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Synthesis, 2D-NMR a...
Synthesis, 2D-NMR and molecular modelling studies of pentacycloundecane lactam-peptides and peptoids as potential HIV-1 wild type C-SA protease inhibitors
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Makatini, Maya M. (author)
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- Petzold, Katja (author)
- School of chemistry, University of KwaZulu Natal, Durban, South Africa
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Alves, Claudio Nahum (author)
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- Arvidsson, Per I. (author)
- Uppsala universitet,Avdelningen för organisk farmaceutisk kemi
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Honarparvar, Bahareh (author)
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Govender, Patrick (author)
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Govender, Thavendran (author)
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Kruger, Hendrik G. (author)
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Sayed, Yasien (author)
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Lameira, Jeronimo (author)
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Maguire, Glenn E. M. (author)
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Soliman, Mahmoud E. S. (author)
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(creator_code:org_t)
- 2012-02-17
- 2013
- English.
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In: Journal of enzyme inhibition and medicinal chemistry (Print). - : Informa UK Limited. - 1475-6366 .- 1475-6374. ; 28:1, s. 78-88
- Related links:
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https://urn.kb.se/re...
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https://doi.org/10.3...
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https://urn.kb.se/re...
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Abstract
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- In this study, eight non-natural peptides and peptoids incorporating the pentacycloundecane (PCU) lactam were designed and synthesized as potential inhibitors of the wild type C-SA HIV-protease. Five of these inhibitors gave IC50 values ranging from 0.5 up to 0.75 mu M against the resistance-prone wild type C-South African HIV-protease. NMR EASY-ROESY studies enabled us to describe the secondary structure of three of these compounds in solution. The 3D structures of the selected cage peptides were also modelled in solution using QM/MM/MD simulations. Satisfactory agreement between the NMR observations and the low energy calculated structures exists. Only one of these inhibitors (11 peptoid), which showed the best IC50 (0.5 mu M), exhibited a definable 3-D structure in solution. Autodock4 and AutodockVina were used to model the potential interaction between these inhibitors and the HIV-PR. It appears that the docking results are too crude to be correlated with the relative narrow range of experimental IC50 values (0.5-10 mu M). The PCU-peptides and peptoides were several orders less toxic (145 mu M for 11 and 102 mu M for 11 peptoid) to human MT-4 cells than lopinavir (0.025 mu M). This is the first example of a polycyclic cage framework to be employed as an HIV-PR transition state analogue inhibitor and can potentially be utilized for other diseases related proteases.
Subject headings
- MEDICIN OCH HÄLSOVETENSKAP -- Medicinska och farmaceutiska grundvetenskaper -- Läkemedelskemi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Basic Medicine -- Medicinal Chemistry (hsv//eng)
Keyword
- pentacycloundecane lactam-peptides
- peptoids
- HIV-1 wild type C-SA protease
- QM/MM/MD simulations
- molecular docking
Publication and Content Type
- ref (subject category)
- art (subject category)
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Makatini, Maya M ...
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Petzold, Katja
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Alves, Claudio N ...
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Arvidsson, Per I ...
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Honarparvar, Bah ...
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Govender, Patric ...
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Govender, Thaven ...
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Kruger, Hendrik ...
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Sayed, Yasien
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Lameira, Jeronim ...
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Maguire, Glenn E ...
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Soliman, Mahmoud ...
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- About the subject
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- MEDICAL AND HEALTH SCIENCES
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MEDICAL AND HEAL ...
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and Basic Medicine
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and Medicinal Chemis ...
- Articles in the publication
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Journal of enzym ...
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Uppsala University
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Umeå University