IP Library Granted Patent US 9,976,147
Granted Patent B2
US 9,976,147 · App. 15/160,865 · Granted May 22, 2018

STAT3 inhibitors and uses thereof

Inventors: Marcin Tomasz Kortylewski (Monrovia, CA); Piotr Marek Swiderski (San Dimas, CA)
Assignee: City of Hope
C12N15/117A61K39/39A61K47/48092C07H21/02C07H21/04C12N15/111A61K2039/55561C12N2310/13C12N2310/17C12N2310/315C12N2310/351C12N2310/3519C12N2320/30C12N2320/32
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Quick Facts
Patent No.
US 9,976,147
App. No.
15/160,865
Granted
May 22, 2018
Kind
B2
Abstract

Described herein, inter alia, are STAT-binding nucleic acids-including compositions and methods of using the same.

Claims (27)

1. A compound comprising a toll-like receptor (TLR)-binding nucleic acid substituent conjugated to a signal transducer and activator of transcription (STAT)-binding nucleic acid substituent, wherein said STAT-binding nucleic acid substituent is capable of binding to a STAT transcription factor.

2. The compound of claim 1 , wherein the TLR-binding nucleic acid substituent is an endosomal TLR-binding nucleic acid substituent.

3. The compound of claim 1 , wherein the TLR-binding nucleic acid substituent conjugated to a STAT-binding DNA substituent is a nucleic acid sequence comprising SEQ ID NO:21, SEQ ID NO:22, SEQ ID NO:23, or SEQ ID NO:24.

4. The compound of claim 1 , wherein the TLR-binding nucleic acid substituent conjugated to a STAT-binding DNA substituent is a nucleic acid sequence comprising SEQ ID NO:23.

5. A compound comprising a toll-like receptor 9 (TLR9)-binding DNA substituent conjugated to a signal transducer and activator of transcription 3 (STAT3)-binding DNA substituent, wherein said STAT3-binding nucleic acid substituent is capable of binding to a STAT3 transcription factor.

6. The compound of claim 5 , wherein the TLR9-binding DNA substituent comprises a CpG motif.

7. The compound of claim 5 , wherein the TLR9-binding DNA substituent comprises a Class A CpG DNA sequence, a Class B CpG DNA sequence or a Class C CpG DNA sequence.

8. The compound of claim 7 , wherein the TLR9-binding DNA substituent is a Class A CpG DNA sequence.

9. The compound of claim 7 , wherein the TLR9-binding DNA substituent is a Class B CpG DNA sequence.

10. The compound of claim 7 , wherein the TLR9-binding DNA substituent is a Class C CpG DNA sequence.

11. The compound of claim 5 , wherein the STAT3-binding DNA substituent comprises a first STAT3-binding DNA sequence covalently bound to a second STAT3-binding DNA sequence by a spacer; and

said spacer is a substituted or unsubstituted alkylene, substituted or unsubstituted heteroalkylene, substituted or unsubstituted cycloalkylene, substituted or unsubstituted heterocycloalkylene, substituted or unsubstituted arylene, or substituted or unsubstituted heteroarylene.

12. The compound of claim 11 , wherein the spacer is a substituted or unsubstituted C 1 -C 40 alkylene, substituted or unsubstituted 2 to 40 membered heteroalkylene, substituted or unsubstituted C 3 -C 8 cycloalkylene, substituted or unsubstituted 3 to 8 membered heterocycloalkylene, substituted or unsubstituted C 6 -C 10 arylene, or substituted or unsubstituted 5 to 10 membered heteroarylene.

13. The compound of claim 11 , wherein the first STAT3-binding DNA sequence and second STAT3-binding DNA sequence form a double-stranded STAT3-binding DNA sequence.

14. The compound of claim 5 , wherein the STAT3-binding DNA substituent preferentially binds phosphorylated STAT3 over unphosphorylated STAT3.

15. The compound of claim 5 , wherein the STAT3-binding DNA substituent comprises a STAT3-binding DNA sequence covalently bonded to a terminal moiety; and

said terminal moiety is a substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl.

16. The compound of claim 15 , wherein the terminal moiety is an R 1 -substituted C 1 -C 40 alkyl, R 1 -substituted 2 to 40 membered heteroalkyl, R 1 -substituted C 3 -C 8 cycloalkyl, R 1 -substituted 3 to 8 membered heterocycloalkyl, R 1 -substituted C 6 -C 10 aryl, or R 1 -substituted 5 to 10 membered heteroaryl; and

R 1 is oxo, oxygen, a detectable moiety, or a therapeutic moiety.

17. The compound of claim 16 , wherein the detectable moiety is a fluorescent dye, electron-dense reagent, enzyme, biotin, digoxigenin, paramagnetic molecule, paramagnetic nanoparticle, contrast agent, magnetic resonance contrast agent, X-ray contrast agent, Gadolinium, radioisotope, radionuclide, fluorodeoxyglucose, gamma ray emitting radionuclide, positron-emitting radionuclide, biocolloid, microbubble, iodinated contrast agent, barium sulfate, thorium dioxide, gold, gold nanoparticle, gold nanoparticle aggregate, fluorophore, two-photon fluorophore, hapten, protein, or fluorescent moiety.

18. The compound of claim 5 , further comprising a linker between the TLR9-binding DNA substituent and the STAT3-binding DNA substituent.

19. The compound of claim 18 , wherein the linker is a substituted or unsubstituted alkyl ene, substituted or unsubstituted heteroalkylene, substituted or unsubstituted cycloalkylene, substituted or unsubstituted heterocycloalkylene, substituted or unsubstituted arylene, or substituted or unsubstituted heteroarylene.

20. The compound of claim 5 , further comprising a phosphorothioate linkage.

21. The compound of claim 5 , wherein the STAT3-binding DNA substituent is a nucleic acid sequence comprising SEQ ID NO:12.

22. The compound of claim 5 , wherein the TLR9-binding DNA substituent is a nucleic acid sequence comprising SEQ ID NO:12, and the STAT3-binding DNA substituent is a nucleic acid sequence comprising SEQ ID NO:23.

23. The compound of claim 5 , comprising nucleic acid SEQ ID NO:6.

24. A pharmaceutical composition comprising a pharmaceutically acceptable excipient and the compound of claim 1 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 10, 2016
From: KORTYLEWSKI, MARCIN TOMASZ; SWIDERSKI, PIOTR MAREK
To: CITY OF HOPE
Reel/Frame 040280/0668 →
Continuity (4)
Continuation PCTUS2014066969 · Nov 21, 2014
Provisional Application 62077035 · Nov 7, 2014
Provisional Application 61907953 · Nov 22, 2013
Related Publication 20160333350A1 · Nov 17, 2016