IP Library Granted Patent US 9,228,225
Granted Patent B2
US 9,228,225 · App. 12/941,931 · Granted Jan 5, 2016

Xanthene dyes

Inventors: Mark Reddington (San Francisco, CA); Matt Lyttle (San Rafael, CA)
Assignee: BIOSEARCH TECHNOLOGIES, INC.
C12Q1/37C07D311/90C07D405/14C07F9/65522C07F9/65586G01N33/582
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 9,228,225
App. No.
12/941,931
Granted
Jan 5, 2016
Kind
B2
Abstract

The invention provides a novel class of xanthene dyes, some of which are functionalized to allow their coupling to conjugation partners of interest, e.g. biomolecules, drugs, toxins and the like. Also provided are conjugates of the dyes, methods of preparing and using the dyes and their conjugates and kits including the dyes and their conjugates.

Claims (125)

1. A xanthene dye having a formula which is

wherein C(O)NR 12 R_is a member selected from the group consisting of:

wherein said DMT is dimethoxytrityl and said CPG is controlled pore glass.

2. A xanthene dye having the formula:

in which

R 1 , R 2 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 and R 11 are independently selected from the group consisting of substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted heterocycloalkyl, halogen, H, NO 2 , CN, NR 15 R 16 and Z 2 R 16 ;

R 3 is NR 15 R 16

wherein

Z 2 is O or S;

R 15 is a member selected from the group consisting of H, substituted or unsubstituted alkyl, and substituted or unsubstituted heteroalkyl;

R 16 is selected from the group consisting of H, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, C(Z 3 )R 17 , and a nitrogen-containing reactive group comprising R 15 and R 16 , together with the nitrogen to which they are attached, wherein said reactive group is a member selected from the group consisting of —NHNH 2 ,—N═C═S and —N═C═O

wherein

Z 3 is a member selected from the group consisting of O, S and NH;

R 17 is a member selected from the group consisting of substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, OR 18 , and NR 19 R 20

wherein

R 19 and R 20 are members independently selected from the group consisting of H, substituted or unsubstituted alkyl and substituted or unsubstituted heteroalkyl;

R 18 is a member selected from the group consisting of H, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl and C(O)R 21

wherein

R 21 is substituted or unsubstituted alkyl or substituted or unsubstituted heteroalkyl;

Y is C(O) or S(O) 2 ;

X is (NR 22 R 23 ) or (O)

wherein

R 22 and R 23 are members independently selected from the group consisting of H, substituted or unsubstituted alkyl and substituted or unsubstituted heteroalkyl;

R 12 and R 13 , together with the nitrogen atom to which they are attached, joined to form a ring, wherein said ring formed from R 12 and R 13 is substituted with:

a member selected from the group consisting of hydroxyl, ester, sulfonate, ether, aldehyde, phosphoramidite, carboxylic acid, acid halides, acyl imidazoles, and thioesters, or

a substituted or unsubstituted alkyl comprising a member selected from the group consisting of hydroxyl, ester, sulfonate, ether, aldehyde, phosphoramidite, carboxylic acid, acid halides, acyl imidazoles, and thioesters, or

a substituted or unsubstituted heteroalkyl moiety comprising a member selected from the group consisting of hydroxyl, ester, sulfonate, ether, aldehyde, phosphoramidite, carboxylic acid, acid halides, acyl imidazoles, and thioesters.

3. The xanthene dye of claim 1 , wherein NR 12 R 13 has the formula:

wherein

h and i are members independently selected from integers such that the sum (h+i) is from 4-8; and

R 25 is:

a member selected from the group consisting of hydroxyl, ester, sulfonate, ether, aldehyde, phosphoramidite, carboxylic acid, acid halides, acyl imidazoles, and thioesters, or

a substituted or unsubstituted alkyl comprising a member selected from the group consisting of hydroxyl, ester, sulfonate, ether, aldehyde, phosphoramidite, carboxylic acid, acid halides, acyl imidazoles, and thioesters, or

a substituted or unsubstituted heteroalkyl moiety comprising a member selected from the group consisting of hydroxyl, ester, sulfonate, ether, aldehyde, phosphoramidite, carboxylic acid, acid halides, acyl imidazoles, and thioesters.

4. The xanthene dye of claim 3 , wherein R 25 is a phosphoramidite, or a substituted or unsubstituted alkyl comprising a phosphoramidite, or a substituted or unsubstituted heteroalkyl moiety comprising a phosphoramidite.

5. The xanthene dye of claim 3 , wherein R 25 is a phosphoramidite.

6. The xanthene dye of claim 3 , wherein h is 2 and i is 2.

7. A xanthene dye having the formula which is a member selected from the group consisting of:

wherein

Y is C(O) or S(O) 2 ;

h and i are members independently selected from integers such that the sum (h+i) is from 4-8; and

R 25 is

a member selected from the group consisting of hydroxyl, ester, sulfonate, ether, aldehyde, phosphoramidite, carboxylic acid, acid halides, acyl imidazoles, and thioesters, or

a substituted or unsubstituted alkyl comprising a member selected from the group consisting of hydroxyl, ester, sulfonate, ether, aldehyde, phosphoramidite, carboxylic acid, acid halides, acyl imidazoles, and thioesters, or

a substituted or unsubstituted heteroalkyl moiety comprising a member selected from the group consisting of hydroxyl, ester, sulfonate, ether, aldehyde, phosphoramidite, carboxylic acid, acid halides, acyl imidazoles, and thioesters.

