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Reseach Article

A Regression Model using K-Means Algorithm to Screen 32 Compound Dataset as COX-2 Inhibitors

by Chunduru Madhava Rao, Yesu Babu Adimulam
International Journal of Computer Applications
Foundation of Computer Science (FCS), NY, USA
Volume 180 - Number 9
Year of Publication: 2018
Authors: Chunduru Madhava Rao, Yesu Babu Adimulam
10.5120/ijca2018916136

Chunduru Madhava Rao, Yesu Babu Adimulam . A Regression Model using K-Means Algorithm to Screen 32 Compound Dataset as COX-2 Inhibitors. International Journal of Computer Applications. 180, 9 ( Jan 2018), 36-42. DOI=10.5120/ijca2018916136

@article{ 10.5120/ijca2018916136,
author = { Chunduru Madhava Rao, Yesu Babu Adimulam },
title = { A Regression Model using K-Means Algorithm to Screen 32 Compound Dataset as COX-2 Inhibitors },
journal = { International Journal of Computer Applications },
issue_date = { Jan 2018 },
volume = { 180 },
number = { 9 },
month = { Jan },
year = { 2018 },
issn = { 0975-8887 },
pages = { 36-42 },
numpages = {9},
url = { https://ijcaonline.org/archives/volume180/number9/28892-2018916136/ },
doi = { 10.5120/ijca2018916136 },
publisher = {Foundation of Computer Science (FCS), NY, USA},
address = {New York, USA}
}
%0 Journal Article
%1 2024-02-07T01:00:13.181069+05:30
%A Chunduru Madhava Rao
%A Yesu Babu Adimulam
%T A Regression Model using K-Means Algorithm to Screen 32 Compound Dataset as COX-2 Inhibitors
%J International Journal of Computer Applications
%@ 0975-8887
%V 180
%N 9
%P 36-42
%D 2018
%I Foundation of Computer Science (FCS), NY, USA
Abstract

COX-2 provided a new class of anti inflammatory, analgesic and antipyretic drugs with significantly reduced side effects. It has been reported that inhibiting COX-2 could also be an important strategy for preventing or treating a number of cancers. A report with modified k-means clustering algorithm to cluster groups of compounds obtained from regression analysis along with few compounds which were non-tested against COX-2 and screened them using regression model. The regression model due to its high predictive ability can be utilized as an alternative aid to the costly and time consuming experiments for recognizing and determining compounds with high COX-2 binding affinity. Hence, a group of new derivatives from literature are subjected to screening utilizing the produced model. A set of 32 compounds with pyrazole ring as main nucleus was selected from a published review paper. In this work, a modification of k-means algorithm that efficiently searches data to cluster points by computing sum of squares within each cluster which makes the program to select the most promising subset of classes for clustering. From a set of 32 compounds, only the top 5 compounds are combined with 58 molecule data set to perform cluster analysis. From the analysis it is evidenced that k-means clustering algorithm is able to group data objects of all molecules based on the 3 centroids provided and all top 5 compounds appear to be centred on one spade whereas Celecoxib appeared in another cluster.

