IP Library Granted Patent US 10,464,952
Granted Patent B2
US 10,464,952 · App. 16/002,363 · Granted Nov 5, 2019

Beta-lactamase inhibitors

Inventors: Christopher J. Burns (Malvern, PA); Daniel C. Pevear (Downingtown, PA); Robert E. Lee Trout (Collegeville, PA); Randy W. Jackson (Livingston, MT); Jodie Hamrick (New Holland, PA); Allison L. Zulli (Chesterbrook, PA); Eugen F. Mesaros (Wallingford, PA); Steven A. Boyd (Chester Springs, PA)
Assignee: VENATORX PHARMACEUTICALS, INC.
C07F5/025A61K31/427A61K31/43A61K31/545A61K31/546A61K31/69A61K45/06A61P31/04A61K2300/00
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Quick Facts
Patent No.
US 10,464,952
App. No.
16/002,363
Granted
Nov 5, 2019
Kind
B2
Abstract

Described herein are compounds and compositions that modulate the activity of beta-lactamases. In some embodiments, the compounds described herein inhibit beta-lactamase. In certain embodiments, the compounds described herein are useful in the treatment of bacterial infections.

Claims (34)

1. A compound of Formula (Ia) or (Ib) or pharmaceutically acceptable salts, isomers, stereoisomers, dimers, trimers, tautomers, or N-oxides thereof:

wherein:

X 1 and X 2 are independently —OR 4 or F; when present;

Z is >C(═O), >C(═S), or >S(═O) 2 ;

R 3 is R 31 , —(R 30 ) q OR 31 , —(R 30 ) q O(R 30 ) q OR 31 , —R 30 OC(═O)R 31 , —R 30 OC(═O)OR 31 , —R 30 OC(═O)NHR 31 , —R 30 OC(═O)N(R 31 ) 2 , optionally substituted alkyloxyalkyl, optionally substituted acyloxyalkyl, optionally substituted alkyloxycarbonyloxyalkyl, optionally substituted cycloalkyloxycarbonyloxyalkyl, optionally substituted aryloxycarbonyloxyalkyl, or optionally substituted alkyl-[1,3]dioxol-2-one;

each q are independently 1, 2, 3, 4, 5, or 6;

each R 30 are independently —CH 2 —, —CH(R 32 )—, or —C(R 32 ) 2 —;

each R 31 are independently optionally substituted C 1 -C 12 alkyl, optionally substituted alkoxyalkyl, optionally substituted C 1 -C 12 alkenyl, optionally substituted C 1 -C 12 alkynyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted alkylcycloalkyl, optionally substituted alkylheterocycloalkyl, optionally substituted alkylaryl, or optionally substituted alkylheteroaryl; or

two R 31 are taken together with the nitrogen to which they are attached to form a heterocycloalkyl;

each R 32 is independently optionally substituted C 1 -C 6 alkyl;

or two R 32 are taken together with the carbon to which they are attached to form a cycloalkyl;

R a , R b , R c are independently hydrogen, fluoro, chloro, bromo, optionally substituted C 1 -C 6 alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, —OR 4 , —N(R 4 R 5 ), or —SR 4 ; and

R d , R 4 , and R 5 are independently hydrogen, —OH, —CN, —CF 3 , optionally substituted C 1 -C 6 alkyl, optionally substituted alkoxyalkyl, optionally substituted hydroxyalkyl, optionally substituted aminoalkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkylalkyl, optionally substituted heterocycloalkylalkyl, optionally substituted aralkyl, optionally substituted heteroaralkyl, (poly-ethylene-glycol)-ethyl, or an optionally substituted saccharide;

or R 4 and R 5 are taken together with the nitrogen to which they are attached to form a heterocycloalkyl.

2. The compound of claim 1 , or pharmaceutically acceptable salts, isomers, stereoisomers, dimers, trimers, tautomers, or N-oxides thereof, wherein R 3 is R 31 , —R 30 OC(═O)R 31 , or —R 30 OC(═O)OR 31 .

3. The compound of claim 1 , or pharmaceutically acceptable salts, isomers, stereoisomers, dimers, trimers, tautomers, or N-oxides thereof, wherein R a , R b , and R c are hydrogen; and R d is hydrogen or C 1 -C 4 alkyl.

