IP Library Granted Patent US 8,877,752
Granted Patent B2
US 8,877,752 · App. 13/661,300 · Granted Nov 4, 2014

4(1H)-quinolones having antimalarial activity with reduced chemical resistance

Inventors: Roman Manetsch (Tampa, FL); Richard Matthew Cross (Brandon, FL); Niranjan Kumar Namelikonda (Tampa, FL); Dennis Edward Kyle (Lithia, FL); Tina Susanna Mutka (Tampa, FL); Alexis Nichole LaCrue (Temple Terrace, FL); Jordany Richarlson Maignan (Tampa, FL); Fabian Ernesto Saenz (Quito, EC)
Assignee: University of South Florida
C07D215/233C07D413/04C07D401/04C07D215/56
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Quick Facts
Patent No.
US 8,877,752
App. No.
13/661,300
Granted
Nov 4, 2014
Kind
B2
Abstract

Provided are 4(1H)-quinolone derivatives effective in inhibiting or eliminating the viability of at least one of the stages in the life-cycle of the malarial parasite, and to show a reduced propensity to induce resistance to the compound by the target parasite. In particular, the compounds can be derivatives of phenoxyethoxy-quinolones, and including, but not only, 7-(2-phenoxyethoxy)quinolin derivatives. These compounds may be administered by themselves, with at least one other derivative compound, or with other antimalarial compounds, to an animal or human subject. The therapeutic compositions can be and formulated to reduce the extent of a Plasmodium infection in the recipient subject, or to reduce the likelihood of the onset or establishment of a Plasmodium infection if administered prior to the parasite contacting the subject. The therapeutic compositions can be formulated to provide an effective single dose amount of an antimalarial compound or multiple doses for administering over a period of time.

Claims (28)

1. A compound having the Formula I or II:

wherein, in Formula I:

R 1 is H, ethyl, an aryl, carboxymethyl, or a halogen;

R 2 is 2-phenoxyethoxy, methoxymethoxy, 3-hydroxy-propoxy, 2-ethyl-3-oxo-butyricacid, 2-morpholino-4-yl-ethoxy-, 2-dimethylamino-ethoxy, or 3-(4-phenyl-piperazin-1-yl)-propoxy;

R 3 is H, butyrate, a halogen, methyl, or methoxy; and

R 4 is H or methyl, and wherein, when R 2 is methoxymethoxy, R 3 is a halogen; and

wherein in Formula II:

R 5 is an H or an alkyl, and

Ar is an aromatic group selected from the group consisting of: phenyl, pyridin-4-yl, pyridin-3-yl, 4-(trifluoromethyl)phenyl, 4-fluorophenoxyphenyl, 4-((4-(trifluoromethoxy)phenoxy)methyl)phenyl), (2-methyl-4-(4-(trifluoromethoxy)phenoxy)phenyl), (2-methyl-4-(trifluoromethyl)phenyl), 2,4-dimethylphenyl), (2-fluoro-4-(trifluoromethyl)phenyl), (4-chloro-2-methylphenyl), and (3,5-dimethylisooxazol-4-yl).

2. The compound of claim 1 having the Formula I.

3. A compound having the Formula I,

wherein:

R 1 is H, ethyl, an aryl, carboxymethyl, or a halogen;

R 2 is 2-phenoxyethoxy, methoxymethoxy, 3-hydroxy-propoxy, 2-ethyl-3-oxo-butyricacid, 2-morpholino-4-yl-ethoxy-, 2-dimethylamino-ethoxy, or 3-(4-phenyl-piperazin-1-yl)-propoxy;

R 3 is H, butyl, a halogen, methyl, or methoxy; and

R 4 is H or methyl, and

wherein the compound is selected from the group consisting of:

6-butyl-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (15), 6-butyl-3-ethyl-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (16), 6-chloro-3-ethyl-2-methyl-7-(2-phenoxy-ethoxy)-1H-quinolin-4-one (17), 3-ethyl-2,6-dimethyl-7-(2-phenoxy-ethoxy)-1H-quiolin-4-one (18), 6-chloro-3-ethyl-7-methoxymethoxy-2-methyl-1H-quinoline-4-one (20), 6-chloro-3-ethyl-7-(3-hydroxy-propoxy)-2-methyl-1H-quinolin-4-one (21), 2-ethyl-3-oxo-butyricacid-3-(6-chloro-3-ethyl-2-methyl-4-oxo-1,4-dihydro-quinolin-7-yloxy)-propyl ester (22), 6-chloro-3-ethyl-2-methyl-7-(2-morpholin-4-yl-ethoxy)-1H-quinolin-4-one (23), 6-chloro-7-(2-dimethylamino-ethoxy)-3-ethyl-2-methyl-1H-quinolin-4-one (24), 6-bromo-3-ethyl-2-methyl-7-(2-phenoxy-ethoxy)-1H-quinolin-4-one (25), and 6-chloro-3-ethyl-2-methyl-7[3-(4-phenyl-piperazin-1-yl)-propoxy]-1H-quinolin-4-one (26).

4. The compound of claim 1 having the Formula II.

5. The compound of claim 1 , wherein R 5 is methyl or ethyl.

6. The compound of claim 4 , wherein the compound is selected from the group consisting of:

6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-phenylquinolin-4(1H)-one (31), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-(pyridin-4-yl)quinolin-4(1H)-one (32), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-(pyridin-3-yl)quinolin-4(1H)-one (33), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-(4-(trifluoromethyl)phenyl)quinolin-4(1H)-one (34), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-(4-(trifluoromethoxy)phenyl)quinolin-4(1H)-one (35), 6-butyl-3-(3-(4-fluorophenoxy)phenyl)-2-methyl-7-(2phenoxyethoxy)quinolin-4(1H)-one (36), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-(4-((4-(trifluoromethoxy)phenoxy)methyl)phenyl) quinolin-4(1H)-one (37), 6-butyl-2-methyl-3-(2-methyl-4-(4-(trifluoromethoxy)phenoxy)phenyl)-7-(2-phenoxyethoxy)-quinolin-4(1H)-one (38), 6-butyl-2-methyl-3-(2-methyl-4-(trifluoromethyl)phenyl)-7-(2-phenoxyethoxy)quinolin-4(1H)-one (39), 6-butyl-3-(2,4-dimethylphenyl)-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (40), 6-butyl-3-(2-fluoro-4-(trifluoromethyl)phenyl)-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (41), 6-butyl-3-(4-chloro-2-methylphenyl)-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (42), and 6-butyl-3-(3,5-dimethylisoxazol-4-yl)-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (43).

7. A pharmaceutically acceptable composition comprising a therapeutic amount of a compound selected from the group consisting of: 6-butyl-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (15), 6-butyl-3-ethyl-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (16), 6-chloro-3-ethyl-2-methyl-7-(2-phenoxy-ethoxy)-1H-quinolin-4one (17), 3-ethyl-2,6-dimethyl-7-(2-phenoxy-ethoxy)-1H-quiolin-4-one (18) 6-chloro-3-ethyl-7-methoxymethoxy-2-methyl-1H-quinoline-4-one (20), 6-chloro-3-ethyl-7-(3-hydroxy-propoxy)-2-methyl-1H-quinolin-4-one (21), 2-ethyl-3-oxo-butyricacid-3-(6-chloro-3-ethyl-2-methyl-4-oxo-1,4-dihydro-quinolin-7-yloxy)-propyl ester (22), 6-chloro-3-ethyl-2-methyl-7-(2-morpholin-4-yl-ethoxy)-1H-quinolin-4-one (23), 6-chloro-7-(2-dimethylamino-ethoxy)-3-ethyl-2-methyl-1H-quinolin-4-one (24), 6-bromo-3-ethyl-2-methyl-7-(2-phenoxy-ethoxy)-1H-quinolin-4-one (25), 6-chloro-3-ethyl-2-methyl-7-[3-(4-phenyl-piperazin-1-yl)-propoxy]-1H-quinolin-4-one (26), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-phenylquinolin-4(1H)-one (31), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-(pyridin-4-yl)quinolin-4(1H)-one (32), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-(pyridin-3-yl)quinolin-4(1H)-one (33), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-(4-(trifluoromethyl)phenyl)quinolin-4(1H)-one (34), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-(4-(trifluoromethoxy)phenyl)quinolin-4(1H)-one (35), 6-butyl-3-(3-(4-fluorophenoxy)phenyl)-2-methyl-7-(2phenoxyethoxy)quinolin-4(1H)-one (36), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-(4-((4-(trifluoromethoxy)phenoxy)methyl)phenyl) quinolin-4(1H)-one (37), 6-butyl-2-methyl-3-(2-methyl-4-(4-(trifluoromethoxy)phenoxy)phenyl)-7-(2-phenoxyethoxy)-quinolin-4(1H)-one (38), 6-butyl-2-methyl-3-(2-methyl-4-(trifluoromethyl)phenyl)-7-(2-phenoxyethoxy)quinolin-4(1H)-one (39), 6-butyl-3-(2,4-dimethylphenyl)-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (40), 6-butyl-3-(2-fluoro-4-(trifluoromethyl)phenyl)-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (41), 6-butyl-3-(4-chloro-2-methylphenyl)-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (42), and 6-butyl-3-(3,5-dimethylisoxazol-4-yl)-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (43) that when administered to a recipient animal or human subject as a single dose or as multiple doses is effective in reducing or preventing a malarial infection in the subject.

