H or C -C3 alkyl.
  • In certain preferred embodiments, therapeutic compounds of the invention are analgesic, sedative and/or anti-inflammatory agents. Preferred therapeutic compounds for use in the invention include compounds in which R19 is X-Y. In a particularly preferred embodiment: R19 is X-Y and R5, R6, R8, R9, R10, R12, R13, R14, R15, R16 are the same or different alkyl groups containing 1-24 carbon atoms which may contain 1-4 ON02 substituents, or Cl or C2 connections to R1-R3 in cyclic derivatives; R1 and R3 are the same or different and selected from H, Cl-C4, alkyl chains, which may inlude one O, linking R1 and R3 to form pentosyl, hexosyl, cyclopentyl, or cycohexyl rings, which rings may optionally bear hydroxyl substituents; R2 and R4, are the same or different and selected from H, a nitrate group, Cl-C4 alkyl optionally bearing 1-3 nitrate groups, and acyl groups (—C(O)R5); R7, R11 are the same or different C1-C8, alkyl or acyl..
  • In certain embodiments in which Rig is X-Y, m, p=1, and n=0. In other embodiments in which Rig is X-Y, X is selected from CH2, O, NH, NMe, CN, NHOH, N2H3, N2H2R13, N2HR13R14, N3, S, SCN, SCN2H2(R15)2, SCN2H3(R15), SC(O)N(R15)2, SC(O)NHR15, SO3M, SH, SR7, SO,M, S(O)R8, S(O)2R9, S(O)OR8, S(O)2OR9, PO3HM, PO3M2, P(O)(OR15)(OR16), P(O)(OR16)(OM), P(O)(R15)(OR8), P(O)(OM)R15, CO2M, CO2H, CO2R11, C(O), C(O)R12, C(O)(OR13), PO?M, P(O)(OR14), P(O)(R13), SO, SO2, C(O)(SR13), SSR4. In another embodiment in which Rig is X-Y, Y is selected from CN, N2H2R13, N2HR13R14, N3, SCN, SCN2H2(R15)2, SC(O)N(R15)2, SC(O)NHR15, SO3M, SR4, SO2M, PO3HM, PO3M2, P(O)(OR15)(OR16), P(O)(OR16)(OM), P(O)(R15)(OR8), P(O)(OM)R15, CO2M, CO2H, CO?R1, C(O)R12, C(O)(SR13), SR5, SSR5, or does not exist. In a further embodiment, X and/or Y contain a sulfur-containing functional group. In certain preferred embodiments, the compound of the invention comprises a heterocyclic functionality, more preferably, a nucleoside or nucleobase. In further preferred embodiments, the compound of the invention comprises a carbocyclic functionality, more preferably, a steroidal or carbohydrate moiety.
  • In another aspect, a therapeutic compound of the invention is represented by the formula (Formula III):
    Figure US20070066575A1-20070322-C00005
  • in which: m is 1-10; R1-18, X, and Y have the meaning as defined above. In certain preferred embodiments, R6 - R16 are the same or different alkyl or acyl groups contaiunig 1-24 carbon atoms which may contain 1-4 ON02 substituents, or Cl - C6 connections to R1-R4 in cyclic derivatives. In certain preferred embodiments, R18 is A and n=1.
  • In preferred embodiments, a therapeutic compound of the invention is represented by the formula (Formula IV):
    Figure US20070066575A1-20070322-C00006
  • in which: R3, R1═H; n, R2 R4-18, X, and Y have the meaning as defined above. In preferred embodiments, X is CH2 or does not exist, and Y is selected from, F, Br, Cl, CH3, CF2H, CF3, OH, NH2, NHR6, NR6R7, CN, NHOH, N2H3, N2H2R13, N2HR13R14, N3, S, SCN, SCN2H2(R15)2, SCN2H3(R15), SC(O)N(R15)2, SC(O)NHR15, SO3M, SH, SR7, SO2M, S(O)R8, S(O)2R9, S(O)OR8, S(O)2O R9, PO2HM, PO3M2, P(O)(OR15)(OR16), P(O)(OR16)(OM), P(O)(Ris)(OR8), P(O)(OM)R15, CO2M, CO2H, CO2R1l, C(O)R12, C(O)(ORi3), C(O)(SR13), SR5, SSR7 or SSR5. In certain preferred embodiments, R2 and R4 are optionally H, a nitrate group or a connection to R5-R16 in cyclic derivatives.
  • In certain preferred embodiments, a compound of the invention is represented by the formula (Formula V):
    Figure US20070066575A1-20070322-C00007
  • in which m, n, R1-18, X, and Y have the meaning as defined above.
  • In another aspect, the invention includes novel compounds useful for treating pain, mitigating inflammation, effecting analgesia and/or providing sedation. The compounds of the invention can be represented by the structures shown hereinbelow, for example, the structures of Formula III, IV and V. Novel compounds of the invention include nitrates IlIr - IIIaj, Vn - Ivt, and Vd-Vag, whose syntheses are described in the following examples.
  • The invention also provides methods for treating a disease state associated with inflammation, comprising administering to a subject an effective amount of a therapeutic compound having a formula set forth above, such that a disease state associated with inflammation is treated.
  • The invention further provides methods for treating a disease state or disorder in which a level of sedation is desired, comprising administering to a subject an effective amount of a sedative therapeutic compound having a formula set forth above, such that a disease state or disorder is treated.
  • The invention provides methods for effecting analgesia comprising administering to a subject an effective amount of a therapeutic compound having a formula set forth above, such that analgesia is effected.
  • The invention father provides novel pharmaceutical compositions for treating pain, mitigating inflammation, effecting analgesia and/or effecting sedation. A said pharmaceutical composition comprises a therapeutic compound of the invention in an effective amount for the particular indication and a pharmaceutically acceptable vehicle.
  • The invention also provides packaged pharmaceutical compositions for treating pain, mitigating inflammation, effecting analgesia and/or effecting sedation. The packaged pharmaceutical compositions include a therapeutic compound of the invention and instructions for using the pharmaceutical composition for treatment of inflammation and/or pain.
    • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a graph showing the effect of IVd neat (diamonds); with added L-cysteine (2mM, triangles); with added dithiothreitol (2 mM, DTr, squares); on soluble GCase activity in rat aorta homogenate normalized to the maximal GTN response. Bars represent the mean±standard errors calculated separately for each point.
  • FIG. 2(a-b) is a graph showing the comparison of GTN (squares), IlIm (circles) and IVh (triangles) with added L-cysteine (1 mM) on soluble GCase activity in rat aorta homogenate (a), and rat hippocampus homogenate (b). Data points represent the mean of duplicate determinations carried out in identical GCase preparations.
  • FIG. 3(a-b) is a graph showing the comparison of GTN (squares), Va (circles) and Vb (triangles) with added L-cysteine(1 mM) on soluble GCase activity in rat aorta homogenate homogenate (a), and rat hippocampus homogenate (b). Data points represent the mean±standard errors calculated separately for each point (n=8-1 1).
  • FIG. 4(a-b) is a graph showing the comparison of cyclic GMP accumulation in isolated rat aorta induced by diluent (basal, open bar), GTN (filled bar), Va (stippled bar), or IIIm (hatched bar). Segments of rat aorta were exposed to diluent, 1 pM drug (a), or 1 0uM drug (b) for 1 min and cyclic GMP content determined by radioinmuunoassay. Data are the mean±standard errors (a, n=8; b, n=5).
  • FIG. 5(a-b) is a graph showing the comparison of cyclic GMP accumulation in isolated rat aorta induced by diluent (basal, open bar), GTN (filled bar), WVk (stippled bar ),Vb (cross-hatched bar), or Vc (hatched bar). Segments of rat aorta were exposed to diluent, 1 tM drug (a), or 10tM drug (b) for 1 mmn and cyclic GMP content determined by radioinmmunoassay. Data are the mean±standard errors (a, n=5; b, n=4).
  • FIG. 6(a-b) is a graph showing cyclic GMP accumulation in rat hippocampal slices induced by diluent (basal, open bar), GTN (filled bar), and Va (stippled bar). Sections of rat hippocampus (400 μm) were prepared and exposed to diluent, 10 μM drug (a) or 100 μM drug (b) for 3 min and cyclic GMP content determined by radioirnmunoassay. Data are the mean±standard errors (a, n=4; b, n=5).
  • FIG. 7 is a graph showing the comparison of relaxation of isolated rat aorta induced by GTN (squares), Va (open triangles), compound I7c (diamonds), compound WVd (open squares), compound IVf (triangles), and compound WVg (open diamonds). Data points represent the mean i standard errors (n=5-8).
  • FIG. 8 is a graph showing the comparison of relaxation of isolated rat aorta induced by GTN (squares), IVk (open triangles), Vb (diamonds), IIIm (open squares), Vc (triangles), and IVh (open diamonds). Data points represent the mean±standard errors (n=3-8).
  • FIG. 9 is a graph showing the comparison of the percent change in mean arterial pressure (MAP) in conscious unrestrained rats after subcutaneous administration of 400 μmol/kg GTN (squares) or Va (open circles). Data points represent the mean i standard errors (n=6).
  • FIG. 10 is a graph showing the comparison of the percent change in mean arterial pressure in Inactin anaesthetized rats after intravenous bolus injection of GTN (squares) or Va (open circles). Data points represent the mean i standard errors (n=4).
  • FIG. 11 is a graph showing the plasma levels (uM) of Vb (circles) and its mononitrate metabolite Vc (open squares) after subcutaneous administration of 200 μmol/kg Vb in conscious unrestrained rats. Data points represent the mean of two experiments.
  • FIG. 12(a-b) is a graph showing the relaxation induced by compound WVd (a) and Ivc (b) in untreated (squares) and GTN-tolerant (circles) isolated rat aorta. Aortae were made tolerant by treatment with 0.5 mM GTN for 30 min. Data points represent the mean±standard deviation (n=3-6).
  • FIG. 13(A-B) is a graph showing the effect of Vm and Va in the mouse writhing test. GT Vm produced a dose-dependent analgesic effect (A). Va also produced analgesia in the mouse writhing test (B). Data are mean i standard errors (n=10-20).
  • FIG. 14(A-B) is a graph showing the effect of Vm on paw flinches in rats after injection of formnalin into the footpad. In comparison to vehicle-treated control animals, Vm decreased the initial pain response to formalin injection (at time=0, *, p<0.05), and the secondary hyperalgia that developed between 20 and 40 minutes after formnalin injection (A). For each animal, a cumulative score (total number of flinches over 60 minutes) was calculated (B). Vm significantly decreased cumulative paw flinches for 60 minutes after formalin injection. Data are mean i standard errors (N=6-7).
  • FIG. 15(A-B) is a graph showing (A) the effects of chlormethiazole (CHLOR) and WVk (200 μM of each) on the membrane current induced by 10 jiM GABA in a Xenopus oocyte expressing the α1β1γ2L isoform of human recombinant GABAA receptors, and (B) the effect of IVk on loss of the righting reflex in mice after intraperitoneal injection of 100 mg/kg and 200 mg/kg. Data in part B are mean +standard error for three animals at each dose.
    • DETAILED DESCRIPTION OF THE INVENTION
  • In accordance with the invention there are provided methods and compositions useful in the treatment of pain. Methods of the invention involve administering to a subject an effective amount of a therapeutic compound which provides analgesia, mitigates inflammation and/or provides sedation. In some embodiments, the invention provides prophylactic methods for avoiding or pre-empting pain, inflammation and the like in a subject. For example, the subject may be susceptible or predisposed to these conditions, e.g., arthritic. Alternatively, the subject may be undergoing a course of treatment, e.g. cancer chemotherapy, which produces pain, inflammation or the like as a side effect. Methods of the invention may be practiced prior to, concurrently with, or after such a course of treatment.
  • In accordance with the invention, analgesic, anti-inflammatory and/or sedative activity can be effected by modulating an interaction with guanylyl cyclase (GCase; the enzyme responsible for cGMP production in various areas of the body), and/or by modulating levels of cGMP and cAMP messenger molecules.
  • As used herein, the term “treating” pain encompasses preventing, ameliorating, mitigating and/or managing pain and/or conditions that may cause pain, such as inflammation. As used herein, “inhibiting” pain or inflammation encompasses preventing, reducing and halting progression of same. The terms “organic nitrate” and “nitrate ester” are used interchangeably herein, with no distinction drawn between them.
  • According to one aspect of the invention, there is provided a method for treating pain in a subject, comprising administering to the subject an effective amount of a compound (nitrate ester) which effects analgesia in the subject. Preferably, analgesia is effected by stimulating GCase. In vivo, GCase activation is effected by nitric oxide (NO), the proximal activator of GCase, which is generated endogenously by enzyme action on arginine in response to many biological triggers (J. R. Stone and M. A. Marletta, Biochemistry (1996) 35, 1093). One of the major targets for organic nitrates is GCase activation, resulting in the production of cGMP. In this respect, organic nitrates act as NO-surrogates. In some cases, there is evidence that organic nitrates may act also as NO-donors, but these two properties should be differentiated and can be modulated by choice of the appropriate organic nitrate.
