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Novel Boronic Chalcone Derivatives and Uses Thereof
Case ID:
C04391
Report of Invention:
1/8/2004
Web Published:
10/7/2014
Technical Details:
A class of anti-cancer agents such as chalcones has shown promising therapeutic efficacy for the management of human cancers. Recent studies have shown that anticancer agents such as chalcones induce apoptosis in variety of cell types, including breast cancers. Biochemical experiments showed that these compounds can disrupt the MDM2/p53 protein complex, releasing p53 from both the p53/MDM2 and DNA-bound p53/MDM2 complexes. However, these carboxylic acid analogs of chalcone are equally toxic to normal cells. In this proposal, a boronic-chalcone strategy is outlined that will overcome this limitation.
Looking for Partners:
The boronic-chalcones are more toxic to breast cancer cells compared to normal breast cells than other known chalcones.
Patent Status:
Granted US Patents
7,829,742
and
8,304,579
Associated Technology:
See JHU Ref. 4085 for additional and distinct boronic-chalcone derivatives.
Associated Technology and Publications:
See
JHU Ref C04391
for additional Boronic Chalcone Derivatives;
J Med Chem. 2003 Jul 3;46(14):2813-5.
;
Bioorg Med Chem. 2006 May 15;14(10):3491-5.
Patent Information:
Title
App Type
Country
Serial No.
Patent No.
File Date
Issued Date
Expire Date
Patent Status
Boronic Acid Aryl Analogs
PCT: Patent Cooperation Treaty
United States
10/596,751
7,829,742
6/22/2006
11/9/2010
7/8/2021
Granted
Boronic Acid Aryl Analogs
DIV: Divisional
United States
12/940,439
8,304,579
11/5/2010
11/6/2012
7/8/2024
Granted
Direct Link:
https://jhu.technologypublisher.com/technology/16321
Inventors:
Category(s):
Clinical and Disease Specializations, Clinical and Disease Specializations > Oncology, Technology Classifications > Therapeutic Modalities > Small Molecules, Technology Classifications > Therapeutic Modalities,
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For Information, Contact:
Vera Sampels
vsampel2@jhu.edu
410-614-0300
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