US2016031893A1PendingUtilityA1

Antimicrobial compounds and methods of making and using the same

39
Assignee: MELINTA THERAPEUTICS INCPriority: Oct 16, 2009Filed: Oct 12, 2015Published: Feb 4, 2016
Est. expiryOct 16, 2029(~3.3 yrs left)· nominal 20-yr term from priority
A61P 31/04A61P 31/00C07D 471/08C07D 519/00C07D 487/04C07D 491/048A61K 31/519A61F 2250/0067A61F 2/82
39
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Claims

Abstract

The present invention relates generally to the field of antimicrobial compounds and to methods of making and using them. These compounds are useful for treating, preventing, and reducing the risk of microbial infections in humans and animals.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A compound having the formula: 
       
         
           
           
               
               
           
         
         wherein -G-H-J alternatively is selected from 
       
       
         
           
           
               
               
           
         
         wherein each H and J are independently selected, 
         C—B-A-, -D-E-F, and -G-H-J are chemical moieties, wherein 
         A, D and G are independently selected from the group consisting of:
 (a) a single bond, (b) —(C 1-8  alkyl)-, (c) —(C 2-8  alkenyl)-, (d) —(C 2-8  alkynyl)-, wherein
 i) 0-4 carbon atoms in any of (b)-(d) immediately above optionally is replaced by a moiety selected from the group consisting of —O—, S(O) p , —NR 6 —, —(C═O)—, —S(O) p NR 6 —, —NR 6 S(O) p —, and —NR 6 S(O) p NR 6 —, 
 ii) any of (b)-(d) immediately above optionally is substituted with one or more R 5  groups, and 
 iii) any of (b)-(d) immediately above optionally is substituted with —(C 1-8  alkyl)-R 5  groups; 
 
 (e) —O—, (f) —NR 6 —, (g) —S(O) p —, (h) —C(O)—, (i) —C(O)O—, (j) —OC(O)—, k) —OC(O)O—, (l) —C(O)NR 6 —, (m) —NR 6 CO—, (n) —NR 6 C(O)NR 6 —, (o) —C(═NR 6 )—, (p) —C(═NR 6 )O—, (q) —OC(═NR 6 )—, (r) —C(═NR 6 )NR 6 —, (s) —NR 6 C(═NR 6 )—, (t) —C(═S)—, (u) —C(═S)NR 6 —, (v) —NR 6 C(═S)—, (w) —C(O)S—, (x) —SC(O)—, (y) —OC(═S)—, (z) —C(═S)O—, (aa) —NR 6 (CNR 6 )NR 6 —, (bb) —CR 6 R 6 C(O)—, (cc) —C(O)NR 6 (CR 6 R 6 ) t —, (dd) a 3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, 
 (ee) a 3-14 member saturated, unsaturated, or aromatic carbocycle, and 
 (ff) —(CR 6 R 6 ) t —, 
 
         wherein (dd) or (ee) is optionally substituted with one or more R 5  groups; 
         B, E, and H are independently selected from the group consisting of:
 (a) a single bond, 
 (b) a 3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, 
 (c) a 3-14 member saturated, unsaturated, or aromatic carbocycle, 
 
         wherein (b) or (c) is optionally substituted with one or more R 5  groups;
 (d) —(C 1-8  alkyl)-, (e) —(C 2-8  alkenyl)-, (f) —(C 2-8  alkynyl)-, wherein
 i) 0-4 carbon atoms in any of (d)-(f) immediately above optionally is replaced by a moiety selected from the group consisting of —O—, —S(O) p —, —NR 6 —, —(C═O)—, —C(═NR 6 )—, —S(O) p NR 6 —, —NR 6 S(O) p —, and —NR 6 S(O) p NR 6 —, 
 ii) any of (d)-(f) immediately above optionally is substituted with one or more R 5  groups, and 
 iii) any of (d)-(f) immediately above optionally is substituted with —(C 1-8  alkyl)-R 5  groups; 
 
