| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Activity cliff for 7-substituted pyrrolo-pyrimidine inhibitors of HCK explained in terms of predicted basicity of the amine nitrogen
|
Yuki, Hitomi
|
|
2017
|
25 |
16 |
p. 4259-4264
6 p.
|
artikel
|
| 2 |
Antitrichomonal activity of δ opioid receptor antagonists, 7-benzylidenenaltrexone derivatives
|
Kutsumura, Noriki
|
|
2017
|
25 |
16 |
p. 4375-4383
9 p.
|
artikel
|
| 3 |
Bistacrines as potential antitrypanosomal agents
|
Schmidt, Ines
|
|
2017
|
25 |
16 |
p. 4526-4531
6 p.
|
artikel
|
| 4 |
Conformational studies of Gram-negative bacterial quorum sensing 3-oxo N-acyl homoserine lactone molecules
|
Crowe, Darren
|
|
2017
|
25 |
16 |
p. 4285-4296
12 p.
|
artikel
|
| 5 |
Conjugates of salicylaldoximes and peripheral site ligands: Novel efficient nonquaternary reactivators for nerve agent-inhibited acetylcholinesterase
|
Wei, Zhao
|
|
2017
|
25 |
16 |
p. 4497-4505
9 p.
|
artikel
|
| 6 |
CRM1 inhibitory and antiproliferative activities of novel 4′-alkyl substituted klavuzon derivatives
|
Kanbur, Tuğçe
|
|
2017
|
25 |
16 |
p. 4444-4451
8 p.
|
artikel
|
| 7 |
Design and synthesis of potent and orally active GPR4 antagonists with modulatory effects on nociception, inflammation, and angiogenesis
|
Miltz, Wolfgang
|
|
2017
|
25 |
16 |
p. 4512-4525
14 p.
|
artikel
|
| 8 |
Design, synthesis and biological evaluation of GPR55 agonists
|
Fakhouri, Lara
|
|
2017
|
25 |
16 |
p. 4355-4367
13 p.
|
artikel
|
| 9 |
Design, synthesis and biological evaluation of novel 4-phenoxyquinoline derivatives containing 3-oxo-3,4-dihydroquinoxaline moiety as c-Met kinase inhibitors
|
Liu, Ju
|
|
2017
|
25 |
16 |
p. 4475-4486
12 p.
|
artikel
|
| 10 |
Design, synthesis, and biological evaluation of some novel indolizine derivatives as dual cyclooxygenase and lipoxygenase inhibitor for anti-inflammatory activity
|
Shrivastava, Sushant K.
|
|
2017
|
25 |
16 |
p. 4424-4432
9 p.
|
artikel
|
| 11 |
Discovery of novel DAPY-IAS hybrid derivatives as potential HIV-1 inhibitors using molecular hybridization based on crystallographic overlays
|
Huang, Boshi
|
|
2017
|
25 |
16 |
p. 4397-4406
10 p.
|
artikel
|
| 12 |
Editorial board
|
|
|
2017
|
25 |
16 |
p. IFC-
1 p.
|
artikel
|
| 13 |
Effect of replacing main-chain ureas with thiourea and guanidinium surrogates on the bactericidal activity of membrane active oligourea foldamers
|
Antunes, Stéphanie
|
|
2017
|
25 |
16 |
p. 4245-4252
8 p.
|
artikel
|
| 14 |
Gerontoxanthone B from Maclura cochinchinensis var. gerontogea exhibits anti-inflammatory potential as an aryl hydrocarbon receptor agonist
|
Nakashima, Ken-ichi
|
|
2017
|
25 |
16 |
p. 4253-4258
6 p.
|
artikel
|
| 15 |
Nanoparticle-macrophage interactions: A balance between clearance and cell-specific targeting
|
Rattan, Rahul
|
|
2017
|
25 |
16 |
p. 4487-4496
10 p.
|
artikel
|
| 16 |
Novel 4-acetamide-2-alkylthio-N-acetanilides resembling nimesulide: Synthesis, cell viability evaluation and in silico studies
|
Catarro, Mafalda
|
|
2017
|
25 |
16 |
p. 4304-4313
10 p.
