nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Anti-cancer activity of m-carborane-containing trimethoxyphenyl derivatives through tubulin polymerization inhibition
|
Kaise, Asako |
|
2019 |
27 |
6 |
p. 1139-1144 |
artikel |
2 |
Anti-cholinesterase hybrids as multi-target-directed ligands against Alzheimer’s disease (1998–2018)
|
Mishra, Pankaj |
|
2019 |
27 |
6 |
p. 895-930 |
artikel |
3 |
Comprehensive kinetic and substrate specificity analysis of an arylsulfatase from Helix pomatia using mass spectrometry
|
Correia, Mário S.P. |
|
2019 |
27 |
6 |
p. 955-962 |
artikel |
4 |
Design, synthesis and biological evaluation of inhibitors of cathepsin K on dedifferentiated chondrocytes
|
Yuan, Xiao-Yu |
|
2019 |
27 |
6 |
p. 1034-1042 |
artikel |
5 |
Design, synthesis and biological evaluation of low molecular weight CXCR4 ligands
|
Sakyiamah, Maxwell M. |
|
2019 |
27 |
6 |
p. 1130-1138 |
artikel |
6 |
Discovery of novel thienoquinoline-2-carboxamide chalcone derivatives as antiproliferative EGFR tyrosine kinase inhibitors
|
Abdelbaset, Mahmoud S. |
|
2019 |
27 |
6 |
p. 1076-1086 |
artikel |
7 |
Discovery of 4′-OH-flurbiprofen Mannich base derivatives as potential Alzheimer’s disease treatment with multiple inhibitory activities
|
Liu, Hongyan |
|
2019 |
27 |
6 |
p. 991-1001 |
artikel |
8 |
Dual inhibitors of RAF-MEK-ERK and PI3K-PDK1-AKT pathways: Design, synthesis and preliminary anticancer activity studies of 3-substituted-5-(phenylamino) indolone derivatives
|
Yu, Zutao |
|
2019 |
27 |
6 |
p. 944-954 |
artikel |
9 |
Editorial Board
|
|
|
2019 |
27 |
6 |
p. ii |
artikel |
10 |
Graphical abstract TOC
|
|
|
2019 |
27 |
6 |
p. I-IV |
artikel |
11 |
Graphical abstract TOC
|
|
|
2019 |
27 |
6 |
p. IBC |
artikel |
12 |
Graphical abstract TOC
|
|
|
2019 |
27 |
6 |
p. OBC |
artikel |
13 |
Highly potent and selective aryl-1,2,3-triazolyl benzylpiperidine inhibitors toward butyrylcholinesterase in Alzheimer's disease
|
de Andrade, Peterson |
|
2019 |
27 |
6 |
p. 931-943 |
artikel |
14 |
Identification of novel lysine demethylase 5-selective inhibitors by inhibitor-based fragment merging strategy
|
Miyake, Yuka |
|
2019 |
27 |
6 |
p. 1119-1129 |
artikel |
15 |
Leucine ureido derivatives as aminopeptidase N inhibitors using click chemistry. Part II
|
Cao, Jiangying |
|
2019 |
27 |
6 |
p. 978-990 |
artikel |
16 |
N’-acyl-N-methylphenylenediamine as a novel proximity labeling agent for signal amplification in immunohistochemistry
|
Sato, Shinichi |
|
2019 |
27 |
6 |
p. 1110-1118 |
artikel |
17 |
New hybrid trifluoromethylquinolines as antiplasmodium agents
|
da Silva, Renata M.R.J. |
|
2019 |
27 |
6 |
p. 1002-1008 |
artikel |
18 |
Optimization of 5,6,7,8-tetrahydropyrido[4,3-d]pyrimidines to generate a highly selective PI3Kδ inhibitor
|
Hamajima, Toshihiro |
|
2019 |
27 |
6 |
p. 1056-1064 |
artikel |
19 |
Structure-activity relationship of leucyladenylate sulfamate analogues as leucyl-tRNA synthetase (LRS)-targeting inhibitors of Mammalian target of rapamycin complex 1 (mTORC1)
|
Yoon, Suyoung |
|
2019 |
27 |
6 |
p. 1099-1109 |
artikel |
20 |
Structure-based virtual screening for insect ecdysone receptor ligands using MM/PBSA
|
Horoiwa, Shinri |
|
2019 |
27 |
6 |
p. 1065-1075 |
artikel |
21 |
4,6-Substituted-1H-Indazoles as potent IDO1/TDO dual inhibitors
|
Yang, Lingling |
|
2019 |
27 |
6 |
p. 1087-1098 |
artikel |
22 |
Synthesis and anti-HSV activity of tricyclic penciclovir and hydroxybutylguanine derivatives
|
Mohammed, Anber F. |
|
2019 |
27 |
6 |
p. 1023-1033 |
artikel |
23 |
Synthesis and urease inhibitory potential of benzophenone sulfonamide hybrid in vitro and in silico
|
Arshia, |
|
2019 |
27 |
6 |
p. 1009-1022 |
artikel |
24 |
Synthesis, antiproliferative and apoptosis induction potential activities of novel bis(indolyl)hydrazide-hydrazone derivatives
|
Sreenivasulu, Reddymasu |
|
2019 |
27 |
6 |
p. 1043-1055 |
artikel |
25 |
Synthesis, biological evaluation, and molecular docking study of novel allyl-retrochalcones as a new class of protein tyrosine phosphatase 1B inhibitors
|
Zhao, Yunjie |
|
2019 |
27 |
6 |
p. 963-977 |
artikel |