Di- and tri-substituted s-triazine derivatives: Synthesis, characterization, anticancer activity in human breast-cancer cell lines, and developmental toxicity in zebrafish embryos-Reference-Cited by-同舟云学术

Di- and tri-substituted s-triazine derivatives: Synthesis, characterization, anticancer activity in human breast-cancer cell lines, and developmental toxicity in zebrafish embryos

Published:2020-01 Issue: Volume:94 Page:103397
ISSN:0045-2068
Container-title:Bioorganic Chemistry
language:en
Short-container-title:Bioorganic Chemistry

Author:

El-Faham Ayman,Farooq Muhammad,Almarhoon Zainab,Alhameed Rakia Abd,Wadaan Mohammad A.M.,de la Torre Beatriz G.,Albericio Fernando

Funder

Deanship of Scientific Research at King Saud University Research

Saudi Arabia; the National Research Foundation

University of KwaZulu-Natal

Spanish Ministry of Science, Innovation, and Universities

Generalitat de Catalunya

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry

Reference44 articles.

1. Exploring the Orthogonal Chemoselectivity of 2,4,6-Trichloro-1,3,5-Triazine (TCT) as a Trifunctional Linker With Different Nucleophiles: Rules of the Game

2. Optimization of the pharmacokinetic properties of potent anti-trypanosomal triazine derivatives

3. Synthesis of New 1,3,5-Triazine-Based 2-Pyrazolines as Potential Anticancer Agents

4. Synthesis of stable benzimidazole derivatives bearing pyrazole as anticancer and EGFR receptor inhibitors

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