Literature DB >> 33624162

Synthesis and Anticancer Properties of Functionalized 1,6-Naphthyridines.

Mallu Lavanya1,2, Chong Lin3, Jincheng Mao4, Dhakshanamurthy Thirumalai5, Sreenath Reddy Aabaka1, Xiaojiang Yang1, Jinhua Mao1, Zhiyu Huang2, Jinzhou Zhao1.   

Abstract

The burgeoning interest in synthesis and biological applications of 1,6-naphthyridines reflects the importance of 1,6-naphthyridines in the synthetic as well as medicinal chemistry fields. Specially, 1,6-naphthyridines are pharmacologically active, with variety of applications such as anticancer, anti-human immunodeficiency virus (HIV), anti-microbial, analgesic, anti-inflammatory and anti-oxidant activities. Although collective recent synthetic developments have paved a path to a wide range of functionalized 1,6-naphthyridines, a complete correlation of synthesis with biological activity remains elusive. The current review focuses on recent synthetic developments from the last decade and a thorough study of the anticancer activity of 1,6-naphthyridines on different cancer cell lines. Anticancer activity has been correlated to 1,6-naphthyridines using the literature on the structure-activity relationship (SAR) along with molecular modeling studies. Exceptionally, at the end of this review, the utility of 1,6-naphthyridines displaying activities other than anticancer has also been included as a glimmering extension.

Entities:  

Keywords:  1,6-Naphthyridines; Anticancer activity; Cancer cell lines; Mechanism of action; Molecular modeling studies; Structural–activity relationship; Synthetic approaches

Mesh:

Substances:

Year:  2021        PMID: 33624162     DOI: 10.1007/s41061-020-00314-6

Source DB:  PubMed          Journal:  Top Curr Chem (Cham)        ISSN: 2364-8961


  84 in total

1.  Comparison of a homologous series of benzonaphthyridine anti-cancer agents in mice: divergence between tumour and plasma pharmacokinetics.

Authors:  Pradeep B Lukka; James W Paxton; Philip Kestell; Bruce C Baguley
Journal:  Cancer Chemother Pharmacol       Date:  2012-06-03       Impact factor: 3.333

2.  Photo- and electrochemical redox behavior of cyclometalated Ru(II) complexes having a 3-phenylbenzo[b][1,6]naphthyridine ligand.

Authors:  Sumanta Kumar Padhi; Koji Tanaka
Journal:  Inorg Chem       Date:  2011-09-28       Impact factor: 5.165

3.  A fluorescence study of new angular polycyclic blue light-emitting pyrazolo[3,4-h][1,6]naphthyridine and their interaction with bovine serum albumin (BSA).

Authors:  Sandeep R Patil; Deepak P Shelar; Ramhari V Rote; Madhukar N Jachak
Journal:  J Fluoresc       Date:  2011-07-14       Impact factor: 2.217

4.  Convenient synthesis of 2,7-naphthyridine Lophocladines A and B and their analogues.

Authors:  Ao Zhang; Chunyong Ding; Chen Cheng; Qizheng Yao
Journal:  J Comb Chem       Date:  2007-10-10

5.  Lophocladines, bioactive alkaloids from the red alga Lophocladia sp.

Authors:  Harald Gross; Douglas E Goeger; Patrice Hills; Susan L Mooberry; David L Ballantine; Thomas F Murray; Frederick A Valeriote; William H Gerwick
Journal:  J Nat Prod       Date:  2006-04       Impact factor: 4.050

Review 6.  A Comprehensive Review of N-Heterocycles as Cytotoxic Agents.

Authors:  Dinesh Kumar; Subheet Kumar Jain
Journal:  Curr Med Chem       Date:  2016       Impact factor: 4.530

7.  Novel topoisomerase I-targeting antitumor agents synthesized from the N,N,N-trimethylammonium derivative of ARC-111, 5H-2,3-dimethoxy-8,9-methylenedioxy-5-[(2-N,N,N-trimethylammonium)ethyl]dibenzo[c,h][1,6]naphthyridin-6-one iodide.

Authors:  Wei Feng; Mavurapu Satyanarayana; Yuan-Chin Tsai; Angela A Liu; Leroy F Liu; Edmond J LaVoie
Journal:  Eur J Med Chem       Date:  2009-02-20       Impact factor: 6.514

8.  Synthesis, molecular modeling and SAR study of novel pyrazolo[5,1-f][1,6]naphthyridines as CB2 receptor antagonists/inverse agonists.

Authors:  Antonio Dore; Battistina Asproni; Alessia Scampuddu; Stefania Gessi; Gabriele Murineddu; Elena Cichero; Paola Fossa; Stefania Merighi; Serena Bencivenni; Gérard A Pinna
Journal:  Bioorg Med Chem       Date:  2016-08-29       Impact factor: 3.641

9.  Synthesis of Natural Product-like Polyheterocycles via One-Pot Cascade Oximation, C-H Activation, and Alkyne Annulation.

Authors:  Liyao Zheng; Yunhui Bin; Yunpeng Wang; Ruimao Hua
Journal:  J Org Chem       Date:  2016-09-26       Impact factor: 4.354

10.  Copper-catalyzed tandem synthesis of indolo-, pyrrolo[2,1-a]isoquinolines, naphthyridines and bisindolo/pyrrolo[2,1-a]isoquinolines via hydroamination of ortho-haloarylalkynes followed by C-2 arylation.

Authors:  Akhilesh K Verma; Rajeev R Jha; Ritu Chaudhary; Rakesh K Tiwari; Kotla Siva K Reddy; Abhinandan Danodia
Journal:  J Org Chem       Date:  2012-09-04       Impact factor: 4.354

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