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Inhibitor designing, virtual screening, and docking studies for methyltransferase: A potential target against dengue virus
AIM: Aim of this work was to design and identify some S-adenosyl-L-homocysteine (SAH) analogs as inhibitors of S-adenosyl-L-methionine-dependent methyltransferase (MTase) protein using computational approaches. INTRODUCTION: According to the current scenario the dengue has been a global burden. The...
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| Publicado no: | J Pharm Bioallied Sci |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4929957/ https://ncbi.nlm.nih.gov/pubmed/27413346 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0975-7406.171682 |
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