Phosphorylated and branched dihydroxy-pentane-dione (DPD) analogs as quorum sensing inhibitors in bacteria
Provided are compositions and methods for modulating quorum sensing in microbes. The compounds are AI-2 analogs and as such have structures similar to 4,5-dihydroxy-2,3-pentanedione that can act as agonists/antagonists of quorum sensing. The compounds are useful for modulating quorum sensing in bacteria and can be used in methods for prophylaxis or therapy of bacterial infections and for reduction of biofilms.
1. A compound having the following structure:
wherein R and R 3 are each are each independently a phosphonate group, sulfonate group, sulfoxide group, or carboxylate group, ii) R is a phosphonate group, sulfonate group, sulfoxide group, or carboxylate group and R 3 is a H or keto group, or iii) R 3 is a phosphonate group, sulfonate group, sulfoxide group, or carboxylate group and R is a H or keto group,
A is selected from the group consisting of: S, NH, CH 2 , O, CZ 2 , and CHZ, where Z is a halogen,
Y is selected from the group consisting of: CH 2 , CZ 2 , and C═O, where Z is a halogen,
X is selected from the group consisting of: CH, C—CH 3 , and N,
R 1 is selected from the group consisting of: H, C 1 to C 16 substituted or unsubstituted branched alkyl group, C 1 to C 16 substituted or unsubstituted linear alkyl group, C 1 to C 16 heterocyclic ring, and C 3 to C 8 carbocyclic ring, and
R 2 is selected from the group of: H and CH 3 ,
wherein, optionally, taken together R 1 —X—R 2 form a C 3 to C 8 carbocyclic ring or heterocyclic ring, and the ring is, optionally, substituted,
wherein, optionally, X is CH, R 1 is CR x R y , and R x is H or C 1 to C 16 substituted or unsubstituted linear alkyl group, R y is H or C 1 to C 16 substituted or unsubstituted linear alkyl group, and the bond between R 1 and X is a double bond,
wherein, optionally, X is CH, and R 1 and X are each bonded to a single O to form an epoxide, wherein, optionally, A is a N, and taken together A and R form a 1,2,5-thiadiazolidin-3-one 1,1-dioxide,
wherein if X is CH, then R 1 and R 2 are not H, and
wherein if X is CH, then R 1 is not H and R 2 is not CH 3 .
2. The compound of claim 1 , wherein the compound has the following structure:
wherein X is selected from the group consisting of: CH, C—CH 3 , and N,
Y is selected from the group consisting of: CH 2 , CZ 2 , and C═O, where Z is a halogen,
R 2 is selected from the group consisting of: H and CH 3 ,
R 4 is selected from the group consisting of: C 1 to C 16 substituted or unsubstituted branched alkyl group, C 1 to C 16 substituted or unsubstituted linear alkyl group, C 3 to C 8 heterocyclic ring, and C 3 to C 8 carbocyclic ring,
R 5 is selected from the group consisting of: C 1 to C 16 substituted or unsubstituted branched alkyl group, C 1 to C 16 substituted or unsubstituted linear alkyl group, C 3 to C 8 heterocyclic ring, and C 3 to C 8 carbocyclic ring.
3. The compound of claim 1 , wherein the compound has the following structure:
wherein X is selected from the group consisting of: CH, C—CH 3 , and N,
Y is selected from the group consisting of: CH 2 , CZ 2 , and C═O, where Z is a halogen, and
wherein taken together R 1 —X—R 2 form a C 3 to C 8 carbocyclic ring or heterocyclic ring, and the ring is optionally substituted.
4. The compound of claim 1 , wherein the compound has the following structure:
wherein X is selected from the group consisting of: CH, and N,
Y is selected from the group consisting of: CH 2 , CZ 2 , and C═O, where Z is a halogen
R 1 is C 1 to C 16 substituted or unsubstituted linear alkyl group,
R 2 is H,
wherein, optionally, where X is CH, R 1 is CR x R y , R x is H or C 1 to C 16 substituted or unsubstituted linear alkyl group, wherein R y is H or C 1 to C 16 substituted or unsubstituted linear alkyl group, and the bond between R 1 and X is a double bond,
wherein, optionally, X is CH, and R 1 and X are each bonded to O to form an epoxide, and
wherein when R is H, X is CH, Y is C═O, R 2 is H, R 3 is H, and R 1 is not C 1 to C 6 unsubstituted linear alkyl group.
