Monoazo dyes with cyclic amine as fluorescence quencers

Patent metadata

Field	Value
Publication number	US-10131789-B2
Application number	US-201815928290-A
Country	US
Kind code	B2
Filing date	Mar 22, 2018
Priority date	Mar 30, 2015
Publication date	Nov 20, 2018
Grant date	Nov 20, 2018

Abstract

The present disclosure provides reactive quencher dyes that can be used in the detection and/or quantification of desirable target molecules, such as proteins, nucleic acids and various cellular organelles. These dyes are essentially non-fluorescent but are efficient quenchers of various fluorescent dyes. Also, provided are methods of using the dyes, bio-probes incorporating dyes and methods of using the bio-probes. The quencher dyes described herein are modified to provide beneficial properties.

First claim

What is claimed is:

1. A compound having the formula:

wherein R 1 and R 8 are each independently H, F, Cl, Br, I, CN, nitro (NO 2 ), azido, hydroxyl, amino, hydrazino, aryl, substituted aryl, aroxyl, substituted aroxyl, alkenyl, alkynyl, alkyl, alkoxy, alkylamino, dialkylamino, arylamino, diarylamino, alkyl(aryl)amino, alkanoylamino, alkylthio, alkylcarbonyl, aryl carbonyl, alkylthiocarbonyl, arylthiocarbonyl, alkyloxycarbonyl, aroxycarbonyl, alkylaminocarbonyl, arylaminocarbonyl, dialkylaminocarbonyl, diarylaminocarbonyl, alkyl(aryl)aminocarbonyl, arylcarboxamido, or Q, wherein the alkyl or alkoxy groups are saturated or unsaturated, linear or branched, unsubstituted or optionally substituted by F, Cl, Br, I, CN, OH, alkenyl, alkynyl, alkylcarbonyl, amide, thioamide, or Q, and the aryl group is optionally substituted by F, Cl, Br, I, CN, OH, alkenyl, alkynyl, alkylcarbonyl, amide, thioamide, or Q;
Q is a carboxyl group (CO 2 − ), a carbonate ester (COER 12 ), a sulfonate ester (SO 2 ER 12 ), a sulfoxide (SOR 12 ), a sulfone (SO 2 CR 12 R 13 R 14 ), a sulfonamide (SO 2 NR 12 R 13 ), a phosphate (PO 4 = ), a phosphate monoester (PO 3 − ER 12 ), a phosphate diester (PO 2 ER 12 ER 13 ), a phosphonate (PO 3 = ) a phosphonate monoester (PO 2 − ER 12 ) a phosphonate diester (POER 12 ER 13 ), a thiophosphate (PSO 3 = ), a thiophosphate monoester (PSO 2 − ER 12 ) a thiophosphate diester (PSOER 12 ER 13 ), a thiophosphonate (PSO 2 = ), a thiophosphonate monoester (PSO − ER 12 ), a thiophosphonate diester (PSER 12 ER 13 ), a phosphonamide (PONR 12 R 13 NR 15 R 16 ) or its thioanalogue (PSNR 12 R 13 NR 15 R 16 ), a phosphoramide (PONR 12 R 13 NR 14 NR 15 R 16 ) or its thioanalogue (PSNR 12 R 13 NR 14 NR 15 R 16 ), or a phosphoramidite (PO 2 R 15 NR 12 R 13 ) or its thioanalogue (POSR 15 NR 12 R 13 ), wherein E is independently O or S;
R 10 is H, a saturated or unsaturated, linear or branched, unsubstituted or further substituted alkyl group, aryl group, alkylcarbonyl, aryl carbonyl, alkylthiocarbonyl, arylthiocarbonyl, alkoxycarbonyl, aroxycarbonyl, alkylaminocarbonyl, arylaminocarbonyl, dialkylaminocarbonyl, diarylaminocarbonyl, alkyl(aryl)aminocarbonyl, arylcarboxamido, or Q, the alkyl or alkoxy portions of which are, alkenyl, alkynyl, alkylcarbonyl, amide, thioamide, or Q, or the aryl portions of which are optionally substituted by F, Cl, Br, I, CN, OH, alkenyl, alkynyl, alkylcarbonyl, amide, thioamide, or Q;
R 12 , R 13 , R 14 , R 15 and R 16 are each independently hydrogen, a halogen, an amino group, a saturated or unsaturated, linear or branched, substituted or unsubstituted alkyl group, a saturated or unsaturated, branched or linear, substituted or unsubstituted alkoxy group, a substituted or unsubstituted aryl group, or
R 12 in combination with R 13 , R 14 in combination with R 16 , R 12 in combination with R 14 , R 12 in combination with R 15 , R 13 in combination with R 16 , and R 14 in combination with R 15 , one or more of which, form a 5- to 10-member ring;

R 3 is nitro;
R 5 is H or OCH 3 ; and
R 6 is H or OCH 3 .

