IP Library › Granted Patent US 12,043,637
Granted Patent B2
US 12,043,637 · App. 17/736,688 · Granted Jul 23, 2024

Fluorescent dyes containing bis-boron fused heterocycles and uses in sequencing

Inventors: Michael Callingham (Cambridge, GB); Nikolai Nikolaevich Romanov (Cambridge, GB); Xiaohai Liu (Cambridge, GB); Justyna Piekos (Cambridge, GB)
Assignee: Illumina Cambridge Limited
C07F5/027C07H23/00
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 12,043,637
App. No.
17/736,688
Granted
Jul 23, 2024
Kind
B2
Abstract

The present application relates to substituted dyes containing bis-boron fused heterocycles and their uses as fluorescent labels. These compounds may be used as fluorescent labels for nucleotides in nucleic acid sequencing applications.

Claims (44)

1. A compound of Formula (I):

a salt or a mesomeric form thereof,

wherein each of R 1 , R 2 , R 3 and R 4 is independently H, unsubstituted or substituted C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkoxy, C 1 -C 6 hydroxyalkyl, (C 1 -C 6 alkoxy)(C 1 -C 6 alkyl), unsubstituted or substituted amino, halo, cyano, carboxyl, hydroxy, nitro, sulfonyl, sulfino, sulfo, sulfonate, S-sulfonamido, N-sulfonamido, unsubstituted or substituted C 3 -C 10 carbocyclyl, unsubstituted or substituted C 6 -C 10 aryl, unsubstituted or substituted 5 to 10 membered heteroaryl, or unsubstituted or substituted 3 to 10 membered heterocyclyl;

each of R a , R b , R c and R d is independently halo, cyano, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, C 6 -C 10 aryl, C 6 -C 10 aryloxy, or —O—C(═O)R 5 ;

R 5 is unsubstituted or substituted C 1 -C 6 alkyl, unsubstituted or substituted C 2 -C 6 alkenyl, unsubstituted or substituted C 6 -C 10 aryl, or unsubstituted or substituted 5 to 10 membered heteroaryl;

alternatively, when both R a and R b are —O—C(═O)R 5 , the two R 5 together with the atoms to which they are attached form an unsubstituted or substituted 6 to 10 membered heterocyclyl;

alternatively, when both R c and R d are —O—C(═O)R 5 , the two R 5 together with the atoms to which they are attached form an unsubstituted or substituted 6 to 10 membered heterocyclyl;

ring A is a 6 to 10 membered heteroaryl optionally substituted with one or more R 6 ;

each R 6 is independently unsubstituted or substituted C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkoxy, C 1 -C 6 hydroxyalkyl, (C 1 -C 6 alkoxy)(C 1 -C 6 alkyl), —NR 7 R 8 , halo, cyano, carboxyl, hydroxy, nitro, sulfonyl, sulfino, sulfo, sulfonate, S-sulfonamido, N-sulfonamido, unsubstituted or substituted C 3 -C 10 carbocyclyl, unsubstituted or substituted C 6 -C 10 aryl, unsubstituted or substituted 5 to 10 membered heteroaryl, or unsubstituted or substituted 3 to 10 membered heterocyclyl; and

each of R 7 and R 8 is independently H, unsubstituted or substituted C 1 -C 6 alkyl, or R 7 and R 8 together with nitrogen atom to which they are attached form an unsubstituted or substituted 3 to 10 membered heterocyclyl;

provided that at least one of R 1 , R 2 , R 3 , R 4 , and ring A comprises a carboxyl group.

2. The compound of claim 1 , having the structure of Formula (Ia) or (Ib):

or a salt or a mesomeric form thereof, wherein m is 0, 1, 2, or 3.

3. The compound of claim 2 , having the structure of Formula (Ic), (Id) or (Ie):

or a salt or a mesomeric form thereof.

4. The compound of claim 1 , wherein each R 6 is independently halo, cyano, carboxyl, unsubstituted or substituted C 1 -C 6 alkyl, unsubstituted phenyl, phenyl substituted with carboxyl, unsubstituted 5 membered heteroaryl, 5 membered heteroaryl substituted with carboxyl, or —NR 7 R 8 .

5. The compound of claim 4 , wherein Reis —NR 7 R 8 , wherein R 7 is H and R 8 is C 1 -C 6 alkyl substituted with one or more substituents selected from the group consisting of carboxyl, sulfo and sulfonate, or R 7 and R 8 together with the nitrogen atom to which they are attached form a 3 to 10 membered heterocyclyl optionally substituted with carboxyl.

6. The compound of claim 5 , wherein R 6 is

wherein each of the ring structure is optionally substituted with carboxyl.

