| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
4-Aryl-5-carbamoyl-3-isoxazolols as competitive antagonists of insect GABA receptors: Synthesis, biological activity, and molecular docking studies
|
Liu, Genyan
|
|
2019
|
27 |
2 |
p. 416-424
|
artikel
|
| 2 |
Design and synthesis of selective CYP1B1 inhibitor via dearomatization of α-naphthoflavone
|
Kubo, Makoto
|
|
2019
|
27 |
2 |
p. 285-304
|
artikel
|
| 3 |
Design, synthesis, and biological evaluation of radioiodinated benzo[d]imidazole-quinoline derivatives for platelet-derived growth factor receptor β (PDGFRβ) imaging
|
Effendi, Nurmaya
|
|
2019
|
27 |
2 |
p. 383-393
|
artikel
|
| 4 |
Discovery of potent, low-absorbable sodium-dependent glucose cotransporter 1 (SGLT1) inhibitor SGL5213 for type 2 diabetes treatment
|
Kuroda, Shoichi
|
|
2019
|
27 |
2 |
p. 394-409
|
artikel
|
| 5 |
Editorial Board
|
|
|
2019
|
27 |
2 |
p. ii
|
artikel
|
| 6 |
Electron injection from mitochondrial transcription factor A to DNA associated with thymine dimer photo repair
|
Hashiya, Fumitaka
|
|
2019
|
27 |
2 |
p. 278-284
|
artikel
|
| 7 |
Elucidating the mode of action for thiophene-based organic D-π-A sensitizers for use in photodynamic therapy
|
Fuse, Shinichiro
|
|
2019
|
27 |
2 |
p. 315-321
|
artikel
|
| 8 |
Evaluation of a non-prime site substituent and warheads combined with a decahydroisoquinolin scaffold as a SARS 3CL protease inhibitor
|
Ohnishi, Kouji
|
|
2019
|
27 |
2 |
p. 425-435
|
artikel
|
| 9 |
Flavone-based natural product agents as new lysine-specific demethylase 1 inhibitors exhibiting cytotoxicity against breast cancer cells in vitro
|
Xu, Xiao
|
|
2019
|
27 |
2 |
p. 370-374
|
artikel
|
| 10 |
Graphical abstract TOC
|
|
|
2019
|
27 |
2 |
p. OBC
|
artikel
|
| 11 |
Graphical abstract TOC
|
|
|
2019
|
27 |
2 |
p. I-IV
|
artikel
|
| 12 |
Graphical abstract TOC
|
|
|
2019
|
27 |
2 |
p. IBC
|
artikel
|
| 13 |
In silico, NMR and pharmacological evaluation of an hydroxyoxindole cholinesterase inhibitor
|
Bacalhau, Patrícia
|
|
2019
|
27 |
2 |
p. 354-363
|
artikel
|
| 14 |
Lamellarin-inspired potent topoisomerase I inhibitors with the unprecedented benzo[g][1]benzopyrano[4,3-b]indol-6(13H)-one scaffold
|
Fukuda, Tsutomu
|
|
2019
|
27 |
2 |
p. 265-277
|
artikel
|
| 15 |
Leucoflavonine, a new bioactive racemic flavoalkaloid from the leaves of Leucosceptrum canum
|
Feng, Ling
|
|
2019
|
27 |
2 |
p. 442-446
|
artikel
|
| 16 |
Metronidazole aryloxy, carboxy and azole derivatives: Synthesis, anti-tumor activity, QSAR, molecular docking and dynamics studies
|
Faghih-Mirzaei, Ehsan
|
|
2019
|
27 |
2 |
p. 305-314
|
artikel
|
| 17 |
Pyrrolidinone-bearing methylated and halogenated benzenesulfonamides as inhibitors of carbonic anhydrases
|
Vaškevičienė, Irena
|
|
2019
|
27 |
2 |
p. 322-337
|
artikel
|
| 18 |
Stability and properties of Z-DNA containing artificial nucleobase 2′-O-methyl-8-methyl guanosine
|
Balasubramaniyam, Thananjeyan
|
|
2019
|
27 |
2 |
p. 364-369
|
artikel
|
| 19 |
Structural and computational basis for potent inhibition of glutamate carboxypeptidase II by carbamate-based inhibitors
|
Barinka, Cyril
|
|
2019
|
27 |
2 |
p. 255-264
|
artikel
|
| 20 |
Synthesis, Antioxidant Activity and Cytotoxicity of N-Functionalized Organotellurides
|
Bandeira, Pamela T.
|
|
2019
|
27 |
2 |
p. 410-415
|
artikel
|
| 21 |
Synthesis of amides from (E)-3-(1-chloro-3,4-dihydronaphthalen-2-yl)acrylic acid and substituted amino acid esters as NorA efflux pump inhibitors of Staphylococcus aureus
|
Rath, Santosh K.
|
|
2019
|
27 |
2 |
p. 343-353
|
artikel
|
| 22 |
Synthesis of novel pyrazoline derivatives and the evaluation of death mechanisms involved in their antileukemic activity
|
Stefanes, Natália Marceli
|
|
2019
|
27 |
2 |
p. 375-382
|
artikel
|
| 23 |
Synthetic approaches to isocarbacyclin and analogues as potential neuroprotective agents against ischemic stroke
|
Abu Deiab, Ghina'a I.
|
|
2019
|
27 |
2 |
p. 338-342
|
artikel
|
| 24 |
Tripeptide analogues of MG132 as protease inhibitors
|
Pehere, Ashok D.
|
|
2019
|
27 |
2 |
p. 436-441
|
artikel
|
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