2. The compound of claim 1 , wherein R 1 is CN or H.

3. A compound having the formula:

wherein
R 10 is H, a saturated or unsaturated, linear or branched, unsubstituted or further substituted alkyl group, aryl group, alkylcarbonyl, aryl carbonyl, alkylthiocarbonyl, arylthiocarbonyl, alkoxycarbonyl, aroxycarbonyl, alkyl aminocarbonyl, arylaminocarbonyl, dialkylaminocarbonyl, diarylaminocarbonyl, alkyl (aryl)aminocarbonyl, arylcarboxamido, or Q, the alkyl or alkoxy portions of which are, alkenyl, alkynyl, alkylcarbonyl, amide, thioamide, or Q, or the aryl portions of which are optionally substituted by F, Cl, Br, I, CN, OH, alkenyl, alkynyl, alkylcarbonyl, amide, thioamide, or Q,
wherein Q is a carboxyl group (CO 2 − ), a carbonate ester (COER 12 ), a sulfonate ester (SO 2 ER 12 ), a sulfoxide (SOR 12 ), a sulfone (SO 2 CR 12 R 13 R 14 ), a sulfonamide (SO 2 NR 12 R 13 ), a phosphate (PO 4 = ), a phosphate monoester (PO 3 − ER 12 ), a phosphate diester (PO 2 ER 12 ER 13 ), a phosphonate (PO 3 = ) a phosphonate monoester (PO 2 − ER 12 ) a phosphonate diester (POER 12 ER 13 ), a thiophosphate (PSO 3 = ), a thiophosphate monoester (PSO 2 − ER 12 ) a thiophosphate diester (PSOER 12 ER 13 ), a thiophosphonate (PSO 2 = ), a thiophosphonate monoester (PSO − ER 12 ), a thiophosphonate diester (PSER 12 ER 13 ), a phosphonamide (PONR 12 R 13 NR 15 R 16 ) or its thioanalogue (PSNR 12 R 13 NR 15 R 16 ), a phosphoramide (PONR 12 R 13 NR 14 NR 15 R 16 ) or its thioanalogue (PSNR 12 R 13 NR 14 NR 15 R 16 ), or a phosphoramidite (PO 2 R 15 NR 12 R 13 ) or its thioanalogue (POSR 15 NR 12 R 13 ), wherein E is independently O or S;

R 12 , R 13 , R 14 , R 15 and R 16 are each independently hydrogen, a halogen, an amino group, a saturated or unsaturated, linear or branched, substituted or unsubstituted alkyl group, a saturated or unsaturated, branched or linear, substituted or unsubstituted alkoxy group, a substituted or unsubstituted aryl group, or
R 12 in combination with R 13 , R 14 in combination with R 16 , R 12 in combination with R 14 , R 12 in combination with R 15 , R 13 in combination with R 16 , and R 14 in combination with R 15 , one or more of which, form a 5- to 10-member ring;

R 1 is CN or H; and
R 5 , R 6 and R 8 are each independently H, CH 3 , or OCH 3 .

4. The compound of claim 3 , wherein
R 5 is H or OCH 3 ; and
R 6 is H or OCH 3 .

5. A compound having the formula:

wherein
R 1 is CN or H;
R 3 is nitro;
R 5 is H;
R 6 is OCH 3 ;
R 8 is H; and
R 10 is H, a saturated or unsaturated, linear or branched, unsubstituted or further substituted alkyl group, aryl group, alkylcarbonyl, aryl carbonyl, alkylthiocarbonyl, arylthiocarbonyl, alkoxycarbonyl, aroxycarbonyl, alkylaminocarbonyl, apylaminocarbonyl, dialkylaminocarbonyl, diarylaminocarbonyl, alkyl(aryl)aminocarbonyl, arylcarboxamido, or Q, the alkyl or alkoxy portions of which are, alkenyl, alkynyl, alkycarbonyl, amide, thioamide, or Q, or the aryl portions of which are optionally substituted by F, Cl, Br, I, CN, OH, alkenyl, alkynyl, alkylcarbonyl, amide, thioamide, or Q,
wherein Q is a carboxyl group (CO 2 − ), a carbonate ester (COER 12 ), a sulfonate ester (SO 2 ER 12 ), a sulfoxide (SOR 12 ), a sulfone (SO 2 CR 12 R 13 R 14 ), a sulfonamide (SO 2 NR 12 R 13 ), a phosphate (PO 4 = ), a phosphate monoester (PO 3 − ER 12 ), a phosphate diester (PO 2 ER 12 ER 13 ), a phosphonate (PO 3 = ) a phosphonate monoester (PO 2 − ER 12 ) a phosphonate diester (POER 12 ER 13 ), a thiophosphate (PSO 3 = ), a thiophosphate monoester (PSO 2 − ER 12 ) a thiophosphate diester (PSOER 12 ER 13 ), a thiophosphonate (PSO 2 = ), a thiophosphonate monoester (PSO − ER 12 ), a thiophosphonate diester (PSER 12 ER 13 ), a phosphonamide (PONR 12 R 13 NR 15 R 16 ) or its thioanalogue (PSNR 12 R 13 NR 15 R 16 ), a phosphoramide (PONR 12 R 13 NR 14 NR 15 R 16 ) or its thioanalogue (PSNR 12 R 13 NR 14 NR 15 R 16 ), or a phosphoramidite (PO 2 R 15 NR 12 R 13 ) or its thioanalogue (POSR 15 NR 12 R 13 ), wherein E is independently O or S.

6. A compound having the formula:

wherein
R 1 is CN or H;
R 3 is nitro;
R 5 is H;
R 6 is OCH 3 ;
R 8 is H; and
R 10 is H, a saturated or unsat

Assignees

• Enzo Biochem Inc

Inventors

• Li Zaiguo
• Pande Praveen
• Raju Natarajan

Classifications

• C12Q2565/101

  Interaction between at least two labels · CPC title

• C12Q1/6876

  Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes · CPC title

• C12Q1/6846

  Common amplification features · CPC title

• C12Q1/68

  involving nucleic acids · CPC title

• C09B56/005

  Azo-nitro dyes · CPC title