Title:1,3,5 and 1,2,4-triazines as Potent Scaffolds for Molecules Potentially Attenuating
Breast Cancer Cell Lines
Volume: 26
Issue: 24
Author(s): Pragya Dubey*, Dharam Pal Pathak, Faraat Ali and Garima Chauhan
Affiliation:
- Department of Pharmaceutical Chemistry, Delhi Institute of Pharmaceutical Sciences and Research, Mehrauli-Badarpur Road, Sector
3, Pushp Vihar, New Delhi, Delhi, 110017, India
Keywords:
Triazine, antiproliferative, inhibitors, breast cancer cell line, structure-activity relationship, molecular target, tumors, docking.
Abstract:
Breast cancer was diagnosed in around 2.3 million women in 2020. Owing to the
alarming rise in the incidence of breast cancer, newer small molecules with targeted therapy
are the need of the hour. A plethora of small molecules has been approved by the USFDA in
the past few years.
Triazine is a six-membered aromatic nitrogen heterocyclic molecule that was investigated for
its various types of biological activities specially anticancer activity.
Triazines are studied in many derivatives having remarkable anti-tumor activity as reported in
this literature. Triazines are reported to possess a variety of biological activities and have been
widely investigated as a scaffold for developing newer anti-tumor agents with an ability to
inhibit various types of cancers, including breast cancers.
Triazine derivatives show anticancer activity by inhibiting various targets like mTOR- kinase, PIP3-kinase, epidermal
growth factor, etc. A limited number of triazine derivatives have also been clinically used for the treatment of
breast cancer. A detailed study of the literature available on various derivatives of triazines with primary applicability
as cytotoxic to breast cancer cell was carried out and is presented in this review. A total of 66 structurally diverse
triazines have been reported in this review along with the structural features responsible for activity against various
breast cancer cell lines. The primary amino residues to which the triazine based molecules bind in the estrogen receptor
alpha and epidermal growth factor receptor 2, as found in various docking studies have also been detailed in
the review.