8. The pharmaceutically acceptable composition of claim 7 , further comprising a pharmaceutically acceptable carrier.

9. A method of reducing the viability of a population of malarial parasites, wherein the method comprises administering to an animal or human subject a therapeutically effective amount of a pharmaceutically acceptable composition comprising a compound selected from the group consisting of: 6-butyl-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (15), 6-butyl-3-ethyl-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (16), 6-chloro-3-ethyl-2-methyl-7-(2-phenoxy-ethoxy)-1H-quinolin-4-one (17), 3-ethyl-2,6-dimethyl-7-(2-phenoxy-ethoxy)-1H-quiolin-4-one (18), 6-chloro-3-ethyl-7-methoxymethoxy-2-methyl-1H-quinoline-4-one (20), 6-chloro-3-ethyl-7-(3-hydroxy-propoxy)-2-methyl-1H-quinolin-4-one (21), 2-ethyl-3-oxo-butyricacid-3-(6-chloro-3-ethyl-2-methyl-4-oxo-1,4-dihydro-quinolin-7-yloxy)-propyl ester (22), 6-chloro-3-ethyl-2-methyl-7-(2-morpholin-4-yl-ethoxy)-1H-quinolin-4-one (23), 6-chloro-7-(2-dimethylamino-ethoxy)-3-ethyl-2-methyl-1H-quinolin-4-one (24), 6-bromo-3-ethyl-2-methyl-7-(2-phenoxy-ethoxy)-1H-quinolin-4-one (25), 6-chloro-3-ethyl-2-methyl-7-[3-(4-phenyl-piperazin-1-yl)-propoxy]-1H-quinolin-4-one (26), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-phenylquinolin-4(1H)-one (31), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-(pyridin-4-yl)quinolin-4(1H)-one (32), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-(pyridin-3-yl)quinolin-4(1H)-one (33), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-(4-(trifluoromethyl)phenyl)quinolin-4(1H)-one (34), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-(4-(trifluoromethoxy)phenyl)quinolin-4(1H)-one (35), 6-butyl-3-(3-(4-fluorophenoxy)phenyl)-2-methyl-7-(2phenoxyethoxy)quinolin-4(1H)-one (36), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-(4-((4-(trifluoromethoxy)phenoxy)methyl)phenyl) quinolin-4(1H)-one (37), 6-butyl-2-methyl-3-(2-methyl-4-(4-(trifluoromethoxy)phenoxy)phenyl)-7-(2-phenoxyethoxy)-quinolin-4(1H)-one (38), 6-butyl-2-methyl-3-(2-methyl-4-(trifluoromethyl)phenyl)-7-(2-phenoxyethoxy)quinolin-4(1H)-one (39), 6-butyl-3-(2,4-dimethylphenyl)-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (40), 6-butyl-3-(2-fluoro-4-(trifluoromethyl)phenyl)-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (41), 6-butyl-3-(4-chloro-2-methylphenyl)-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (42), and 6-butyl-3-(3,5dimethylisoxazol-4-yl)-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (43).

