Exploration of structural requirements for azole chemicals towards human aromatase CYP19A1 activity: Classification modeling, structure-activity relationships and read-across study. (June 2022)

• Record Type: Journal Article
• Authors: Caballero Alfonso, Ana Y.; Mora Lagares, Liadys; Novic, Marjana; Benfenati, Emilio; Kumar, Anil; Chayawan,
• Is Part Of: Toxicology in vitro. Volume 81(2022)
• Publication Date: 2022-06
• Subjects: Human aromatase -- Agonist -- Antagonist -- Azoles -- Structural alerts -- Classification model -- Structure-activity relationship (SAR) -- Read-across; Toxicity testing -- In vitro -- Periodicals; Toxicology -- Periodicals; 615.9
• DOI: 10.1016/j.tiv.2022.105332
• Languages: English
• ISSNs: 0887-2333

Abstract

Abstract: Human aromatase, also called CYP19A1, plays a major role in the conversion of androgens into estrogens. Inhibition of aromatase is an important target for estrogen receptor (ER)-responsive breast cancer therapy. Use of azole compounds as aromatase inhibitors is widespread despite their low selectivity. A toxicological evaluation of commonly used azole-based drugs and agrochemicals with respect to CYP19A1 is currently requested by the European Union- Registration, Evaluation, Authorization and Restriction of Chemicals (EU-REACH) regulations due to their potential as endocrine disruptors. In this connection, identification of structural alerts (SAs) is an effective strategy for the toxicological assessment and safe drug design. The present study describes the identification of SAs of azole-based chemicals as guiding experts to predict the aromatase activity. Total 21 SAs associated with aromatase activity were extracted from dataset of 326 azole-based drugs/chemicals obtained from Tox21 library. A cross-validated classification model having high accuracy (error rate 5%) was proposed which can precisely classify azole chemicals into active/inactive toward aromatase. In addition, mechanistic details and toxicological properties (agonism/antagonism) of azoles with respect to aromatase were explored by comparing active and inactive chemicals using structure-activity relationships (SAR). Lastly, few structural alerts were applied to form chemical categories for read-across applications. Graphical abstract: Unlabelled Image Highlights: Structural alerts of azoles have been identified for Human CYP19A1 activity. SAR analysis distinguished between agonist and antagonist activities of azoles. 2-Amino-benzothiazoles/-1, 3 thiazoles associated with the agonist/toxic effects. Imidazolium ionic liquids were CYP19A1 enzyme inhibitors/antagonists. Xanthine and β -lactum based drugs, mostly, do not interfere with Human aromatase.