IP Library Granted Patent US 8,426,618
Granted Patent B2
US 8,426,618 · App. 13/374,728 · Granted Apr 23, 2013

Luminescence quenching compounds

Inventors: Zhenjun Diwu (Sunnyvale, CA); Jianheng Zhang (Santa Clara, CA); Yi Tang (Sunnyvale, CA)
Assignee: AnaSpec Incorporated
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Quick Facts
Patent No.
US 8,426,618
App. No.
13/374,728
Granted
Apr 23, 2013
Kind
B2
Abstract

The quenching compounds of the invention are weakly luminescent cyanines that are substituted by one or more heteroaromatic quenching moieties. The quenching compounds of the invention exhibit little or no observable luminescence and efficiently quench a broad spectrum of luminescent compounds. The chemically reactive quenching compounds possess utility for labeling a wide variety of substances, including biomolecules. These labeled substances are highly useful for a variety of energy-transfer assays and applications.

Claims (14)

1. A method of labeling a nucleic acid, wherein the method involves conjugation of the nucleic acid with a compound having the following structure:

wherein R 1 to R 3 , R 6 , R 8 to R 11 and R 13 to R 16 are hydrogen, alkyl having from 1-20 carbons, alkoxy having from 1-20 carbons, trifluoromethyl, halogen, methylthio, sulfonyl, carbonyl, hydroxyl, amino, thiol, or nitro, and wherein R 4 is a chemically reactive group, and wherein R 5 is an alkyl having from 1-20 carbons, and wherein R 7 is a thiophene or a substituted thiophene,

and wherein the conjugation comprises covalent attachment of the compound to a functional group on the nucleic acid using the chemically reactive group.

2. The method according to claim 1 , wherein the chemically reactive group is a carboxylic acid, an activated carboxylic ester, a sulfonyl chloride, an isocyanate, an isothiocyanate, an acyl azide, an aldehyde, an anhydride, an acyl chloride, an aziridine, an epoxide, a halotriazine, an imido ester, a haloacetamide, a maleimide, an alcohol, a phosphoramidite, an aryl azide, a reactive platinum complex or psoralen.

3. The method according to claim 2 , wherein R 15 and R 16 are hydrogen or alkyl having from 1-20 carbons.

4. The method according to claim 2 , wherein R 13 is trifluoromethyl, halogen, methylthio, sulfonyl, carbonyl, hydroxyl, amino, thiol, or nitro.

5. The method according to claim 2 , wherein R 1 to R 3 are hydrogen.

6. The method according to claim 2 , wherein R 8 to R 11 are hydrogen.

7. The method according to claim 3 , wherein R 15 and R 16 are alkyl having from 1-20 carbons.

8. The method according to claim 7 , wherein the chemically reactive group is a carboxylic acid, an activated carboxylic ester, an acyl azide or a haloacetamide.

9. The method according to claim 8 , wherein R 13 is trifluoromethyl, halogen, methylthio, sulfonyl, carbonyl, hydroxyl, amino, thiol, or nitro.

10. The method according to claim 9 , wherein R 1 to R 3 are hydrogen.

11. A method of labeling a nucleic acid, wherein the method involves conjugation of the nucleic acid with a compound having the following structure:

wherein R 1 to R 3 , R 6 , R 8 to R 11 and R 13 to R 16 are hydrogen, alkyl having from 1-20 carbons, alkoxy having from 1-20 carbons, trifluoromethyl, halogen, methylthio, sulfonyl, carbonyl, hydroxyl, amino, thiol, or nitro, and wherein R 4 is a chemically reactive group, and wherein R 5 is an alkyl having from 1-20 carbons, and wherein R 7 is a thiophene or a substituted thiophene.

Continuity (4)
Continuation 12807180 · Aug 30, 2010
Continuation 11222049 · Sep 7, 2005
Provisional Application 60608817 · Sep 10, 2004
Related Publication 20120123109A1 · May 17, 2012