8. The xanthene dye of claim 7 , wherein h is 2 and i is 2.

9. The xanthene dye of claim 7 , wherein R 25 is a phosphoramidite, or a substituted or unsubstituted alkyl comprising a phosphoramidite, or a substituted or unsubstituted heteroalkyl moiety comprising a phosphoramidite.

10. The xanthene dye of claim 7 , wherein R 25 is a phosphoramidite.

11. The xanthene dye of claim 7 , having a formula which is:

wherein

h is 2 and i is 2; and R 25 is a phosphoramidite, or a substituted or unsubstituted alkyl comprising a phosphoramidite, or a substituted or unsubstituted heteroalkyl moiety comprising a phosphoramidite.

12. The xanthene dye of claim 7 , having a formula which is:

wherein

h is 2 and i is 2; and R 25 is a phosphoramidite, or a substituted or unsubstituted alkyl comprising a phosphoramidite, or a substituted or unsubstituted heteroalkyl moiety comprising a phosphoramidite.

13. The xanthene dye of claim 7 , having a formula which is:

wherein

h is 2 and i is 2;and R 25 is a phosphoramidite, or a substituted or unsubstituted alkyl comprising a phosphoramidite, or a substituted or unsubstituted heteroalkyl moiety comprising a phosphoramidite.

14. A xanthene dye having the formula:

in which

R 1 , R 2 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 and R 11 are independently selected from the group consisting of substituted or unsubstituted alkyl, substituted or unsubstituted. heteroalkyl, substituted or unsubstituted aryl, substituted or unsubstituted. heteroaryl, substituted or unsubstituted heterocycloalkyl, halogen, H, NO 2 , CN, NR 15 R 16 and Z 2 R 16 ;

R 3 is Z 2 R 16 or NR 15 R 16

wherein

Z 2 is O or S;

R 15 is a member selected from the group consisting of H. substituted or unsubstituted alkyl, and substituted or unsubstituted heteroalkyl;

R 16 is selected from the group consisting of H, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, C(Z 3 )R 17 , and a nitrogen-containing reactive group comprising R 15 and R 16 , together with the nitrogen to which they are attached, wherein said reactive group is a member selected from —NHNH 2 , —N═C═S and —N═C═O

wherein

Z 3 is a member selected from the group consisting of O, S and NH;

R 17 is a member selected from the group consisting of substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, OR 18 , and NR 19 R 20

wherein

R 18 is a member selected from the group consisting of H, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl and C(O)R 21

wherein

 R 21 is substituted or unsubstituted. alkyl or substituted or unsubstituted heteroalkyl;

R 19 and R 20 are members independently selected from the group consisting of H, substituted or unsubstituted alkyl and substituted or unsubstituted heteroalkyl

Y is C(O) or S(O) 2 ;

X is (NR 22 R 23 ) or (O)

wherein

R 22 and R 23 are members independently selected from the group consisting of H, substituted or unsubstituted alkyl and substituted or unsubstituted heteroalkyl;

R 12 and R 13 , together with the nitrogen atom to which they are attached, are joined to form a ring, wherein said ring formed from R 12 and R 13 is substituted with a member selected from the group consisting of hydroxyl, ester, sulfonate, ether, aldehyde, phosphoramidite, carboxylic acid, acid halides, acyl imidazoles, and thioesters, or a substituted or unsubstituted alkyl bearing a member selected from the group consisting of hydroxyl, ester, sulfonate, ether, aldehyde, phosphoramidite, carboxylic acid, acid halides, acyl imidazoles, and thioesters, or substituted or unsubstituted heteroalkyl moiety bearing a member selected from the group consisting of hydroxyl, ester, sulfonate, ether, aldehyde, phosphoramidite, carboxylic acid, acid halides, acyl imidazoles, and thioesters.

15. The xanthene dye of claim 14 , wherein NR 12 R 13 as the formula:

wherein

h and i are members independently selected from integers such that the sum (h+i) is from 4-8; and

R 25 is a member selected from the group consisting of hydroxyl, ester, sulfonate, ether, aldehyde, phosphoramidite, carboxylic acid, acid halides, acyl imidazoles, and thioesters, or a substituted or unsubstituted alkyl bearing a member selected from the group consisting of hydroxyl, ester, sulfonate, ether, aldehyde, phosphoramidite, carboxylic acid, acid halides, acyl imidazoles, and thioesters, or substituted or unsubstituted heteroalkyl moiety bearing a member selected from the group consisting of hydroxyl, ester, sulfonate, ether, aldehyde, phosphoramidite, carboxylic acid, acid halides, acyl imidazoles, and thioesters.