10. The method of claim 9 , wherein the compound is selected from the group consisting of:

6-butyl-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (15), 6-butyl-3-ethyl-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (16), 6-chloro-3-ethyl-2-methyl-7-(2-phenoxy-ethoxy)-1H-quinolin-4-one (17), 3-ethyl-2,6-dimethyl-7-(2-phenoxy-ethoxy)-1H-quiolin-4-one (18), (19), 6-chloro-3-ethyl-7-methoxymethoxy-2-methyl-1H-quinoline-4-one (20), 6-chloro-3-ethyl-7-(3-hydroxy-propoxy)-2-methyl-1H-quinolin-4-one (21), 2-ethyl-3-oxo-butyricacid-3-(6-chloro-3-ethyl-2-methyl-4-oxo-1,4-dihydro-quinolin-7-yloxy)-propyl ester (22), 6-chloro-3-ethyl-2-methyl-7-(2-morpholin-4-yl-ethoxy)-1H-quinolin-4-one (23), 6-chloro-7-(2-dimethylamino-ethoxy)-3-ethyl-2-methyl-1H-quinolin-4-one (24), 6-bromo-3-ethyl-2-methyl-7-(2-phenoxy-ethoxy)-1H-quinolin-4-one (25), and 6-chloro-3-ethyl-2-methyl-7-[3-(4-phenyl-piperazin-1-yl)-propoxy]-1H-quinolin-4-one (26).

11. The method of claim 9 , wherein the compound is selected from the group consisting of: 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-phenylquinolin-4(1H)-one (31), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-(pyridin-4-yl)quinolin-4(1H)-one (32), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-(pyridin-3-yl)quinolin-4(1H)-one (33), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-(4-(trifluoromethyl)phenyl)quinolin-4(1H)-one (34), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-(4-(trifluoromethoxy)phenyl)quinolin-4(1H)-one (35), 6-butyl-3-(3-(4-fluorophenoxy)phenyl)-2-methyl-7-(2phenoxyethoxy)quinolin-4(1H)-one (36), 6-butyl-2-methyl-7-(2-phenoxyethoxy)-3-(4-((4-(trifluoromethoxy)phenoxy)methyl)phenyl) quinolin-4(1H)-one (37), 6-butyl-2-methyl-3-(2-methyl-4-(4-(trifluoromethoxy)phenoxy)phenyl)-7-(2-phenoxyethoxy)-quinolin-4(1H)-one (38), 6-butyl-2-methyl-3-(2-methyl-4-(trifluoromethyl)phenyl)-7-(2-phenoxyethoxy)quinolin-4(1H)-one (39), 6-butyl-3-(2,4-dimethylphenyl)-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (40), 6-butyl-3-(2-fluoro-4-(trifluoromethyl)phenyl)-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (41), 6-butyl-3-(4-chloro-2-methylphenyl)-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (42), and 6-butyl-3-(3,5-dimethylisoxazol-4-yl)-2-methyl-7-(2-phenoxyethoxy)quinolin-4(1H)-one (43).

Assignments (3)
CONFIRMATORY LICENSE Recorded Jan 12, 2015
From: UNIVERSITY OF SOUTH FLORIDA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 034750/0689 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 29, 2013
From: MANETSCH, ROMAN; CROSS, RICHARD MATTHEW; NAMELIKONDA, NIRANJAN KUMAR; KYLE, DENNIS EDWARD; MUTKA, TINA SUSANNA; LACRUE, ALEXIS NICHOLE; MAIGNAN, JORDANY RICHARLSON; SAENZ, FABIAN ERNESTO
To: UNIVERSITY OF SOUTH FLORIDA (A FLORIDA NON-PROFIT CORPORATION)
Reel/Frame 029709/0304 →
CONFIRMATORY LICENSE Recorded Dec 18, 2012
From: UNIVERSITY OF SOUTH FLORIDA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 029490/0747 →
Continuity (2)
Provisional Application 61552609 · Oct 28, 2011
Related Publication 20130123258A1 · May 16, 2013