IP Library Granted Patent US 10,370,385
Granted Patent B2
US 10,370,385 · App. 15/325,320 · Granted Aug 6, 2019

Tricyclic mosquitocides and methods of making and using thereof

Inventors: Jon Njardarson (Tucson, AZ); Jun Isoe (Tuscon, AZ); Roger Miesfeld (Tucson, AZ)
Assignee: Arizona Board of Regents on Behalf of the University of Arizona
C07D495/04A01N43/90
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,370,385
App. No.
15/325,320
Granted
Aug 6, 2019
Kind
B2
Abstract

Compounds that inhibit digestion in blood-ingesting pests are described herein. In one embodiment, the compounds described herein block entry of blood into the midgut and thereby inhibit digestion and nutrient processing. In another embodiment, the compounds described herein prevent pathogens contained in the blood meal from entering the midgut where they could cross the epithelial cell layer and infect the mosquito. The compounds can be administered to a population of blood-ingesting pests, such as mosquitos, directly or indirectly in an effective amount to prevent mosquitoes from transmitting diseases such as malaria, dengue fever, West Nile virus and lymphatic filariasis. Preferably, the compounds are lethal to blood-ingesting pests. The compounds can be combined with one or more excipients to prepare compositions.

Claims (47)

1. A composition comprising a compound having the formula:

wherein

X is O, S, CR 10 R 11 , SiR 10 R 11 , or NR 10 ;

Y is O, S, CR 10 R 11 ;

Z is O, S, CR 10 R 11 ;

R 1 -R 11 are each independently selected from the group consisting of hydrogen, hydroxyl, cyano, nitro, halogen, NH 2 , SH, SR 12 , OR 12 , N(R 12 ) 2 , OCON(R 12 ) 2 , C(═O)R 12 , OC(═O)R 12 , C(═O)OR 12 , COOH, COO − M + , CONH 2 , CON(R 12 ) 2 , C(═O)H, substituted or unsubstituted linear, branched, or cyclic alkyl, alkenyl, or alkynyl; substituted or unsubstituted linear, branched, or cyclic heteroalkyl, heteroalkenyl, or heteroalkynyl, substituted or unsubstituted aryl or heteroaryl, SOR 12 , SOOR 12 , SO 3 R 12 , SO 4 R 12 , NR 12 COR 13 , phosphoryl, sulfamoyl, and sulfonamido; wherein each occurrence of R 12 or R 13 is selected from the group consisting of hydrogen, substituted or unsubstituted linear, branched, or cyclic alkyl, alkenyl, or alkynyl; substituted or unsubstituted linear, branched, or cyclic heteroalkyl, heteroalkenyl, or heteroalkynyl, and substituted or unsubstituted aryl or heteroaryl;

wherein the dotted line represents a bond that is either present or absent;

and

wherein the compound is in an effective amount to inhibit digestion or nutrient processing in at least 40% of a population of blood-ingesting pests, reduce follicle size in female blood-ingesting pests compared to the follicle size when the pests are not exposed to the compound, or provide a lethal concentration against pest larvae, or a combination thereof, and

wherein the compound is in a concentration of less than 0.25 mM.

2. The composition of claim 1 , wherein the compound has the following stereochemistry

3. The composition of claim 1 , wherein

X is sulfur;

Y is oxygen;

Z is oxygen; or

X is sulfur and Y and Z are both oxygen.

4. The composition of claim 1 , wherein R 1 is a substituted or unsubstituted alkyl.

5. The compound of claim 4 , wherein

R 1 is methyl;

R 2 is hydrogen;

R 3 is hydrogen;

R 6 is hydrogen;

R 7 is hydrogen; or

R 4 and R 5 are hydrogen.

6. The composition of claim 1 , wherein R 8 is a substituted or unsubstituted aryl.

7. The composition of claim 6 , wherein R 8 is a substituted or unsubstituted phenyl.

8. The composition of claim 7 , wherein R 8 is an unsubstituted phenyl.

9. The composition of claim 1 , wherein the compound is:

10. The composition of claim 1 , wherein the compound has the formula:

11. The composition of claim 1 , in the form of a liquid is selected from the group consisting of a solution, suspension, dispersion, and an emulsion.