  • Experimental evidence obtained in a number of in vivo model systems supports the notion that elevated levels of cGMP help effect analgesia. Sodium nitroprusside (SNP), which releases NO non-enzymatically, blocked the hyperalgesic effect of prostaglandin (PGE2) in a rat paw pressure test (Ferreira et al., 1991). Moreover, this effect was potentiated by an inhibitor of cGMP phosphodiesterase, and blocked by an inhibitor of GCase (Ferreira et al., 1991). The peripheral analgesic effects of morphine were attributed to elevations of cGMP levels in sensory nerve fibres (Ferreira et al., 1991; Granados-Soto et al., 1997) in both the rat paw pressure and formalin tests, since inhibition of GCase activity attenuated the analgesic effects of locally applied morphine. Activation of the NO-cGMP system by NO donors such as SNP has also been reported to potentiate beta-endorphin-induced analgesia in thermal tail-flick test in mice (Xu et al., 1995), an effect that was potentiated by a selective inhibitor (zaprinast) of a cGMP-specific phosphodiesterase.
  • Sensitization of sensory nerve fibres leading to hyperalgesia is assumed to involve increased concentrations of cAMP and calcium ions in sensory neurons, a process that may be attenuated or counteracted by activation of the NO-cGMP pathway (Ferreira, 1993; Cunha et al., 1999).
  • In accordance with another embodiment of the invention, administration of an effective amount of a therapeutic compound to a subject effects analgesia in the subject by modulating levels of cAMP and/or cGMP. For example, it has been shown that NO-donors modulate hyperalgesia via modulation of levels of cAMP, separately from and in addition to modulation of cGMP levels, in rat models of pain and nociceptor sensitization (Aley et al. 1998). Thus, modulation of cAMP/cGMP levels is expected to be effective in inducing analgesia and in pain management in individuals suffering injury, disease or aging.
  • In a futher embodiment of the invention, there is provided a method for treating or hibitng imflammation in a subject, comprising administering to the subject an effective amount of a compound which mitigates inflammation in the subject. Preferably, inflammation is mitigated by modulation of levels of cGMP/cAMP. Inflammatory hyperalgesia has been shown to be linked directly to the NO-cGMP pathway (Ferreira, 1993).
  • We have shown in our co-pending application U.S. Ser. No. 09/267,379, filed Mar. 15, 1999, now U.S. Pat. No. 6,310,052, which is hereby incorporated by reference, that novel nitrate esters have differential effects to activate soluble GCase and to cause cGMP accumulation in vascular and brain tissue. Further, we have shown that the structure of the organic nitrate can be varied to alter potency and efficacy towards both activation of GCase and accumulation of cGMP and effects resulting from these processes in intact tissue, such as aortic strip relaxation. Activation of GCase and accumulation of cGMP have been shown to be important in the induction of analgesia. We show herein that novel organic nitrates are effective analgesics in animal models of pain management. The mouse writhing model, with a relatively short time course of minutes, is a preclinical model of acute pain; whereas formalin injection in the rat paw is a preclinical model of acute and sensitization pain with a time course of minutes to hours, which effectively mnimics the hyperalgesia/allodynia underlying pain due to tissue damage (Yaksh, 1999).
  • In a further embodiment, the invention relates to a method for providing sedation and/or anaesthesia in a subject, comprising administering to the subject an effective amount of a compound (organic nitrate) which effects sedation or anaesthesia in the subject. In certain aspects, the invention provides methods and compositions useful for reducing anxiety, and/or aiding or inducing sleep.
  • γ-Aminobutyric acid (GABA) is the major inhibitory neurotransmitter in the mammalian (including human) central nervous system. GABA acts on three major classes of neurotransmitter receptor, designated type A (GABAA), type B (GABAB) and type C (GABAC). GABAA receptors play an important role in regulating many behavioural and physiological functions. Thus, drugs that modulate GABAA receptor function are among the most widely used in clinical medicine. For example, drugs that selectively potentiate GABAA receptor function (such as the benzodiazepines) are extensively used to relieve anxiety, produce sedation and induce sleep. Given the importance of this receptor mechanism in clinical medicine, there is a constant search for new chemical entities that modulate GABAA function, as the currently available drugs have several side effects, including ataxia, amnesia, tolerance and physical dependence. We show herein that organic nitrates that act as positive allosteric modulators of GABAA receptor function have sedative properties in the whole animal that are comparable to known drugs. This effect of organic nitrates has not previously been recognized or reported. Our findings provide direct evidence that nitrate esters are useful as sedative agents. Such agents are useful as therapeutics for treating conditions such as, for example, anxiety and pain associated with disease states; and as hypnotic agents. According to the invention, nitrate esters may also be employed prophylactically, to prevent or reduce anxiety, or to aid sleep.
  • Therapeutic compounds of the invention comprise at least one nitrate group. The nitrate groups(s) can optionally be covalendy bound to a carrier (e.g., an aromatic group, an aliphatic group, peptide, steroid, nucleobase, nucleoside, peptidomimetic, steroidomimetic, or nucleoside analogue, or the like). In addition to functioning as a carrier for the nitrate functionality, the carrier molecule can enable the compound to traverse biological membranes and to be biodistributed preferentially, without excessive or premature metabolism. Further, in addition to functioning as a carrier for the nitrate functionality, the carrier molecule can enable the compound to exert amplified analgesic, sedative, or anti-inflammatory effects through synergism with the nitrate functionality.
  • In one embodiment, the invention provides a method comprising administering to a subject an effective amount of a therapeutic compound which has at least one nitrate group and is capable of effecting analgesia. In another embodiment, the therapeutic compound is capable of mitigating inflammation. In a further embodiment, the therapeutic compound is capable of effecting sedation. In the respective embodiments, the therapeutic compound has the formula (Formula I):
    Figure US20070066575A1-20070322-C00008
  • wherein: E, F1, F2, G1, G2 are the same or different organic radicals which may be joined in cyclic ring systems, and which may contain inorganic counterions.
  • In further aspects of the invention, therapeutic compounds of the invention effect analgesia, effect sedation and/or mitigate inflammation in a subject to which the therapeutic compound is administered, and have the formula (Formula II).
    Figure US20070066575A1-20070322-C00009
  • in which: m, n, p are integers from 0 to 10; R3,17 are each independently hydrogen; a nitrate group; or A; R1,4 are each independently hydrogen; or A; where A is selected from: a substituted or unsubstituted aliphatic group (preferably a branched, or straight-chain aliphatic moiety having from 1 to 24 carbon atoms in the chain, which optionally may contain O, S, NR6 and unsaturations in the chain, optionally bearing from 1 to 4 hydroxy, or nitrate, or amino or aryl, or heterocyclic groups; an unsubstituted or substituted cyclic aliphatic moiety having from 3 to 7 carbon atoms in the aliphatic ring, which optionally may contain O, S, NR6 and unsaturations in the ring, optionally bearing from 1 to 4 hydroxy, or nitrate, or ammno or aryl, or heterocyclic groups; an unsubstituted or substituted aliphatic moiety constituting a linkage of from 0 to 5 carbons, between R1 and R3 and/or between R17 and R4, which optionally may contain O, S, NR6 and unsaturations in the linkage, and optionally bearing from 1 to 4 hydroxy, or nitrate, or amino or aryl, or heterocyclic groups); a substituted or unsubstituted aliphatic group (preferably a branched, cyclic or straight-chain aliphatic moiety having from 1 to 24 carbon atoms in the chain), containing carbonyl linkages (e.g., C═O, C═S, C═NOH), which optionally may contain O, S, NR6 and unsaturations in the chain, optionally bearing from 1 to 4 hydroxy, or nitrate, or ammno or aryl, or heterocyclic groups; a substituted or unsubstituted aryl group; a heterocyclic group; amino (including alkylamino, dialkylamino, such as cyclic amino, diamino and triamnuo moieties), arylamifno, diarylamnino, and alkylarylarnino); hydroxy; alkoxy; a substituted or unsubstituted aryloxy ; R2, R5, R18, R19 are optionally hydrogen; or A; or X-Y; where X is F, Br, Cl, NO2, CH2, CF2, O, NH, NMe, CN, NHOH, N2H3, N2H2R13, N2HR13R14, N3, S, SCN, SCN2H2(R15)2, SCN2H3(R15), SC(O)N(R15)2, SC(O)NHR15, SO3M, SH, SR7, SO-M, S(O)R8, S(O)2R9, S(O)OR8, S(O)20R9, PO2HM, PO3HM, PO3M2, P(O)(OR15)(OR16), P(O)(OR16)(OM), P(O)(R15)(OR8), P(O)(OM)R15, CO2M, CO2H, CO2R1, C(O), C(O)R12, C(O)(OR13), PO2H, PO2M, P(O)(OR14), P(O)(R13), SO, SO2, C(O)(SR13), SR5, SSR7 or SSR5; Y is F, Br, Cl, CH3, CF2H, CF3, OH, NH2, NHR6, NR6R7, CN, NHOH, N2H3, N2H2R13, N2HR13R14, N3, S, SCN, SCN2H2(R15)2, SCN2H3(R15), SC(O)N(R15)2, SC(O)NHR15, SO3M, SH, SR7, SOM, S(O)R8, S(O)2R9, S(O)OR8, S(O)2O R9, PO2HM, PO3M2, P(O)(OR15)(OR16), P(O)(OR16)(OM), P(O)(R15)(OR8), P(O)(OM)R15, CO2M, CO2H, CO2R11, C(O)R12, C(O)(OR13), C(O)(SR13), SR5, SSR7 or SSR5, or does not exist; R6, R7, R8, R9, R10, R11, R12, R13, R14, R15, R16 are the same or different alkyl or acyl groups containing 1-24 carbon atoms which may contain 1-4 ONO2 substituents; or C1-C6 connections to R1-R4 in cyclic derivatives; or are each independently hydrogen; a nitrate group; or A; M is H, Na+, K+, NH4+, N+HkR11 where k is 0-3, or other pharmaceutically acceptable counterion.
  • Preferred therapeutic compounds for use in the invention include compounds in which R19 is X-Y. In a particularly preferred embodiment: R19 is X-Y and R5, R6, R8, R9, R10, R12, R13, R14, R15, 19 R16 are the same or different alkyl groups containing 1-24 carbon atoms which may contain 1-4 ON02 substituents, or Cl or C2 connections to R1-R3 in cyclic derivatives; R1 and R3 are the same or different and selected from H, Cl-C4, alkyl chains, which may inlude one 0, linking R1 and R3 to form pentosyl, hexosyl, cyclopentyl, or cycohexyl rings, which rings may optionally bear hydroxyl substituents; R2 and R4, are the same or different and selected from H, a nitrate group, Cl-C4 alkyl optionally bearing 1-3 nitrate group, and acyl groups (-C(O)R5); R7, R11 are the same or different Cl - C8, a,l or acyl.
  • In certain embodiments in which Rig is X-Y, m, p=1, and n=0. In other embodiments in which Rig is X-Y, X is selected from CH2, O, NH, NMe, CN, NHOH, N2H3, N2H2R13, N2HR13R14, N3, S, SCN, SCN2H2(R5)2, SCN2H3(R15), SC(O)N(RI5)2, SC(O)NHR15, SO3M, SH, SR7, SO?M, S(O)R8, S(O)2R9, S(O)OR8, S(O)2O R9, PO3HM, PO3M2, P(O)(OR15)(OR16), P(O)(OR16)(OM), P(O)(R15)(ORB), P(O)(OM)R15, CO2M, CO2H, CO2R11, C(O), C(O)R12, C(O)(OR13), PO2M, P(O)(OR14), P(O)(R13), SO, SO2, C(O)(SR13), SSR4. In another embodiment in which Rig is X-Y, Y is selected from CN, N2H2R13, N2HR13R14, N3, SCN, SCN2H2(R15)2, SC(O)N(R15)2, SC(O)NHR15, SO3M, SR4, SO?M, PO3HM, PO3M2, P(O)(OR15)(OR16), P(O)(OR16)(OM), P(O)(R15)(OR8), P(O)(OM)R15, CO2M, CO2H, CO2R1l, C(O)R12, C(O)(SR13), SR5, SSR5, or does not exist. In a further embodiment, X and/or Y contain a sulfur-containing functional group. In certain preferred embodiments, the compound of the invention comprises a heterocyclic functionality, more preferably, a nucleoside or nucleobase. In further preferred embodiments, the compound of the invention comprises a carbocyclic functionality, more preferably, a steroidal or carbohydrate moiety.
