| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel series of enoyl reductase inhibitors targeting the ESKAPE pathogens, Staphylococcus aureus and Acinetobacter baumannii
|
Kwon, Jieun
|
|
2018
|
26 |
1 |
p. 65-76
|
artikel
|
| 2 |
Antitussive and expectorant activities of licorice and its major compounds
|
Kuang, Yi
|
|
2018
|
26 |
1 |
p. 278-284
|
artikel
|
| 3 |
Bioluminescence probe for γ-glutamyl transpeptidase detection in vivo
|
Lin, Yuxing
|
|
2018
|
26 |
1 |
p. 134-140
|
artikel
|
| 4 |
Bisindolylmethane thiosemicarbazides as potential inhibitors of urease: Synthesis and molecular modeling studies
|
Taha, Muhammad
|
|
2018
|
26 |
1 |
p. 152-160
|
artikel
|
| 5 |
Design and synthesis of aminoester heterodimers containing flavone or chromone moieties as modulators of P-glycoprotein-based multidrug resistance (MDR)
|
Dei, Silvia
|
|
2018
|
26 |
1 |
p. 50-64
|
artikel
|
| 6 |
Design and synthesis of highly selective pyruvate dehydrogenase complex E1 inhibitors as bactericides
|
Zhou, Yuan
|
|
2018
|
26 |
1 |
p. 84-95
|
artikel
|
| 7 |
Design, synthesis and biological evaluation of novel indole-xanthendione hybrids as selective estrogen receptor modulators
|
Singla, Ramit
|
|
2018
|
26 |
1 |
p. 266-277
|
artikel
|
| 8 |
Design, synthesis and evaluation against Mycobacterium tuberculosis of azole piperazine derivatives as dicyclotyrosine (cYY) mimics
|
El-wahab, Hend A.A. Abd
|
|
2018
|
26 |
1 |
p. 161-176
|
artikel
|
| 9 |
Design, synthesis and pharmacological evaluation of some novel indanone derivatives as acetylcholinesterase inhibitors for the management of cognitive dysfunction
|
Piplani, Poonam
|
|
2018
|
26 |
1 |
p. 215-224
|
artikel
|
| 10 |
Discovery of novel purine nucleoside derivatives as phosphodiesterase 2 (PDE2) inhibitors: Structure-based virtual screening, optimization and biological evaluation
|
Qiu, Xiaoxia
|
|
2018
|
26 |
1 |
p. 119-133
|
artikel
|
| 11 |
Editorial Board
|
|
|
2018
|
26 |
1 |
p. ii
|
artikel
|
| 12 |
Evaluation of alkylating pyrrole-imidazole polyamide conjugates by a novel method for high-throughput sequencer
|
Kashiwazaki, Gengo
|
|
2018
|
26 |
1 |
p. 1-7
|
artikel
|
| 13 |
Exploiting a water network to achieve enthalpy-driven, bromodomain-selective BET inhibitors
|
Shadrick, William R.
|
|
2018
|
26 |
1 |
p. 25-36
|
artikel
|
| 14 |
Graphical abstract TOC
|
|
|
2018
|
26 |
1 |
p. OBC
|
artikel
|
| 15 |
Graphical abstract TOC
|
|
|
2018
|
26 |
1 |
p. IBC
|
artikel
|
| 16 |
Identification of potent lysophosphatidic acid receptor 5 (LPA5) antagonists as potential analgesic agents
|
Kawamoto, Yuichiro
|
|
2018
|
26 |
1 |
p. 257-265
|
artikel
|
| 17 |
Lead identification and optimization of bacterial glutamate racemase inhibitors
|
Malapati, Prasanthi
|
|
2018
|
26 |
1 |
p. 177-190
|
artikel
|
| 18 |
7-Methylguanosine monophosphate analogues with 5′-(1,2,3-triazoyl) moiety: Synthesis and evaluation as the inhibitors of cNIIIB nucleotidase
|
Kozarski, Mateusz
|
|
2018
|
26 |
1 |
p. 191-199
|
artikel
|
| 19 |
Microwave-assisted diastereoselective two-step three-component synthesis for rapid access to drug-like libraries of substituted 3-amino-β-lactams
|
Janssen, Guido V.
|
|
2018
|
26 |
1 |
p. 41-49
|
artikel
|
| 20 |
Mitochondria-targeted cationic porphyrin-triphenylamine hybrids for enhanced two-photon photodynamic therapy
|
Hammerer, Fabien
|
|
2018
|
26 |
1 |
p. 107-118
|
artikel
|
| 21 |
N-Arylsulfonylsubstituted-1H indole derivatives as small molecule dual inhibitors of signal transducer and activator of transcription 3 (STAT3) and tubulin
|
Zhou, Qiang
|
|
2018
|
26 |
1 |
p. 96-106
|
artikel
|
| 22 |
Novel sulfenamides and sulfonamides based on pyridazinone and pyridazine scaffolds as CB1 receptor ligand antagonists
|
Murineddu, Gabriele
|
|
2018
|
26 |
1 |
p. 295-307
|
artikel
|
| 23 |
Studies on interactions of carbazole derivatives with DNA, cell image, and cytotoxicity
|
Hao, Guoyan
|
|
2018
|
26 |
1 |
p. 285-294
|
artikel
|
| 24 |
Synthesis and anti-influenza virus evaluation of triterpene-sialic acid conjugates
|
Tsuji, Mitsuru
|
|
2018
|
26 |
1 |
p. 17-24
|
artikel
|
| 25 |
Synthesis and bioevaluation study of novel N-methylpicolinamide and thienopyrimidine derivatives as selectivity c-Met kinase inhibitors
|
Wang, Linxiao
|
|
2018
|
26 |
1 |
p. 245-256
|
artikel
|
| 26 |
Synthesis and biological evaluation of novel synthetic chalcone derivatives as anti-tumor agents targeting Cat L and Cat K
|
Wang, Yali
|
|
2018
|
26 |
1 |
p. 8-16
|
artikel
|
| 27 |
Synthesis and evaluation of a potent, well-balanced EP2/EP3 dual agonist
|
Kinoshita, Akihiro
|
|
2018
|
26 |
1 |
p. 200-214
|
artikel
|
| 28 |
Synthesis and evaluation of biaryl derivatives for structural characterization of selective monoamine oxidase B inhibitors toward Parkinson’s disease therapy
|
Yeon, Seul Ki
|
|
2018
|
26 |
1 |
p. 232-244
|
artikel
|
| 29 |
Synthesis and evaluation of 18F-hexafluorophosphate as a novel PET probe for imaging of sodium/iodide symporter in a murine C6-glioma tumor model
|
Jiang, Huailei
|
|
2018
|
26 |
1 |
p. 225-231
|
artikel
|
| 30 |
Synthesis, in vitro and in silico evaluation of novel trans-stilbene analogues as potential COX-2 inhibitors
|
Regulski, Miłosz
|
|
2018
|
26 |
1 |
p. 141-151
|
artikel
|
| 31 |
TLR8 activation and inhibition by guanosine analogs in RNA: Importance of functional groups and chain length
|
Hu, Tiannan
|
|
2018
|
26 |
1 |
p. 77-83
|
artikel
|
| 32 |
UVA irradiation of BrU-substituted DNA in the presence of Hoechst 33258
|
Saha, Abhijit
|
|
2018
|
26 |
1 |
p. 37-40
|
artikel
|
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