Effective anti-aromatase therapy to battle against estrogen-mediated breast cancer: Comparative SAR/QSAR assessment on steroidal aromatase inhibitors

被引:15
作者
Adhikari, Nilanjan [1 ]
Baidya, Sandip Kumar [1 ]
Jha, Tarun [1 ]
机构
[1] Jadavpur Univ, Dept Pharmaceut Technol, Div Med & Pharmaceut Chem, Nat Sci Lab, POB 17020, Kolkata 700032, W Bengal, India
关键词
Estrogen-mediated breast tumor; Aromatase; Steroidal aromatase inhibitor; Structure-activity relationship (SAR); Quantitative structure-activity relationship (QSAR); HUMAN PLACENTAL AROMATASE; ACTIVATED IRREVERSIBLE INHIBITORS; TIME-DEPENDENT INACTIVATION; MOLECULAR DOCKING; MICROSOMAL CYTOCHROME-P-450; BIOLOGICAL AROMATIZATION; ANDROSTENEDIONE ANALOGS; POSTMENOPAUSAL PATIENTS; BIOCHEMICAL EVALUATION; SIGNALING PATHWAYS;
D O I
10.1016/j.ejmech.2020.112845
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A large number of world women populations are suffering from breast cancer. It is increasing day by day that is quite alarming. The major reason behind breast tumors is upregulation of estrogen which is dependent on aromatase. Aromatase inhibitors (AIs) have opened up a new era to combat the battle against estrogen-mediated breast cancer. Despite several advantages, various adverse effects have limited the use of AIs. Therefore, it is still a demanding and challenging job to design selective AIs with fewer adverse effects. In this article, comparative quantitative structure-activity relationship (QSAR) study of steroidal aromatase inhibitors (SAIs) have been discussed in details to get an insight into the structural and physicochemical properties of SAIs controlling the aromatase inhibitory activity. This study reflects that SAIs should possess smaller shape and size with less bulky substituents having lesser polarity and less steric effect along with greater hydrophobicity for the higher aromatase inhibitory activity. This study will obviously shed light into the newer idea for the medicinal chemists to design and discover novel, effective and less toxic SAIs to combat the life-threatening breast cancer as well as to initiate a modern era in breast cancer drug discovery. (C) 2020 Elsevier Masson SAS. All rights reserved.
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页数:47
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