References
  1. Jouzeau JY, Terlain B, Abid A, Nedelec E, Netter P. Cyclo-oxygenaseisoenzymes. How recent findings affect thinking about nonsteroidal anti-inflammatory drugs. Drugs. 1997;53(4):563-82
  2. K. T. Moreland, J. D. Procknow, R. S. Sprague, J. L. Iverson, A. J. Lonigro and A.,H.Stephenson. 2007. Cyclooxygenase (COX)-1 and COX-2 Participate in 5, 6-Epoxyeicosatrienoic Acid-Induced Contraction of Rabbit Intralobar Pulmonary Arteries J. Pharmacol. Exp. Ther., 321(2): 446 – 454.
  3. S. S. Reuben and E. F. Ekman. 2005. The Effect of Cyclooxygenase-2 Inhibition on Analgesia and Spinal Fusion J. Bone Joint Surg. Am.; 87(3): 536 – 542.
  4. H Sano, T Hla, J A Maier, L J Crofford, J P Case, T Maciag, and R L Wilder. 1992. In vivo cyclooxygenase expression in synovial tissues of patients with rheumatoid arthritis and osteoarthritis and rats with adjuvant and streptococcal cell wall arthritis. J Clin Invest.; 89(1): 97–108
  5. Reitz, D. B. 1995. Isakson, P. C. Cyclooxygenase-2 Inhibitors. Curr. Pharm. Des, 1, 211-220.
  6. Subbaramaiah, K.; Zakim, D.; Weksler, B. B.; Dannenberg A. J.1997. Inhibition of Cyclooxygenase: A Novel Approach to Cancer Prevention. Proc. Soc. Exp. Biol. Med, 216, 201-210.
  7. Pasinetti, G. M. Cyclooxygenase and Inflammation in Alzheimer’s Disease.1998. Experimental Approaches and Clinical Intervention. J. Neurosci. Res, 54, 1-6
  8. Futaki, N.; Yoshikawa, K.; Hamasaka, Y.; Arai, I.; Higuchi, S.; Iizuka, H.; Otomo, S. NS398.1993. a Novel Nonsteroidal Anti inflammatory Drug with Potent Analgesic and Antipyretic Effects, which Causes Minimal Stomach Lesions. Gen. Pharmacol, 24, 105-110.
  9. Gans, K.; Galbraith, W.; Roman, R.; Haber, S.; Kerr, J.; Schmidt, W.; Smith, C.; Hewes, W.; Ackerman, N. 1990. Antiinflammatory and Safety Profile of DuP697, a Novel Orally Prostaglandin Synthesis Inhibitor. J. Pharm. Exp. Ther. 254, 180-187.
  10. Kalgutkar, A. S.; Marnett, A. B.; Crews, B. C.; Remmel, R. P.; Marnett, L. J. Ester and Amide Derivatives of the Nonsteroidal Anti inflammatory Drug, Indomethacin, as Selective Cyclooxygenase-2 Inhibitors. J. Med. Chem. 2000, 43, 2860-2870.
  11. Khanna, I. K.; Weier, R. M.; Yu, Y.; Collins, P. W.; Miyashiro, J. M.; Koboldt, C. M.; Veenhuizen, A. W.; Currie, J. L.; Seibert, K.; Isakson, P. C. 1,2-Diarylpyrroles as Potent and Selective Inhibitors of Cyclooxygenase-2. J. Med. Chem. 1997, 40, 1619-1633.
  12. [12 ]Khanna, I. K.; Weier, R. M.; Yu, Y.; Xu, X. D.; Koszyk, F. J.; Collins, P. W.; Koboldt, C. M.; Veenhuizen, A. W.; Perkins, W.E.; Casler, J. J.; Masferrer, J. L.; Zhang, Y. Y.; Gregory, S. A.; Seibert, K.; Isakson, P. C. 1,2-Diarylimidazoles as Potent, Cyclooxygenase-2 Selective, and Orally Active Antiinflammatory Agents. J. Med. Chem. 1997, 40, 1634-1647.
  13. Reitz, D. B.; Li, J. J.; Norton, M. B.; Reinhart, E. J.; Collins, J.T.; Anderson, G. D.; Gregory, S. A.; Koboldt, C. M.; Perkins, W.E.; Seibert, K.; Isakson, P. C. Selective Cyclooxygenase Inhibitors: Novel 1,2-Diarylcyclopentenes are Potent and Orally Active COX-2 Inhibitors. J. Med. Chem. 1994, 38, 3878-3881.
  14. enning, T. D.; Talley, J. J.; Bertenshaw, S. R.; Carter, J. S.; Collins, P. W.; et al. Synthesis and Biological Evaluation of the 1,5-Diarylpyrazole Class of Cyclooxygenase-2 Inhibitors: Identification of 4-[5-(4-Methylphenyl)-3-(trifluoromethyl)-1Hpyrazol-1-yl]benzenesulfonamide (SC-58635, Celecoxib). J. Med. Chem. 1997, 40, 1347-1365.
  15. Huang, H. C.; Li, J. J.; Garland, D. J.; Chamberlain, T. S.; Reinhart, E. J.; Manning, R. E.; Seibert, K.; Koboldt, C. M.; et al. Diarylspiro[2.4] heptenes as Orally Active, Highly Selective Cyclooxygenase-2 inhibitors: Synthesis and Structure-Activity Relationships. J. Med. Chem. 1996, 39, 253-266.
  16. [16 ]Talley J. J.; Brown, D. L.; Carter, J. S.; Graneto, M. J.; Koboldt, C. M.; Masferrer, J. L.; Perkins, W. E.; Rogers, R. S.; Shaffer, A. F.; Zhang, Y. Y.; Zweifel, B. S.; Seibert, K. 4-[5-Methyl-3- phenylisoxazol-4-yl]-benzenesulfonamide, Valdecoxib: a Potent and Selective Inhibitor of COX-2. J. Med. Chem. 2000, 43, 775-777.
  17. [17 ]Zhong Chen et al. Design, synthesis, biological evaluation and molecular modeling of dihydropyrazolesulfonamide derivatives as potential COX-1/COX-2 inhibitors. Bioorganic & Medicinal Chemistry Letters 25 (2015) 1947–1951.
  18. Abdellatif, K.R.A. et al. Synthesis, cyclooxygenase inhibition, anti-inflammatory evaluation and ulcerogenic liability of novel triarylpyrazoline derivatives as selective COX-2 inhibitors, Bioorganic & Medicinal Chemistry Letters 2015; 25(24):5787-91.
  19. Abdellatif, K.R.A. et al. Synthesis, cyclooxygenase inhibition, anti-inflammatory evaluation and ulcerogenic liability of new 1,3,5-triarylpyrazoline and 1,5-diarylpyrazole derivatives as selective COX-2 inhibitors. Bioorganic & Medicinal Chemistry Letters 2016; 26(2):406-12.
  20. Yu, M., Yang, H., Wu, K., Ji, Y., Ju, L. and Lu, X., 2014.Novel pyrazoline derivatives as bi-inhibitor of COX-2 and B-Raf in treating cervical carcinoma.Bioorganic & medicinal chemistry, 22(15), pp.4109-4118.
  21. Ruth Pérez-Fernández,Pilar Goya, and José Elguero. A review of recent progress (2002-2012) on the biological activities of pyrazoles.ARKIVOC 2014 (ii) 233-293.
  22. [22 Pablo A Jaskowiak et al. On the selection of appropriate distances for gene expression data clustering. BMC Bioinformatics 2014, 15(Suppl 2):S2 doi:10.1186/1471-2105-15-S2-S2.
Index Terms

Computer Science
Information Sciences

Keywords

COX-2 Cluster analysis k-means phylogenetic tree