System Biology Approach to Identify Potential Receptor for Targeting Cancer and Biomolecular Interaction Studies of Indole[2,1-a]Isoquinoline Derivative as Anticancerous Drug Candidate Against it
- PMID: 28748401
- DOI: 10.1007/s12539-017-0249-0
System Biology Approach to Identify Potential Receptor for Targeting Cancer and Biomolecular Interaction Studies of Indole[2,1-a]Isoquinoline Derivative as Anticancerous Drug Candidate Against it
Abstract
Cancer is a public health concern which is spreading throughout the world. Different approaches have been employed to combat this disease. System biology approach has been used to understand the molecular mechanisms of drugs targeting cancer cell's receptor which have opened-up a window to develop effective drugs for it. We have demonstrated biomolecular interaction studies using the rational drug design of indole[2,1-a]isoquinoline derivative as a potent inhibitor against identified cancerous protein PIK3CA -a catalytic sub-unit of PI3K family protein-and compared its affinity with FDA approved drugs for receptors such as dactolisib, idelalisib, and several others such afatinib, avastin, ceritinib and crizotinib, etc.; by docking against potential receptor to set a cutoff value for our screening. Isoquinolines are small alkaloids with a vast variety of substitution depending upon their biogenetic pattern. Isoquinoline derivatives have been reported for their antimalarial, antibacterial, antifungal and anticancerous activities. The results obtained from the present studies conclude that membrane protein is an efficient drug that can be used to target cancer. Moreover, comparative study with ADMET prediction concludes that isoquinoline can be a potent drug for cancer treatment.
Keywords: Anticancerous; Biomolecular interaction; Isoquinoline; System biology.
Similar articles
-
Design, synthesis, and testing of an isoquinoline-3-carboxylic-based novel anti-tumor lead.Bioorg Med Chem Lett. 2015 Oct 15;25(20):4434-6. doi: 10.1016/j.bmcl.2015.09.014. Epub 2015 Sep 7. Bioorg Med Chem Lett. 2015. PMID: 26386603
-
A historical overview of protein kinases and their targeted small molecule inhibitors.Pharmacol Res. 2015 Oct;100:1-23. doi: 10.1016/j.phrs.2015.07.010. Epub 2015 Jul 21. Pharmacol Res. 2015. PMID: 26207888 Review.
-
Anticancer and Reversing Multidrug Resistance Activities of Natural Isoquinoline Alkaloids and their Structure-activity Relationship.Curr Med Chem. 2018;25(38):5088-5114. doi: 10.2174/0929867324666170920125135. Curr Med Chem. 2018. PMID: 28933285 Review.
-
Naturally occurring plant isoquinoline N-oxide alkaloids: their pharmacological and SAR activities.Phytomedicine. 2015 Jan 15;22(1):183-202. doi: 10.1016/j.phymed.2014.11.002. Epub 2014 Nov 20. Phytomedicine. 2015. PMID: 25636889 Review.
-
Design, synthesis, cytotoxicities and DNA cleavage activities of dibenzoxepine and isoquinoline derivatives starting from dehydroabietylamine.J Asian Nat Prod Res. 2016 Dec;18(12):1169-1177. doi: 10.1080/10286020.2016.1232251. Epub 2016 Sep 26. J Asian Nat Prod Res. 2016. PMID: 27696913
Cited by
-
Computational advances of tumor marker selection and sample classification in cancer proteomics.Comput Struct Biotechnol J. 2020 Jul 17;18:2012-2025. doi: 10.1016/j.csbj.2020.07.009. eCollection 2020. Comput Struct Biotechnol J. 2020. PMID: 32802273 Free PMC article. Review.
-
Identification of Potential Cytokinin Responsive Key Genes in Rice Treated With Trans-Zeatin Through Systems Biology Approach.Front Genet. 2022 Feb 7;12:780599. doi: 10.3389/fgene.2021.780599. eCollection 2021. Front Genet. 2022. PMID: 35198001 Free PMC article.
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous