IP Library Granted Patent US 8,410,255
Granted Patent B2
US 8,410,255 · App. 12/852,387 · Granted Apr 2, 2013

Dark quenchers for donor-acceptor energy transfer

Inventors: Ronald M. Cook (Novato, CA); Matt Lyttle (San Rafael, CA); Daren Dick (San Rafael, CA)
Assignee: Biosearch Technologies, Inc.
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Quick Facts
Patent No.
US 8,410,255
App. No.
12/852,387
Granted
Apr 2, 2013
Kind
B2
Abstract

The present invention provides a family of dark quenchers, termed Black Hole Quenchers (“BHQs”), that are efficient quenchers of excited state energy but which are themselves substantially non-fluorescent. Also provided are methods of using the BHQs, probes incorporating the BHQs and methods of using the probes.

Claims (48)

1. A quencher of excited state energy having a formula which is a member selected from:

2. A quencher of excited state energy, having the formula:

wherein

X 5 is —NR′R″,

in which R′ and R″ are members independently selected from unsubstituted alkyl and substituted alkyl,

with the proviso that at least one of R′ and R″ is selected such that it bears a reactive functional group.

3. A quencher of excited state energy, having the formula:

wherein

X 5 is —NR′R″,

in which R′ and R″ are members independently selected from unsubstituted alkyl and substituted alkyl,

with the proviso that at least one of R′ and R″ is selected such that it bears a reactive functional group,

wherein said reactive functional group is a member selected from carboxy, N-hydroxysuccinimide ester, N-hydroxybenztriazole ester, acid halide, acyl imidazole, thioester, p-nitrophenyl ester, alkyl ester, alkenyl ester, alkynyl ester, aromatic ester, and —NH 2 .

4. A quencher of excited state energy, having the formula:

wherein X 5 is

wherein

X 1 is —CH 3 ;

X 2 is —OP(OX 3 )N(X 4 ) 2 ,

wherein X 3 is cyanoethyl; and X 4 is isopropyl; and

p and q are numbers independently selected from 1 to 20, inclusive.

5. A quencher of excited state energy, having the formula:

wherein

X 5 and X 6 are each —NR′R″,

in which R′ and R″ are members independently selected from unsubstituted alkyl and substituted alkyl,

with the proviso that for at least one of X 5 and X 6 at least one of R′ and R″ is selected such that it bears a reactive functional group.

6. The quencher of excited state energy according to claim 2 , having a formula which is a member selected from:

7. The quencher of excited state energy according to claim 5 , having a formula which is a member selected from:

8. The quencher of excited state energy according to claim 2 , wherein R′ is unsubstituted alkyl and R″ is substituted alkyl.

9. The quencher of excited state energy according to claim 8 , wherein said reactive functional group is a member selected from carboxy, N-hydroxysuccinimide ester, N-hydroxybenztriazole ester, acid halide, acyl imidazole, thioester, p-nitrophenyl ester, alkyl ester, alkenyl ester, alkynyl ester, aromatic ester, and —NH 2 .

10. The quencher of excited state energy according to claim 8 , wherein X 5 is

wherein

X 1 is —CH 3 ;

X 2 is —OP(OX 3 )N(X 4 ) 2 ,

wherein X 3 is cyanoethyl; and X 4 is isopropyl; and

p and q are numbers independently selected from 1 to 20, inclusive.

11. The quencher of excited state energy according to claim 3 , wherein R′ is unsubstituted alkyl and R″ is substituted alkyl.

12. The quencher of excited state energy according to claim 5 ,

wherein

for X 6 , R′ and R″ are each unsubstituted alkyl.

13. The quencher of excited state energy according to claim 12 ,

wherein

for X 5 , R′ is unsubstituted alkyl and R″ is substituted alkyl.

14. The quencher of excited state energy according to claim 13 , wherein said reactive functional group is a member selected from carboxy, N-hydroxysuccinimide ester, N-hydroxybenztriazole ester, acid halide, acyl imidazole, thioester, p-nitrophenyl ester, alkyl ester, alkenyl ester, alkynyl ester, aromatic ester, and —NH 2 .

15. The quencher of excited state energy according to claim 13 , wherein X 5 is

wherein

X 1 is —CH 3 ;

X 2 is —OP(OX 3 )N(X 4 ) 2 ,

wherein X 3 is cyanoethyl; and X 4 is isopropyl; and

p and q are numbers independently selected from 1 to 20, inclusive.

Assignments (5)
RELEASE OF SECURITY INTEREST IN PATENTS PREVIOUSLY RECORDED AT REEL/FRAME (035957/0976) Recorded Mar 8, 2016
From: HSBC CORPORATE TRUSTEE COMPANY (UK) LIMITED
To: BIOSEARCH TECHNOLOGIES, INC.
Reel/Frame 038037/0669 →
CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT APPL. NO. 61/996,902 PREVIOUSLY RECORDED AT REEL: 035957 FRAME: 0976. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Aug 11, 2015
From: BIOSEARCH TECHNOLOGIES, INC.
To: HSBC CORPORATE TRUSTEE COMPANY (UK) LIMITED, AS SECURITY AGENT
Reel/Frame 036335/0516 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 30, 2015
From: BIOSEARCH TECHNOLOGIES, INC.
To: HSB CORPORATE TRUST COMPANY (UK) LIMITED, AS SECURITY AGENT
Reel/Frame 035957/0976 →
CORRECTIVE ASSIGNMENT TO CORRECT THE THE ASSIGNOR'S NAME PREVIOUSLY RECORDED ON REEL 026085 FRAME 0194. ASSIGNOR(S) HEREBY CONFIRMS THE THE ASSIGNMENT. Recorded Apr 20, 2011
From: COOK, RONALD M.; LYTTLE, MATT; DICK, DAREN
To: BIOSEARCH TECHNOLOGIES, INC.
Reel/Frame 026159/0808 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 6, 2011
From: COOK, RONALD M.; LYTTLE, MATT; DICK, DARREN
To: BIOSEARCH TECHNOLOGIES, INC.
Reel/Frame 026085/0194 →
Continuity (7)
Continuation 12546927 · Aug 25, 2009
Continuation 11437991 · May 19, 2006
Division 11192705 · Jul 29, 2005
Continuation 09567863 · May 9, 2000
Continuation 12765844 · Apr 22, 2010
Continuation 12546927
Related Publication 20110178280A1 · Jul 21, 2011