[HTML][HTML] Comprehensive review on current developments of quinoline-based anticancer agents

S Jain, V Chandra, PK Jain, K Pathak, D Pathak… - Arabian Journal of …, 2019 - Elsevier
Among heterocyclic compounds, quinoline scaffold has become an important construction
motif for the development of new drugs. Quinoline and its derivatives possess many types of …

Recent development of sulfonyl or sulfonamide hybrids as potential anticancer agents: A key review

KP Rakesh, SM Wang, J Leng… - Anti-Cancer Agents …, 2018 - ingentaconnect.com
Cancer is the second leading cause of death worldwide. There is always a huge demand for
novel anticancer drugs and diverse new natural or synthetic compounds are developed …

Oxidative Phosphorylation—an Update on a New, Essential Target Space for Drug Discovery in Mycobacterium tuberculosis

CSY Foo, K Pethe, A Lupien - Applied Sciences, 2020 - mdpi.com
New drugs with new mechanisms of action are urgently required to tackle the global
tuberculosis epidemic. Following the FDA-approval of the ATP synthase inhibitor …

Discovery of high in vitro and in vivo antitumor activities of organometallic ruthenium (II)–arene complexes with 5, 7-dihalogenated-2-methyl-8-quinolinol

T Meng, QP Qin, ZL Chen, HH Zou, K Wang… - Dalton …, 2019 - pubs.rsc.org
This paper reports the synthesis, structure characterization, and anticancer properties of 13
organometallic Ru (II)–arene complexes:[Ru (η6-p-cymene) Cl-(L1)](1),[Ru (η6-p-cymene) …

An overview of privileged scaffold: quinolines and isoquinolines in medicinal chemistry as anticancer agents

Y Mao, K Soni, C Sangani, Y Yao - Current Topics in Medicinal …, 2020 - ingentaconnect.com
Cancer is one of the most difficult diseases and causes of death for many decades. Many
pieces of research are continuously going on to get a solution for cancer. Quinoline and …

Small organic molecules targeting the energy metabolism of Mycobacterium tuberculosis

M Urban, V Šlachtová, L Brulikova - European Journal of Medicinal …, 2021 - Elsevier
Causing approximately 10 million incident cases and 1.3–1.5 million deaths every year,
Mycobacterium tuberculosis remains a global health problem. The risk is further …

Design, synthesis and investigation of the mechanism of action underlying anti-leukemic effects of the quinolinequinones as LY83583 analogs

HI Ciftci, N Bayrak, M Yıldız, H Yıldırım, B Sever… - Bioorganic …, 2021 - Elsevier
Literature conclusively shows that one of the quinolinequinone analogs (6-anilino-5, 8-
quinolinequinone), referred to as LY83583 hereafter, an inhibitor of guanylyl cyclase, was …

Structure based design, synthesis, and evaluation of anti-CML activity of the quinolinequinones as LY83583 analogs

N Bayrak, HI Ciftci, M Yıldız, H Yıldırım, B Sever… - Chemico-Biological …, 2021 - Elsevier
Quinone-based small molecules are the promising structures for antiproliferative drug
design and can induce apoptosis in cancer cells. Among them, one of the …

Design, synthesis and biological evaluation of novel naphthoquinone derivatives as IDO1 inhibitors

L Pan, Q Zheng, Y Chen, R Yang, Y Yang, Z Li… - European Journal of …, 2018 - Elsevier
Abstract Indoleamine 2, 3-dioxygenase 1 (IDO1) mediated kynurenine pathway of
tryptophan degradation is identified as an appealing and novel target in immunotherapy for …

Betulin-1, 4-quinone hybrids: Synthesis, anticancer activity and molecular docking study with NQO1 enzyme

M Kadela-Tomanek, E Bębenek, E Chrobak… - European Journal of …, 2019 - Elsevier
Abstract Betulin-1, 4-quinone hybrids were obtain by connecting two active structures with a
linker. This strategy allows for obtaining compounds showing a high biological activity and …