Improvement of conventional anti-cancer drugs as new tools against multidrug resistant tumors

S Dallavalle, V Dobričić, L Lazzarato, E Gazzano… - Drug Resistance …, 2020 - Elsevier
Multidrug resistance (MDR) is the dominant cause of the failure of cancer chemotherapy.
The design of antitumor drugs that are able to evade MDR is rapidly evolving, showing that …

[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 …

Quinoline as a privileged scaffold in cancer drug discovery

VR Solomon, H Lee - Current medicinal chemistry, 2011 - ingentaconnect.com
Quinoline (1-azanaphthalene) is a heterocyclic aromatic nitrogen compound characterized
by a double-ring structure that contains a benzene ring fused to pyridine at two adjacent …

Solvent-free heterocyclic synthesis

MAP Martins, CP Frizzo, DN Moreira, L Buriol… - Chemical …, 2009 - ACS Publications
Heterocycles form, by far, the largest of the classical divisions of organic chemistry.
Moreover, they are of immense importance not only biologically and industrially but also to …

Phenazine natural products: biosynthesis, synthetic analogues, and biological activity

JB Laursen, J Nielsen - Chemical reviews, 2004 - ACS Publications
The medicine man of prehistoric time knew of the healing capacity of leaves, oils, extracts,
roots, etc. from the surrounding flora. A widely acknowledged example of natural medicine …

Potential antitumor agents. 59. Structure-activity relationships for 2-phenylbenzimidazole-4-carboxamides, a new class of minimal DNA-intercalating agents which …

WA Denny, GW Rewcastle… - Journal of medicinal …, 1990 - ACS Publications
A series of substituted 2-phenylbenzimidazole-4-carboxamides has been synthesized and
evaluated for in vitro and in vivo antitumor activity. These compounds represent the logical …

Acridine and acridone derivatives, anticancer properties and synthetic methods: where are we now?

P Belmont, J Bosson, T Godet… - Anti-Cancer Agents in …, 2007 - ingentaconnect.com
Acridine derivatives are interesting chemotherapeutic agents that were first used as
antibacterial and antiparasite agents. In this review we wish to concentrate our attention on …

Potential antitumor agents. 57. 2-Phenylquinoline-8-carboxamides as minimal DNA-intercalating antitumor agents with in vivo solid tumor activity

GJ Atwell, BC Baguley, WA Denny - Journal of medicinal chemistry, 1989 - ACS Publications
A series of phenyl-substituted derivatives of the “minimal” DNA-intercalating agent IV-[2-
(dimethylamino)-ethyl]-2-phenylquinoline-8-carboxamide (1) have been synthesized and …

Natural and synthetic acridines/acridones as antitumor agents: their biological activities and methods of synthesis

G Cholewiński, K Dzierzbicka, AM Kołodziejczyk - Pharmacological reports, 2011 - Elsevier
Acridine derivatives constitute a class of compounds that are being intensively studied as
potential anticancer drugs. Acridines are well-known for their high cytotoxic activity; …

Structure− activity relationships for substituted bis (acridine-4-carboxamides): a new class of anticancer agents

SA Gamage, JA Spicer, GJ Atwell… - Journal of Medicinal …, 1999 - ACS Publications
A series of acridine-substituted bis (acridine-4-carboxamides) linked by a (CH2) 3N
(Me)(CH2) 3 chain have been prepared by reaction of the isolated imidazolides of the …