  • In another aspect of the invention, a therapeutic compound of the invention is represented by the formula (Formula III):
    Figure US20070066575A1-20070322-C00010
  • in which: m, n are 1-10; R1-18, X, and Y have the meaning as defined above. In certain preferred embodiments, R6 - R16 are the same or different alkyl or acyl groups containing 1-24 carbon atoms which may contain 1-4 ON02 substituents, or C1-C6 connections to R1-R4 in cyclic derivatives. In certain preferred embodiments, R18 is A and m=n=1. In further preferred embodiments, therapeutic compounds of the invention have a formula selected from (Formulae IIIa-IIIam):
    Figure US20070066575A1-20070322-C00011
    Figure US20070066575A1-20070322-C00012
    Figure US20070066575A1-20070322-C00013
    Figure US20070066575A1-20070322-C00014
    Figure US20070066575A1-20070322-C00015
    Figure US20070066575A1-20070322-C00016
  • In a further aspect of the invention, a therapeutic compound of the invention is represented by the formula (Formula IV):
    Figure US20070066575A1-20070322-C00017
  • in which n=0, X is CH2 or does not exist, and Y is selected from, F, Br, Cl, CH3, CF2H, CF3, OH, NH2, NHR6, NR6R7, CN, NHOH, N2H3, N2H2R13, N2HR13R14, N3, S, SCN, SCN2H2(R15)2, SCN2H3(R15), SC(O)N(R15)2, SC(O)NHRi5, SO3M, SH, SR7, SO-M, S(O)Rg, S(O)2R9, S(O)ORg, S(O)2O R9, PO2HM, PO3M2, P(O)(OR15)(OR16), P(O)(OR16)(OM), P(O)(Ri5)(OR8), P(O)(OM)R15, CO2M, CO2H, CO2R1l, C(O)RI2, C(O)(OR13), C(O)(SR13), SR5, SSR7 or SSR5. R2, R4, R5, R6, R7, Rg, Rg, Rio, Ril, R12, R13, R14, R15, and R16 are as defined above. In certain preferred embodiments, R2 and R4 are optionally H, a nitrate group or a connection to R5-R16 in cyclic derivatives.
  • In certain preferred embodiments, a compounds of the invention is represented by the formula (Formulae IVa-IVt):
    Figure US20070066575A1-20070322-C00018
    Figure US20070066575A1-20070322-C00019
    Figure US20070066575A1-20070322-C00020
  • In a further aspect of the invention, compounds according to the invention are represented by the formula (Formula V):
    Figure US20070066575A1-20070322-C00021
  • in which R2 is optionally H or a connection to R5 in cyclic derivatives, R4 is H or a nitrate group, and R5 is as described above.
  • In certain preferred embodiments, compounds of the invention are represented by the formula (Formulae Va-Vag):
    Figure US20070066575A1-20070322-C00022
    Figure US20070066575A1-20070322-C00023
    Figure US20070066575A1-20070322-C00024
    Figure US20070066575A1-20070322-C00025
    Figure US20070066575A1-20070322-C00026
  • In another aspect, the invention provides novel compounds which can be represented by structures of Formula III, Formula IV, and Formula V. Table 1 lists data associated with these compounds using art-recognized characterization techniques. Further, the invention provides novel pharmaceutical compositions comprising a therapeutic compound (nitrate ester) of the invention and a pharmaceutically acceptable vehicle.
    TABLE 1
    1H NMR 13C NMR
    IIIa (CDCl3): 5.34-5.57(1H, dm, 3JHF 20.6), (CDCl3): 79.47(d, 1JCF 177),
    4.53-4.87(4H, superposition several multiplets, O2NO—CH 2+CH 2F, 76.73(d, 2JCF 20.6), 67.84(d,
    2JHF 46.7, 4JHF 0.66) 3JCF 6.87)
    IIIc (CDCl3): δ 5.7(1H, t, 2JHF 54), 5.45(1H, m), (CDCl3): δ 75.55, 68.05, 60.76
    4.5-4.9(2H, m), 4.15-4.35(1H, m)
    IIId (CDCl3): δ 5.46(1H, m), 4.80-4.87(1H, dd, J 3.5, (CDCl3): δ 77.24, 68.57, 39.86
    12.9), 4.65-4.72(1H, dd, J 6.2, 12.9), 3.7-3.8(2H, m)
    IIIf (CDCl3) δ 8.72(s, 1H), 5.38(t, 1H), 4.6(d, 2H), —
    2.45(s, 3H)
    IIIg (DMSOd6) CHONO2 only: δ 4.8-5.8 (DMSOd6) CONO2 only: δ
    85.68, 84.17, 82.47, 76.50
    IIIh (CD3OD) δ 4.85(3H, m), 3.5(1H, m) (CD3OD) δ 70.61, 36.74
    IIIi (CDCl3): δ 6.95(dd, 1H), 6.71(dd, 1H), 6.09(m, (CDCl3): δ 137.9, 132.5, 76.6,
    1H), 3.80(dd, 1H), 3.32(dd, 1H) 52.9
    IIIj (CDCl3): δ 5.62(2H, m), 3.60(4H, m) (CDCl3): δ 77.87, 25.22
    IIIk (CD3CN): δ 3.45(m, 2H), 5.72(m, 2H) (CD3CN): δ 79.98, 28.87
    IIIl — (CD3CN): δ 79.48, 33.45, 28.47
    IIIm (DMSOd6): δ 5.97(m, 2H), 3.80(m, 4H) (DMSOd6): δ 78.84, 52.60
    IIIn (CDCl3): δ 5.73(m, 1H), 4.62(m, 1H), 3.96-3.77(m, (CDCl3): δ 81.47, 57.85, 53.50,
    1H), 3.58-3.32(m, 1H) 38.75
    IIIo — (CDCl3): δ 81.24, 69.79, 33.26,
    27.24
    IIIp (CDCl3): δ 5.36(m, 1H), 3.11-3.60(m, 4H), 2.33(m, (CDCl3): δ 78.92, 33.66, 30.64,
    2H) 27.36
    IIIq (CDCl3): δ 5.47(m, 1H), 3.53-3.05(m, 4H), 2.29(m, (CDCl3): δ 81.32, 37.12, 32.97,
    2H) 30.98
    IIIw (CDCl3, 300MHz): 5.31-5.45(m, 1H), 3.92-4.08(m, (CDCl3, 75MHz): 76.83,
    31P(CDCl3, 162MHz) 4H), 3.63-3.81(m, 2H), 2.03-2.30(m, 2H), 62.15(d, J 6.37), 43.77(d, J 8.95),
    24.60 1.16-1.24(superposition of 2 t, 6H, J 7) 27.08(d, J 142.00), 15.99(d, J
    5.88)
    IIIx 31P(CD3OD, (CD3OD, 300MHz): 5.38-5.63(m, 1H), (CD3OD, 75MHz): 81.14,
    122MHz) 17.62 3.75-4.25(superposition of 2 m, 4H), 1.88-2.20(m, 2H), 61.17(d, J 5.41), 45.56(d, J
    1.12-1.28(t, 3H) 5.94), 29.35(d, J 131.74),
    17.00(d, J 6.75)
    IIIak 1H(CD3CN, 300MHz): 7.8(s, 1H), 5.75-5.85(m, 13C(CD3CN, 75MHz) (for
    1H), 4.90-4.97(dd, 1H, J 12.87, 3.39), 4.54-4.76(m, polynitrated chain): 78.51,
    3H), 3.46(s, 3H), 3.27(s, 3H) 70.58, 46.01, 30.10, 28.18
    Ivi (CDCl3): δ 5.45(1H, m), 4.83(1H, dd), 4.65(1H, (CD3OD): δ 116.44, 75.37,
    dd), 2.9(2H, m) 71.20, 19.19
    Ivk (CDCl3) δ 8.55(s, 1H), 4.55(t, 2H), 3.15(t, 2H), (CDCl3) δ 150.9, 150.7, 125.3,
    2.37(s, 3H) 72.53, 24.47, 15.18
    Ivm (CDCl3): δ 7.5-8.0(arom, 5H), 5.7(1H, m), (CDCl3): δ 135.45, 134.79,
    4.94(1H, dd), 4.62(1H, dd), 3.5(2H, m) 129.81, 27.95, 73.08, 70.04,
    54.73
    Ivs 1H-NMR(CDCl3, 300MHz): 5.23-5.32(1H, m), 13C-NMR: (CDCl3, 75.48MHz):
    4.87(1H, dd, J 12.82, 3.22), 4.68(1H, dd, J 12.83, 79.39, 69.30, 23.68
    6.09), 2.77-2.94(2H, m), 1.66(1H, t, J 9.07)
    Ivt 1H-NMR(CDCl3, 300MHz): 5.29-5.38(1H, m), 13C-NMR: (CDCl3, 75.48MHz):
    4.76(1H, dd, J 12.94, 3.11), 4.55(1H, dd, J 12.94, 194.10, 77.00, 69.79,
    6.37), 3.30(1H, dd, J 14.06, 5.98), 3.13(1H, dd, J 30.42, 27.78
    14.61, 6.35)
    Vb (CDCl3) δ 5.56(m, 2H), 3.38-2.95(m, 4H) (CD3OD) δ 85.93, 32.77
    Vc (CDCl3): δ 5.85-5.91(1H, m), 4.50-4.58(1H, m), (CDCl3): δ 87.6, 74.96, 36.20,
    3.22-3.29(1H, dd, J 5.47, 12.78), 2.97-3.05(1H, dd, 31.54
    J 4.6, 11.88), 2.82-2.90(1H, dd, J 2.87, 12.78),
    2.74-2.83(1H, dd, J 3.15, 11.9)
    Ve (CDCl3): δ 7.44-7.51(m, arom 2H), 7.17-7.24(d, (CDCl3): δ 21.53, 36.78, 69.82,
    arom 2H, J 7.91), 5.47-5.59(m, 1H), 4.83-4.93(dd, 77.68, 130.52, 130.62, 132.55,
    1H, J 12.81, 2.78), 4.57-4.67(dd, 1H, J 12.82, 5.71), 139.23
    3.02-3.12(dd, 1H, J 14.48, 6.01), 2.9-2.99(dd, 1H, J
    14.47, 7.72), 2.38(s, 3H)
    Vf (CDCl3): δ 7.48-7.57(m, arom 2H), 7.48-7.57(m, (CDCl3): δ 36.57, 55.87, 69.75,
    arom 2H), 5.49-5.59(m, 1H), 4.84-4.93(dd, 1H, J 77.76, 115.47, 126.71, 133.76,
    12.79, 2.79), 4.58-4.68(dd, 1H, J 12.79, 5.75), 160.94.
    3.84(s, 3H), 3.02-3.12(dd, 1H, J 14.47, 5.8),
    2.89-2.99(dd, 1H, J 14.46, 7.99).
    Vg (CDCl3): δ 7.47-7.54(m, arom 2H), 7.32-7.38(m, (CDCl3): δ 36.87, 69.80, 77.5,
    arom 2H), 5.45-5.55(m, 1H), 4.84-4.97(dd, 1H, J 129.98, 130.85, 134.51, 134.79.
    12.86, 2.92), 4.58-4.68(dd, 1H, 12.86, 5.68),
    2.91-3.11(m, 2H).
    Vh (CDCl3): δ 8.21-8.27(m, arom 2H), 7.67-7.74(m, (CDCl3): δ 37.24, 69.75, 77.41,
    arom 2H), 5.44-5.54(m, 1H), 4.86-4.94(dd, 1H, J 124.82, 127.26, 144.83
    12.92, 3.11), 4.61-4.70(dd, 1H, J 12.92, 5.56),
    3.01-3.16(m, 2H).
    Vi (CDCl3): δ 7.40-7.55(m, arom 4H), 5.44-5.55(m, (CDCl3): δ 36.87, 69.79, 77.48,
    1H), 4.85-4.92(dd, 1H, J 12.87, 2.91), 4.60-4.70(dd, 122.72, 130.93, 132.90, 135.15.
    1H, J 12.86, 5.66), 2.92-3.11(m, 2H).
