IP Library Granted Patent US 12,098,117
Granted Patent B2
US 12,098,117 · App. 17/312,858 · Granted Sep 24, 2024

Compositions and methods for the treatment of cancer

Inventors: Dennis J. Thiele (Chapel Hill, NC); Bushu Dong (Durham, NC); Alexander M. Jaeger (Cambridge, MA); Philip F. Hughes (Chapel Hill, NC); Timothy Haystead (Durham, NC); Jiyong Hong (Durham, NC)
Assignee: Duke University
C07C275/30A61P35/00C07C211/40C07C255/60C07C275/28C07C275/34C07C275/40C07C275/42C07C279/18C07C279/28C07C281/06C07C311/46C07C317/36C07C317/42C07D213/40C07D213/75C07D223/04C07D229/02C07D231/56C07D233/64C07D241/24C07D249/14C07D271/12C07D285/10C07D317/66C07D333/20C07D333/36C07D333/72C07D405/04C07D405/12C07D417/12
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Quick Facts
Patent No.
US 12,098,117
App. No.
17/312,858
Granted
Sep 24, 2024
Kind
B2
Abstract

This disclosure relates to compounds, pharmaceutical compositions comprising them, and methods of using the compounds and compositions for treating diseases related to Heat Shock Transcription Factor 1 (HSF1) activity and/or function. More particularly, this disclosure relates to methods of inhibiting HSF1 activity with these compounds and pharmaceutical compositions thereof, and methods of treating diseases associated with HSF1 activity and/or function, such as cancer.

Claims (10)

1. A method of treating cancer associated with an elevated HSF1 activity in a subject in need thereof, the method comprising administering to the subject an effective amount of an HSF1 inhibiting compound selected from the group consisting of:

and combinations thereof,

wherein the cancer is selected from the group consisting of breast cancer, prostate cancer, colon cancer, squamous cell cancer, small-cell lung cancer, non-small cell lung cancer, ovarian cancer, cervical cancer, gastrointestinal cancer, pancreatic cancer, glioblastoma, liver cancer, bladder cancer, hepatoma, colorectal cancer, uterine cervical cancer, endometrial carcinoma, salivary gland carcinoma, mesothelioma, kidney cancer, vulval cancer, pancreatic cancer, thyroid cancer, hepatic carcinoma, skin cancer, melanoma, brain cancer, neuroblastoma, myeloma, head and neck cancer, leukemia (including but not limited to acute lymphoblastic leukemia and acute myeloid leukemia), sarcoma, carcinoma, stromal cancer, testicular cancer, neurofibroma, hepatocellular carcinoma, lymphoma, Ewing sarcoma and peripheral neuroepithelioma.

2. The method of claim 1 , wherein the compound binds directly to an HSF1 protein to inhibit HSF1 activity in the subject.

3. The method of claim 2 , wherein inhibiting HSF1 activity comprises inhibition of HSF1 homo-trimerization, inhibition of HSF1 target gene expression, inhibition of HSF1 target protein expression, inhibition of HSF1-mediated genome-wide transcriptional regulation, inhibition of protein chaperone activity, or a combination thereof.

4. The method of claim 2 , wherein the binding of the compound increases the melting temperature of the HSF1 protein by at least 1° C. when compared with the melting temperature of the HSF1 protein prior to binding.

5. The method of claim 2 , wherein the binding of the compound decreases the melting temperature of the HSF1 protein by at least 1° C. when compared with the melting temperature of the HSF1 protein prior to binding.

6. The method of claim 1 , wherein the cancer is prostate cancer.

7. A compound having the structure of

or a pharmaceutically acceptable salt thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 26, 2024
From: THIELE, DENNIS J.; DONG, BUSHU; JAEGER, ALEXANDER M.; HUGHES, PHILIP F.; HAYSTEAD, TIMOTHY; HONG, JIYONG
To: DUKE UNIVERSITY
Reel/Frame 067956/0657 →
Continuity (2)
Provisional Application 62777831 · Dec 11, 2018
Related Publication 20220106265A1 · Apr 7, 2022