Premium
sp 3 ‐Rich Glycyrrhetinic Acid Analogues Using Late‐Stage Functionalization as Potential Breast Tumor Regressing Agents
Author(s) -
Kallepu Shivakrishna,
Neeli Praveen Kumar,
Mallappa Sreevidya,
Nagendla Narendra Kumar,
Reddy Mudiam Mohana Krishna,
Mainkar Prathama S.,
Kotamraju Srigiridhar,
Chandrasekhar Srivari
Publication year - 2020
Publication title -
chemmedchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.817
H-Index - 100
eISSN - 1860-7187
pISSN - 1860-7179
DOI - 10.1002/cmdc.202000400
Subject(s) - chemistry , mitochondrion , surface modification , glutathione , breast cancer , apoptosis , cancer research , stereochemistry , superoxide , pharmacology , biochemistry , cancer , biology , medicine , enzyme
Late‐stage functionalization (LSF) aids drug discovery efforts by introducing functional groups onto C−H bonds on pre‐existing skeletons. We adopted the LSF strategy to synthesize analogues of the abundantly available triterpenoid, glycyrrhetinic acid (GA), by introducing aryl groups in the A‐ring, expanding the A‐ring and selectively activating one methyl group of the gem ‐dimethyl groups. Intriguingly, two compounds were found to preferentially accumulate in the mitochondrial compartment of MDA‐MB‐231 breast cancer cells, to cause depolarization of mitochondrial membrane potential and to induce antiproliferative and anti‐invasive effects through enhanced mitochondrial superoxide production with parallel depletion of GSH levels. Furthermore, intraperitoneal administration of these two compounds, in comparison with GA, greatly regressed breast tumor growth and metastasis in a SCID mouse model bearing labeled MDA‐MB‐231 cells.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom