| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
4-(3-Alkyl-2-oxoimidazolidin-1-yl)-N-phenylbenzenesulfonamides as new antimitotic prodrugs activated by cytochrome P450 1A1 in breast cancer cells
|
Chavez Alvarez, Atziri Corin
|
|
2018
|
26 |
18 |
p. 5045-5052
|
artikel
|
| 2 |
Andrographolide derivative as STAT3 inhibitor that protects acute liver damage in mice
|
Chen, Shao-Ru
|
|
2018
|
26 |
18 |
p. 5053-5061
|
artikel
|
| 3 |
A new phenolic series of indenopyridinone as topoisomerase inhibitors: Design, synthesis, and structure-activity relationships
|
Shrestha, Aarajana
|
|
2018
|
26 |
18 |
p. 5212-5223
|
artikel
|
| 4 |
A reusable magnetic nickel nanoparticle based catalyst for the aqueous synthesis of diverse heterocycles and their evaluation as potential anti-bacterial agent
|
Bhattacharjee, Deboshikha
|
|
2018
|
26 |
18 |
p. 5018-5028
|
artikel
|
| 5 |
A truncated RHAMM protein for discovering novel therapeutic peptides
|
Hauser-Kawaguchi, Alexandra
|
|
2018
|
26 |
18 |
p. 5194-5203
|
artikel
|
| 6 |
Compromising the plasma membrane as a secondary target in photodynamic therapy-induced necrosis
|
Thompson, Sebastian A.
|
|
2018
|
26 |
18 |
p. 5224-5228
|
artikel
|
| 7 |
Design, synthesis, and biological evaluation of novel selective peptide inhibitors of 11β-hydroxysteroid dehydrogenase 1
|
Boudon, Stephanie
|
|
2018
|
26 |
18 |
p. 5128-5139
|
artikel
|
| 8 |
Design, synthesis and in vitro study of densely functionalized oxindoles as potent α-glucosidase inhibitors
|
Luthra, Tania
|
|
2018
|
26 |
18 |
p. 4996-5005
|
artikel
|
| 9 |
Development of 13H-benzo[f]chromeno[4,3-b][1,7]naphthyridines and their salts as potent cytotoxic agents and topoisomerase I/IIα inhibitors
|
Arepalli, Sateesh Kumar
|
|
2018
|
26 |
18 |
p. 5181-5193
|
artikel
|
| 10 |
Development of matrix metalloproteinase-13 inhibitors – A structure-activity/structure-property relationship study
|
Fuerst, Rita
|
|
2018
|
26 |
18 |
p. 4984-4995
|
artikel
|
| 11 |
Discovery and structural characterization of peficitinib (ASP015K) as a novel and potent JAK inhibitor
|
Hamaguchi, Hisao
|
|
2018
|
26 |
18 |
p. 4971-4983
|
artikel
|
| 12 |
Discovery of a non-toxic [1,2,4]triazolo[1,5-a]pyrimidin-7-one (WS-10) that modulates ABCB1-mediated multidrug resistance (MDR)
|
Chang, Liming
|
|
2018
|
26 |
18 |
p. 5006-5017
|
artikel
|
| 13 |
Discovery of DS-6930, a potent selective PPARγ modulator. Part II: Lead optimization
|
Shinozuka, Tsuyoshi
|
|
2018
|
26 |
18 |
p. 5099-5117
|
artikel
|
| 14 |
Discovery of DS-6930, a potent selective PPARγ modulator. Part I: Lead identification
|
Shinozuka, Tsuyoshi
|
|
2018
|
26 |
18 |
p. 5079-5098
|
artikel
|
| 15 |
Discovery of natural flavonoids as activators of Nrf2-mediated defense system: Structure-activity relationship and inhibition of intracellular oxidative insults
|
Li, Yan-Ru
|
|
2018
|
26 |
18 |
p. 5140-5150
|
artikel
|
| 16 |
Editorial Board
|
|
|
2018
|
26 |
18 |
p. ii
|
artikel
|
| 17 |
Graphical abstract TOC
|
|
|
2018
|
26 |
18 |
p. IBC
|
artikel
|
| 18 |
Graphical abstract TOC
|
|
|
2018
|
26 |
18 |
p. OBC
|
artikel
|
| 19 |
Graphical abstract TOC
|
|
|
2018
|
26 |
18 |
p. I-V
|
artikel
|
| 20 |
Identification of N-(5-(phenoxymethyl)-1,3,4-thiadiazol-2-yl)acetamide derivatives as novel protein tyrosine phosphatase epsilon inhibitors exhibiting anti-osteoclastic activity
|
Ku, Bonsu
|
|
2018
|
26 |
18 |
p. 5204-5211
|
artikel
|
| 21 |
Novel autophagy modulators: Design and synthesis of (+)-epogymnolactam analogues and structure-activity relationship
|
Ueda, Kazuki
|
|
2018
|
26 |
18 |
p. 5159-5168
|
artikel
|
| 22 |
Novel 4-(2-pyrimidinylamino)benzamide derivatives as potent hedgehog signaling pathway inhibitors
|
Xin, Minhang
|
|
2018
|
26 |
18 |
p. 5029-5036
|
artikel
|
| 23 |
N-Thiazolylamide-based free fatty-acid 2 receptor agonists: Discovery, lead optimization and demonstration of off-target effect in a diabetes model
|
Hoveyda, Hamid R.
|
|
2018
|
26 |
18 |
p. 5169-5180
|
artikel
|
| 24 |
Oximes short-acting CB1 receptor agonists
|
Malamas, Michael S.
|
|
2018
|
26 |
18 |
p. 4963-4970
|
artikel
|
| 25 |
Pyrrolo[2,1-c][1,4] benzodiazepine-3,11-diones protect SHSY-5Y cells from Cd-induced apoptosis involving suppression of endoplasmic reticulum stress
|
Ma, Chao
|
|
2018
|
26 |
18 |
p. 5151-5158
|
artikel
|
| 26 |
Structure-activity relationship of novel (benzoylaminophenoxy)phenol derivatives as anti-prostate cancer agents
|
Kazui, Yuko
|
|
2018
|
26 |
18 |
p. 5118-5127
|
artikel
|
| 27 |
Synthesis and biological evaluation of novel heteroring-annulated pyrrolino-tetrahydroberberine analogues as antioxidant agents
|
Mari, Giacomo
|
|
2018
|
26 |
18 |
p. 5037-5044
|
artikel
|
| 28 |
Synthesis of oxidative metabolites of CRA13 and their analogs: Identification of CRA13 active metabolites and analogs thereof with selective CB2R affinity
|
Hassan, Ahmed H.E.
|
|
2018
|
26 |
18 |
p. 5069-5078
|
artikel
|
| 29 |
Thiazole- and selenazole-comprising high-affinity inhibitors possess bright microsecond-scale photoluminescence in complex with protein kinase CK2
|
Vahter, Jürgen
|
|
2018
|
26 |
18 |
p. 5062-5068
|
artikel
|
Tijdschrift beschrijving