Molecular docking and molecular dynamics studies reveal structural basis of inhibition and selectivity of inhibitors EGCG and OSU-03012 toward glucose regulated protein-78 (GRP78) overexpressed in glioblastoma.
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Multi-kinase inhibitors can associate with heat shock proteins through their NH2-termini by which they suppress chaperone functionA Review of the Antiviral Role of Green Tea Catechins.Drugs currently under investigation for the treatment of invasive candidiasis.Endoplasmic reticulum stress signaling and chemotherapy resistance in solid cancers.Novel galeterone analogs act independently of AR and AR-V7 for the activation of the unfolded protein response and induction of apoptosis in the CWR22Rv1 prostate cancer cell model.Recent Developments and Applications of the MMPBSA Method.Glucose-regulated protein 78 substrate-binding domain alters its conformation upon EGCG inhibitor binding to nucleotide-binding domain: Molecular dynamics studies.Computational Molecular Docking and X-ray Crystallographic Studies of Catechins in New Drug Design Strategies
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P2860
Molecular docking and molecular dynamics studies reveal structural basis of inhibition and selectivity of inhibitors EGCG and OSU-03012 toward glucose regulated protein-78 (GRP78) overexpressed in glioblastoma.
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2015 nî lūn-bûn
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2015年の論文
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
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name
Molecular docking and molecula ...... overexpressed in glioblastoma.
@en
type
label
Molecular docking and molecula ...... overexpressed in glioblastoma.
@en
prefLabel
Molecular docking and molecula ...... overexpressed in glioblastoma.
@en
P2860
P1476
Molecular docking and molecula ...... overexpressed in glioblastoma.
@en
P2093
Rituparna Bhattacharjee
P2860
P2888
P356
10.1007/S00894-015-2801-3
P577
2015-09-29T00:00:00Z