    Vj (CDCl3): δ 7.55-7.62(d, arom 2H, J 7.16), (CDCl3): δ 36.97, 69.88, 77.61,
    7.29-7.44(m, arom 3H), 5.46-5.58(m, 1H), 4.82-4.92(dd, 128.60, 129.50, 129.85, 136.02
    1H, J 12.85, 2.79), 4.57-4.67(dd, 1H, J 12.86, 5.67),
    3.01-3.13(dd, 1H, J 14.51, 6.24), 2.92-3.02(dd, 1H,
    J 14.52, 7.4)
    Vk (CDCl3, 300MHz): 8.09(1H, dd, J 8.12, 0.36), (CDCl3, 75.48MHz): 166.21,
    8.02(1H, dd, J 7.8, 1.15), 7.51-7.59(1H, m, J 7.24, 1.44), 140.41, 132.78, 131.46, 127.63,
    7.21-7.29(1H, m, J 7.35, 0.54), 5.40-5.49(1H, m), 125.48, 77.25, 71.03, 61.42,
    4.70-4.78(1H, dd, J 13.04, 2.95), 4.33-4.45(3H, m, 32.51, 28.29, 14.17
    superposition of 1H from CH2—ONO2 and quartet
    from O—CH2—CH3), 2.66-2.87(2H, quartet, J 6.92),
    1.39(3H, t, J 7.14)
    Vl (CDCl3, 300MHz): δ 7.97(s, 1H), 7.48-7.51(d, 1H), (CDCl3, 75.48MHz): δ 14.17,
    7.17-7.22(m, 1H), 6.84-6.89(d, 1H), 6.05(s, 2H), 36.27, 62.15, 69.71, 76.57,
    5.48-5.58(m, 1H), 4.81-4.89(dd, 1H), 4.53-4.61(dd, 101.77, 108.27, 110.31, 125.20,
    1H), 4.25-4.4(m, 2H), 3.05-3.10(m, 2H), 127.55, 127.87, 146.87, 147.811,
    1.35-1.45(t, 3H). 149.76, 165.89
    Vm (CDCl3, 300MHz): δ 8.04-8.11(m, arom 2H), (CDCl3, 75.48MHz): δ 14.17,
    7.55-7.62(m, arom 1H), 7.30-7.34(m, arom 1H), 26.23, 35.95, 61.55, 69.54,
    5.43-5.54(m, 1H), 4.88-4.97(dd, 1H, J 12.95, 2.79), 77.24, 125.56, 125.92, 127.91,
    4.62-4.71(dd, 1H, J 12.94, 5.35), 4.45-4.39(q, 2H, 131.52, 132.93, 139.56, 166.189
    J 7.12), 2.92-3.08(m, 2H), 1.39-1.47(t, 3H, J 7.13)
    Vn (CDCl3, 300MHz): δ 8.92-8.97(m, arom 1H), (CDCl3, 75.48MHz): δ 36.06,
    8.07-8.23(m, arom 2H), 7.46-7.77(m, arom 3H), 69.62, 70.24, 77.42, 121.97,
    5.53-5.62(m, 1H), 4.91-4.99(dd, 1H, J 12.98, 2.77), 125.65, 126.43, 126.70, 128.52,
    4.61-4.7(dd, 1H, J 12.98, 5.35), 3-3.18(m, 2H) 135.31, 136.37, 145.62, 149.65
    Vo (CDCl3, 300MHz): δ 7.55-7.59(m, arom 1H), (CDCl3, 75.48MHz): δ 37.10,
    7.40-7.45(m, arom 1H), 7.25-7.36(m, arom 2H), 69.87, 77.44, 126.80, 128.38,
    5.45-5.55(m, 1H), 4.85-4.95(dd, 1H, J 12.98, 3), 128.52, 130.83, 135.76, 138.01
    4.59-4.69(dd, 1H, J 12.89, 6.67), 2.95-3.12(m, 2H)
    Vp (CDCl3, 300MHz): δ 7.65-7.67(d, arom 1H J 2.15), (CDCl3 75.48MHz): δ 36.59,
    7.44-7.47(d, arom 1H, J 7.42), 7.28-7.49(m, arom 69.32, 76.90, 127.49, 129.86,
    1H), 5.46-5.54(m, 1H), 4.87-4.94(dd, 1H, J 12.89, 131.04, 132.31, 133.59, 135.65
    2.99), 4.61-4.68(dd, 1H, J 12.88, 5.65),
    2.95-3.12(m, 2H)
    Vq (CDCl3, 300MHz): δ 7.2-7.6(m, arom 8H),
    5.42-5.56(m, 2H), 4.82-4.95(dd, 2H), 4.55-4.67(dd,
    2H), 2.93-3.15(m, 4H)
    Vr (CDCl3, 300MHz): δ 8.63(s, arom 1H),
    8.01-8.13(m, arom 2H), 7.57-7.65(m arom 1H),
    7.26-7.37(m, arom 1H), 5.42-5.51(m, arom 1H),
    4.88-4.97(dd, 1H, J 12.9, 2.7), 4.62-4.71(dd, 2H, J 12.9,
    5.1), 4.49-4.57(t, 2H, J 6.6), 3.23-3.32(t, 2H, J
    6.6), 2.91-3.08(m, 2H), 2.45(s, 3H)
    Vs (d6-acetone), 300MHz): 8.16-8.23(1H, d, J 7.72), (d6-acetone, 100.62MHz):
    8.07-8.13(1H, dd, J 7.72, 1.11), 7.63-7.72(1H, m, J 167.74, 134.01, 132.64, 126.62,
    8.38, 1.26), 7.33-7.42(1H, m, J 7.33), 5.67-5.76(1H, 126.21, 78.90, 71.69, 36.79
    m), 5.09-5.17(1H, dd, J 12.91, 2.68), 4.83-4.93(1H,
    dd, J 12.91, 5.91), 3.18-3.32(2H, m)
    Vt (CDCl3, 300MHz): δ 7.53-7.59(d, arom 1H, J 8.35), (CDCl3, 75.48MHz): δ 19.01,
    7.46-7.49(d, arom 1H, J 1.82), 7.37-7.43(m, arom 37.10, 70.01, 77.46, 115.27,
    1H), 6.24(s, 1H), 5.46-5.55(m, 1H), 4.86-4.94(dd, 115.34, 119.52, 123.07, 125.83,
    1H, 12.92, 2.92), 4.61-4.69(dd, 1H, J 12.93, 5.75), 141.13, 152.38, 154.25, 160.51
    3.0-3.15(m, 2H), 2.42(s, 3H)
    Vu (CDCl3, 300MHz): δ 7.55-7.58(m, arom 1H), (CDCl3, 75.48MHz): δ
    7.40-7.45(m, arom 1H), 7.27-7.32(m, arom 2H), 37.08, 69.83, 77.40, 126.80,
    5.46-5.54(m, 1H), 4.86-4.94(dd, 1H, J 12.88, 2.92), 128.40, 128.54, 130.83,
    4.59-4-68(dd, 1H, J 12.88, 5.65), 2.95-3.13(m, 2H) 135.78, 137.98
    Vv (CDCl3, 300MHz): 8.09-8.14(1H, d, J 8.15), (CDCl3, 75.48MHz): 166.34,
    7.98-8.04(1H, dd, J 7.75, 0.91), 7.52-7.59(1H, m, J 8.22, 140.25, 132.90, 131.49, 127.67,
    1.19), 7.22-7.28(1H, m, J 7.65), 4.53-4.61(1H, dd, J 125.60, 74.34, 66.83, 61.53,
    11.33, 3.63), 4.42-4.50(1H, m, J 11.33, 6.27), 40.89, 14.20
    4.32-4.41(2H, qu., J 7.13), 4.16-4.25(1H, m),
    2.74-2.84(2H, m), 2.55-2.73(1H, br.s.), 1.34-1.42(3H, t, J
    7.13)
    Vx (CDCl3, 300MHz): δ 5.49-5.61(m, 1H), (CDCl3, 75.48MHz): δ 17.39,
    4.88-4.90(m, 1H), 4.62-4.74(m, 1H), 4.40-4.55(m, 1H), 25.20, 29.40, 36.41/36.51,
    3.59-3.78(m, superpos. 5H), 2.69-3.21(m, superpos. 38.55, 41.94/42.19, 47.32,
    5H), 2.14-2.29(m, 1H), 1.90-2.12(m, 3H), 52.56, 59.12,
    1.22-1.28(d, 3H) 69.90/70.29, 77.89/78.00,
    173.01, 173.48
    Vy (CDCl3, 300MHz): δ 8.5(s, 1H), 2.94-3.02(t, (CDCl3, 75.48MHz): δ 15.41,
    2H), 2.62-2.72(q, 2H), 2.33(s, 3H), 1.38-1.45(t, 26.41, 31.51, 39.72, 129.36,
    1H). 149.90
    Vz (CD3CN, 300MHz): 4.60-4.68(1H, dd, J 11.44, (CD3CN, 75.48MHz): 76.33,
    3.36), 4.43-4.52(1H, dd, J 11.35, 6.97), 67.34, 42.74
    4.11-4.21(1H, m), 2.80-3.00(2H, m)
    Vaa (CDCl3, 300MHz): δ 8.05-8.15(m, arom 2H), (CDCl3, 5.48MHz): δ 36.42,
    7.55-7.65(m, arom 1H), 7.25-7.35(m, arom 1H), 52.87, 69.98, 77.69, 126.07,
    5.40-5.55(m, 1H), 4.85-4.95(dd, 1H), 4.60-4.70(dd, 1H), 126.45, 128.01, 132.06, 133.53,
    3.95(s, 3H), 2.90-3.10(m, 2H) 140.161, 167.10
    Vab (CDCl3, 300MHz): δ 7.30-7.39(m, arom 5H), (CDCl3, 75.48MHz): δ 32.01,
    5.28-5.37(m, 1H), 4.72-4.78(dd, 1H, J 12.86, 2.79), 35.997, 43.66, 69.89, 77.72,
    4.45-4.53(dd, 1H, J 12.86, 5.9), 3.95(s, 2H), 128.33, 129.22, 129.81, 137.22
    2.44-2.52(dd, 1H, J 14.38, 6.1), 2.33-2.42(dd, 1H, J 14.38,
    7.34)
    Vac 1H-NMR(CDCl3, 300MHz): 5.48-5.58(1H, m), 13C-NMR: (CDCl3, 75.48MHz):
    4.89(1H, ddd, J 12.91, 2.91, 1.21), 4.56-4.70(2H, 77.30, 74.22, 69.46,
    m), 4.48(1H, dd, J 11.41, 6.4), 4.16-4.26(1H, m), 69.38, 66.90, 66.78, 42.12,
    2.94-3.12(2H, m), 2.81-2.91(2H, m) 41.99, 36.82, 36.59
    Vad (CDCl3, 400MHz): 5.55-5.65(m, 1H), (CDCl3, 400MHz): 76.74,
    4.87-4.94(dd, 1H, J 12.94, 2.94), 4.62-4.70(m, 1H, J 12.88), 69.46/69.42, 36.65/36.63
    3.13-3.30(m, 2H)
  • It will be noted that the structure of some of the compounds of this invention include asymmetric carbon atoms. It is to be understood accordingly that the isomers (e.g., enantiomers, diastereomers) arising from such asymmetry are included within the scope of this invention. Such isomers can be obtained in substantially pure form by classical separation techniques and by asymmetric synthesis (for example, see below in Example 21). Unless expressly noted to the contrary, compounds referred to herein shall be construed to include both the R and S stereolsomers at each stereogenic centre.
  • In certain embodiments, a therapeutic compound of the invention comprises a cation (i.e., in certain embodiments, one of X or Y includes a cation, e.g., in the compound of formula IVd). If the cationic group is a proton, then the compound is considered an acid. If the proton is replaced by a metal ion or its equivalent, the compound is a salt. Pharmaceutically acceptable salts of the therapeutic compound are within the scope of the invention. For example, M can be a pharmaceutically acceptable alkali metal (e.g., Li, Na, K), ammonium, alkaline earth metal (e.g., Ca, Ba, Mg), higher valency cation, or polycationic counter ion (e.g., polyammonium cation) (see e.g., Berge et al. (1977)). It will be appreciated that the stoichiometry of an anionic portion of the compound to a salt-forming cation will vary depending on the charge of the anionic portion of the compound and the charge of the counterion. Preferred pharmaceutically acceptable salts include a sodium, potassium, or calcium salt, but other salts are also contemplated within their pharmaceutically acceptable range.
  • Therapeutic compounds of the invention can be administered in a pharmaceutically acceptable vehicle. As used herein “pharmaceutically acceptable vehicle” includes any and all solvents, excipients, dispersion media, coatings, antibacterial and antifuangal agents, isotonic and absorption delaying agents, and the like which are compatible with the activity of the compound and are physiologically acceptable to the subject. An example of a pharmaceutically acceptable vehicle is buffered normal saline (0.15 M NaCi). The use of such media and agents for pharmaceutically active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the therapeutic compound, use thereof in the compositions suitable for pharmaceutical administration is contemplated. Supplementary active compounds can also be incorporated into the compositions.