4. The compound of claim 1 , or pharmaceutically acceptable salts, isomers, stereoisomers, dimers, trimers, tautomers, or N-oxides thereof, wherein X 1 and X 2 are —OH; when present and Z is >C(═O).

5. The compound of claim 1 , wherein the compound is:

or pharmaceutically acceptable salts, isomers, stereoisomers, dimers, trimers, tautomers, or N-oxides thereof, wherein the compound is present in a closed form, an open form, or mixtures thereof.

6. A pharmaceutical composition comprising at least one compound of claim 1 , or pharmaceutically acceptable salts, isomers, stereoisomers, dimers, trimers, tautomers, or N-oxides thereof, and a pharmaceutically acceptable excipient.

7. A method of treating a bacterial infection in a subject, comprising administering to the subject a compound of claim 1 , or pharmaceutically acceptable salts, isomers, stereoisomers, dimers, trimers, tautomers, or N-oxides thereof.

8. A compound of Formula (IVa) or (IVb) or pharmaceutically acceptable salts, isomers, stereoisomers, dimers, trimers, tautomers, or N-oxides thereof:

wherein:

X 1 and X 2 are independently —OR 4 or F; when present;

Z is >C(═O), >C(═S), or >S(═O) 2 ;

R a , R b , R c are independently hydrogen, fluoro, chloro, bromo, optionally substituted C 1 -C 6 alkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, —OR 4 , —N(R 4 R 5 ), or —SR 4 ; and

R d , R 4 , and R 5 are independently hydrogen, —OH, —CN, —CF 3 , optionally substituted C 1 -C 6 alkyl, optionally substituted alkoxyalkyl, optionally substituted hydroxyalkyl, optionally substituted aminoalkyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkylalkyl, optionally substituted heterocycloalkylalkyl, optionally substituted aralkyl, optionally substituted heteroaralkyl, (poly-ethylene-glycol)-ethyl, or an optionally substituted saccharide;

or R 4 and R 5 are taken together with the nitrogen to which they are attached to form a heterocycloalkyl.

9. The compound of claim 8 , or pharmaceutically acceptable salts, isomers, stereoisomers, dimers, trimers, tautomers, or N-oxides thereof, wherein R a , R b , and R c are hydrogen; and R d is hydrogen or C 1 -C 4 alkyl.

10. The compound of claim 8 , or pharmaceutically acceptable salts, isomers, stereoisomers, dimers, trimers, tautomers, or N-oxides thereof, wherein X 1 and X 2 are —OH; when present; and Z is >C(═O).

11. The compound of claim 8 , wherein the compound is:

or pharmaceutically acceptable salts, isomers, stereoisomers, dimers, trimers, tautomers, or N-oxides thereof, wherein the compound is present in a closed form, an open form, or mixtures thereof.

12. A pharmaceutical composition comprising at least one compound of claim 8 , or pharmaceutically acceptable salts, isomers, stereoisomers, dimers, trimers, tautomers, or N-oxides thereof, and a pharmaceutically acceptable excipient.

13. A method of treating a bacterial infection in a subject, comprising administering to the subject a compound of claim 8 , or pharmaceutically acceptable salts, isomers, stereoisomers, dimers, trimers, tautomers, or N-oxides thereof.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 25, 2026
From: VENATORX PHARMACEUTICALS, INC.
To: BASILEA PHARMACEUTICA INTERNATIONAL AG, ALLSCHWIL
Reel/Frame 074177/0939 →
LICENSE Recorded Dec 9, 2024
From: VENATORX PHARMACEUTICALS INC
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 069545/0974 →
CONFIRMATORY LICENSE Recorded Feb 7, 2023
From: VENATORX PHARMACEUTICALS INC
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 062667/0362 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2018
From: BURNS, CHRISTOPHER J.; PEVEAR, DANIEL C.; TROUT, ROBERT E. LEE; JACKSON, RANDY W.; HAMRICK, JODIE; ZULLI, ALLISON L.; MESAROS, EUGEN F.; BOYD, STEVEN A.
To: VENATORX PHARMACEUTICALS, INC.
Reel/Frame 046692/0776 →
Continuity (3)
Continuation PCTUS2016065771 · Dec 9, 2016
Provisional Application 62265843 · Dec 10, 2015
Related Publication 20180291039A1 · Oct 11, 2018
Cited By (1)
US 12,544,395