 and (g) —(CR 6 R 6 ) t —, 
 
         C, F, and J are independently selected from the group consisting of:
 (a) hydrogen, (c) F, (d) Cl, (e) Br, (f) I, (g) —CF 3 , (h) —CN, (i) —N 3  (j) —NO 2 , (k) —NR 6 (CR 6 R 6 ) t R 8 , (l) —OR 8 , (m) —S(O) p (CR 6 R 6 ) t R 8 , (n) —C(O)(CR 6 R 6 ) t R 8 , (o) —OC(O)(CR 6 R 6 ) t R 8 , (p) —SC(O)(CR 6 R 6 ) t R 8 , (q) —C(O)O(CR 6 R 6 ) t R 8 , (r) —NR 6 C(O)(CR 6 R 6 ) t R 8 , (s) —C(O)NR 6 (CR 6 R 6 ) t R 8 , (t) —C(═NR 6 )(CR 6 R 6 ) t R 8 , (u) —C(═NNR 6 R 6 )(CR 6 R 6 ) t R 8 , (v) —C(═NNR 6 C(O)R 6 )(CR 6 R 6 ) t R 8 , (w) —C(═NOR 8 )(CR 6 R 6 ) t R 8 , (x) —NR 6 C(O)O(CR 6 R 6 ) t R 8 , (y) —OC(O)NR 6 (CR 6 R 6 ) t R 8 , (z) —NR 6 C(O)NR 6 (CR 6 R 6 ) t R 8 , (aa) —NR 6 S(O) p (CR 6 R 6 ) t R 8 , (bb) —S(O) p NR 6 (CR 6 R 6 ) t R 8 , (cc) —NR 6 S(O) p NR 6 (CR 6 R 6 ) t R 8 , (dd) —NR 6 R 8 , (ee) —NR 6 (CR 6 R 6 )R 8 , (ff) —OH, (gg) —NR 8 R 8 , (hh) —OCH 3 , (ii) —S(O) p R 8 , (jj) —NC(O)R 8 , (kk) —NR 6 C(NR 6 )NR 6 R 8 , (ll) a C 1-8  alkyl group, (mm) a C 2-8  alkenyl group, (nn) a C 2-8 alkynyl group, (oo) a 3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, (pp) a 3-14 member saturated, unsaturated, or aromatic carbocycle, (qq) —(CR 6 R 6 ) t NR 6 (CR 6 R 6 ) t R 8 , (rr) —N[(CR 6 R 6 ) t R 8 ][C═O(CR 6 R 6 ) t R 8 ], (ss) —(CR 6 R 6 ) t N[(CR 6 R 6 ) t R 8 ][(CR 6 R 6 ) t R 8 ], (tt) —(CR 6 R 6 ) t NR 6 (C═O)(CR 6 R 6 ) t R 8 , (uu) -haloalkyl, (vv) —C(O)(CR 6 )[(CR 6 R 6 ) t R 8 ]R 8 , (ww) —(CR 6 R 6 ) t C(O)NR 8 R 8 , (xx) —(CR 6 R 6 ) t C(O)O(CR 6 R 6 ) t R 8 , (yy) —NR 6 C(O)CR 8 R 8 R 8 , (zz) —N[(CR 6 R 6 ) t R 8 ]C(O)R 8 , and (aaa) —S(O) p NR 8 R 8 ; 
 
         wherein (ll) through (pp) is optionally substituted with one or more R 7  groups; 
         R 5  is selected from (a) hydrogen, (b) F, (c) Cl, (d) Br, (e) I, (f) —CF 3 , (g) —CN, (h) —N 3  (i) —NO 2 , (j) —NR 6 R 6 , (k) —OR, (l) —NR 6 (CNR 6 )NR 6 R 6 , (m) —C 1-8  alkyl, (n) —C 1-8  alkenyl, (o) —C 1-8  alkynyl, (p) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur), (q) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic carbocycle), (r) -haloalkyl, (s) —SR 6 , (t) -3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, and (u) -3-14 member saturated, unsaturated, or aromatic carbocycle; alternatively, two R 5  groups are taken together to form a carbocycle
 wherein (m) through (r) and (t) through (u) is optionally substituted with one or more R 8 ; 
 
         R 6  is selected from (a) hydrogen, (b) —C 1-8  alkyl or alternatively two R 6  groups are taken together to form a carbocycle, (c) -haloalkyl, (d) -3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, and (e) -3-14 member saturated, unsaturated, or aromatic carbocycle; 
         wherein (b) through (e) is optionally substituted with one or more R 8 ; 
         R 7  is selected from (a) hydrogen, (b) F, (c) Cl, (d) Br, (e) I, (f) —CF 3 , (g) —CN, (h) —N 3  (i) —NO 2 , (j) —NR 6 R 6 , (k) —OR 6 , (l) —NR 6 (CNR 6 )NR 6 R 6 , (m) —C 1-8  alkyl, (n) —C 1-8  alkenyl, (o) —C 1-8  alkynyl, (p) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur), (q) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic carbocycle), (r) -haloalkyl, (s) —NR 6 R 8 , (t) —OR 8 , (u) —(CR 6 R 6 ) t NR 6 R 8 , (v) —CR 6 R 8 R 8 , (w) —SR 6 , (x) -3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, (y) -3-14 member saturated, unsaturated, or aromatic carbocycle, (z) —(CR 6 R 6 ) t C(O)NR 8 R 8 , (aa) —S(O) p R 8 , (bb) —NR 6 C(O)NR 6 R 6 , (cc) —NR 6 C(O)R 6 , and (dd) —C(═NR 6 )NR 6 R 6 ;
 wherein (m) through (q) and (x) through (y) are optionally substituted with one or more R 9 ; 
 
