Anti-inflammatory and protein kinase inhibitor compositions and related methods for downregulation of detrimental cellular responses and inhibition of cell death
A novel class of pyridazine compositions and related methods of use.
1. An N-heterocyclic compound of the structural formula
wherein
A is a first pyridazinyl component; and R 3 is a component selected from the group consisting of hydrogen, alkyl and substituted alkyl moieties, arylalkyl and substituted arylalkyl moieties; phenyl and substituted phenyl moieties;
R 4 is a component selected from the group consisting of hydrogen, halogen, alkyl, substituted alkyl, amino, arylalkyl and substituted arylalkyl moieties, phenyl and substituted phenyl moieties, or alkyl and substituted alkyl moieties as can provide a carbocyclic or a heterocyclic moiety with R 5 ;
R 5 is a component selected from the group consisting of hydrogen, halogen, alkyl, substituted alkyl; phenyl, substituted phenyl, heterocyclic and substituted heterocyclic moieties, arylalkyl and substituted arylalkyl moieties, or alkyl and substituted alkyl moieties as can provide a carbocyclic or a heterocyclic moiety with R 4 or R 6 ;
R 6 is a component selected from the group consisting of hydrogen, halogen, alkyl, substituted alkyl, phenyl, substituted phenyl, heterocyclic and substituted heterocyclic moieties, arylalkyl and substituted arylalkyl moieties, or a substituted phenyl moiety providing a carbocyclic or a heterocyclic moiety with R 5 ;
R 2 is a divalent component coupling A and G, said component selected from the group consisting of alkyl, cycloalkyl, acyl, alkylacyl, amido, alkylamido moieties, and further including said moieties having at least one unsaturated carbon-carbon bond sequence;
G is a divalent component coupling R 2 and B, said component selected from the group consisting of alkyl, cycloalkyl, acyl, alkylacyl, amido, alkylamido, ureido, sulfonamido, thio, and primary, secondary and tertiary amine moieties; and
B is a second pyridazinyl component of the structural formula
wherein R 3 ′ is a component selected from the group consisting of hydrogen, alkyl and substituted alkyl; phenyl and substituted phenyl, and arylalkyl and substituted arylalkyl moieties;
R 4 ′ is a component selected from the group consisting of hydrogen, halogen, alkyl, substituted alkyl, amino, arylalkyl and substituted arylalkyl moieties, phenyl and substituted phenyl moieties, or alkyl and substituted alkyl moieties as can provide a carbocyclic or a heterocyclic moiety with R 5 ′;
R 5 ′ is a component selected from the group consisting of hydrogen, halogen, alkyl, substituted alkyl; phenyl, substituted phenyl, heterocyclic and substituted heterocyclic moieties, arylalkyl and substituted arylalkyl moieties, or alkyl and substituted alkyl moieties as can provide a carbocyclic or a heterocyclic moiety with R 4 ′ or R 6 ′;
R 6 ′ is a component selected from the group consisting of hydrogen, halogen, alkyl, substituted alkyl, phenyl, substituted phenyl, heterocyclic and substituted heterocyclic moieties, arylalkyl and substituted arylalkyl moieties, or a substituted phenyl moiety providing a carbocyclic or a heterocyclic moiety with R 5 ′;
wherein B is coupled with the G component at one of the 1-, 2-, 3-nitrogen- and 4-positions thereof.
2. An N-heterocyclic compound of claim 1 , wherein B is coupled with the G component at the 3-nitrogen thereof.
3. A compound of claim 2 , wherein R 6 is a halogen moiety.
4. A compound of claim 3 , wherein R 6 is a chlorine moiety.
5. A compound of claim 2 , wherein G is an acyl or amido moiety.
6. A compound of claim 3 , wherein G is an acyl or amido moiety.
7. A compound of claim 4 , wherein G is an acyl or amido moiety.
8. A compound of claim 3 , wherein R 2 is a (CH 2 ) n alkyl moiety and n is 10.
9. A compound of claim 5 , wherein R 2 is a (CH 2 ) n alkyl moiety and n is 10.
10. A compound of claim 6 , wherein R 2 is a (CH 2 ) n alkyl moiety and n is 10.
11. An N-heterocyclic compound of claim 6 , wherein R 2 is a (CH 2 ) n alkyl moiety and n is 4-12; R 3 , R 4 , R 5 , R 3 ′ and R 5 ′ are hydrogen, and R 4 ′ is hydrogen or alkyl.
12. An N-heterocyclic compound of claim 10 , wherein R 3 , R 4 , R 5 , R 3 ′, R 4 ′, and R 5 ′ are hydrogen.
13. An N-heterocyclic compound of claim 12 , wherein R 6 ′ is phenyl or substituted phenyl.
14. A compound of the following structural formula:
15. A pharmaceutical composition comprising a compound of claim 1 and a pharmaceutically acceptable diluent, carrier, adjuvant or vehicle.
16. A pharmaceutical composition comprising a compound of claim 14 and a pharmaceutically acceptable diluent, carrier, adjuvant or vehicle.
17. A method for treating or reducing acute lung injury in a subject comprising administering to the subject a compound of claim 1 .
18. A method for treating complications from mechanical ventilation in a subject comprising administering to the subject a compound of claim 1 .
19. A method for treating or reducing acute lung injury in a subject comprising administering to the subject a compound of claim 14 .
20. A method for treating complications from mechanical ventilation in a subject comprising administering to the subject a compound of claim 14 .