Title |
Molecular docking analysis of piperine with CDK2, CDK4, Cyclin D and Cyclin T proteins
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Authors |
Umaphathy Vidhya Rekha1,*, M. Anita1, Govindaraj Jayamathi2, K. Sadhana1, Subramanian Deepa3, Sajid Hussain3, J. Bhuvaneswari3, V. Ramya3, Jayaraman Selvaraj4
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Affiliation |
1Department of Public
Health Dentistry, Sree Balaji Dental College and Hospital,
Pallikaranai, Chennai-600 100, India; 2Department of
Biochemistry, Sree Balaji Dental College and Hospital, Pallikaranai,
Chennai-600 100, India; 3Department of Periodontics, Sree
Balaji Dental
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Dr. Umaphathy Vidhya Rekha - Email: drvidhyarekha@gmail.com; *Corresponding author
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Article Type |
Research Article
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Date |
Received March 3, 2019; Revised April 1, 2020, Accepted April 10, 2020; Published May 31, 2020
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Abstract |
Piperine is a component of Piper nigrum (Black pepper). It is well known in ayurvedic formulations. Piperine is a bioenhancer as it reduces the activity of drug-metabolizing enzymes in rodents and thereby enhancing the plasma concentrations of several drugs, including the Pglycoprotein substrates. Therefore, it is of interest to understand the molecular docking interactions of piperine with several cell cycle proteins such as Cyclin dependent kinase 2 (CDK2), Cyclin-dependent kinase 4 (CDK4), Cyclin D and Cyclin T for further consideration in drug discovery related to oral cancer.
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Keywords |
Piperine, CDK2, CDK4, Cyclin D and Cyclin T, cell cycle regulators, oral cancer, molecular docking
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Citation |
Vidhya Rekha et al. Bioinformation 16(5): 359-362 (2020)
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Edited by |
P Kangueane
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ISSN |
0973-2063
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Publisher |
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License |
This is an Open Access article which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. This is distributed under the terms of the Creative Commons Attribution License.
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