Tetracycline derivatives with reduced antibiotic activity and neuroprotective benefits
The present disclosure is directed to compositions and methods which utilize the tetracycline scaffold, preferably the scaffold of tetracycline or minocycline, and which significantly lack antibiotic activity. The compounds have neuroprotective attributes without interfering with the drugs capacity to pass through the blood brain barrier. These compounds have neuroprotective activity because of their inhibition of neuronal cell cycle progression. The compounds are characterized in part by a fifth ring joining positions 9 and 10.
1. A compound having the formula:
wherein R 4 , R 6 , R 9 , and R 10 are defined as follows:
R 4 is a substitution selected from the group consisting of —N(CH 3 ) 2 , NH(CH 2 CH 2 OH), and amino alkanol, or else R 4 is a disubstitution selected from the group consisting of (i) a first substitution of —N(CH 3 ) 2 and a second substitution of substituted alkyl, and (ii) a first substitution of amino alkyl and a second substitution of lower alkyl;
R 6 is H or —CH 2 —S—R″, wherein R″ is aryl or substituted aryl; and
R 10 and R 9 , taken together with the atoms to which they are attached, form a 5 or 6 membered heteroalkyl ring, wherein said heteroalkyl ring is substituted with an oxygen atom;
or a pharmaceutically acceptable salt thereof.
2. The compound of claim 1 , wherein R 4 is —N(CH 3 ) 2 .
3. The compound of claim 2 , wherein the compound is an up epimer at R 4 .
4. The compound of claim 1 , wherein R 6 is a substituent that reduces antibiotic potency.
5. The compound of claim 1 , wherein R 6 is —CH 2 —S—R″.
6. The compound of claim 5 , wherein R″ at R 6 is benzyl or phenyl.
7. The compound of claim 1 , wherein R 6 is H.
8. The compound of claim 1 , wherein R 9 contains nitrogen.
9. The compound of claim 8 , wherein R 9 and R 10 have the formula (from R 10 to R 9 ) —O—Y—HN—, wherein Y is C═O.
10. The compound of claim 8 , wherein R 9 and R 10 have the formula (from R 10 to R 9 ) —O—CH 2 —C(═O)—HN—.
11. The compound of claim 9 , wherein R 4 is —N(CH 3 ) 2 .
12. The compound of claim 11 , wherein the compound is an up epimer at R 4 .
13. The compound of claim 9 , wherein R 6 is a substituent that reduces antibiotic potency.
14. The compound of claim 9 , wherein R 6 is —CH 2 —S—R″.
15. The compound of claim 13 , wherein R″ at R 6 is benzyl or phenyl.
16. The compound of claim 9 , wherein R 6 is H.
17. The compound of claim 1 , wherein said compound has the formula:
or a pharmaceutically acceptable salt thereof.
18. The compound of claim 1 , wherein said compound has the formula:
or a pharmaceutically acceptable salt thereof.
19. A compound having the formula:
wherein R 4 , R 6 , R 9 , and R 10 are defined as follows:
R 4 is a substitution selected from the group consisting of —N(CH 3 ) 2 , NH(CH 2 CH 2 OH), and amino alkanol, or else R 4 is a disubstitution selected from the group consisting of (i) a first substitution of —N(CH 3 ) 2 and a second substitution of substituted alkyl, and (ii) a first substitution of amino alkyl and a second substitution of lower alkyl;
R 6 is —CH 2 —S—R″, wherein R″ is aryl or substituted aryl; and
R 10 and R 9 , taken together with the atoms to which they are attached, form a 5 or 6 membered heteroalkyl ring, wherein said heteroalkyl ring is optionally substituted with an oxygen atom;
or a pharmaceutically acceptable salt thereof.
20. The compound of claim 19 , wherein R″ at R 6 is benzyl or phenyl.