Diarylether‐Amino Acid Conjugates as New Class of Anticancer Agents

Author:

Thanh Le Thanh1ORCID,Huy Vo Vinh2,Thanh Huong Le Thi34,Huy Hoang Vo Nguyen5,Loc Le Xuan6,Hong Tuoi Do Thi7,Y Vu Thien5,Hung Nguyen Phu34,Duy Vo Duc8910,Le Tin Thanh2

Affiliation:

1. Faculty of Petroleum Engineering PetroVietnam University 762 Cach Mang Thang Tam Street, Long Toan Ward Ba Ria City Ba Ria Vung Tau Province Viet Nam

2. Department of Organic Chemistry Faculty of Chemistry Ho Chi Minh City University of Education 280 An Duong Vuong Street, Ward 4, District 5 Ho Chi Minh City Viet Nam

3. Faculty of Biotechnology TNU-University of Sciences Tan Thinh Ward Thai Nguyen City Viet Nam

4. Center for Interdisciplinary Science and Education -CISE Thai Nguyen University Tan Thinh Ward Thai Nguyen City Viet Nam

5. Faculty of Pharmacy Ton Duc Thang University Ho Chi Minh City Viet Nam

6. School of Medicine Vietnam National University Ho Chi Minh City Linh Trung Ward, Thu Duc District Ho Chi Minh City Viet Nam

7. Department of Pharmacology Faculty of Pharmacy University of Medicine and Pharmacy at Ho Chi Minh City 41 Dinh Tien Hoang Street, Ben Nghe Ward, District 1 Ho Chi Minh City Viet Nam

8. Department of Cell and Molecular Biology Biomedical Centre Uppsala University Husargatan 3 75237 Uppsala Sweden

9. Department of Chemistry Biomedical Centre Uppsala University Husargatan 3 75237 Uppsala Sweden

10. School of Applied Chemistry Tra Vinh University 126 Nguyen Thien Thanh Street, Ward 5 Tra Vinh City Viet Nam

Abstract

AbstractDiarylether (DE) is a privileged structure found in both natural products and synthetic compounds including small molecule drugs. We present the synthesis of a series of 13 new DE‐amino acid conjugates which were screened for cancer cells antiproliferation activity. Structure‐activity relationship suggests ester and phenyl groups in DE‐Phe‐OEt 4c are important for the activity. Compound 4c inhibited strongly MCF‐7 3D tumor sphere formation and have favourable calculated physical chemical properties according to Lipinski's rule of 5. Docking study suggests estrogen receptor and/ or 3a‐HSD type 3 protein could be the target(s) for anticancer activity of this class of compounds.

Publisher

Wiley

Subject

General Chemistry

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