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In silico evaluation of some 4-(quinolin-2-yl)pyrimidin-2-amine derivatives as potent V600E-BRAF inhibitors with pharmacokinetics ADMET and drug-likeness predictions

Abstract Background The resistance of V600E-BRAF to the vemurafenib and the side effects of the identified inhibitors trigger the research for a novel and more potent anti-melanoma agents. In this study, virtual docking screening along with pharmacokinetics ADMET and drug-likeness predictions were c...

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Bibliografski detalji
Glavni autori: Abdullahi Bello Umar, Adamu Uzairu, Gideon Adamu Shallangwa, Sani Uba
Format: Artigo
Jezik:Inglês
Izdano: SpringerOpen 2020-09-01
Serija:Future Journal of Pharmaceutical Sciences
Teme:
Online pristup:http://link.springer.com/article/10.1186/s43094-020-00084-4
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