IP Library Granted Patent US 10,280,447
Granted Patent B2
US 10,280,447 · App. 15/800,649 · Granted May 7, 2019

Substituted imidazo[1,2-A]pyrazines tethered to energy acceptors

Inventors: Mary Hall (Waunakee, WI); Thomas Kirkland (Atascadero, CA); Thomas Machleidt (Madison, WI); Anton Shakhmin (Santa Clara, CA); Joel R. Walker (San Luis Obispo, CA); Keith V. Wood (Mount Horeb, WI); Wenhui Zhou (San Luis Obispo, CA)
Assignee: Promega Corporation
C12Q1/66A61K49/0052C07D487/04C07D491/22C07D498/14C07D519/00G01N21/763
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Quick Facts
Patent No.
US 10,280,447
App. No.
15/800,649
Granted
May 7, 2019
Kind
B2
Abstract

Described are substituted imidazo[1,2-a]pyrazine compounds of formula (I), which are coelenterazine analogs, methods for making the compounds, kits comprising the compounds, and methods of using the compounds for the detection of luminescence in luciferase-based assays.

Claims (41)

1. A compound of formula (I)

or a tautomer, or a pharmaceutically acceptable salt thereof, wherein

R 1 is;

R 2 is absent or a substituent selected from the group consisting of alkyl, haloalkyl, halogen, —OH, and —NH 2 ;

A 1 is aryl, heteroaryl, heterocyclyl, or cycloalkyl, wherein the aryl, heteroaryl, heterocyclyl, and cycloalkyl are unsubstituted or substituted with 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 substituents, each independently selected from the group consisting of halogen, oxo, thioxo, cyano, nitro, fluoroalkyl, alkoxyfluoroalkyl, fluoroalkoxy, alkyl, alkenyl, alkynyl, haloalkyl, haloalkoxy, heteroalkyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkylalkyl, heteroarylalkyl, arylalkyl, hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, aryloxy, benzyloxy, amino, alkylamino, dialkylamino, acylamino, aminoalkyl, arylamino, sulfonylamino, sulfinylamino, alkylsulfonyl, arylsulfonyl, aminosulfonyl, —COOH, amide, carbamate, silyl, t-butyldimethylsilyl, alkylsulfanyl, and acyl;

T 1 is alkyl, alkenyl, alkynyl, or heteroalkyl, wherein the alkyl, alkenyl, alkynyl, and heteroalkyl are unsubstituted or substituted with 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 substituents, each independently selected from the group consisting of halogen, oxo, thioxo, cyano, nitro, fluoroalkyl, alkoxyfluoroalkyl, fluoroalkoxy, alkyl, alkenyl, alkynyl, haloalkyl, haloalkoxy, heteroalkyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkylalkyl, heteroarylalkyl, arylalkyl, hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, aryloxy, benzyloxy, amino, alkylamino, dialkylamino, acylamino, aminoalkyl, arylamino, sulfonylamino, sulfinylamino, alkylsulfonyl, arylsulfonyl, aminosulfonyl, —COOH, ketone, amide, carbamate, silyl, t-butyldimethylsilyl, alkylsulfanyl, and acyl;

E 1 is an energy acceptor, wherein the energy acceptor is a fluorescent dye, a quencher, a fluorescent particle, a luminescent metal complex, or a combination of any of the foregoing; and

q is 0, 1, or 2.

2. The compound of claim 1 , or a tautomer, or a pharmaceutically acceptable salt thereof, wherein A 1 is phenyl optionally substituted with 0, 1, 2, 3, or 4 substituents, each independently selected from the group consisting of halogen, cyano, nitro, fluoroalkyl, alkoxyfluoroalkyl, fluoroalkoxy, alkyl, alkenyl, alkynyl, haloalkyl, haloalkoxy, heteroalkyl, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heterocyclyl, cycloalkylalkyl, heteroarylalkyl, arylalkyl, hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, aryloxy, benzyloxy, amino, alkylamino, dialkylamino, acylamino, aminoalkyl, arylamino, sulfonylamino, sulfinylamino, alkylsulfonyl, arylsulfonyl, aminosulfonyl, —COOH, amide, carbamate, silyl, t-butyldimethylsilyl, alkylsulfanyl, and acyl.

