Design, synthesis, and antiproliferative evaluation of novel dehydroabietic acid-1,2,3-triazole-oxazolidinone hybrids-Reference-Cited by-同舟云学术

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Design, synthesis, and antiproliferative evaluation of novel dehydroabietic acid-1,2,3-triazole-oxazolidinone hybrids

Published:2024 Issue:2 Volume:15 Page:561-571
ISSN:2632-8682
Container-title:RSC Medicinal Chemistry
language:en
Short-container-title:RSC Med. Chem.

Author:

Wu Yaju¹,Huang Lin¹,Ma Xianli¹,Zhou Xiaoqun¹,Li Qian¹,Li Fangyao¹^ORCID

Affiliation:

1. Guangxi Key Laboratory of Drug Discovery and Optimization, Guangxi Engineering Research Center for Pharmaceutical Molecular Screening and Druggability Evaluation, School of Pharmacy, Guilin Medical University, Guilin 541199, PR China

Abstract

Compound 4p blocked the cell cycle of MGC-803 cells in G1 phase stage and induced cell apoptosis.

Funder

Natural Science Foundation of Guangxi Province

Guilin Medical University

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/MD/D3MD00550J

Reference33 articles.

1. PAX1 and SEPT9 methylation analyses in cervical exfoliated cells are highly efficient for detecting cervical (pre)cancer in hrHPV-positive women

2. Recent advances (2015–2016) in anticancer hybrids

3. Antitumor Drugs and Their Targets

4. Natural Products as Inducers of Non-Canonical Cell Death: A Weapon against Cancer

5. Anti-Virulence Strategy of Novel Dehydroabietic Acid Derivatives: Design, Synthesis, and Antibacterial Evaluation

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