Compounds and methods to treat organophosphorus poisoning
Organophosphate (OP) nerve agents and pesticides are potent inhibitors of acetylcholinesterase (AChE). Though oxime nucleophiles can reactivate an AChE-phosphyl adduct, the adduct can undergo a reaction called aging, leading to an aged-AChE adduct. The invention provides compounds and methods that can be used to reactivate an aged-AChE adduct. Such compounds and methods are useful to counteract organophosphorus poisoning.
1. A method for reactivating an aged-AChE adduct comprising contacting the aged-AChE adduct with an alkylating agent that reactivates the aged-AChE adduct to provide an AChE-OP adduct, wherein the alkylating agent is a compound of formula (I):
wherein:
R 1 is C 1 -C 3 )alkyl that is optionally substituted with one or more halo;
each R 2 is independently H, halo, cyano, or (C 1 -C 3 )alkyl that is optionally substituted with one or more halo; and
X is − BF 4 , CF 3 SO 3 − , F − , Cl − , Br − , I − , monobasic sulfate, dibasic sulfate, monobasic phosphate, dibasic phosphate, or tribasic phosphate, NO 3 − , PF 6 − , NO 2 − , C e F f SO 3 − (where e=2−10 and f=2e+1), or arylsulfonyl, wherein aryl is optionally substituted with one or more groups independently selected from halo, cyano, nitro, carboxy, hydroxy, (C 1 -C 3 )alkyl, (C 1 -C 3 )alkoxy, (C 1 -C 3 )alkanoyl, (C 1 -C 3 )alkoxycarbonyl, (C 2 -C 3 )alkanoyloxy, and (C 1 -C 3 )alkylthio, wherein any (C 1 -C 3 )alkyl, (C 1 -C 3 )alkoxy, (C 1 -C 3 )alkanoyl, (C 1 -C 3 )alkoxycarbonyl, (C 2 -C 3 )alkanoyloxy, and (C 1 -C 3 )alkylthio can optionally be substituted with one or more halo.
2. A method for reactivating an aged-AChE adduct in an animal having organophosphorus poisoning comprising administering to the animal an amount of an alkylating agent effective to reactivate aged-AChE to provide an AChE-OP adduct, wherein the alkylating agent is a compound of formula (I):
wherein:
R 1 is C 1 -C 3 )alkyl that is optionally substituted with one or more halo;
each R 2 is independently H, halo, cyano, or (C 1 -C 3 )alkyl that is optionally substituted with one or more halo; and
X is − BF 4 , CF 3 SO 3 − , F − , Cl − , Br − , I − monobasic sulfate, dibasic sulfate, monobasic phosphate, dibasic phosphate, or tribasic phosphate, NO 3 − , PF 6 − , NO 2 − , C e F f SO 3 − (where e=2−10 and f=2e+1), or arylsulfonyl, wherein aryl is optionally substituted with one or more groups independently selected from halo, cyano, nitro, carboxy, hydroxy, (C 1 -C 3 )alkyl, (C 1 -C 3 )alkoxyl, (C 1 -C 3 )alkanoyl, (C 1 -C 3 )alkoxycarbonyl, (C 2 -C 3 )alkanoyloxy, and (C 1 -C 3 )alkylthio, wherein any (C 1 -C 3 )alkyl, (C 1 -C 3 )alkoxy, (C 1 -C 3 )alkanoyl, (C 1 -C 3 )alkoxycarbonyl, (C 2 -C 3 )alkanoyloxy, and (C 1 -C 3 )alkylthio can optionally be substituted with one or more halo.
3. A method for increasing acetylcholinesterase activity in an animal comprising administering to the animal an amount of an alkylating agent effective to reactivate aged-AChE to provide an AChE-OP adduct and administering to the animal an agent capable of reactivating the AChE-OP adduct and increasing acetylcholinesterase activity in the animal, wherein the alkylating agent is a compound of formula (I):
wherein:
R 1 is C 1 -C 3 )alkyl that is optionally substituted with one or more halo;
each R 2 is independently H, halo, cyano, or (C 1 -C 3 )alkyl that is optionally substituted with one or more halo; and
X is − BF 4 , CF 3 SO 3 − , F − , Cl −, Br − , I − monobasic sulfate, dibasic sulfate, monobasic phosphate, dibasic phosphate, or tribasic phosphate, NO 3 − , PF 6− , NO 2− , C e F f SO 3 − (where e=2−10 and f=2e+1), or arylsulfonyl, wherein aryl is optionally substituted with one or more groups independently selected from halo, cyano, nitro, carboxy, hydroxy, (C 1 -C 3 )alkyl, (C 1 -C 3 )alkoxy, (C 1 -C 3 )alkanoyl, (C 1 -C 3 )alkoxycarbonyl, (C 2 -C 3 )alkanoyloxy, and (C 1 -C 3 )alkylthio, wherein any (C 1 -C 3 )alkyl, (C 1 -C 3 )alkoxy, (C 1 -C 3 )alkanoyl, (C 1 -C 3 )alkoxycarbonyl, (C 2 -C 3 )alkanoyloxy, and (C 1 -C 3 )alkylthio can optionally be substituted with one or more halo.
4. The method of claim 2 further comprising administering to the animal an agent capable of reactivating the AChE-OP adduct.
5. The method of claim 4 wherein the agent capable of reactivating the AChE-OP adduct is a nucleophilic oxime.
6. The method of claim 4 wherein the agent capable of reactivating the AChE-OP adduct is 2-PAM.
7. The method of claim 2 further comprising administering an acetylcholine receptor antagonist to the animal.
8. The method of claim 7 wherein the acetylcholine receptor antagonist is atropine.
9. The method of claim 2 further comprising administering an antiseizure agent to the animal.
10. The method of claim 9 wherein the antiseizure agent is diazepam.