3. The compound of claim 1 , or a tautomer, or a pharmaceutically acceptable salt thereof, wherein A 1 is phenyl optionally substituted with 0, 1, 2, 3, or 4 substituents, wherein each substituent independently is halogen.

4. The compound of claim 1 , or a tautomer, or a pharmaceutically acceptable salt thereof, wherein T 1 is heteroalkyl.

5. The compound of claim 1 , or a tautomer, or a pharmaceutically acceptable salt thereof, wherein T 1 is

6. The compound of claim 1 , or a tautomer, or a pharmaceutically acceptable salt thereof, wherein T 1 is —(O—CR 1a R 1b —CR 1a R 1b ) m -Q- or —O—(CR 1a R 1b ) n -Q-, and wherein

m is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30;

n is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30;

Q at each occurrence is independently —NH—CO—, —CO—NH—, —CO—O—, —O—CO—, or —O—CO—NH—; and

R 1a and R 1b at each occurrence is independently hydrogen or C 1 -C 4 alkyl.

7. The compound of claim 1 , or a tautomer, or a pharmaceutically acceptable salt thereof, wherein R 2 is absent.

8. The compound of claim 1 , or a tautomer, or a pharmaceutically acceptable salt thereof, wherein the energy acceptor is a fluorescent non-chloro TOM dye.

9. The compound of claim 1 , or a tautomer, or a pharmaceutically acceptable salt thereof, wherein the energy acceptor has the formula:

10. The compound of claim 1 , wherein the compound has formula (I-a), or a tautomer, or a pharmaceutically acceptable salt thereof:

wherein R 3 is absent or halogen.

11. The compound of claim 1 , wherein the compound has formula (I-b), or a tautomer, or a pharmaceutically acceptable salt thereof:

wherein n is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30.

12. The compound of claim 11 , or a tautomer, or a pharmaceutically acceptable salt thereof, wherein n is 6 or 8.

13. The compound of claim 1 , wherein the compound has formula (I-c) or formula (I-d), or a tautomer, or a pharmaceutically acceptable salt thereof:

14. The compound of claim 1 , which is TAK-0043 or TAK-0052:

or a tautomer, or a pharmaceutically acceptable salt thereof.

15. A bioluminescence resonance energy transfer system comprising a compound of claim 1 , or a tautomer, or a pharmaceutically acceptable salt thereof.

16. A method of detecting an enzyme in a sample, the method comprising:

(a) contacting the sample with a compound of claim 1 , or a tautomer, or a pharmaceutically acceptable salt thereof; and

(b) detecting luminescence in the sample.

17. A method for detecting luminescence in a sample, the method comprising:

(a) contacting a sample with a compound of claim 1 , or a tautomer, or a pharmaceutically acceptable salt thereof;

(b) contacting the sample with a coelenterazine-utilizing luciferase, if it is not present in the sample; and

(c) detecting luminescence.

18. The method of claim 17 , wherein the sample contains live cells.

19. The method of claim 17 , wherein the sample contains a coelenterazine-utilizing luciferase.

20. A method for detecting luminescence in a transgenic animal expressing a coelenterazine-utilizing luciferase, the method comprising:

(a) administering to the transgenic animal a compound of claim 1 , or a tautomer, or a pharmaceutically acceptable salt thereof; and

(b) detecting luminescence.

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 May 14, 2018
From: HALL, MARY; KIRKLAND, THOMAS; MACHLEIDT, THOMAS; SHAKHMIN, ANTON; WALKER, JOEL; WOOD, KEITH V.; ZHOU, WENHUI
To: PROMEGA CORPORATION
Reel/Frame 045796/0076 →
Continuity (2)
Provisional Application 62415671 · Nov 1, 2016
Related Publication 20180119200A1 · May 3, 2018