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US Patent 11918592 Inhibitors of cyclin dependent kinase 7 (CDK7)

Patent 11918592 was granted and assigned to Syros Pharmaceuticals on March, 2024 by the United States Patent and Trademark Office.

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Contents

Is a
Patent
Patent
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Patent attributes

Patent Applicant
Syros Pharmaceuticals
Syros Pharmaceuticals
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Current Assignee
Syros Pharmaceuticals
Syros Pharmaceuticals
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Patent Jurisdiction
United States Patent and Trademark Office
United States Patent and Trademark Office
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Patent Number
119185920
Patent Inventor Names
Michael Bradley0
Anzhelika Kabro0
Kenneth Matthew Whitmore0
Jason J. Marineau0
Stephane Ciblat0
Henri Piras0
Kate-Lyn Lund0
Claudio Edmundo Chuaqui0
Date of Patent
March 5, 2024
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Patent Application Number
169628090
Date Filed
January 16, 2019
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Patent Citations
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US Patent 9012462 Phosphorous derivatives as kinase inhibitors
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US Patent 7615562 2-aminopyrimidine derivatives and their medical use
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US Patent 9561228 ERK inhibitors and uses thereof
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Patent Primary Examiner
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Samira J Jean-Louis
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CPC Code
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A61P 35/00
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C07D 413/14
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C07D 403/14
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C07D 403/04
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Patent abstract

The present invention provides, inter alia, compounds having the structures of formulas described herein; pharmaceutically acceptable salts, solvates, hydrates, tautomers, and isotopic forms thereof; and compositions (e.g., pharmaceutical compositions and kits) containing one or more of the foregoing. Also provided are methods of administering and uses involving the compounds and/or pharmaceutical compositions for treating or preventing disease. The disease can be a proliferative disease, such as a cancer (e.g., a blood cancer (e.g., a leukemia or lymphoma), a brain cancer, a breast cancer, melanoma, multiple myeloma, or an ovarian cancer) a benign neoplasm, pathologic angiogenesis, or a fibrotic disease. While no aspect of the invention is limited by the biological events that may transpire, administering a compound or other composition described herein may selectively inhibit the aberrant expression or activity of cyclin-dependent kinase 7 (CDK7) and, thereby, induce cellular apoptosis and/or inhibit the transcription of disease-related genes in the patient (or in a biological sample).

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