         R is selected from (a) hydrogen, (b) F, (c) Cl, (d) Br, (e) I, (f) —CF 3 , (g) —CN, (h) —N 3  (i) —NO 2 , (j) —NR 6 R 9 , (k) —OR 9 , (l) —NR 6 (CNR 6 )NR 6 R 6 , (m) —C 1-8  alkyl, (n) —C 1-8  alkenyl, (o) —C 1-8  alkynyl, (p) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur), (q) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic carbocycle), (r) -3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, (s) -3-14 member saturated, unsaturated, or aromatic carbocycle, (t) -haloalkyl, (u) —C(O)(CR 6 R 6 ) t R 9 , (v) —SR 6 , (w) —OC(O)(CR 6 R 6 ) t R 9 , (x) —NR 6 C(O)NR 6 R 9 , (y) —NR 6 C(O)R 9 , (z) —NR 6 (CNR 9 )(NR 6 R 6 ), (aa) —ONR 6 (CNR 6 )NR 6 R 6 , (bb) —C(═NR 9 )NR 6 R 6 , (cc) —S(O) p R 9 , (dd) —(CR 6 R 6 ) t C(O)NR 6 R 9 , (ee) —(CR 6 R 6 ) t OR 9 , and (ff) —(CR 6 R 6 ) t NR 6 R 9 ;
 wherein (m) through (s) is optionally substituted with one or more R 9 ; 
 
         R 9  is selected from (a) hydrogen, (b) F, (c) Cl, (d) Br, (e) I, (f) —CF 3 , (g) —CN, (h) —N 3  (i) —NO 2 , (j) —NR 6 R 10 , (k) —OR 6 , (l) —NR 6 (CNR 6 )NR 6 R 6 , (m) —C(O)(CR 6 R 6 ) t NR 6 R 6 , (n) —C 1-8  alkyl, (o) —C 1-8  alkenyl, (p) —C 1-8  alkynyl, (q) -3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, (r) -3-14 member saturated, unsaturated, or aromatic carbocycle, (s) -haloalkyl, (t) —(CR 6 R 6 ) t OR 6 , (u) —O(CR 6 R 6 ) t NR 6 R 10 , (v) —C(O)R 6 , (w) —SR 6 , (x) —C(O)OR 10 , (y) —S(O) p R 6 , (z) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur), (aa) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic carbocycle), (bb) —O(CR 6 R 6 ) t OR 6 , (cc) —C(═NR 6 )NR 6 R 6 , (dd) —ONR 6 R 6 , (ee) —NR 6 C(O)NR 6 R 6 , (ff) —O(CR 6 R 6 ) t OR 6 , (gg) —NR 6 C(O)R 6 , and (hh) —(CR 6 R 6 ) t NR 6 R 10 ;
 wherein (n) through (r) and (z) through (aa) is optionally substituted with one or more R 10 ; 
 
         R 10  is selected from (a) hydrogen, (b) F, (c) Cl, (d) Br, (e) I, (f) —CF 3 , (g) —CN, (h) —N 3  (i) —NO 2 , (j) —NR 6 R 6 , (k) —OR 6 , (l) —NR 6 (CNR 6 )NR 6 R 6 , (m) —C(O)(CR 6 R 6 ) t NR 6 R 6 , (n) —C 1-8  alkyl, (o) —C 1-8  alkenyl, (p) —C 1-8  alkynyl, (q) -3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, (r) -3-14 member saturated, unsaturated, or aromatic carbocycle, (s) -haloalkyl, (t) —(CR 6 R 6 ) t OR 6 , (u) —O(CR 6 R 6 ) t NR 6 R 6 , (v) —C(O)R 6 , (w) —SR 6 , (x) —C(O)OR 6 , (y) —S(O) p R 6 , (z) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur), (aa) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic carbocycle), (bb) —O(CR 6 R 6 ) t OR 6 , (cc) —C(═NR 6 )NR 6 R 6 , (dd) —ONR 6 R 6 , (ee) —NR 6 C(O)NR 6 R 6 , (ff) —O(CR 6 R 6 ) t OR 6 , (gg) —NR 6 C(O)R 6 , and (hh) —(CR 6 R 6 ) t NR 6 R 6 ;
 optionally, wherein either the group -D-E-F or the group -G-H-J is absent, but both -D-E-F and -G-H-J are not simultaneously absent; 
 
         p is 0, 1, or 2, and 
         t is 0, 1, 2, or 3, 
         or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof. 
       
