Araştırma Makalesi

Designing potential HIV-1 integrase inhibitors: An In silico approach

Cilt: 3 Sayı: 2 30 Aralık 2021
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Designing potential HIV-1 integrase inhibitors: An In silico approach

Öz

Human immunodeficiency virus is a spectrum of conditions caused by infection with the human immunodeficiency virus. In 2019, about 38 million people worldwide were living with HIV and 690,000 deaths had occurred in that year. To date, for the treatment of HIV-1 disease, many compounds have been synthesized and some of them was approved by FDA. However, the use of these drugs has been limited due to reasons such as resistance caused by the misuse of drugs and bad side effects. We describe herein designing 48 novel compounds as a potential inhibitor of HIV-1 integrase through in silico studies such as molecular docking, target analysis, toxicity prediction and ADME prediction. The online web-based platform, SwissADME, also predicts these molecules solubility, pharmacodynamics property and target accuracy.

Anahtar Kelimeler

Kaynakça

  1. 1. O. Delelis, K. Carayon, A. Saib, E. Deprez, J.F. Mouscadet, Integrase and integration: biochemical activities of HIV-1 integrase, Retrovirology 5, 2008, 114-127.
  2. 2. N. Neamati, Z. Lin, R.G. Karki, A. Orr, K. Cowansage, D. Strumberg, Metal-dependent inhibition of HIV-1 integrase, J Med Chem, 45, 2002, 5661-5670.
  3. 3. T. Kawasuji, T. Yoshinaga, A. Sato, M. Yodo, T. Fujiwara, R. Kiyama, A platform for designing HIV integrase inhibitors. Part 1: 2-hydroxy-3-heteroaryl acrylic acid derivatives as novel HIV integrase inhibitor and modeling of hydrophilic and hydrophobic pharmacophores, Bioorg Med Chem, 14, 2006, 8430-8445.
  4. 4. B.A. Johns, A.C. Svolto, Advances in two-metal chelation inhibitors of HIV integrase, Expert Opin Ther Pat, 18, 2008, 1225-1237.
  5. 5. M. Rowley, The discovery of raltegravir, an integrase inhibitor for the treatment of HIV infection, Prog Med Chem, 46, 2008, 1-28.
  6. 6. M. Sato, H. Kawakami, T. Motomura, H. Aramaki, T. Matsuda, M. Yamashita, Quinolone carboxylic acids as a novel monoketo acid class of human immunodeficiency virus type 1 integrase inhibitors, J Med Chem, 52, 2009, 4869-4882.
  7. 7. C. Katlama, R. Murphy, Dolutegravir for the treatment of HIV, Expert Opin Investig Drugs, 21, 2008, 523-530.
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Ayrıntılar

Birincil Dil

İngilizce

Konular

Analitik Kimya

Bölüm

Araştırma Makalesi

Yayımlanma Tarihi

30 Aralık 2021

Gönderilme Tarihi

9 Haziran 2021

Kabul Tarihi

14 Ekim 2021

Yayımlandığı Sayı

Yıl 2021 Cilt: 3 Sayı: 2

Kaynak Göster

APA
Mermer, A. (2021). Designing potential HIV-1 integrase inhibitors: An In silico approach. Turkish Journal of Analytical Chemistry, 3(2), 45-53. https://doi.org/10.51435/turkjac.950248
AMA
1.Mermer A. Designing potential HIV-1 integrase inhibitors: An In silico approach. TurkJAC. 2021;3(2):45-53. doi:10.51435/turkjac.950248
Chicago
Mermer, Arif. 2021. “Designing potential HIV-1 integrase inhibitors: An In silico approach”. Turkish Journal of Analytical Chemistry 3 (2): 45-53. https://doi.org/10.51435/turkjac.950248.
EndNote
Mermer A (01 Aralık 2021) Designing potential HIV-1 integrase inhibitors: An In silico approach. Turkish Journal of Analytical Chemistry 3 2 45–53.
IEEE
[1]A. Mermer, “Designing potential HIV-1 integrase inhibitors: An In silico approach”, TurkJAC, c. 3, sy 2, ss. 45–53, Ara. 2021, doi: 10.51435/turkjac.950248.
ISNAD
Mermer, Arif. “Designing potential HIV-1 integrase inhibitors: An In silico approach”. Turkish Journal of Analytical Chemistry 3/2 (01 Aralık 2021): 45-53. https://doi.org/10.51435/turkjac.950248.
JAMA
1.Mermer A. Designing potential HIV-1 integrase inhibitors: An In silico approach. TurkJAC. 2021;3:45–53.
MLA
Mermer, Arif. “Designing potential HIV-1 integrase inhibitors: An In silico approach”. Turkish Journal of Analytical Chemistry, c. 3, sy 2, Aralık 2021, ss. 45-53, doi:10.51435/turkjac.950248.
Vancouver
1.Arif Mermer. Designing potential HIV-1 integrase inhibitors: An In silico approach. TurkJAC. 01 Aralık 2021;3(2):45-53. doi:10.51435/turkjac.950248

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