7. The compound of claim 1 , wherein each of R 1 , R 2 and R 3 is independently H or unsubstituted C 1 -C 6 alkyl.

8. The compound of claim 7 , wherein each of R 1 and R 3 is methyl and R 2 is ethyl.

9. The compound of claim 1 , wherein two of R 1 , R 2 and R 3 are H or unsubstituted C 1 -C 6 alkyl, and one of R 1 , R 2 and R 3 is halo, carboxyl or a C 1 -C 6 alkyl substituted with carboxyl.

10. The compound of claim 1 , wherein R 4 is H, unsubstituted C 1 -C 6 alkyl, C 1 -C 6 alkyl substituted with a carboxyl, or phenyl substituted with a carboxyl.

11. The compound of claim 1 , wherein each of R a and R b is independently fluoro, cyano, methyl, trifluoromethyl, methoxy, or —O-acyl (—OC(═O)CH 3 ).

12. The compound of claim 1 , wherein both R a and R b are —OC(═O)R 5 , and the two R 5 together with the atoms to which they are attached form a 6 membered heterocyclyl having the structure

13. The compound of claim 1 , wherein each of R c and R d is independently fluoro, cyano, methyl, trifluoromethyl, methoxy, or —O-acyl (—OC(═O)CH 3 ).

14. The compound of claim 1 , wherein both R c and R d are —OC(═O)R 5 , and the two R 5 together with the atoms to which they are attached form a 6 membered heterocyclyl having the structure

15. The compound of claim 1 , selected from the group consisting of:

or salts or mesomeric forms thereof.

16. A nucleotide labeled with a compound of Formula (I) according to claim 1 .

17. The labeled nucleotide of claim 16 , wherein the compound of Formula (I) is attached to the nucleotide via a carboxyl group of the compound of Formula (I).

18. The labeled nucleotide of claim 16 , comprising a 3′ hydroxy blocking group covalently attached to the ribose or deoxyribose sugar of the nucleotide.

19. An oligonucleotide or polynucleotide comprising the labeled nucleotide according to claim 16 incorporated thereto.

20. The oligonucleotide or polynucleotide of claim 19 , wherein the oligonucleotide or polynucleotide is at least partially complementary and hybridized to a target polynucleotide immobilized on a surface of a solid support.

21. The oligonucleotide or polynucleotide of claim 20 , wherein the solid support comprises an array of a plurality of target polynucleotides immobilized thereon.

22. A kit comprising a first type of labeled nucleotide according to claim 16 .

23. The kit of claim 22 , wherein the kit comprises four types of nucleotides, wherein a first type of nucleotide is a labeled nucleotide according to any one of claims 16 to 18 , a second type of nucleotide carries a second label, a third type of nucleotide carries a third label, and a fourth type of nucleotide is unlabeled (dark).

24. The kit of claim 22 , wherein the kit comprises four types of nucleotides, wherein a first type of nucleotide is a labeled nucleotide according to any one of claims 16 to 18 , a second type of nucleotide carries a second label, a third type of nucleotide comprises a mixture of third type of nucleotides carry two labels, and a fourth type of nucleotide is unlabeled (dark).

25. The kit according to claim 22 , further comprising a DNA polymerase and one or more buffer compositions.

26. A method of determining the sequences of a plurality of target polynucleotides, comprising:

(a) contacting a solid support with a solution comprising sequencing primers under hybridization conditions, wherein the solid support comprises a plurality of different target polynucleotides immobilized thereon; and the sequencing primers are complementary to at least a portion of the target polynucleotides;

(b) contacting the solid support with an aqueous solution comprising DNA polymerase and one or more of four different types of nucleotides under conditions suitable for DNA polymerase-mediated primer extension, wherein one type of nucleotide is a nucleotide of claim 24 having a 3′ hydroxy blocking group covalently attached to the deoxyribose sugar of the nucleotide, and each type of nucleotide has a 3′ hydroxy blocking group;

(c) incorporating one type of nucleotides into the sequencing primers to produce extended copy polynucleotides; and

(d) performing one or more fluorescent measurements of the extended copy polynucleotides to determine the identity of the incorporated nucleotides.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 2, 2023
From: CALLINGHAM, MICHAEL; ROMANOV, NIKOLAI NIKOLAEVICH; LIU, XIAOHAI; PIEKOS, JUSTYNA
To: ILLUMINA CAMBRIDGE LIMITED
Reel/Frame 062577/0561 →
Continuity (2)
Provisional Application 63184429 · May 5, 2021
Related Publication 20220380389A1 · Dec 1, 2022