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US 2023/0406831 A1Published application
Compounds and methods of inhibiting bacterial chaperonin systems
AssigneesThe Trustees of Indiana University, Arizona Board of Regents on Behalf of the University of Arizona
InventorsSteven JOHNSON, Eli CHAPMAN
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Abstract
The present disclosure relates to compounds and methods of killing or inhibiting the growth of bacteria by disrupting chaperonin-mediated refolding of proteins.
Claims26
A compound of formula I
- wherein
- R′ is C1-C6 alkyl or
- R1 is H, —OH, —OC1-C6 alkyl, —NHC(O)C1-C6 alkyl, —C(O)PC1-C6 alkyl, —C(O)OH, C1-C6 alkyl, —S-heteroaryl, or
- wherein each hydrogen atom in C1-C6 alkyl is optionally substituted by —CN,
- R2 is H or halo,
- each of R3, R4, R5, and R6 is independently H, —OH, halo, —C1-C6 alkyl, —O—C1-C6 alkyl, —NO2, or —NH2,
- R7 is H or C1-C6 alkyl,
- X is —O—, —S—, —C(R9)(R9)m—, or —C(R9)(R10)mO—, optionally X is —O—, —S—, or —C(R9)(CN);
- R8 is halo,
- R9 is H or —CN,
- R10 is H or —CN,
- m is 1 or 2, and
- n is 0, 1, or 2;
- or a pharmaceutically acceptable salt thereof, provided the compound of formula (I) is not
11 more elements
4-9. (canceled)
(canceled)
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A method of killing or inhibiting the growth of bacteria, said method comprising contacting the bacteria with a compound of the formula I
- wherein
- R′ is C1-C6 alkyl or
- R1 is H, —OH, —OC1-C6 alkyl, —NHC(O)C1-C6 alkyl, —C(O)OC1-C6 alkyl, —C(O)OH, C1-C6 alkyl, —S-heteroaryl, or
- wherein each hydrogen atom in C1-C6 alkyl is optionally substituted by —CN,
- R2 is H or halo,
- each of R3, R4, R5, and R6 is independently H, —OH, halo, —C1-C6 alkyl, —O—C1-C6 alkyl, —NO2, or —NH2,
- R7 is H or C1-C6 alkyl,
- X is —O—, —S—, —C(R9)(R9)m—, or —C(R9)(R10)mO—, optionally X is —O—, —S—, or —C(R9)(CN);
- R8 is halo,
- R9 is H or —CN,
- R10 is H or —CN,
- m is 1 or 2, and
- n is 0, 1, or 2;
- or a pharmaceutically acceptable salt thereof, provided the compound of formula (I) is not
11 more elements
(canceled)
(Canceled)
22-26. (canceled)
Dependencies are inferred from the claim text.