Enhancement of tigecycline potency using efflux pump inhibitors
View Patent ↗Disclosed herein are Efflux Pump Inhibitor (EPI) compounds that can be co-administered with antimicrobial agents for the treatment of infections caused by drug resistant pathogens. The EPI compounds are soft drugs which exhibit a reduced propensity for tissue accumulation. It is demonstrated that the EPIs can be used to increase the potency, decrease bacterial resistance and development of bacterial resistance, and increase killing effectivness of tigecycline. Also disclosed are methods of treatment and pharmaceutical compositions for co-administering tigecylcine with an EPI.
1. A method of increasing susceptibility of a bacterium to tigecycline, comprising contacting the bacterium with an efflux pump inhibitor, wherein the efflux pump inhibitor is a compound having the structure of Formula (III) or a pharmaceutically acceptable salt thereof:
wherein:
R 1 is:
X 1 is selected from the group consisting of —O— and —S—;
m 1 is an integer from 0 to 4;
n 1 is an integer from 0 to 1;
R 11 is selected from the group consisting of —NH 2 , —NH—CH(═NH), —NH—C(CH 3 )(═NH), —CH(═NH)NH 2 , and —NH—C(═NH)NH 2 ;
R 3 is selected from the group consisting of:
X 3 is selected from the group consisting of —CH 2 —, —C(CH 3 ) 2 — —O—, and —S—;
m 3 is an integer from 1 to 2;
n 3 is an integer from 0 to 2;
R 31 is selected from the group consisting of C 1-10 alkyl, C 1-10 alkenyl, C 1-10 alkynyl, and C 1-10 cycloalkyl;
R 4 is selected from the group consisting of hydrogen, optionally substituted C 1-6 alkyl, and optionally substituted C 3-7 cycloalkyl;
Ar is an optionally substituted phenyl, and
R 5 is selected from the group consisting of:
each optionally substituted with methyl, ethyl, n-propyl, isopropyl, cyclopropyl, tert-butyl, hydroxyl, methoxyl, ethoxyl, hydroxymethyl, trifluoromethyl, trifluoromethoxyl, or halogen moieties, and
wherein:
each A 5 is separately selected from the group consisting of ═CH— and ═N—, with the proviso that each A 5 containing ring contains no more than four ═N— groups;
each B 5 is separately selected from the group consisting of —C═, —N═, —O—, —S—, —NH—, and —N(R 6 )—, with the proviso that each B 5 containing ring contains no more than three heteroatoms;
R 6 is selected from the group consisting of hydrogen, C 1-6 alkyl, and C 3-6 cycloalkyl;
R 51 is selected from the group consisting of hydrogen, methyl, ethyl, and cyclopropyl;
m 5 is an integer from 1 to 3;
n 5 is an integer from 0 to 2;
p 5 is an integer from 0 to 4; and
any amino groups present in R 1 are optionally acyated with a natural or artificial amino acid residue having an (S)-configuration selected from aspartic acid and glutamic acid.
2. The method of claim 1 , wherein the efflux pump inhibitor is selected from the group consisting of:
pharmaceutically acceptable salt thereof.
3. A method of treating a subject having a bacterial infection, comprising co-administering to the subject tigecycline and an efflux pump inhibitor, wherein the efflux pump inhibitor is a compound having the structure of Formula (III) or a pharmaceutically acceptable salt thereof:
wherein:
R 1 is:
X 1 is selected from the group consisting of —O— and —S—;
m 1 is an integer from 0 to 4;
n 1 is an integer from 0 to 1;
R 11 is selected from the group consisting of —NH 2 , —NH—CH(═NH), —NH—C(CH 3 )(═NH), —CH(═NH)NH 2 , and —NH—C(═NH)NH 2 ;
R 3 is selected from the group consisting of:
X 3 is selected from the group consisting of —CH 2 —, —C(CH 3 ) 2 — —O—, and —S—;
m 3 is an integer from 1 to 2;
n 3 is an integer from 0 to 2;
R 31 is selected from the group consisting of C 1-10 alkyl, C 1-10 alkenyl, C 1-10 alkynyl, and C 1-10 cycloalkyl;
R 4 is selected from the group consisting of hydrogen, optionally substituted C 1-6 alkyl, and optionally substituted C 3-7 cycloalkyl;
Ar is an optionally substituted phenyl,
R 5 is selected from the group consisting of:
each optionally substituted with methyl, ethyl, n-propyl, isopropyl, cyclopropyl, tert-butyl, hydroxyl, methoxyl, ethoxyl, hydroxymethyl, trifluoromethyl, trifluoromethoxyl, or halogen moieties, and
wherein:
each A 5 is separately selected from the group consisting of ═CH— and ═N—, with the proviso that each A 5 containing ring contains no more than four ═N— groups;
each B 5 is separately selected from the group consisting of —C═, —N═, —O—, —S—, 13 NH—, and —N(R 6 )—, with the proviso that each B 5 containing ring contains no more than three heteroatoms;
R 6 is selected from the group consisting of hydrogen, C 1-6 alkyl, and C 3-6 cycloalkyl;
R 51 is selected from the group consisting of hydrogen, methyl, ethyl, and cyclopropyl;
m 5 is an integer from 1 to 3;
n 5 is an integer from 0 to 2;
p 5 is an integer from 0 to 4; and
any amino groups present in R 1 are optionally acylated with a natural or artificial amino acid residue having an (S)-configuration selected from aspartic acid and glutamic acid.