5. The compound of claim 1 , wherein the compound has the following structure:
wherein X is selected from the group consisting of: CH, C—CH 3 , and N,
Y is selected from the group consisting of: CH 2 , CZ 2 , and C═O, where Z is a halogen,
A is selected from the group consisting of: NH, CH 2 , CF 2 , CHF and O,
R is selected from the group consisting of: phosphonate group, sulfonate group,
sulfoxide group, and carboxylate group,
R 1 is selected from the group consisting of: C 1 to C 16 substituted or unsubstituted branched alkyl group, C 1 to C 16 substituted or unsubstituted linear alkyl group, and C 3 to C 8 carbocyclic ring,
and R 2 is selected from the group consisting of: H or CH 3 ,
wherein, optionally, taken together R 1 and R 2 form a C 3 to C 8 carbocyclic ring or heterocyclic ring,
wherein the ring is, optionally, substituted,
wherein, optionally, where X is CH, R 1 is CR x R y , R x is H or C 1 to C 16 substituted or unsubstituted linear alkyl group, wherein R y is H or C 1 to C 16 substituted or unsubstituted linear alkyl group, and the bond between R 1 and X is a double bond, and
wherein, optionally, where X is CH, and R 1 and X are each bonded to 0 to form an epoxide,
wherein, optionally, where A is N, and taken together A and R form a 1,2,5-thiadiazolidin-3-one 1,1-dioxide.
6. The compound of claim 1 , wherein the compound has one of the following structures:
wherein A + is H + , alkali metal cation, divalent cation, trivalent cation, or ammonium cation.
7. A method for modulating quorum sensing (QS) in a population of bacteria comprising contacting the population of bacteria with a composition comprising a compound having the following structure (I):
wherein i) R and R 3 are each are each independently a phosphonate group, sulfonate group, sulfoxide group, or carboxylate group, ii) R is a phosphonate group, sulfonate group, sulfoxide group, or carboxylate group and R 3 is a H or keto group, or iii) R 3 is a phosphonate group, sulfonate group, sulfoxide group, or carboxylate group and R is a H or keto group,
A is selected from the group consisting of: S, NH, CH 2 , O, CZ 2 , and CHZ, where Z is a halogen;
Y is selected from the group consisting of: CH 2 , CZ 2 , and C═O, where Z is a halogen;
X is selected from the group consisting of: CH, C—CH 3 , and N;
R 1 is selected from the group consisting of: H, C 1 to C 16 substituted or unsubstituted branched alkyl group, C 1 to C 16 substituted or unsubstituted linear alkyl group, C 1 to C 16 heterocyclic ring, and C 3 to C 8 carbocyclic ring, and
R 2 is selected from the group of: H and CH 3 ,
wherein, optionally, taken together R 1 —X—R 2 form a C 3 to C 8 carbocyclic ring or heterocyclic ring, and the ring is, optionally, substituted,
wherein, optionally, X is CH, R 1 is CR x R y , and R x is H or C 1 to C 16 substituted or unsubstituted linear alkyl group, R y is H or C 1 to C 16 substituted or unsubstituted linear alkyl group, and the bond between R 1 and X is a double bond,
wherein, optionally, X is CH, and R 1 and X are each bonded to a single O to form an epoxide,
wherein, optionally, A is a N, and taken together A and R form a 1,2,5-thiadiazolidin-3-one 1,1-dioxide, and
wherein if X is CH, then R 1 and R 2 are not H, and
wherein if X is CH, then R 1 is not H and R 2 is not CH 3 .
8. A pharmaceutical preparation comprising a composition a compound having the following structure (I):
wherein i) R and R 3 are each are each independently a phosphonate group, sulfonate group, sulfoxide group, or carboxylate group, ii) R is a phosphonate group, sulfonate group, sulfoxide group, or carboxylate group and R 3 is a H or keto group, or iii) R 3 is a phosphonate group, sulfonate group, sulfoxide group, or carboxylate group and R is a H or keto group,
A is selected from the group consisting of: S, NH, CH 2 , O, CZ 2 , and CHZ, where Z is a halogen;
Y is selected from the group consisting of: CH 2 , CZ 2 , and C═O, where Z is a halogen;
X is selected from the group consisting of: CH, C—CH 3 , and N;
R 1 is selected from the group consisting of: H, C 1 to C 16 substituted or unsubstituted branched alkyl group, C 1 to C 16 substituted or unsubstituted linear alkyl group, C 1 to C 16 heterocyclic ring, and C 3 to C 8 carbocyclic ring, and
R 2 is selected from the group of: H and CH 3 ,
wherein, optionally, taken together R 1 —X—R 2 form a C 3 to C 8 carbocyclic ring or heterocyclic ring, and the ring is, optionally, substituted,
wherein, optionally, X is CH, R 1 is CR x R y , and R x is H or C 1 to C 16 substituted or unsubstituted linear alkyl group, R y is H or C 1 to C 16 substituted or unsubstituted linear alkyl group, and the bond between R 1 and X is a double bond,
wherein, optionally, X is CH, and R 1 and X are each bonded to a single O to form an epoxide,
wherein, optionally, A is a N, and taken together A and R form a 1,2,5-thiadiazolidin-3-one 1,1-dioxide, and
wherein if X is CH, then R 1 and R 2 are not H, and
wherein if X is CH, then R 1 is not H and R 2 is not CH 3 .