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PubPharm (391)
91
Design, synthesis and evaluation of rivastigmine and curcumin hybrids as site-activated multitarget-directed ligands for Alzheimer’s disease therapy
enthalten in:
Bioorganic & medicinal chemistry
| 2014
von
Li, Y.
|
Peng, P.
|
Tang, L.
| +3
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92
Design, synthesis and biological evaluation of thienopyridinones as Chk1 inhibitors
enthalten in:
Bioorganic & medicinal chemistry
| 2014
von
Song, P.
|
Peng, P.
|
Han, M.
| +5
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93
Design, synthesis and biological evaluation of novel tripeptidyl epoxyketone derivatives constructed from β-amino acid as proteasome inhibitors
enthalten in:
Bioorganic & medicinal chemistry
| 2014
von
Zhang, J.
|
Cao, J.
|
Xu, L.
| +4
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94
Design, synthesis and biological evaluation of novel tripeptidyl epoxyketone derivatives constructed from β-amino acid as proteasome inhibitors
enthalten in:
Bioorganic & medicinal chemistry
| 2014
von
Zhang, J.
|
Cao, J.
|
Xu, L.
| +4
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95
Novel DPP-4 inhibitors against diabetes
enthalten in:
Future medicinal chemistry
| 2014
von
Liu, Y.
|
Hu, Y.
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96
Cap-dependent translation initiation factor, eIF4E, is the target for Ouabain-mediated inhibition of HIF-1α
enthalten in:
Biochemical pharmacology
| 2014
von
Cao, J.
|
He, L.
|
Lin, G.
| +8
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97
Cap-dependent translation initiation factor, eIF4E, is the target for Ouabain-mediated inhibition of HIF-1α
enthalten in:
Biochemical pharmacology
| 2014
von
Cao, J.
|
He, L.
|
Lin, G.
| +8
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98
Integrating docking scores, interaction profiles and molecular descriptors to improve the accuracy of molecular docking : toward the discovery of novel Akt1 inhibitors
enthalten in:
European journal of medicinal chemistry
| 2014
von
Zhan, W.
|
Li, D.
|
Che, J.
| +5
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99
Integrating docking scores, interaction profiles and molecular descriptors to improve the accuracy of molecular docking: Toward the discovery of novel Akt1 inhibitors
enthalten in:
European journal of medicinal chemistry
| 2014
von
Zhan, W.
|
Li, D.
|
Che, J.
| +5
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100
Structure-based design, synthesis and biological evaluation of diphenylmethylamine derivatives as novel Akt1 inhibitors
enthalten in:
European journal of medicinal chemistry
| 2014
von
Liu, T.
|
Zhan, W.
|
Wang, Y.
| +4
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10
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