A Comprehensive Review of N-Heterocycles as Cytotoxic Agents

被引:78
|
作者
Kumar, Dinesh [1 ]
Jain, Subheet Kumar [1 ]
机构
[1] Guru Nanak Dev Univ, Dept Pharmaceut Sci, Amritsar 143005, Punjab, India
关键词
N-Heterocycles; Cytotoxic Agents; Fusion; Natural leads; IC50; Oxadiazoles; PHASE-II TRIAL; TYROSINE KINASE INHIBITORS; POLY(ADP-RIBOSE) POLYMERASE PARP; ANTICANCER ACTIVITY EVALUATION; SPIN-LABELED DERIVATIVES; VITRO ANTITUMOR-ACTIVITY; ESTROGEN-RECEPTOR-ALPHA; GROWTH-FACTOR RECEPTOR; CELL LUNG-CANCER; BIOLOGICAL EVALUATION;
D O I
10.2174/0929867323666160809093930
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Scientific community is striving to understand the role of heterocycles and fused heterocycles in drug discovery programme due to its impact on multi-drug resistance (MDR) of anticancer drugs. Architecting of various scaffolds for cancer treatment has become gradually increased in many years. Till now there is no treatment which is so proficient that it can cure the cancer from the roots. Hence, it is very necessary to design novel anticancer agents with minimum side effects. Synthesis of hybrids from natural leads is one of the rationale approaches in medicinal chemistry. It remains a big challenge to invent new efficient drugs to beat cancer. The design and synthesis of fused molecules as anticancer agents is one of the great innovations of modern era. In drug discovery archetype, a variety of heterocycles have been considered for the development of novel lead compounds. This article presents some recent advancements in the field of anticancer heterocyclic agents all around the world and also attracted the structure activity relationship along with the structure of the most promising molecules along with IC50 values against various human cancer cell lines.
引用
收藏
页码:4338 / 4394
页数:57
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