     
     
         2 . The compound according to  claim 1  having the formula: 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof. 
     
     
         3 . The compound according to  claim 2  having the formula: 
       
         
           
           
               
               
           
         
       
       wherein D and E are single bonds and F is hydrogen, or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof. 
     
     
         4 . The compound according to  claim 3 , wherein
 A is selected from
 (a) a 3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, 
 (b) a 3-14 member saturated, unsaturated, or aromatic carbocycle, and 
 (c) a single bond, 
   wherein (a) or (b) is optionally substituted with one or more R 5  groups;   B is selected from (a) —(C 1-8  alkyl)-, (b) —(C 2-8  alkenyl)-, (c) —(C 2-8  alkynyl)-, (d) a single bond, wherein
 i) 0-4 carbon atoms in any of (a)-(c) immediately above optionally is replaced by a moiety selected from the group consisting of —O—, —S(O) p —, —NR 6 —, —(C═O)—, —C(═NR 6 )—, —S(O) p NR 6 —, and —NR 6 S(O) p NR 6 —, 
 ii) any of (a)-(c) immediately above optionally is substituted with one or more R 5  groups, and 
 iii) any of (a)-(c) immediately above optionally is substituted with —(C 1-8  alkyl)-R 5  groups, and 
   C is selected from (a) NH 2 , (b) —NHC(═NH)NH 2  and (c) hydrogen,   or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof.   
     
     
         5 . The compound according to  claim 4 , wherein
 A is selected from azepanyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, phenyl, pyridyl, cyclohexenyl, cyclohexadienyl, dihydropyridyl, furanyl, tetrahydrofuranyl, tetrahydropyridyl, azetidinyl, pyrrolidinyl, piperidinyl, and piperidenyl,   wherein any of A immediately above optionally is substituted with one or more R 5  groups;   alternatively, A is a single bond;   B is selected from (a) —(C 1-8  alkyl)-, wherein
 i) 0-4 carbon atoms in (a) immediately above optionally is replaced by a moiety selected from the group consisting of —O—, —S(O) p —, —NR 6 —, —(C═O)—, —S(O) p NR 6 —, and —NR 6 S(O) p NR 6 —, 
 ii) (a) immediately above optionally is substituted with one or more R 5  groups, and 
 iii) (a) immediately above optionally is substituted with —(C 1-8  alkyl)-R 5  groups; and 
   alternatively, B is a single bond;   C is selected from (a) NH 2 , (b) —NHC(═NH)NH 2  and (c) hydrogen;   or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof.   
     
     
         6 . The compound according to  claim 5 , wherein C—B-A- is selected from the group consisting of:
 hydrogen, 
 
       
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof. 
     
     
         7 . The compound according to  claim 3 , wherein G is selected from
 (a) a 3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, and   (b) a 3-14 member saturated, unsaturated, or aromatic carbocycle,   (c) a single bond;   
       wherein (a) or (b) is optionally substituted with one or more R 5  groups, or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof. 
     
     
         8 . The compound according to  claim 4 , wherein R 5  is selected from (a) hydrogen, (b) F, (c) Cl, (d) Br, (e) I, (f) —CF 3 , (g) —CN, (h) —N 3  (i) —NO 2 , (j) —NH 2 , (k) —OR 6 , (l) —NHC(═NH)NH 2 , (m) —C 1-8  alkyl, (n) —C 1-8  alkenyl, (o) —C 1-8  alkynyl, (p) —(C 1-8  alkyl) -(3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur), (q) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic carbocycle), (r) -haloalkyl, (s) —SR 6 , (t) -3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, and (u) -3-14 member saturated, unsaturated, or aromatic carbocycle; alternatively, two R 5  groups are taken together to form a carbocycle; or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof. 
     
     
         9 . The compound according to  claim 4 , wherein R 6  is selected from (a) hydrogen, (b) —C 1-8  alkyl or alternatively two R 6  groups are taken together to form a carbocycle, (c) -haloalkyl, (d) -3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, and (e) -3-14 member saturated, unsaturated, or aromatic carbocycle; or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof. 
     
     
         10 . The compound according to  claim 7 , wherein G is selected from azepanyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, phenyl, pyridyl, cyclohexenyl, cyclohexadienyl, dihydropyridyl, furanyl, tetrahydrofuranyl, tetrahydropyridyl, azetidinyl, pyrrolidinyl, piperidinyl, piperidenyl, and a single bond; or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof. 
     