16. The xanthene dye of claim 15 , wherein R 25 is a phosphoramidite, or a substituted or unsubstituted alkyl bearing a phosphoramidite, or a substituted or unsubstituted heteroalkyl moiety bearing a phosphoramidite.

17. The xanthene dye of claim 15 , wherein R 25 is a phosphoramidite.

18. The xanthene dye of claim 15 , wherein h is 2 and i is 2.

19. The xanthene dye of claim 15 , wherein the xanthene dye has the formula which is a member selected from the group consisting of:

wherein

h and i are members independently selected from integers such that the sum (h+i) is from 4-8; and

R 25 is a member selected from the group consisting of hydroxyl, ester, sulfonate, ether, aldehyde, phosphoramidite, carboxylic acid, acid halides, acyl imidazoles, and thioesters, or a substituted or unsubstituted alkyl bearing a member selected from the group consisting of hydroxyl, ester, sulfonate, ether, aldehyde, phosphoramidite, carboxylic acid, acid halides, acyl imidazoles, and thioesters, or substituted or unsubstituted heteroalkyl moiety bearing a member selected from the group consisting of hydroxyl, ester, sulfonate, ether, aldehyde, phosphoramidite, carboxylic acid, acid halides, acyl imidazoles, in thioesters.

20. The xanthene dye of claim 19 , wherein h is 2 and i is 2.

21. The xanthene dye of claim 19 , wherein R 25 is a phosphoramidite, or a substituted or unsubstituted alkyl comprising a phosphoramidite, or a substituted or unsubstituted heteroalkyl moiety comprising a phosphoramidite.

22. The xanthene dye of claim 19 , wherein R 25 is a phosphoramidite.

23. The xanthene dye of claim 19 , having a formula which is:

wherein

h is 2 and i is 2; and R 25 is a phosphoramidite, or a substituted or unsubstituted alkyl comprising a phosphoramidite, or a substituted or unsubstituted heteroalkyl moiety comprising a phosphoramidite.

24. The xanthene dye of claim 19 , having a formula which is:

wherein

h is 2 and i is 2; and R 25 is a phosphoramidite, or a substituted or unsubstituted alkyl comprising a phosphoramidite, or a substituted or unsubstituted heteroalkyl moiety comprising a phosphoramidite.

25. The xanthene dye of claim 19 , having a formula which is:

wherein

h is 2 and i is 2; and R 25 is a phosphoramidite, or a substituted or unsubstituted alkyl comprising a phosphoramidite, or a substituted or unsubstituted heteroalkyl moiety comprising a phosphoramidite.

26. The xanthene dye of claim 2 , wherein said ester is N-hydroxysuccinimide ester, N-hydroxybenztriazole ester, p-nitrophenyl ester, alkyl ester, alkenyl ester, alkynyl ester, or aromatic ester.

27. The xanthene dye of claim 14 , wherein said ester is N-hydroxysuccinimide ester, N-hydroxybenztriazole ester, p-nitrophenyl ester, alkyl ester, alkenyl ester, alkynyl ester, or aromatic ester.

28. The xanthene dye of claim 19 , wherein said ester is N-hydroxysuccinimide ester, N-hydroxybenztriazole ester, p-nitrophenyl ester, alkyl ester, alkenyl ester, alkynyl ester, or aromatic ester.

29. A xanthene dye having a formula which is:

wherein C(O)NR 12 R 13 is a member selected from the group consisting of:

wherein said DMT is dimethoxytrityl and said CPG is controlled pore glass.

30. A xanthene dye having a formula which is:

wherein C(O)NR 12 R 13 is a member selected from the group consisting of:

wherein said DMT is dimethoxytrityl and said CPG is controlled pore glass.

31. A xanthene dye having a formula which is:

wherein C(O)NR 12 R 13 is a member selected from the group consisting of:

wherein said DMT is dimethoxytrityl and said CPG is controlled pore glass.

32. A xanthene dye having a formula which is:

wherein C(O)NR 12 R 13 is

33. A xanthene dye having a formula which is:

wherein C(O)NR 12 R 13 is

34. A xanthene dye having a formula which is:

wherein C(O)NR 12 R 13 is a member selected from the group consisting of:

wherein said DMT is dimethoxytrityl and said CPG is controlled pore glass.

35. A xanthene dye having a formula which is:

wherein C(O)NR 12 R 13 is

36. A xanthene dye having a formula which is:

wherein C (O)NR 12 R 13 is

37. The xanthene dye of claim 7 , having the formula:

Assignments (4)
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 14, 2010
From: REDDINGTON, MARK; LYTTLE, MATT
To: BIOSEARCH TECHNOLOGIES, INC.
Reel/Frame 025489/0169 →
Continuity (4)
Continuation 12036926 · Feb 25, 2008
Continuation 10824175 · Apr 13, 2004
Provisional Application 60541686 · Feb 3, 2004
Related Publication 20110054165A1 · Mar 3, 2011