  • Carrier or substituent moieties useful in the present invention may also include moieties which allow a therapeutic compound to be selectively delivered to a target organ. For example, delivery of a therapeutic compound to the brain may be enhanced by a carrier moiety using either active or passive transport (a “targeting moiety”). Illustratively, the carrier molecule may be a redox moiety, as described in, for example, U.S. Pat. Nos. 4,540,654 and 5,389,623, both to Bodor. These patents disclose drugs linked to dihydropyridine moieties which can enter the brain, where they are oxidized to a charged pyridinium species which is trapped in the brain. Thus drugs accumulate in 45 the brain. Other carrier moieties include compounds, such as amino acids or thyroxine, which can be passively or actively transported in vivo. Such a carrier moiety can be metabolically removed in vivo, or can remain intact as part of an active compound. Structural mimics of amino acids (and other actively transported moieties) including peptidomimetics, are also useful in the invention. As used herein, the term “peptidomimetic” is intended to include peptide analogs which serve as appropriate substitutes for peptides in interactions with e.g., receptors and enzymes. The peptidomimetic must possess not only affinity, but also efficacy and substrate function. That is, a peptidomimetic exhibits functions of a peptide, without restriction of structure to amino acid constituents. Peptidomimetics, methods for their preparation and use are described in Morgan et al., (1989) “Approaches to the discovery of non-peptide ligands for peptide receptors and peptidases”. In Annual sorts in Medicinal Chemistg (Vinick, FJ., ed.) pp. 243-252, Academic Press, San Diego, Calif. Many targeting moieties are known, and include, for example, asialoglycoproteins (see e.g., Wu, U.S. Pat. No. 5,166,320) and other ligands which are transported into cells via receptor-mediated endocytosis (see below for further examples of targeting moieties which may be covalendy or non-covalently bound to a target molecule).
  • In the methods of the invention, pain and/or inflammation in a subject is mitigated by administering an analgesic, sedative or anti-inflammatory therapeutic compound of the invention to the subject. The term “subject” is intended to include living organisms in which pain can occur. Examples of subjects include humans, apes, monkeys, cows, sheep, goats, dogs, cats, mice, rats, and transgenic species thereof. Administration of the compositions of the present invention to a subject to be treated can be carried out using known procedures, at dosages and for periods of time effective to alleviate pain in the subject. An effective amount of the therapeutic compound necessary to achieve a therapeutic effect may vary according to factors such as the subject, the age, sex, and weight of the subject, and the ability of the therapeutic compound to mitigate pain and inflammation in the subject. Dosage regimens can be adjusted to provide the optimum therapeutic response. For example, several divided doses may be administered daily or the dose may be proportionally reduced as indicated by the exigencies of the therapeutic situation. A non-limiting example of an effective dose range for a therapeutic compound of the invention (e.g., Va) is between 0.5 and 5000 mg/kg of body weight/per day, preferably between 50 and 1000 mg/kg/day, and still more preferably between 250 and 750 mg/kg/day. In an aqueous composition, preferred concentrations for the active compound (i.e., the therapeutic compound that can mitigate pain) are 46 between 5 and 500 mM, more preferably between 10 and 100 mM, and still more preferably between 20 and 50 mM.
  • According to the invention, therapeutic compounds are administered to a subject by a route which is effective for mitigating inflammation, effecting analgesia and/or effecting sedation. Suitable routes of administration include but are not limited to sublingual, oral, buccal, transdermal, nasal, subcutaneous, intraocular, intravenous, intramuscular and intraperitoneal (e.g., by injection). Preferred routes of administration are oral and transdermal. The therapeutic compounds can be administered with a pharmaceutically acceptable vehicle. Depending on the route of administration, the active compound may be coated in a material to protect the compound from the action of acids, enzymes and other natural conditions which may inactivate the compound.
  • Therapeutic compounds of the invention can be formulated to ensure proper distribution in tivo. For example, the blood-brain barrier (BBB) excludes many highly hydrophilic compounds. To ensure that the therapeutic compounds of the invention cross the BBB, they can be formulated, for example, in liposomes. For methods of manufacturing liposomes, see, e.g., U.S. Patents 4,522,811; 5,374,548; and 5,399,331. The liposomes may comprise one or more moieties which are selectively transported into specific cells or organs (“targeting moieties”), thus providing targeted drug delivery (see, e.g., Ranade et al., 1989). Exemplary targeting moieties include folate or biotin (see, e.g., U.S. Patent 5,416,016 to Low et al.); mannosides (Umezawa et al., 1988); antibodies (Bloeman et al., 1995; Owais et al., 1995); surfactant protein A receptor (Briscoe et al., 1995). In a preferred embodiment, therapeutic compounds of the invention are formulated in liposomes; in a more preferred embodiment, the liposomes include a targeting moiety.
  • Delivery and in tvito distribution can also be affected by alteration of an anionic group of compounds of the invention. For example, anionic groups such as phosphonate or carboxylate can be esterified to provide compounds with desirable pharmocokinetic, pharmacodynamic, biodistributive, or other properties. Exemplary compounds include Mi and pharmaceutically acceptable salts or esters thereof To administer a therapeutic compound by other than parenteral administration, it may be necessary to coat the compound with, or co-administer the compound with, a material to prevent its inactivation. For example, a therapeutic compound may be administered to a subject in an appropriate carrier, for example, liposomes, or a diluent. Pharmaceutically acceptable diluents include saline and aqueous buffer solutions. Liposomes include water-in-oil-in-water CGF emulsions as well as conventional liposomes (Strejan et al, J. Neuroimmunol. (1984) 7, 27). 47
  • A therapeutic compound may also be administered parenterally (e.g., intramuscularly, intravenously, intraperitoneally, intraspinally, or intracerebrally). Dispersions can be prepared in glycerol, liquid polyethylene glycols, lactose, dextrose and mixtures thereof and in oils. Under ordinary conditions of storage and use, these preparations may contain a preservative to prevent the growth of microorganisms. Pharmaceutical compositions suitable for injectable use include sterile aqueous solutions (where water soluble) or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersion. In all cases, the composition must be sterile and must be fluid to the extent that easy syringability exists. It must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms such as bacteria and fungi. The vehicle can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (for example, glycerol, propylene glycol, dextrose, and liquid polyethylene glycol, and the like), suitable mixtures thereof, and vegetable oils. The proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants.
  • Prevention of the action of microorganisms can be achieved by various antibacterial and antifungal agents, for example, parabens, chlorobutanol, phenol, ascorbic acid, thimerosal, and the like. In some cases, it will be preferable to include isotonic agents, for example, sugars, sodium chloride, or polyalcohols such as mannitol and sorbitol, in the composition. Prolonged absorption of the injectable compositions can be brought about by including in the composition an agent which delays absorption, for example, aluminum monostearate or gelatin.
  • Sterile injectable solutions can be prepared by incorporating a therapeutic compound in the required amount in an appropriate solvent with one or a combination of ingredients enumerated above, as required, followed by filter sterilization. Generally, dispersions are prepared by incorporating the therapeutic compound into a sterile vehicle which contains a basic dispersion medium and the required other ingredients from those enumerated above. In the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum drying and freeze-drying which yields a powder of the active ingredient (i.e., the therapeutic compound) plus any additional desired ingredient from a previously sterile-filtered solution thereof.
  • A therapeutic compound can be orally administered, for example, with an inert diluent or an assimilable edible carrier. A therapeutic compound and other ingredients may also be enclosed in a hard or soft shell gelatin capsule, compressed into tablets, or incorporated directly into the subject's diet. For oral therapeutic administration, a therapeutic compound may be incorporated with 48 excipients and used in the form of ingestible tablets, buccal tablets, troches, capsules, elixirs, suspensions, syrups, wafers, and the like. The percentage of therapeutic compound in the compositions and preparations may, of course, be varied. The amount of therapeutic compound in such therapeutically useful compositions is such that a suitable dosage will be obtained.
  • It is especially advantageous to formulate parenteral compositions in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used herein refers to physically discrete units suited as unitary dosages for the subjects to be treated; each unit containing a predetermined quantity of therapeutic compound calculated to produce the desired therapeutic effect in association with the required pharmaceutical vehicle. The specification for the dosage unit forms of the invention are dictated by and directly dependent on (a) the unique characteristics of the therapeutic compound and the particular therapeutic effect to be achieved, and (b) the limitations inherent in the art of compounding such a therapeutic compound for the treatment of pain and inflammation in subjects, or effecting sedation.
  • A therapeutic composition can be administered in time-release or depot form, to obtain sustained release of a therapeutic compound over time. A therapeutic compound of the invention can also be administered transdermally (e.g., by providing a therapeutic compound, with a suitable carrier, in patch form, or in an unguent or cream).
  • Active compounds are administered at a therapeutically effective dosage sufficient to mitigate pain and/or inflammation in a subject. The ability of a compound to mitigate pain or inflammation can be evaluated in model systems that may be predictive of analgesia and anti-inflammation in human diseases, such as animal model systems known in the art (including, e.g., the preclinical acute pain writhing model in the mouse; and the formalin-sensitization model of tissue injury pain in the rat) or by in mitro methods, (including, e.g., the assays described above and below, tide infra). The ability of a compound to effect sedation can be evaluated in model systems that may be predictive of sedation of use in treatment of human diseases, such as animal model systems known in the art (including, e.g., the loss of the righting reflex in the mouse as described, tide infra) or by in vitro methods, (including, e.g., modulation of the activity of GABAA receptors as described above and below, tide infra).
  • It will be appreciated that the ability of a compound of the invention to mitigate pain and/or inflammation, in certain embodiments, be evaluated by observation of one or more symptoms or signs associated with pain and inflammation in vivo. Thus, for example, the ability of a compound to alleviate pain may be associated with an observable improvement in a clinical manifestation of the 49 underlying pain or inflammation related disease state or condition, or a slowing or delay in progression of symptoms of the condition. Thus, monitoring of clinical manifestations of disease can be usefuil in evaluating the analgesic, sedative and anti-inflammatory efficacy of a compound of the invention.
  • Treating or mitigating pain may involve effecting analgesia, effecting sedation, inhibiting or preventing inflammation, and/or ameliorating the manifestations or impact of pain inducing stimuli. Modulating a biological process such as the biological levels of cGMP or cAMP, or activity of soluble GCase, includes regulating increases and decreases in such activity, and inhibition, potentiation, agomism, or antagonism of the biological process.
  • Methods of the invention are useful for treating pain and/or inflammation associated with any disease in which pain or inflammation occurs. Clinically, pain and inflammation can be associated with, but not limited to, tissue injury, post-operative tissue injury, nerve injury, post-herpetic neuralgia, phantom limb pain, diabetic neuropathy, arthritis, dysmenorthea, endometriosis, cancer, chemotherapy, myocardial infarction, cerebral vascular occlusion, or result from surgical procedures.
  • Certain compounds for use in the methods of the invention are commercially available, whereas others are novel (see hereinbelow and applicants' co-pending application U.S. Ser. No. 09/267,379, filed Mar. 15, 1999, now U.S. Pat. No. 6,310,052). Both types can be synthesized by standard techniques known in the art. In general, nitrate esters can be prepared from the corresponding alcohol, oxirane or alkene by standard methods that include: nitration of alcohols and oxiranes, mixed aqueous/organic solvents using mixtures of nitric and sulfuric acid and/or their salts, with temperature control (see Yang et al., 1996); nitration of alcohols and oxiranes in acetic anhydride using nitric acid or its salts with or without added acid catalyst, with temperature control (see, e.g., Louw, et al., 1976); nitration of an alcohol with a nitronium salt, e.g., a tetrafluoroborate; nitration of an alkene with thallium nitrate in an appropriate solvent (Ouellette et al., 1976). Compounds of the present invention also can be prepared as described below.
  • The contents of all scientific publications and patent documents cited herein are hereby incorporated herein by reference in their entirety.
  • The following Examples further illustrate the present invention and are not intended to be limiting in any respect.
    • EXAMPLES Example 1
  • Characterization of Guanylyl Cyclase Activation
  • Activation of soluble guanylyl cyclase (GCase) by nitrates IIIm, IVa, IVb, WVd, IVe, WVf, Ig, WVj, Va, Vb, and GTN was assayed employing partially purified enzyme freshly prepared from the 105,000 g supernatant fraction of rat aorta homogenates, using the radioimmunoassay method described by Bennett et al. (1992). Dose-response curves were obtained for GCase activation by nitrates IVa, IVb, IVd, IVe, IVf, IVg, IVj, and GTN in the presence and absence of cysteine and dithiothreitol (DTT; both 2mM). In all cases, data were normalized to the maximal GTN response carried out in identical GCase preparations. Experimental incubations were performed at 37° C for 10 min. The data for WVd is summarized in FIG. 1. The GCase assay data show that WVd activates GCase, with a submiulimolar EC-50 (effective concentration for 50% of the subjects) in the absence of any added thiol, in contrast to GTN, which requires added cysteine. Compounds WVd also activates GCase in the presence of DTT, in contrast to GTN, which, emgmatically, does not. Relative to GTN itself, a wide range of potency was observed for these novel nitrate esters. No activation of GCase by glycerol mononitrates was observed in this assay at the concentrations of nitrate employed.
  • Activation of GCase, in titrv, by some of these organic nitrates is via release of NO, since in the presence of cysteine, substantial NO is released at rates which are measurable amperometrically, using the method described by Artz and Thatcher (1998). By comparison, nitroglycerin, which is currently understood by others skilled in the art to act only as an NO-donor therapeutic agent, does not release NO at a rate measurable amperometrically, in the absence nor the presence of cysteine. Relative rates for NO release, at 37° C, pH 7.4, in the presence of cysteine (2mM) from nitrates Vj, Vu, Vi, Vh, Vg, Vf, and Ve, (lmM) were 1.0, 1.0, 1.8, 0, 1.2, 0.5, 1.8, respectively. Thus modification of the structure of these organic nitrates can be used to control their NO-releasing ability and also to modulate GCase activity.