     
         11 . The compound according to  claim 10 , wherein -G-H-J is selected from:
 hydrogen,   
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof. 
     
     
         12 . The compound according to  claim 11 , wherein each -G-H-J is selected from: hydrogen, 
       
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         
           
           
               
               
           
         
       
       wherein n is 0, 1, or 2, 
       further wherein R 5  is as defined in  claim 8 , 
       or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof. 
     
     
         13 . The compound according to any of  claims 1  to  12  that binds to a ribosome. 
     
     
         14 . The compound according to  claim 13 , wherein the ribosome is a bacterial ribosome. 
     
     
         15 . The compound according to any of the compounds in Table 1 or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof. 
     
     
         16 . The pharmaceutical composition comprising a compound according to any one of  claims 1 - 15 , or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof, and a pharmaceutically acceptable carrier. 
     
     
         17 . A method for treating, preventing, or reducing the risk of a disease state in a human or animal comprising administering to a human or animal in need thereof an effective amount of a compound according to any one of  claims 1 - 15 , or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof. 
     
     
         18 . A method of treating a microbial infection in a human or animal comprising administering to the human or animal an effective amount of a compound according to any one of  claims 1 - 15 , or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof. 
     
     
         19 . The use of a compound according to any one of  claims 1 - 15 , or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof, in the manufacture of a medicament for treating a microbial infection in a human or animal. 
     
     
         20 . A method of treating, preventing, or reducing the risk of a microbial infection in a human or animal comprising administering to the human or animal an effective amount of a compound according to any one of  claims 1 - 15 , or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof, wherein the microbial infection is selected from the group consisting of:
 a skin infection, a Gram positive infection, a Gram negative infection, nosocomial pneumonia, community acquired pneumonia, post-viral pneumonia, hospital acquired pneumonia/ventilator associated pneumonia, a respiratory tract infection such as chronic respiratory tract infection (CRTI), acute pelvic infection, a complicated skin and skin structure infection, a skin and soft tissue infection (SSTI) including uncomplicated skin and soft tissue infections (uSSTI)s and complicated skin and soft tissue infections, an abdominal infection, a complicated intra-abdominal infection, a urinary tract infection, bacteremia, septicemia, endocarditis, an atrio-ventricular shunt infection, a vascular access infection, meningitis, surgical prophylaxis, a peritoneal infection, a bone infection, a joint infection, a methicillin-resistant  Staphylococcus aureus  infection, a vancomycin-resistant Enterococci infection, a linezolid-resistant organism infection, a  Bacillus anthracis  infection, a  Francisella tularensis  infection, a  Yersinia pestis  infection, and tuberculosis.   
     
     
         21 . The method or use according to any one of  claims 17 - 20  wherein the compound, or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof, is administered otically, ophthalmically, nasally, orally, parenterally, topically, or intravenously. 
     
     
         22 . A method of synthesizing a compound according to any of  claims 1 - 15 , or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof. 
     
     
         23 . A medical device containing a compound according to any one of  claims 1 - 15 , or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof. 
     
     
         24 . The medical device according to  claim 23 , wherein the device is a stent. 
     
     
         25 . A compound having the formula: 
       
         
           
           
               
               
           
         
         wherein   represents a fused 5 to 7 member saturated, unsaturated, or aromatic carbocyclic or heterocyclic ring system, 
         wherein T 1  is a carbon atom or N, such that when T 1  is N, -D-E-F is absent, 
         wherein T 2  is a carbon atom or N, such that when T 2  is N, -G-H-J is absent, 
         wherein both T 1  and T 2  are not both simultaneously N, 
         wherein V is independently selected from —CR 4a — or —N—, 
         W is O, NR 1 , NOR 1 , or S, alternatively W═ is selected from the combination of HO— and H— both attached to the same carbon atom or the combination of (C 1-8  alkyl)O— and H— both attached to the same carbon atom; 
       
       
         
           
           
               
               
           
         
       
       represents a single bond or a double bond such that when 
       
         
           
           
               
               
           
         
       
       is a single bond, X is selected from O, NR 2 , and S(O) and Y is C—R 3 , and when 
       
         
           
           
               
               
           
         
       
       is a double bond, X is N and Y is a carbon atom,
 Z is selected from the group consisting of O, NR 4 , S(O) n , or NH, 
 R 1  is selected from H and C 1-8  alkyl, 
 R 2  is selected from H and C 1-8  alkyl, 
 R 3  is selected from H and C 1-8  alkyl, 
 R 4  is selected from H and C 1-8  alkyl, 
 R 4a  is selected from H and C 1-8  alkyl, 
 n is 0, 1, or 2, 
 alternatively -G-H-J is selected from 
 
