IP Library Granted Patent US 10,428,075
Granted Patent B2
US 10,428,075 · App. 15/982,514 · Granted Oct 1, 2019

Coelenterazine analogues

Inventors: Mary Hall (Waunakee, WI); Thomas Kirkland (Atascadero, CA); Thomas Machleidt (Madison, WI); Anton Shakhmin (Grover Beach, CA); Joel R. Walker (San Luis Obispo, CA)
Assignee: PROMEGA CORPORATION
C07D487/04A61K49/0021C07D519/00C09K11/06C12Q1/66C12Y113/12005C12Y113/12013C09K2211/1011C09K2211/1018
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 10,428,075
App. No.
15/982,514
Granted
Oct 1, 2019
Kind
B2
Abstract

Described are coelenterazine analogues, methods for making the analogues, kits comprising the analogues, and methods of using the compounds for the detection of luminescence in luciferase-based assays.

Claims (29)

1. A method for in vivo bioluminescent imaging, the method comprising:

contacting a live cell with a compound of Formula I or Formula II:

wherein R 5 and R 5a are hydrogen;

R 6 and R 6a are aryl optionally substituted with 1, 2, 3, 4, or 5 substituents independently selected from the group consisting of halogen, hydroxy, cyano, nitro, amino, alkylamino, dialkylamino, acyl amino, aminoalkyl, alkyl, fluoroalkyl, alkoxyfluoroalkyl, fluoroalkoxy, alkenyl, alkynyl, haloalkyl, haloalkoxy, heteroalkyl, alkoxy, sulfonylamino, sulfonyl, alkylsulfonyl, amide, carbamate, silyl, substituted silyl, acyl, or aminosulfonyl;

R 8 and R 8a are optionally substituted aryl, heteroaryl, alkyl substituted with aryl, or alkyl substituted with heteroaryl;

R x is halogen, hydroxy, cyano, nitro, amino, alkylamino, dialkylamino, alkyl, alkenyl, alkynyl, alkoxy, or heteroalkyl; and

p is 0, 1, 2, 3, 4, or 5;

provided that the following compounds are excluded from formula (I): 8-benzyl-2-(furan-2-ylmethyl)-6-phenylimidazo[1,2-a]pyrazin-3(7H)-one; and

8-benzyl-2-(furan-2-ylmethyl)-6-(4-hydroxyphenyl)imidazo[1,2-a]pyrazin-3(7H)-one; and

R x is not 4-hydroxy when p is 1, R 5a is not hydrogen, or R 8a is not benzyl, or any combination thereof;

and

detecting luminescence; wherein the live cell expresses a coelenterazine-utilizing luciferase.

2. The method of claim 1 , wherein:

R 6 and R 6a are phenyl optionally substituted with 1, 2, 3, 4, or 5 substituents independently selected from the group consisting of halogen, hydroxy, cyano, nitro, amino, alkylamino, dialkylamino, acyl amino, aminoalkyl, alkyl, fluoroalkyl, alkoxyfluoroalkyl, fluoroalkoxy, alkenyl, alkynyl, haloalkyl, haloalkoxy, heteroalkyl, alkoxy, sulfonylamino, sulfonyl, alkylsulfonyl, amide, carbamate, silyl, substituted silyl, acyl, or aminosulfonyl.

3. The method of claim 1 , wherein

R 6 and R 6a are

X 1 -X 5 are each independently CR 11 ; and

R 11 , at each occurrence, is independently selected from the group consisting of hydrogen, halogen, hydroxy, cyano, amino, nitro, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkyl, C 1 -C 6 -haloalkoxy, C 1 -C 6 -alkylamino, C 1 -C 6 -dialkylamino, and C 1 -C 6 -heteroalkyl.

4. The method of claim 3 , wherein R 8 and R 8a are selected from the group consisting of:

5. The method of claim 3 , wherein the compound is of formula (I); R 11 at X 1 , X 3 , X 4 , and X 5 is hydrogen; and the R 11 at X 2 is hydrogen, hydroxy, amino, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, C 1 -C 6 -alkylamino, C 1 -C 6 -dialkylamino, or C 1 -C 6 -heteroalkyl.

6. The method of claim 3 , wherein the compound is of formula (I); and R 6 is selected from the group consisting of:

7. The method of claim 5 , wherein R 8 is selected from the group consisting of:

8. The method of claim 5 , wherein R 8 is

9. The method of claim 7 , wherein the compound is

10. The method of claim 1 , wherein the live cell is in an animal.

11. The method of claim 1 , wherein the coelenterazine-utilizing luciferase is selected from the group of a Oplophorus luciferase or variant thereof and a Renilla luciferase or a variant thereof.

12. The method of claim 1 , wherein the coelenterazine-utilizing luciferase is expressed as a fusion protein.

13. The method of claim 12 , wherein the fusion protein comprises the coelenterazine-utilizing luciferase and a protein of interest.

14. The method of claim 13 , wherein the coelenterazine-utilizing luciferase is selected from the group of a Oplophorus luciferase or variant thereof and a Renilla luciferase or a variant therof.

Assignments (2)
SECURITY INTEREST Recorded Apr 3, 2019
From: PROMEGA CORPORATION; PROMEGA BIOSCIENCES, LLC; TERSO SOLUTIONS, INC.; ORION SEVEN, LLC; PROMEGA AVIATION LLC
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 048790/0259 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 26, 2018
From: HALL, MARY; KIRKLAND, THOMAS; MACHLEIDT, THOMAS; SHAKHMIN, ANTON; WALKER, JOEL R.
To: PROMEGA CORPORATION
Reel/Frame 047325/0767 →
Continuity (3)
Continuation 15661582 · Jul 27, 2017
Provisional Application 62367689 · Jul 28, 2016
Related Publication 20180334463A1 · Nov 22, 2018