  • To test for potential differences in GCase activation by nitrates, the effects of IlIm, IVh, Va, Vb, and GTN were assayed in brain and vascular tissue. WI) had no effect on GCase activity in either rat aorta or rat hippocampus (FIG. 2). IIm had greater efficacy to stimulate GCase activity compared to GTN in both rat aorta and rat hippocampus (FIG. 2). Vb was found to be equivalent to GTN in efficacy and potency for activation of GCase in both rat aorta and rat hippocampus (FIG. 3). Va was found to have greater efficacy, but equal potency, to GTN in rat aorta (FIG. 3a). In contrast, Va had greater efficacy and greater potency to stimulate GCase in rat hippocampus (FIG. 3b). These data illustrate that nitrates have differential effects on GCase activation that are dependent on both structure of the compound and the tissue assayed for GCase activity, supporting the notion that effects of nitrates elicited through GCase activation, such as analgesia and vasodilation, are separable and may be regulated in a tissue-specific and/or activity-specific manner, by appropriate choice of organic nitrate.
  • As further examples of the potential for modulating potency, efficacy and tissue selectivity for activation of GCase, by choice of an appropriate organic nitrate, nitrates Vaa and Vt were assayed in brain and vascular tissue. In the presence (+) and absence (-) of lmM cysteine, the potency (EC-50 values) and efficacy (maximal activation) were measured for activation of GCase from rat hippocampus (Table 2).
    TABLE 2
    maximal (hipp.), maximal (aorta),
    1 mM cysteine EC-50 (hipp.), M EC-50 (aorta), M relative to GTNa relative to GTNa
    Vaa + 1.4 × 10−4 1.8 × 10−4 5.1 2.2
    Vaa − 5.7 × 10−5 1.8 × 10−4 2.1 1.0
    Vt + 5.1 × 10−5 6.5 × 10−5 3.0 2.3
    Vt − 1.7 × 10−5 1.8 × 10−6 1.8 1.7

    aNormalized to GTN + 1 mM cysteine maximal response.
    • Example 2
  • Characterization of Cyclic GMP Accumulation
  • In order to extend the GCase data further, the effects of nitrates Va, IlIm, Vb, Vc, and WVk on cyclic GMP accumulation in intact isolated rat aorta were examined (FIGS. 4, 5). Thoracic aortic strips were prepared from male Sprague-Dawley rats (Charles-River, Canada) as described in McGuire et al. (1994) and Stewart et al. (1989). Tissues were contracted submaximally with phenylephrine (0.1CtM) and exposed to various concentrations of drug for 1 min. Cyclic GMP accumulation was determined using the radioitnmunoassay method described by Bennett et al. (1992). At concentrations of 1 liM and 10 AM, GTN and WVk significantly increased cGMP accumulation (FIGS. 5). At a concentration of 1 AM, Va, IIlm, Vb, and Vc did not significantly increase cyclic GMP accumulation (FIGS. 4a, 5a). At a concentration of 10 [tM, Va, Vb, and WVk significantly increased cyclic GMP accumulation whereas IIIm and Vc did not (FIGS. 4b, 5b).
  • Sections of rat hippocampus (400 lim) were prepared and incubated in oxygenated Krebs solution at 37° C. After a 60-min equilibration period, the brain slices were stimulated with different concentrations of Va or GTN for 3-trin. Cyclic GMP accumulation was determined as described above for aortic strips. FIG. 6 shows that Va causes a concentration-dependent increase in the tissue levels of cGMP in rat hippocampal brain slices in vitro, and that at high concentration (100 lM) Va is more effective than GTN in elevating cGMP levels in hippocampal brain slices in vitm. These data are in very good agreement with the differential effects of Va and GTN on hippocampal GCase activity shown in FIG. 3 b.
    • Example 3
  • Characterization of Relaxation of Isolated Blood Vessels
  • In order to extend the GCase data, the relaxing effects of nitrates Illm, WVc, WVd, WVf, WVg, WVh, Wk, Va, Vb, and Vc on rat aortic tissue were examined. Thoracic aortic strips were prepared from male Sprague-Dawley rats (Charles-River, Canada) as described in McGuire et al. (1994), and Stewart et al. (1989). Tissues were contracted submaximally with phenylephrine (0.1 pM) and exposed to various concentrations of nitrovasodilator to obtain concentration-response curves. In this intact tissue assay, all of the nitrates were observed to cause relaxation of the tissue with a maximal relaxant response equal to that obtained with GTN. However, the compounds differed in potency, with EC-50 values of 7.87 nM, 94.3 nM, 6.59 ,M, 25.2 tM, 11.0 μM, and 0.203 μM, for GTN and compounds Va, IVd, IVg, WVf, and IVc, respectively (FIG. 7,8). In another series of experiments, the EC-50 values for relaxation were 0.61 nM, 3.19 nM, 8.40 nM, 0.153 μM, 0.437 μM and 6.89 lM for GTN, WVk, Vb, IIIm, Vc, and IVh, respectively (FIG. 7,8). Compounds WVd and WVc were tested for their ability to cause vascular relaxation in tissues that had been made tolerant to the relaxant effect of GTN. GTN tolerance was induced by incubating tissues with high concentrations of GTN (0.5 mM GTN for 30 min). Under these conditions, the maximal relaxant effects of WVd (FIG. 12 a) and WVc (FIG. 12 b) were not significantly different to that of untreated tissue. The EC-50 for relaxation was imcreased approximately threefold, but the difference was not statistically significant.
    • Example 4
  • Characterization of Blood Pressure Changes in the Whole Animal
  • To test for differential effects of nitrates on blood pressure responses, Va and GTN were injected into rats in which the abdominal aorta was cannulated for blood pressure recording. In the first experiment, Va and GTN were injected subcutaneously at a dose of 400 lmol/kg body weight into conscious, freely moving animals. GTN caused a small and transient decrease in blood pressure in these animals, whereas Va had no discernable effect on arterial blood pressure (FIG. 9). Va and GTN were subsequently tested in anesthetized rats in which the abdominal vena cava was also cannulated to allow for bolus intravenous injection of drugs. In this preparation, GTN caused a substantial and dose-dependent decrease in arterial blood pressure. In contrast, Va at equal doses had very modest effects on blood pressure at doses lower than 2 lmol/kg body weight (FIG. 10). These data are in very good agreement with the results obtained for these two agents using the isolated blood vessel preparation.
  • The plasma levels of nitrates Vb and Vc (the denitrated metabolite of Vb) were measured to gain insight into the handling of these molecules in the body. Cannulas were placed in the abdominal aorta for blood sampling. After a two-day recovery period, a single subcutaneous dose of Vb (200 lmol/kg) was administered and blood samples collected over a period of six hours. Samples were centrifuged, the plasma collected, and the concentration of Vb and Vc determined by gas-liquid chromatography by the method of McDonald and Bennett (1990). The data obtained for Vb and Vc indicate that nitrates achieve maximal plasma levels within 30 minutes after subcutaneous injection, and therafter decline at a steady rate (FIG. 11). These data suggest that nitrates have excellent bioavailability after subcutaneous injection.
    • Example 5
  • Characterization of the Analgesic Effects of Novel Organic Nitrates in a Model of Acute Pain
  • Injection of dilute acetic solutions into the peritoneum of a mouse induces writhing movements that can be quantified. We adopted the methodology described by Bak et al. (1998) to test for analgesic effects of organic nitrates in this mouse model. Each mouse was given an intraperitoneal injection of 0.5 mL of a 0.6% solution of acetic acid in distilled water. After a 5 minute delay, the number of writhing movements was counted over a 10 minute period. To test the efficacy of novel organic nitrates in this model, drugs were administered at doses of 100-500 mg/kg given by subcutaneous injection) 15 minutes before the intraperitoneal injection of acetic acid. In this model of acute pain, Vm induced a significant, dose-dependent analgesic effect, manifested as a decrease in the number of writhes per 10 minute period after intraperitoneal injection of dilute acetic acid (FIG. 13 a). Va was also able to act as an analgesic (decreased writhing) in this experimental model when administered at a dose of 500 mg/kg subcutaneously (FIG. 13b).
    • Example 6
  • Characterization of the Analgesic Effects of Novel Organic Nitrates in a model of Hyperalgesia/Allodymia
  • Under light halothane anesthesia, male Sprague-Dawley rats were injected subcutaneously with 0.05 mL of 5% formnalin into the dorsal surface of one hind paw as described in Malmberg and Yaksh (Anesthesiology (1993) 79, 270-281). The number of spontaneous paw flinches was determined in 1 minute blocks at 5 minute intervals for 60 minutes. Fortnalin injection in the paw produces two distinct phases of pain; an acute phase occurring within the first 5-10 minutes, and a delayed phase that develops between 15-30 minutes after formalin injection. The acute phase of the pain response to formalin is caused by activation of peripheral nociceptive sensory afferents (C-fibres) by the peripheral stimulus. The delayed pain response is considered to be a hyperalgesia/allodynia caused by a combination of sensitization of peripheral sensory afferents and sensitization of synaptic connections in the spinal cord. The formalin test in the rat is considered to be an appropriate model for tissue injury pain occurring in humans (Tjolsen et al., Pain (1992) 51, 5-17; Yaksh, 77PS (1999) 20, 329-337). In this experimental model of inflammatory tissue injury pain, Vm (500 mg/kg) significantly reduced both phases of the pain response to formalin injection (FIG. 14a,b).
    • Example 7
  • Synthesis of IIIe
  • To acetic anhydride (3 iL) was added gradually, with strring, 70% nitric acid (0.26 mL), while keeping the temperature between 20-300 by external cooling. With continuous vigorous stiring the mixture was cooled to -30-350 and 2′,3′-dideoxy-3-thiocytosine (0.25 g) was added. After 10 nrn at -35o, the reaction mixture was heated up to -200 and then stirred at -20-100 for 15 min and 10 min at 00. The resulting reaction mixture was poured into ice-water, stirred for 1 h, then NaHCO3 was added by portions until CO2 evolution ceased. The water solution was extracted with 3×20 mL of ethyl acetate. Combined extracts were dried (MgSO4) and concentrated. 0.38 g of slightly yellowish oil was obtained. The oil crystallized in a day and was recrystallized from CHCl3. Yield 52%. Conversion to the nitrate was evidenced by the significant downfield shift of the C5′ proton multiplet from 6 3.6 to 4.85 ppm.
    • Example 8
  • Synthesis of Nitrate IIIf
  • 0.26 mL (4.15 rumol) conc. HNO3 was added to 2 mL acetic anhydride such that the temperature did not exceed 25-30° C. The mixture was cooled at 0-5° C. and 0.3 g (1.88 mmol) of 5-(1,2-dihydroxyethyl)-4-methylthiazole was added in several portions, the temperature being kept below 5 OC. The reaction mixture was stirred at 0-5° C. for 45 min and then 0.45 mL water was added. The mixture was stirred for 30 rnin and then rotavary evaporated. The residue was neutralized by adding 5 mL of saturated NaHCO3 solution and the organic product was extracted with ethyl acetate. The organic layer was concentrated and the dinitrate Illf was purified through column chromatography (silica gel/ethyl acetate eluant). A slightly yellow solid was obtained. Yield: 0.150 g (32%).
    • Example 9
  • Synthesis of Nitrate IIIi
  • Nitrate IIIi was obtained by two routes. Route I proceeded from the elimination reaction of IIIm in basic solution. Route II proceeded from nitration of trans-3-bromo-4-hydroxytetrahydrothiophene-1,1-dioxide, yielding nitrate Illn, followed by reaction with a weak base, e.g., sodium thiocyanate in 2-butanone. Purification may be achieved with silica flash column chromatography using 1:1 hexane:ethyl acetate as eluant.
    • Example 10
  • Synthesis of Nitrate HIIj 1,4-Dibromo-2,3-butanediol may be nitrated: (a) using a nitration mixture prepared from HNO3 and H2SO4 over 2 days; or (b) using acetyl nitrate reacting for 2 hours. Work-up requires quenching of the reaction mixture in ice-water for an hour, extraction, drying, and evaporation. Successful purification of the title compound by silica gel column chromatography is achieved on a 25 g scale using a mixture of 70% hexane and 30% CH2CI2 as eluent.
