IP Library Granted Patent US 7,439,341
Granted Patent B2
US 7,439,341 · App. 10/987,608 · Granted Oct 21, 2008

Fluorescence quenching azo dyes, their methods of preparation and use

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 7,439,341
App. No.
10/987,608
Granted
Oct 21, 2008
Kind
B2
Abstract

Disclosed is a group of azo quencher compositions useful as fluorescence quenchers having the general structure of formula 1, methods of making or using the compositions, and kits comprising the composition.

Claims (29)

1. A chemical composition for quenching light having the structure of Formula 1:

wherein R 1-6 on the conjugated ring system are individually an electron withdrawing group, alkyl group, aryl group, hydrogen, heteroaryl group, or a five or six member ring structure formed from the R 1 , R 2 pair, the R 3 , R 4 pair, the R 4 , R 5 pair, or the R 5 , R 6 pair; and wherein R 7 is an unsubstituted or substituted aryl or heteroaryl group, the aryl or heteroaryl group being selected from the group consisting of phenyl, xylyl, tolyl, pyridyl, and anilyl groups, with the proviso that the aryl group is not an unsubstituted phenyl or tolyl, and wherein the anilyl group is a group of Formula 2:

wherein L and L′ are the same or different and are a C 1-10 group, —C 1-10 —O—R 8 , or —C 1-10 —O—R 9 , wherein C 1-10 is a C 1-10 alkyl group, and wherein R 8 and R 9 are independently a hydrogen, trityl, alkoxytrityl, silyl, cyanoethylphosphoramidite, or phosphoramidite with the proviso that L and L′ are not both methyl, and when L or L′ is ethyl, then the other is not hydroxyethyl.

2. The composition of claim 1 wherein the electron withdrawing groups are selected from the group consisting of halogen, NO 2 , CN, NCS, keto, and alkoxy groups.

3. The composition of claim 1 , wherein at least one of R 1-6 on the conjugated ring system is an electron withdrawing group.

4. The composition of claim 1 , wherein at least one of R 1-6 on the conjugated ring system is an alkyl group.

5. The composition of claim 1 , wherein the alkyl group has from one to ten carbon atoms.

6. The composition of claim 1 , wherein at least one of R 1-6 on the conjugated ring system is an aryl group.

7. The composition of claim 1 , wherein at least one of R 1-6 on the conjugated ring system is a heteroaryl group.

8. The composition of claim 1 , wherein at least one of R 1-6 on the conjugated ring system is a hydrogen.

9. The composition of claim 1 , wherein at least one of the R 1 , R 2 pair, the R 3 , R 4 pair, the R 4 , R 5 pair, or the R 5 , R 6 pair are combined to form a ring structure having five or six ring members.

10. The composition of claim 9 , wherein the ring has six ring members.

11. The composition of claim 1 , wherein the composition is of Formula 13,

wherein CEP is cyanoethylphosphoramidite, and C 1-10 is a C 1-10 alkyl group.

12. The composition of claim 1 , wherein the composition is of Formula 14,

wherein trityl is an alkoxytrityl group, CEP is cyanoethylphosphoramidite, and C 1-10 is a C 1-10 alkyl group.

13. The composition comprising a dye pair comprising a fluorescent dye and a chemical composition for quenching light of claim 1 having the structure of Formula 1.

14. The composition comprising the dye pair of claim 13 , wherein the composition quenches the fluorescence of the fluorescent dye by about 90% or more.

15. The composition comprising the dye pair of claim 13 , wherein the composition quenches the fluorescence of the fluorescent dye by about 95% or more.

16. The composition comprising the dye pair of claim 14 , wherein the fluorescent dye is fluorescein.

17. A kit comprising a container comprising a composition of claim 1 and instructions for its use.

18. The composition of claim 1 , wherein L or L′ is hydroxyethyl.

19. The composition of claim 1 , wherein R 8 or R 9 is hydrogen.

20. The composition of claim 1 , wherein R 8 or R 9 is trityl.

21. The composition of claim 1 , wherein R 8 or R 9 is alkoxytrityl.

22. The composition of claim 21 , wherein R 8 or R 9 is dimethoxytrityl.

23. The composition of claim 1 , wherein R 8 or R 9 is silyl.

24. The composition of claim 1 , wherein R 8 or R 9 is phosphoramidite.

25. The composition of claim 1 , wherein —C 1-10 —O—R 8 and —C 1-10 —O—R 9 are —CH 2 CH 2 —O—R 8 and CH 2 CH 2 —O—R 9 .

Assignments (1)
RELEASE OF SECURITY INTEREST Recorded Oct 5, 2017
From: JPMORGAN CHASE BANK, N.A.
To: INTEGRATED DNA TECHNOLOGIES, INC.
Reel/Frame 043800/0186 →