       
         
           
           
               
               
           
         
         wherein each H and J are independently selected, 
         C—B-A-, -D-E-F, and -G-H-J are chemical moieties, wherein 
         A, D and G are independently selected from the group consisting of:
 (a) a single bond, (b) —(C 1-8  alkyl)-, (c) —(C 2-8  alkenyl)-, (d) —(C 2-8  alkynyl)-, wherein
 i) 0-4 carbon atoms in any of (b)-(d) immediately above optionally is replaced by a moiety selected from the group consisting of —O—, —S(O) p —, —NR 6 —, —(C═O)—, —S(O) p NR 6 —, —NR 6 S(O) p —, and —NR 6 S(O) p NR 6 —, 
 ii) any of (b)-(d) immediately above optionally is substituted with one or more R 5  groups, and 
 iii) any of (b)-(d) immediately above optionally is substituted with —(C 1-8  alkyl)-R 5  groups; 
 
 (e) —O—, (f) —NR 6 —, (g) —S(O) p —, (h) —C(O)—, (i) —C(O)O—, (j) —OC(O)—, k) —OC(O)O—, (l) —C(O)NR 6 —, (m) —NR 6 CO—, (n) —NR 6 C(O)NR 6 —, (o) —C(═NR 6 )—, (p) —C(═NR 6 )O—, (q) —OC(═NR 6 )—, (r) —C(═NR 6 )NR 6 —, (s) —NR 6 C(═NR 6 )—, (t) —C(═S)—, (u) —C(═S)NR 6 —, (v) —NR 6 C(═S)—, (w) —C(O)S—, (x) —SC(O)—, (y) —OC(═S)—, (z) —C(═S)O—, (aa) —NR 6 (CNR 6 )NR 6 —, (bb) —CR 6 R 6 C(O)—, (cc) —C(O)NR 6 (CR 6 R 6 ) t —, (dd) a 3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, 
 (ee) a 3-14 member saturated, unsaturated, or aromatic carbocycle, and 
 (ff) —(CR 6 R 6 ) t —, 
 
         wherein (dd) or (ee) is optionally substituted with one or more R 5  groups; 
         B, E, and H are independently selected from the group consisting of:
 (a) a single bond, 
 (b) a 3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, 
 (c) a 3-14 member saturated, unsaturated, or aromatic carbocycle, 
 
         wherein (b) or (c) is optionally substituted with one or more R 5  groups;
 (d) —(C 1-8  alkyl)-, (e) —(C 2-8  alkenyl)-, (f) —(C 2-8  alkynyl)-, wherein
 i) 0-4 carbon atoms in any of (d)-(f) immediately above optionally is replaced by a moiety selected from the group consisting of —O—, —S(O) p —, —NR 6 —, —(C═O)—, —C(═NR 6 )—, —S(O) p NR 6 —, —NR 6 S(O) p —, and —NR 6 S(O) p NR 6 —, 
 ii) any of (d)-(f) immediately above optionally is substituted with one or more R 5  groups, and 
 iii) any of (d)-(f) immediately above optionally is substituted with —(C 1-8  alkyl)-R 5  groups; 
 