    • Example 11
  • Synthesis of Nitrate Ve
  • 4-Methylbenzenethiol was obtained by adaptation of literature procedures from p-toluidine (.-P. Morizur, Bull Soc. Chim. Fr. (1964) 1338-1342; Bourgeois, Recl. Trav. Chim. Pays-Bas (1899) 18, 445-450). p-Toluidine hydrochloride (14.2 g, 0.098 mole) was diazotised at 5OC with concentrated hydrocloric acid (16.5 mL) and sodium nitrite (7.2 g, 0.104 mole) in water (12 mL). The solution of diazonium salt was added over 1.5 h to a solution of ethyl xanthate (24 g, 0.149 mole) in water (30 niL) at 45-500C. The mixture was kept at this temperature, under strring, for a further 1 h. The xanthate ester was separated as a maroon oil, washed with 50 mL 10% NaOH and with water to neutral pH and dried over MgSO4 (20g of crude product). The crude xanthate was dissolved in 60 mL absolute ethanol and to this solution 20 g KOH (pellets) were added in portions. The reaction mixture was refluxed under stiring and Ar for 8 h, then concentrated under vacuum. The concentrate was taken up in 50 niL H 20 and extracted with 3x100 mL diethyl ether. The aqueous layer was acidified with a 6N H2SO4 solution and extracted with 3x100 mL CH2Cl2. The combined extracts were washed with water, dried over MgSO4, evaporated and flash columned on silica gel, eluant hexanes:ethyl acetate=9:1, giving 10 g (81.56%/0) of 4-methylbenzenethiol. 1H-NMR(CDCl3, 300 MHz):7.18-7.24 (m, arom 2H), 7.04-7.11 (d, arom 2H,J 7.93), 3.41(s, 1 H), 2.32(s, 3H). 13C-NMR(75.48 MHz): 21.34, 128.95, 130.24,130.29,136.05.
  • The dinitrate WVd (9.67 mmoles) was dissolved in 10 niL distilled water and the solution kept under Ar for 30 minutes. To this solution, a solution of 0.8 g (6.46 rnnoles) of 4-methylbenzenethiol and 7 nL 1M NaOH was added dropwise. The resulting emulsion was stirred for 15 min and then extracted with 3×20 mL CH2Cl2. The combined organic extracts were washed with H2O, dried over MgSO4 and concentrated under vacuum. The remaining oil was purified by flash column chromatography on silica gel, eluant hexanes: ethyl acetate=9:1, giving the product Ve (1.097 g, 52.22%). 1H-NMR(CDCl3, 300 MHz):7.44-7.51 (m, atom 2H), 7.17-7.24 (d, atom 2H,J 7.91), 5.47-5.59 (m, 1H), 4.83-4.93 (dd, 1H,J 12.81, 2.78), 4.57-4.67 (dd, 1H,J 12.82, 5.71), 3.02-3.12 (dd, 1H,J 14.48, 6.01), 2.9-2.99 (dd, 1H,J 14.47, 7.72), 2.38 (s, 3H). 13C-NMR(75.48 MHz): 21.53, 36.78, 69.82, 77.68, 130.52, 130.62, 132.55, 139.23.
    • Example 12
  • Synthesis of Nitrate IIIm 3,4-Epoxytetrahydrothiophene-1,1-dioxide (250 mg,1.9 nmnol) was refluxed for 24 h in 10 miL of water and 25mg of toluenesulfonic acid. After the first 6 h, another 25 mg of the acid was added. The reaction was monitored by thin layer chromatography (LLC) (5% methanol in dichloromethane). Purification was by Si flash column chromatography using 5% methanol/CH2Ck2 as eluent to afford 200 mg of diol. The diol was nitrated in a cooled solution of conc. sulfuric acid (2 mol eq.), nitric acid (70%, 2 mol eq.) in an ice bath. The temperature was maintained as close to O° C as possible. The ice bath was removed and the mixture was allowed to stir for 1 hour (reaction was monitored by TLC, 100% CH2Cl2 eluent). The acid layer was removed and the organic layer washed with: (i) water; (ii) 10% sodium carbonate; (iii) 100% urea; (iv) water. Drying over sodium sulfate, filtration and concentration, yielded crude product which was purified by flash column chromatography, with dichloromethane as eluent. An alternative route involves direct nitration of 3,4-epoxytetrahydrothiophene-1,1-dioxide in a similar nitration mixture.
    • Example 13
  • Synthesis of Nitrate IVk
  • 1.17 niL (18.2 nmuol) concentrated HNO3 was added, under stirring and cooling (0-5 OC), to 1 mL (18.2 mmol) concentrated H2SO4 and then 2 g (14 mmol) of 4-methyl-5-(2-hydroxyethyl)thiazole was added dropwise into the nitration mixture, the temperature being kept under 10 OC. The mixture was stirred for 3 hours at room temperature, diluted with 10 niL of water and neutralized with solid NaHCO3. The organic product was extracted with ethyl acetate and purified by column chromatography (silica gel/ ethyl acetate eluant) to produce a colorless oily product. Yield: 1.18 g (45%).
    • Example 14
  • Synthesis of Nitrate IVi
  • 0.03 g (0.035 niL) of allyl cyanide was added to a stirred suspension of 0.22 g (0.5 mmol) of Tl (NO3)3.3H2O in 2 mL of pentane. After 20 min of vigorous stirring the pentane solution was decanted and evaporated to dryness. After evaporation the residual oil (0.44 g) was columned (CH2Cl2, Rf 0.64 (CH2Cl2). Clean oil rmmediately crystalized during attempt to dissolve it in CDCl3. Yield 0.065 g (76%). The structure of IVn was confirmed by X-ray analysis. IR (film): 1297.03, 1678.91, 2258.91 (CN). Mass spec. m/z (CI+, fragment, %): 191.9 (M+H, 2.44), 129.0 (16.41), 81.9 (100). Calculated for C4H5N306 191.02.
    • Example 15
  • Synthesis of Nitrate IVm
  • 0.9 g (0.75 nL, 4.92 mmol) of allyphenyl sulfone was added dropwise to a stirred suspension of 2.43 g (5.47 mmol) of T1 (NO3)3.3H20 in 10 mL of pentane. The resulting mixture was stirred overnight. The pentane solution was decanted. 2x10 mL of methanol were added to the reaction mixture, stirred for 10 minutes and extracts were added to the pentane solution. The combined extracts evaporated to dryness and purified by silica flash column chromatography using CH2CI2 as eluant. Yield 0.08 g (15%). IR (KBr): 1152.39, 1290.91, 1273.12, 1353.83, 1646.08. Mass spec. m/z (CI+fragment, %): 307.0 (M+1, 66.5), 244.0 (100%). Calculated for CgHloN208S 306.02.
    • Example 16
  • Synthesis of Nitrate Va
  • 2.2 g (7.3 nmmol) of nitrate IVd was dissolved in 5 g of cold H202 (30%, 0° C) and then 1 g of 10% H2SO4 was added. The mixture was stirred at 0-5 ° C. until a white oil separated (ca. 30-60 min). The aqueous layer was discarded and the oil was dissolved in dichloromethane, washed successively with water, then NaHCO3 solution and finally water. The organic solution was dried over MgSO4. Removal of the solvent produced 1.3 g of the crude product which was purified by column chromatography (Silicagel, CH2Cl2/hexanes: 70/30). Yield: 0.650 g (45%).
    • Example 17
  • Synthesis of Nitrate Vc
  • 3 g (8.88 nimol) of 1,4-dibromo-2,3-dinitrobutanediol and 2.81 g (18 inmol) of Na2S2O3.5H2O were dissolved in the mixture of 100 niL of methanol and 45 mL of H2O. The resulting solution was heated during 4 days at 40-45°. After this time the reaction mixture was partially evaporated to reduce the volume of solvents. The resulting mixture was extracted 4x50 niL of ethyl ether. The extracts were combined, washed (H20), dried (MgSO4) and evaporated to minimum. Column chromatography afforded the title compound in 10% yield, seperated from Vb the major product.
    • Example 18
  • Synthesis of Nitrate Vy
  • The title compound was synthesised by the reaction of rVd with 4-methyl-5-thiazole ethanthiol, in a similar procedure to that used in Example 11. The crude product was purified by column chromatography (Silicagel, ethyl acetate eluant) to give product (50 mg, 27.32%). 1H-NMR(CDCl3, 300 MHz): 8.22 (s, 1H), 5.49-5.6 (m, 1H), 4.9-5.00 (dd,1H), 4.64-4.78 (dd, 1H), 3.14-3.22 (t, 2H), 2.89-3.07 (m, 4F), 2.45 (s, 3F). Mass spec., m/z (EI+, fragment, %): 355.0 .Calculated for C9H13N3O6S3: 355.0. The 4-Methyl-5-tdliazole precursor was obtained from 4-methyl-5-thiazole ethanol, thiourea and hydrobromic acid by adaptation of literature procedures (R.L. Frank, P. V. Smith, J. Am. Chem. Soc. (1946) 68, 2103-2104). A mixture of 2 g 4-methyl-5-thiazole ethanol (13.965 mmoles), 1.063 g(13.965 mmoles) thiourea and 9.45 g (56 nimoles) hydrogen bromide as 48 % hydrobromic acid was refluxed for 7 h with stirring, under Ar. A solution of 2.24 g (56 mmoles) of NaOH in 20 mL of water was then added and the mixture was refluxed without stirring for 2 h. The layers were separated, and the acidified aqueous layer was extracted with three 30 mL portions of CH2Cl2. The extracts and original organic layer were combined, dried over MgSO4 and concentrated under vacuum to afford 1.9 g crude product which was purified by column chromatography using ethyl acetate as eluent (Yield 1.6 g, 75%). 1H-NMR(CDCl3, 300MHz): 8.5 (s, 1H), 2.94-3.02 (t, 2H),2.62-2.72 (q, 2H), 2.33 (s, 3H), 1.38-1.45 (t, 1H). 13C-NMR(75.48 MHz): 15.41, 26.41, 31.51, 39.72, 129.36, 149.90
    • Example 19
  • Synthesis of Nitrate IIIk and IIIl
  • Synthesis from dinitrate IIIj proceeded by refluxing with sodium ot potassium thiocyanate (2 eq.) in 2-butanone for 8 h. After cooling, a precipitate was removed by filtration and the filtrate was concentrated. Nitrates li1k and IIIl were separated by silica flash column chromatography with hexane/dichloromethane as eluent.
    • Example 20
  • Synthesis of Nitrate Vk.
  • IVd ( 0.43 g, 1.37 mmol) was dissolved in 10 mL of distilled water and the emulsion of 0.23 g (1.28 mmol) of the ethyl ester of thiosalycilic acid in 1.3 niL of 1 M NaOH was added. The resulting solution immediately became turbid and was stirred for 3 min, then extracted with ethyl acetate (4x15 iL). The resulting extracts were washed with H2O, dried (MgSO4), and concentrated by evaporation. The residue was flash columned on silica gel, eluant hexane:ethyl acetate=9:1 Rf 0.23), giving 0.27 g (55%) of Vk. 1H-NMR(CDCl3, 300 MHz): 8.06-8.12 (1H, dd,J 8.12, 0.36), 7.99-8.04 (IH, dd,J 7.8, 1.15), 7.51-7.59 (1H, m,J 7.24, 1.44), 7.21-7.29 (IH, m,J 7.35, 0.54), 5.40-5.49 (1H, m), 4.70-4.78 (1H, dd,J 13.04, 2.95), 4.33-4.45 (3H, m, superposition of dd a 13.08, 6.01) of 11H from CH2-ON02 and quart. from O-CI,-CH3), 2.66-2.87 (2H, m), 2.06-2.15 (2H, quart.,J 6.92), 1.35-1.43 (3H, t,J 7.14). 13C-NMR: (CDCl3, 75.48 MHz): 166.21, 140.41, 132.78, 131.46, 127.63, 125.48, 77.25, 71.03, 61.42, 32.51, 28.29, 14.17. Mass spec. m/z (EI+, fragment, %): 392.3 (M+, 3.69), 153 (100). Calculated for C13Hl6N208S2392.03 .
    • Example 21
  • Chiral Synthesis of Nitrate IVd
  • A 50 mnL round-bottom flask, equipped with a magnetic stirrer, was charged with 10 niL of tert-butyl alcohol, 10 m]L of water, and 2.8 g of a catalyst (AD-mix-B, Aldrich: K.B.Sharpless, W.Amberg, Y.L.Bennani, G.A.Crispino, J.Hartung, K.-S.Jeong, H.-L.Kwong, K.Morikawa, Z.-M.Wang, D.Xu, X.-L.Zhang,J.Otg.Chem. (1992) 57, 2768-2771). Stifling at room temperature produced two clear phases; the lower aqueous phase appears bright yellow. The mixture was cooled to 40 and 0.2 mL (2 mmol) of allylbromide was added at once, and the heterogeneous slurry was stirred vigorously at 4-50 for 2.5 h (monitoring by TLC hexane:methanol=1:9). While the mixture was stirred at 0° C , solid sodium sulfite (3 g) was added and the mixture was allowed to warm to room temperature and stirred for 1 h. Then 20 niL of ethyl acetate was added to the reaction mixture, and after separation of the layers, the aqueous phase was further extracted with ethyl acetate. The combined organic extracts were dried (MgSO4), concentrated in vacuo and purified by flash chromatography on silica (hexane:methanol=1:9, Rf 0.5), to yield chiral 1-bromo-2,3-propanediol. Yield 0.2 g (55.5%). Optical rotation: minus. Nitration to 1-bromo-2,3-dinitroxypropane was achieved using reaction in HNO3/H2SO4 (K. Yang, J.D. Artz, J. Lock, C. Sanchez, B.M. Bennett, A.B. Fraser, G.RJ. Thatcher,J.Chem.Soc., Perkin Trans. (1996) 1, 1073-1075) and the product was purified by flash chromatography on silica gel (hexane:CH2Cl2=2:3, Rf 0.5). Yield 55.5%. Optical rotation: minus. The dinitrate IVd was synthesised from chiral 1-bromo-2,3-propanediol by our usual procedure (K. Yang, J.D. Artz, J. Lock, C. Sanchez, B.M. Bennett, A.B. Fraser, G.RJ. Thatcher,J.Chem.Soc., Perkin Trans. (1996) 1, 1073-1075). and purified by flash chromatography on silica (ethyl acetate:methanol=9:1). Yield 2.27%. Optical rotation: plus.
