4-dedimethylamino tetracycline compounds
View Patent ↗The present invention pertains, at least in part, to novel substituted 4-dedimethylamino tetracycline compounds. These tetracycline compounds can be used to treat numerous tetracycline compound-responsive states, such as bacterial infections and neoplasms, as well as other known applications for minocycline and tetracycline compounds in general, such as blocking tetracycline efflux and modulation of gene expression.
1. A tetracycline compound of formula IV:
wherein:
X is CHC(R 13 Y′Y), or CR 6′ R 6 ;
R 2 is hydrogen, alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, arylalkyl, aryl, heterocyclic or heteroaromatic;
R 7′ and R 7″ are each alkyl;
R 4 and R 4′ are each independently alkyl, alkenyl, alkynyl, aryl, hydroxyl, alkoxy, halogen, hydrogen, or taken together to form the oxygen of a carbonyl;
R 2′ , R 3 , R 10 , R 11 and R 12 are each hydrogen;
R 5 is hydroxyl hydrogen, thiol, alkanoyl, aroyl, alkaroyl, aryl, heteroaromatic, alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, arylalkyl, alkyl carbonyloxy, or aryl carbonyloxy;
R 6 and R 6′ are independently hydrogen, methylene, hydroxyl, halogen, thiol, alkyl, alkenyl, alkynyl, aryl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, or an arylalkyl;
R 7 is NR 7′ R 7″ ;
R 9 is alkyl, alkenyl, alkynyl, aryl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, arylalkyl, amido, acyl, arylalkenyl, arylalkynyl, thionitroso, or —(CH 2 ) 0-3 NR 9c C(=Z′)ZR 9a ;
Z is CR 9d R 9e , S, NR 9b or O;
Z′ is NR 9f , O or S;
R 9a , R 9b , R 9c , R 9d , R 9e and R 9f are each independently hydrogen, acyl, alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, arylalkyl, aryl, heterocyclic or heteroaromatic;
R 8 is hydrogen, hydroxyl, thiol, alkyl, alkenyl, alkynyl, aryl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, or an arylalkyl;
R 13 is hydrogen, hydroxyl, alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, or an arylalkyl;
Y′ and Y are each independently hydrogen, halogen, hydroxyl, cyano, sulfhydryl, amino, alkyl, alkenyl, alkynyl, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, or an arylalkyl, and pharmaceutically acceptable salts, esters and amides thereof.
2. The tetracycline compound of claim 1 , wherein R 9 is acyl.
3. The tetracycline compound of claim 2 , wherein R 9 is acetyl.
4. The tetracycline compound of claim 1 , wherein R 4 and R 4′ are each hydrogen or the oxygen of a carbonyl group; X is CR 6 R 6′ ; R 2 , R 2′ , R 5 , R 6 , R 6′ , R 8 , R 10 , R 11 , and R 12 are each hydrogen; and R 7′ and R 7″ are each lower alkyl.
5. A tetracycline compound of claim 1 , wherein the compound is:
6. The tetracycline compound of claim 1 , wherein R 7 is dimethylamino.
7. The tetracycline compound of claim 1 , wherein R 9 is substituted or unsubstituted aryl.
8. The tetracycline compound of claim 1 , wherein R 9 is substituted or unsubstituted alkyl.
9. The tetracycline compound of claim 1 , wherein R 9 is substituted or unsubstituted alkynyl.
10. The tetracycline compound of claim 1 , wherein R 4 , R 4′ , and R 5 are each hydrogen.
11. A substituted tetracycline compound selected from the group consisting of:
and pharmaceutically acceptable salts, esters and amides thereof.
12. A pharmaceutical composition comprising a therapeutically effective amount of a tetracycline compound of claim 1 and a pharmaceutically acceptable carrier.