 and (g) —(CR 6 R 6 ) t —, 
 
         C, F, and J are independently selected from the group consisting of:
 (a) hydrogen, (c) F, (d) Cl, (e) Br, (f) I, (g) —CF 3 , (h) —CN, (i) —N 3  (j) —NO 2 , (k) —NR 6 (CR 6 R 6 ) t R 8 , (l) —OR 8 , (m) —S(O) p (CR 6 R 6 ) t R 8 , (n) —C(O)(CR 6 R 6 ) t R 8 , (o) —OC(O)(CR 6 R 6 ) t R 8 , (p) —SC(O)(CR 6 R 6 ) t R 8 , (q) —C(O)O(CR 6 R 6 ) t R 8 , (r) —NR 6 C(O)(CR 6 R 6 ) t R 8 , (s) —C(O)NR 6 (CR 6 R 6 ) t R 8 , (t) —C(═NR 6 )(CR 6 R 6 ) t R 8 , (u) —C(═NNR 6 R 6 )(CR 6 R 6 ) t R 8 , (v) —C(═NNR 6 C(O)R 6 )(CR 6 R 6 ) t R 8 , (w) —C(═NOR 8 )(CR 6 R 6 ) t R 8 , (x) —NR 6 C(O)O(CR 6 R 6 ) t R 8 , (y) —OC(O)NR 6 (CR 6 R 6 ) t R 8 , (z) —NR 6 C(O)NR 6 (CR 6 R 6 ) t R 8 , (aa) —NR 6 S(O) p (CR 6 R 6 ) t R 8 , (bb) —S(O) p NR 6 (CR 6 R 6 ) t R 8 , (cc) —NR 6 S(O) p NR 6 (CR 6 R 6 ) t R 8 , (dd) —NR 6 R 8 , (ee) —NR 6 (CR 6 R 6 )R 8 , (ff) —OH, (gg) —NR 8 R 8 , (hh) —OCH 3 , (ii) —S(O) p R 8 , (jj) —NC(O)R 8 , (kk) —NR 6 C(NR 6 )NR 6 R 8 , (ll) a C 1-8  alkyl group, (mm) a C 2-8  alkenyl group, (nn) a C 2-8 alkynyl group, (oo) a 3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, (pp) a 3-14 member saturated, unsaturated, or aromatic carbocycle, (qq) —(CR 6 R 6 ) t NR 6 (CR 6 R 6 ) t R 8 , (rr) —N[(CR 6 R 6 ) t R 8 ][C═O(CR 6 R 6 ) R 8 ], (ss) —(CR 6 R 6 ) t N[(CR 6 R 6 ) t R 8 ][(CR 6 R 6 ) t R 8 ], (tt) —(CR 6 R 6 ) t NR 6 (C═O)(CR 6 R 6 ) t R 8 , (uu) -haloalkyl, (vv) —C(O)(CR 6 )[(CR 6 R 6 ) t R 8 ]R 8 , (ww) —(CR 6 R 6 ) t C(O)NR 8 R 8 , (xx) —(CR 6 R 6 ) t C(O)O(CR 6 R 6 ) t R 8 , (yy) —NR 6 C(O)CR 8 R 8 R 8 , (zz) —N[(CR 6 R 6 ) t R 8 ]C(O)R 8 , and (aaa) —S(O) p NR 8 R 8 ; 
 
         wherein (ll) through (pp) is optionally substituted with one or more R 7  groups; 
         R 5  is selected from (a) hydrogen, (b) F, (c) Cl, (d) Br, (e) I, (f) —CF 3 , (g) —CN, (h) —N 3  (i) —NO 2 , (j) —NR 6 R 6 , (k) —OR 8 , (l) —NR 6 (CNR 6 )NR 6 R 6 , (m) —C 1-8  alkyl, (n) —C 1-8  alkenyl, (o) —C 1-8  alkynyl, (p) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur), (q) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic carbocycle), (r) -haloalkyl, (s) —SR 6 , (t) -3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, and (u) -3-14 member saturated, unsaturated, or aromatic carbocycle; alternatively, two R 5  groups are taken together to form a carbocycle;
 wherein (m) through (r) and (t) through (u) is optionally substituted with one or more R 8 ; 
 
         R 6  is selected from (a) hydrogen, (b) —C 1-8  alkyl or alternatively two R 6  groups are taken together to form a carbocycle, (c) -haloalkyl, (d) -3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, and (e) -3-14 member saturated, unsaturated, or aromatic carbocycle; 
         wherein (b) through (e) is optionally substituted with one or more R 8 ; 
         R 7  is selected from (a) hydrogen, (b) F, (c) Cl, (d) Br, (e) I, (f) —CF 3 , (g) —CN, (h) —N 3  (i) —NO 2 , (j) —NR 6 R 6 , (k) —OR 6 , (l) —NR 6 (CNR 6 )NR 6 R 6 , (m) —C 1-8  alkyl, (n) —C 1-8  alkenyl, (o) —C 1-8  alkynyl, (p) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur), (q) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic carbocycle), (r) -haloalkyl, (s) —NR 6 R 8 , (t) —OR 8 , (u) —(CR 6 R 6 ) t NR 6 R 8 , (v) —CR 6 R 8 R 8 , (w) —SR 6 , (x) -3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, (y) -3-14 member saturated, unsaturated, or aromatic carbocycle, (z) —(CR 6 R 6 ) t C(O)NR 8 R 8 , (aa) —S(O) p R 8 , (bb) —NR 6 C(O)NR 6 R 6 , (cc) —NR 6 C(O)R 6 , and (dd) —C(═NR 6 )NR 6 R 6 ;
 wherein (m) through (q) and (x) through (y) are optionally substituted with one or more R 9 ; 
 