12. The composition of claim 1 , wherein the effective amount of the compound is non-toxic to plants, animals, and/or arthropods that do not function as vectors of human pathogens.

13. A method of preventing the spread of mosquito-borne illnesses, comprising administering to a site or region containing one or more mosquitoes an effective amount of a composition comprising a compound having the formula:

wherein

X is O, S, CR 10 R 11 , SiR 10 R 11 , or NR 10 ;

Y is O, S, CR 10 R 11 ;

Z is O, S, CR 10 R 11 ;

R 1 -R 11 are each independently selected from the group consisting of hydrogen, hydroxyl, cyano, nitro, halogen, NH 2 , SH, SR 12 , OR 12 , N(R 12 ) 2 , OCON(R 12 ) 2 , C(═O)R 12 , OC(═O)R 12 , C(═O)OR 12 , COOH, COO − M + , CONH 2 , CON(R 12 ) 2 , C(═O)H, substituted or unsubstituted linear, branched, or cyclic alkyl, alkenyl, or alkynyl; substituted or unsubstituted linear, branched, or cyclic heteroalkyl, heteroalkenyl, or heteroalkynyl, substituted or unsubstituted aryl or heteroaryl, SOR 12 , SOOR 12 , SO 3 R 12 , SO 4 R 12 , NR 12 COR 13 , phosphoryl, sulfamoyl, and sulfonamido; wherein each occurrence of R 12 or R 13 is selected from the group consisting of hydrogen, substituted or unsubstituted linear, branched, or cyclic alkyl, alkenyl, or alkynyl; substituted or unsubstituted linear, branched, or cyclic heteroalkyl, heteroalkenyl, or heteroalkynyl, and substituted or unsubstituted aryl or heteroaryl;

wherein the dotted line represents a bond that is either present or absent; and

wherein the compound is in an effective amount to inhibit digestion or nutrient processing in at least 40% of a population of blood-ingesting pests, reduce follicle size in female blood-ingesting pests compared to the follicle size when the pests are not exposed to the compound, or provide a lethal concentration against pest larvae, or a combination thereof, and

wherein the compound is in a concentration of less than 0.25 mM.

14. The method of claim 13 , wherein the site or region is a body of water or contains standing water.

15. The method of claim 13 , wherein the compound is:

16. The composition of claim 1 , wherein the composition formed by introducing pellets comprising the compound into a continuous aqueous phase.

17. The composition of claim 1 , wherein the composition formed by introducing flakes comprising the compound into a continuous aqueous phase.

18. The composition of claim 1 , wherein the composition is in the form of a liquid, and wherein the compound is dispersed or dissolved in an aqueous continuous phase.

19. The composition of claim 1 , further comprising a wetting agent, surfactant, or carrier, or a combination thereof.

20. The compound of claim 19 , wherein the composition comprises a surfactant, and wherein the surfactant is an anionic, cationic, amphoteric, or nonionic surface-active agent.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE LAST NAME OF THIRD ASSIGNOR PREVIOUSLY RECORDED AT REEL: 040936 FRAME: 0603. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Apr 21, 2017
From: NJARDARSON, JON; ISOE, JUN; MIESFELD, ROGER
To: THE ARIZONA BOARD OF REGENTS ON BEHALF OF THE UNIVERSITY OF ARIZONA
Reel/Frame 042310/0270 →
CONFIRMATORY LICENSE Recorded Feb 23, 2017
From: UNIVERSITY OF ARIZONA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 041785/0200 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 10, 2017
From: NJARDARSON, JON; ISOE, JUN; MIESFELD, ROGERT
To: THE ARIZONA BOARD OF REGENTS ON BEHALF OF THE UNIVERSITY OF ARIZONA
Reel/Frame 040936/0603 →
Continuity (2)
Provisional Application 62022771 · Jul 10, 2014
Related Publication 20170166580A1 · Jun 15, 2017