Molecular docking and ADME properties of bioactive molecules against human acid-beta-glucosidase enzyme, cause of Gaucher’s disease

Gaucher disease is one of the common lysosomal storage diseases widespread all over the world. It is divided into three types such as type 1 (non-neuropathic), type 2 (acute infantile neuropathic) and type 3 (chronic neuropathic). This is caused by the deficiency of glucocerebrosidases from the midp...

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Vydáno v:In Silico Pharmacol
Hlavní autoři: Subramaniyan, Vijayakumar, Mathiyalagan, Sathiya, Praveenkumar, Arulmozhi, Srinivasan, Prabhu, Palani, Manogar, Ravichandran, Vinothkannan, Nallasamy, Parameswari
Médium: Artigo
Jazyk:Inglês
Vydáno: Springer Berlin Heidelberg 2018
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Original Research
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6314663/
https://ncbi.nlm.nih.gov/pubmed/30607316
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s40203-018-0039-3
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