         R 8  is selected from (a) hydrogen, (b) F, (c) Cl, (d) Br, (e) I, (f) —CF 3 , (g) —CN, (h) —N 3  (i) —NO 2 , (j) —NR 6 R 9 , (k) —OR 9 , (l) —NR 6 (CNR 6 )NR 6 R 6 , (m) —C 1-8  alkyl, (n) —C 1-8  alkenyl, (o) —C 1-8  alkynyl, (p) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur), (q) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic carbocycle), (r) -3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, (s) -3-14 member saturated, unsaturated, or aromatic carbocycle, (t) -haloalkyl, (u) —C(O)(CR 6 R 6 ) t R 9 , (v) —SR 6 , (w) —OC(O)(CR 6 R 6 ) t R 9 , (x) —NR 6 C(O)NR 6 R 9 , (y) —NR 6 C(O)R 9 , (z) —NR 6 (CNR 9 )(NR 6 R 6 ), (aa) —ONR 6 (CNR 6 )NR 6 R 6 , (bb) —C(═NR 9 )NR 6 R 6 , (cc) —S(O) p R 9 , (dd) —(CR 6 R 6 ) t C(O)NR 6 R 9 , (ee) —(CR 6 R 6 ) t OR 9 , and (ff) —(CR 6 R 6 ) t NR 6 R 9 ;
 wherein (m) through (s) is optionally substituted with one or more R 9 ; 
 
         R 9  is selected from (a) hydrogen, (b) F, (c) Cl, (d) Br, (e) I, (f) —CF 3 , (g) —CN, (h) —N 3  (i) —NO 2 , (j) —NR 6 R 10 , (k) —OR 6 , (l) —NR 6 (CNR 6 )NR 6 R 6 , (m) —C(O)(CR 6 R 6 ) t NR 6 R 6 , (n) —C 1-8  alkyl, (o) —C 1-8  alkenyl, (p) —C 1-8  alkynyl, (q) -3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, (r) -3-14 member saturated, unsaturated, or aromatic carbocycle, (s) -haloalkyl, (t) —(CR 6 R 6 ) t OR 6 , (u) —O(CR 6 R 6 ) t NR 6 R 10 , (v) —C(O)R 6 , (w) —SR 6 , (x) —C(O)OR 10 , (y) —S(O) p R 6 , (z) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur), (aa) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic carbocycle), (bb) —O(CR 6 R 6 ) t OR 6 , (cc) —C(═NR 6 )NR 6 R 6 , (dd) —ONR 6 R 6 , (ee) —NR 6 C(O)NR 6 R 6 , (ff) —O(CR 6 R 6 ) t OR 6 , (gg) —NR 6 C(O)R 6 , and (hh) —(CR 6 R 6 ) t NR 6 R 10 ;
 wherein (n) through (r) and (z) through (aa) is optionally substituted with one or more R 10 ; 
 
         R 10  is selected from (a) hydrogen, (b) F, (c) Cl, (d) Br, (e) I, (f) —CF 3 , (g) —CN, (h) —N 3  (i) —NO 2 , (j) —NR 6 R 6 , (k) —OR 6 , (l) —NR 6 (CNR 6 )NR 6 R 6 , (m) —C(O)(CR 6 R 6 ) t NR 6 R 6 , (n) —C 1-8  alkyl, (o) —C 1-8  alkenyl, (p) —C 1-8  alkynyl, (q) -3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur, (r) -3-14 member saturated, unsaturated, or aromatic carbocycle, (s) -haloalkyl, (t) —(CR 6 R 6 ) t OR 6 , (u) —O(CR 6 R 6 ) t NR 6 R 6 , (v) —C(O)R 6 , (w) —SR 6 , (x) —C(O)OR 6 , (y) —S(O) p R 6 , (z) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic heterocycle containing one or more heteroatoms selected from the group consisting of nitrogen, oxygen, and sulfur), (aa) —(C 1-8  alkyl)-(3-14 member saturated, unsaturated, or aromatic carbocycle), (bb) —O(CR 6 R 6 ) t OR 6 , (cc) —C(═NR 6 )NR 6 R 6 , (dd) —ONR 6 R 6 , (ee) —NR 6 C(O)NR 6 R 6 , (ff) —O(CR 6 R 6 ) t OR 6 , (gg) —NR 6 C(O)R 6 , and (hh) —(CR 6 R 6 ) t NR 6 R 6 ;
 optionally, wherein either the group -D-E-F or the group -G-H-J is absent, but both -D-E-F and -G-H-J are not simultaneously absent; 
 
         p is 0, 1, or 2, and 
         t is 0, 1, 2, or 3, 
         or a pharmaceutically acceptable salt, ester, tautomer, or prodrug thereof.

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