    • Example 22
  • Chiral Synthesis of Nitrate Vk
  • The same procedure as described above for racemic Vk was utilized for the stereospecific synthesis of Vk from the sterechemically resolved, chiral dinitrate IVd.
    • Example 23
  • Synthesis of Tetranitrate Vx
  • The tide compound was synthesised by the reaction of IVd (0.345 g, 1.15 mmoles) with captopril methyl ester (0.2 g, 0.865 mmoles) in the presence of 1 mL of 1M NaOH. The crude product was purified by column chromatography (Silicagel, ethyl acetate) to afford 0.1 g (18.03%) of unsymmetrical disulphide. 1H-NMR(CDCl3, 300MHz): 5.49-5.61 (m, 11), 4.88-4.90 (m, 11H), 4.62-4.74 (m, 1H),4.40-4.55 (m, 1H),3.59-3.78 (m, superpos. 5H), 2.69-3.21 (m, superpos. 5H), 2.14-2.29 (m, 1H), 1.90-2.12 (m, 3H), 1.22-1.28 (d, 311). 13C-NMR(75.48 MHz): a mixture of enantiomers can be seen: 17.39, 25.20, 29.40, 36.41, 36.51, 38.55, 41.94, 42.19, 47.32, 52.56, 59.12, 69.90, 70.29,77.89, 78.00, 173.01, 173.48.
    • Example 24
  • Synthesis of Nitrate Vq
  • The tide compound was synthesised by the reaction of Bunte salt (2.4 g, 8 mtnoles) with 4,4′-thiobisbenzenetliol (0.5 g, 2 mmoles) in the presence of 4.4 mL of 1M NaOH. The crude product was purified by column chromatography (silica gel, hexanes/CH2CI2: 3/7) to afford 0.28 g (21.82%) disulphide. 1H-NMR(CDCl3, 300 MHz): 7.2-7.6 (m, arom 8H), 5.42-5.56 (m, 2H), 4.82-4.95 (dd, 2H), 4.55-4.67 (dd, 2H), 2.93-3.15 (m, 411).
    • Example 25
  • Synthesis of Nitrate Vr
  • The title compound was synthesised by the reaction of IVd (0.5 g, 1.58 mmoles) with ethyl 2-mercapto-3-(3′,4′-methylenedioxy-phenyl) propenoate (0.2 g, 0.8 rmmoles). The crude product was purified by column chromatography (Silicagel, hexanes/CH2Cl2: 3/7) to give Vr (0.1 g, 28.09%). 1H-NMR(CDCl3, 300 MHz):7.97 (s, 1H), 7.48-7.51 (d, 1H), 7.17-7.22 (m, 1H), 6.84-6.89 (d, 1H), 6.05 (s, 2F), 5.48-5.58(m, 1H), 4.81-4.89 (dd, 1H), 4.53-4.61 (dd, 1H), 4.25-4.4 (m, 2H), 3.05-3.10 (m, 2H), 1.35-1.45 (t, 3H). 13C-NMR(75.48 MHz): 14.17, 36.27, 62.15, 69.71, 76.57, 101.77, 108.27, 110.31, 125.20, 127.55, 127.87, 146.87, 147.811, 149.76, 165.89.
  • Ethyl 2-mercapto-3-(3′,4′-methylenedioxy-phenyl) propenoate was obtained by the following route:
    • (1) Ethylisothiocyanate (10 g, 0.115 moles), 7.9 g(O.086 moles) mercaptoacetic acid and 5 mL pyridine in C6H6 was refluxed, cooled and filtered yielding 3-ethylrhodanine, which was used in the next step without any further purification. Reaction of 3-ethylrodanine with piperonal in the presence of sodium acetate was performed in CH30H under refluxing for 1 h. The yellow precipitate obtained after cooling and filtration, was washed several times with CH30H on the filter and crystallizated from CH3OH to give 3-ethyl-5-piperilidenerodanine. 1H-NMR(DMSO-d6, 300 MHz):7.72 (s, 1H), 7.1-7.3 (m, 3H), 6.14 (s, 2H), 3.95-4.15(q, 2H), 1.15-1.20 (t, 3H). 13C-NMR(75.48 MHz): 12.76, 40.28, 103.07, 110.21, 110.47, 120.68, 127.89, 128.07, 134.01, 149.23, 150.74, 167.57, 193.68.
    • (2) 3-Ethyl-5-piperilidene- rodanine (lg, 3.4 mimoles) was added to a stirred solution of 0.16 g (6.8 mmoles) in 8 mL abs. ethanol and the mixture was refluxed for 30 min. To the solution cooled to room temperature 5 mL H 20 were added and the mixture was hydrolized with 10% HCl and extracted with ether. The ether phase was separated, dried (MgSO4) and evaporated to an oil. Since the investigation by TLC of the crude reaction mixture indicated the presence of piperonal, the reaction mixture was dissolved in CH2Cl2 and the obtained solution was washed with 1M NaOH. The aqueous phase was extracted twice with CH2Cl2 and then neutralized with dilute HCl. Free thiol was extracted with ethyl ether. After concentration, the product was purified by column cromatography eluating with hexane/ethyl ether:8/2. Yield 0.4 g (62.4%). 1H-NMR(CDCl3, 300 MHz):7.69 (s, 1H), 7.7.25-7.29 (d, 1H,J 1.46), 7.1-7.18 (m, 1H), 6.85-6.9 (d, 1H, J 8.13), 6.01 (s, 2H), 4.75 (s, 1H), 4.28-4.38 (q, 2H,J 7.12 ), 1.35-1.42 (t, 3H, J 7.13). 13C-NMR(75.48 MHz): 14.20, 62.5, 101.41, 108.37, 109.43, 121.06, 125.45, 129.20, 134.68, 147.80, 148.05, 165.43.
    Example 26
  • Synthesis of Nitrate IVs
  • The title compound was synthesised by the reaction of IVb with dithiothreitol in CH30H and was isolated as an oil in 15-20% yield (CAUTION: stench). 1H-NMR(CDCl3, 300 MHz): 5.23-5.32 (1H, m), 4.87 (1H, dd,J 12.82, 3.22), 4.68 (1H, dd,J 12.83, 6.09), 2.77-2.94 (2H, m), 1.66 (1H, t,J 9.07). 13C-NMR: (CDCl3, 75.48 MHz): 79.39, 69.30, 23.68.
    • Example 27
  • Synthesis of Nitrate IVt
  • The title compound was synthesised by the reaction of nitrate IVs with acetyl chloride in CHCl3. Isolated yield 50%. 1H-NMR(CDCl3, 300 MHz): 5.29-5.38 (1 H.m), 4.76 (1 H.dd, J 12.94, 3.11), 4.55 (1H, dd, J 12.94, 6.37), 3.30 (IH, dd, J 14.06, 5.98), 3.13 (lH, dd, J 14.61, 6.35). 13C-NMR: (CDCl3, 75.48 MHz): 194.10, 77.00, 69.79, 30.42, 27.78. Mass spec. m/z (EI+, fragment, %): 240.0 (M+, 1.17), 193.9 (N-NO2, 10.86), 148.8 (100). Calculated for C5H8N2O7S 240.01.
    • Example 28
  • Synthesis of Nitrate IIIw
  • Diethyl 1-chloro-2-tnmethylsiloxypropylphosphonate was obtained by adaptation of literature methods (T.Azuhata, Y.Okamoto, Synthesis (1983) 916-917). This phosphonate was quantitatively converted to diethyl 1-chloro-2-hydroxypropylphosphonate using CH30H. After stirring for 15 min the resulting reaction mixture was evaporated to a minimum and subjected to nitration with a mixture of HNO3 and H2SO4 Work-up and flash column chromatography on silica (ethyl acetate eluant) yielded pure product in 25% yield. 31P (CDCl3, 162 MHz): 24.60. 1H (CDCl3, 300 MHz): 5.31-5.45 (m, 1R), 3.92-4.08 (m, 4R), 3.63-3.81 (m, 2H), 2.03-2.30 (m, 2R), 1.16-1.24 (superposition of 2 t, 6H,J 7). 13C (CDCl3, 75 MHz): 76.83, 62.15 (d,J 6.37), 43.77 (d,J 8.95), 27.08 (d,J 142.00), 15.99 (d,J 5.88).
    • Example 29
  • Synthesis of Nitrate IIIx
  • Treatment of IIw with 1 mole of Me3SiBr for 1 h with subsequent addition of CH30H provided the monodealkylated phosphonic acid in high purity. Transformation of the free acid to its sodium salt IIIx was achieved using the cation-exchange resin Amberlite IR-122-Na+form. 31p (CD3OD, 122 MHz): 17.62. 1H (CD3OD, 300 MHz): 5.38-5.63 (m, 1H), 3.75-4.25 (superposition of 2 m, 4H), 1.88-2.20 (m, 211), 1.12-1.28 (t, 3H). 13C (CD 30D, 75 MHz): 81.14, 61.17 (d, J 5.41), 45.56 (d,J 5.94), 29.35 (d,J 131.74), 17.00 (d,J 6.75)
    • Example 30
  • The effect of WVk was tested in Xenopus oocytes expressing human recombinant GABAA receptors by the two-electrode voltage clamp technique as described in Reynolds and Maitra (EurpeanJournalofPharmacologv (1996) 314, 151-156.). The control GABA response was substantially potentiated by the positive control drug, chlormethiazole, at a concentration of 200 EM (FIG. 15a). In contrast, a concentration of 200 HM of WVk produced a smaller, but still significant, potentiation of the control GABA response in the same oocyte (FIG. 15a). A decreased efficacy with Wk suggests the possibility that it is a partial allosteric modulator of GABAA receptor function, and may therefore have more selective behavioural effects than more efficacious compounds.
  • The effect of a drug that induces brief periods of sedation/hypnosis in animals is characterized by loss of the righting reflex (loss of the ability of the animal to right its posture when placed on its back). The “loss of the righting reflex” response is a commonly used test for sedative-hypnotic agents. Wk produced a dose-dependent and reversible loss of the righting reflex in mice when given by intraperitoneal injection at doses of 100 and 200 mg/kg (FIG. 15b). Thus, the organic nitrate WVk exhibits the activity of a sedative/hypnotic, and represents a novel class of compounds that may have utility as new anti-anxiety, sedative and/or hypnotic agents.
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Claims (1)

1. A method for treating pain in a subject in need thereof, comprising administering to the subject an effective amount of a therapeutic compound, wherein said therapeutic compound is of the formula (Ia):
Figure US20070066575A1-20070322-C00027
F2 is a nitrate group or an organic radical which may be joined in a cyclic ring system with
G2, and which may contain inorganic counterions;
E is a methylene group;
G1 is a methylene group or does not exist;
F1 is H; and
G2 is joined with F2 to form a cyclic system or is RN-ZN; wherein RN is an organic radical possessing a heteroaryl group containing a P or S atom, where said P or S is positioned β, γ, or δ to a nitrate group; and ZN is WN nwn-XN nn-YN oo; wherein
mm, nn, oo are 0 or 1 and WN, XN, YN are NH, NRNN, CO, O, or CH2; wherein
RNN is a C1-C12 alkyl group.
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DE60016460T2 (en) 2005-12-22
WO2001049275A2 (en) 2001-07-12
EP1246625B1 (en) 2004-12-01
AU2335101A (en) 2001-07-16
ES2233489T3 (en) 2005-06-16
IL150487A0 (en) 2002-12-01
EP1518553A2 (en) 2005-03-30
PT1246625E (en) 2005-03-31
HK1050144A1 (en) 2003-06-13
ATE283695T1 (en) 2004-12-15
EP1246625A2 (en) 2002-10-09
JP2003519176A (en) 2003-06-17
DE60016460D1 (en) 2005-01-05
CA2394184A1 (en) 2001-07-12
AU782489C (en) 2006-04-27
US7115661B1 (en) 2006-10-03

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