|
artikel
|
| 17 |
Novel analogs of N-acylhydroxyethylaminomethyl-4H-chromen-4-one scaffold as IL-5 inhibitors
|
Yang, Hyun-Sun
|
|
2017
|
25 |
16 |
p. 4330-4338
9 p.
|
artikel
|
| 18 |
Novel 3H-[1,2,3]triazolo[4,5-c]pyridine derivatives as GPR119 agonists: Synthesis and structure-activity/solubility relationships
|
Matsuda, Daisuke
|
|
2017
|
25 |
16 |
p. 4339-4354
16 p.
|
artikel
|
| 19 |
Phenylsulfonylfuroxan NO-donor phenols: Synthesis and multifunctional activities evaluation
|
Xie, Yundong
|
|
2017
|
25 |
16 |
p. 4407-4413
7 p.
|
artikel
|
| 20 |
Phosphonodifluoropyruvate is a mechanism-based inhibitor of phosphonopyruvate decarboxylase from Bacteroides fragilis
|
Pallitsch, Katharina
|
|
2017
|
25 |
16 |
p. 4368-4374
7 p.
|
artikel
|
| 21 |
Selective opioid growth factor receptor antagonists based on a stilbene isostere
|
Stockdale, David P.
|
|
2017
|
25 |
16 |
p. 4464-4474
11 p.
|
artikel
|
| 22 |
Stable C–N axial chirality in 1-aryluracil scaffold and differences in in vitro metabolic clearance between atropisomers of PDE4 inhibitor
|
Hasegawa, Futoshi
|
|
2017
|
25 |
16 |
p. 4506-4511
6 p.
|
artikel
|
| 23 |
Stereospecific inhibition of nitric oxide production in macrophage cells by flavanonols: Synthesis and the structure-activity relationship. Part 2
|
Jiang, Wen-Jun
|
|
2017
|
25 |
16 |
p. 4277-4284
8 p.
|
artikel
|
| 24 |
Structure-activity relationships of 3-O-β-chacotriosyl oleanic acid derivatives as entry inhibitors for highly pathogenic H5N1 influenza virus
|
Li, Sumei
|
|
2017
|
25 |
16 |
p. 4384-4396
13 p.
|
artikel
|
| 25 |
Structure-activity relationship studies of G9a-like protein (GLP) inhibitors
|
Xiong, Yan
|
|
2017
|
25 |
16 |
p. 4414-4423
10 p.
|
artikel
|
| 26 |
Structure-activity relationship studies on thiaplidiaquinones A and B as novel inhibitors of Plasmodium falciparum and farnesyltransferase
|
Cadelis, Melissa M.
|
|
2017
|
25 |
16 |
p. 4433-4443
11 p.
|
artikel
|
| 27 |
Synthesis and biological activity of cyclolinopeptide A analogues modified with γ4-bis(homo-phenylalanine)
|
Jędrzejczak, Karol
|
|
2017
|
25 |
16 |
p. 4265-4276
12 p.
|
artikel
|
| 28 |
Synthesis and characterization of monophosphinic acid DOTA derivative: A smart tool with functionalities for multimodal imaging
|
Chilla, Satya Narayana Murthy
|
|
2017
|
25 |
16 |
p. 4297-4303
7 p.
|
artikel
|
| 29 |
Synthesis and evaluation of (E)-2-(5-phenylpent-2-en-4-ynamido)cyclohex-1-ene-1-carboxylate derivatives as HCA2 receptor agonists
|
Bobileva, Olga
|
|
2017
|
25 |
16 |
p. 4314-4329
16 p.
|
artikel
|
| 30 |
Targeting progesterone metabolism in breast cancer with l-proline derived new 14-azasteroids
|
Singh, Jyotsana
|
|
2017
|
25 |
16 |
p. 4452-4463
12 p.
|
artikel
|
| 31 |
The medicinal chemistry of Chikungunya virus
|
da Silva-Júnior, Edeildo F.
|
|
2017
|
25 |
16 |
p. 4219-4244
26 p.
|
artikel
|
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