4. The method of claim 3 , wherein the efflux pump inhibitor is selected from the group consisting of:
pharmaceutically acceptable salt thereof.
5. The method of claim 1 , wherein the bacterium is selected from the group consisting of an enterobacteriaceae, acinetobacter, burkholderia, stenotrophomonas , and staphylococcus bacterium.
6. The method of claim 1 , wherein the bacterium is selected from the group consisting of Klebsiella pneumonia, Proteus mirabilis , and Morganella morganii.
7. The method of claim 1 , wherein the bacterium is P. aeruginosa.
8. The method of claim 1 , further comprising contacting the bacterium with tigecycline.
9. The method of claim 3 , wherein the bacterial infection comprises infection with a bacteria selected from the group consisting of an enterobacteriaceae, acinetobacter, burkholderia, stenotrophomonas , and staphylococcus bacteria.
10. The method of claim 3 , wherein the bacterial infection comprises infection with a bacteria selected from the group consisting of Klebsiella pneumonia, Proteus mirabilis , and Morganella morganii.
11. The method of claim 3 , wherein the bacterial infection comprises infection with P. aeruginosa.
12. A method of increasing susceptibility of a bacterium to tigecycline, comprising contacting the bacterium with an efflux pump inhibitor, wherein the efflux pump inhibitor is a compound having the structure selected from the group consisting of:
a pharmaceutically acceptable salt thereof.
13. The method of claim 12 , wherein the bacterium is selected from the group consisting of an enterobacteriaceae, acinetobacter, burkholderia, stenotrophomonas , and staphylococcus bacterium.
14. The method of claim 12 , wherein the bacterium is selected from the group consisting of Klebsiella pneumonia, Proteus mirabilis , and Morganella morganii.
15. The method of claim 12 , wherein the bacterium is P. aeruginosa.
16. The method of claim 12 , further comprising contacting the bacterium with tigecycline.
17. A method of treating a subject having a bacterial infection, comprising co-administering to the subject tigecycline and an efflux pump inhibitor, wherein the efflux pump inhibitor is selected from the group consisting of:
a pharmaceutically acceptable salt thereof.
18. The method of claim 17 , wherein the bacterial infection comprises infection with a bacteria selected from the group consisting of an enterobacteriaceae, acinetobacter, burkholderia, stenotrophomonas , and staphylococcus bacteria.
19. The method of claim 17 , wherein the bacterial infection comprises infection with a bacteria selected from the group consisting of Klebsiella pneumonia, Proteus mirabilis , and Morganella morganii.
20. The method of claim 17 , wherein the bacterial infection comprises infection with P. aeruginosa.
21. A method of increasing susceptibility of a bacterium to tigecycline, comprising contacting the bacterium with an efflux pump inhibitor, wherein the efflux pump inhibitor is a compound having the structure selected ton the group consisting of:
or pharmaceutically acceptable salt thereof.
22. A method of increasing susceptibility of a bacterium to tigecycline, comprising contacting the bacterium with an efflux pump inhibitor, wherein the efflux pump inhibitor is a compound having the structure:
or pharmaceutically acceptable salt thereof.
23. A method of treating a subject having a bacterial infection, comprising co-administering to the subject tigecycline and an efflux pump inhibitor, wherein the efflux pump inhibitor is selected from the group consisting of:
or pharmaceutically acceptable salt thereof.
24. A method of treating a subject having a bacterial infection, comprising co-administering to the subject tigecycline and an efflux pump inhibitor, wherein the efflux pump inhibitor is a compound having the structure:
or a pharmaceutically acceptable salt thereof.