| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Antiplasmodial activities of gold(I) complexes involving functionalized N-heterocyclic carbenes
|
Hemmert, Catherine
|
|
2016
|
24 |
13 |
p. 3075-3082
8 p.
|
artikel
|
| 2 |
Antiproliferative activity and apoptosis inducing effects of nitric oxide donating derivatives of evodiamine
|
Zhao, Nan
|
|
2016
|
24 |
13 |
p. 2971-2978
8 p.
|
artikel
|
| 3 |
Bismuth(III) complexes with 2-acetylpyridine- and 2-benzoylpyridine-derived hydrazones: Antimicrobial and cytotoxic activities and effects on the clonogenic survival of human solid tumor cells
|
Ferreira, Isabella P.
|
|
2016
|
24 |
13 |
p. 2988-2998
11 p.
|
artikel
|
| 4 |
Comparing the efficacy of photodynamic and sonodynamic therapy in non-melanoma and melanoma skin cancer
|
McEwan, Conor
|
|
2016
|
24 |
13 |
p. 3023-3028
6 p.
|
artikel
|
| 5 |
Corrigendum to “Purinylpyridinylamino-based DFG-in/αC-helix-out B-Raf inhibitors: Applying mutant versus wild-type B-Raf selectivity indices for compound profiling” [Bioorg. Med. Chem. 24 (2016) 2215–2234]
|
Liu, Longbin
|
|
2016
|
24 |
13 |
p. 3093-
1 p.
|
artikel
|
| 6 |
Design, biological evaluation and 3D QSAR studies of novel dioxin-containing triaryl pyrazoline derivatives as potential B-Raf inhibitors
|
Yang, Yu-Shun
|
|
2016
|
24 |
13 |
p. 3052-3061
10 p.
|
artikel
|
| 7 |
Design, synthesis and anticonvulsant activity of new hybrid compounds derived from N-phenyl-2-(2,5-dioxopyrrolidin-1-yl)-propanamides and -butanamides
|
Kamiński, Krzysztof
|
|
2016
|
24 |
13 |
p. 2938-2946
9 p.
|
artikel
|
| 8 |
Design, synthesis and biological evaluation of novel tetrahydroisoquinoline quaternary derivatives as peripheral κ-opioid receptor agonists
|
Guo, Ting
|
|
2016
|
24 |
13 |
p. 2964-2970
7 p.
|
artikel
|
| 9 |
Dihydrochelerythrine and its derivatives: Synthesis and their application as potential G-quadruplex DNA stabilizing agents
|
Malhotra, Rajesh
|
|
2016
|
24 |
13 |
p. 2887-2896
10 p.
|
artikel
|
| 10 |
Discovery of a novel covalent non-β-lactam inhibitor of the metallo-β-lactamase NDM-1
|
Christopeit, Tony
|
|
2016
|
24 |
13 |
p. 2947-2953
7 p.
|
artikel
|
| 11 |
Discovery of new [1,4]dioxino[2,3-f]quinazoline-based inhibitors of EGFR including the T790M/L858R mutant
|
Qin, Xuemei
|
|
2016
|
24 |
13 |
p. 2871-2881
11 p.
|
artikel
|
| 12 |
Editorial board
|
|
|
2016
|
24 |
13 |
p. IFC-
1 p.
|
artikel
|
| 13 |
Identification, synthesis and evaluation of SARS-CoV and MERS-CoV 3C-like protease inhibitors
|
Kumar, Vathan
|
|
2016
|
24 |
13 |
p. 3035-3042
8 p.
|
artikel
|
| 14 |
Inhibitors of secreted phospholipase A2 suppress the release of PGE2 in renal mesangial cells
|
Vasilakaki, Sofia
|
|
2016
|
24 |
13 |
p. 3029-3034
6 p.
|
artikel
|
| 15 |
New trans dichloro (triphenylphosphine)platinum(II) complexes containing N-(butyl),N-(arylmethyl)amino ligands: Synthesis, cytotoxicity and mechanism of action
|
Dalla Via, Lisa
|
|
2016
|
24 |
13 |
p. 2929-2937
9 p.
|
artikel
|
| 16 |
Novel free fatty acid receptor 1 (GPR40) agonists based on 1,3,4-thiadiazole-2-carboxamide scaffold
|
Krasavin, Mikhail
|
|
2016
|
24 |
13 |
p. 2954-2963
10 p.
|
artikel
|
| 17 |
Novel sulfonamide bearing coumarin scaffolds as selective inhibitors of tumor associated carbonic anhydrase isoforms IX and XII
|
Chandak, Navneet
|
|
2016
|
24 |
13 |
p. 2882-2886
5 p.
|
artikel
|
| 18 |
Optimization of the phenylurea moiety in a phosphoinositide 3-kinase (PI3K) inhibitor to improve water solubility and the PK profile by introducing a solubilizing group and ortho substituents
|
Kawada, Hatsuo
|
|
2016
|
24 |
13 |
p. 2897-2906
10 p.
|
artikel
|
| 19 |
Pyrazolylbenzo[d]imidazoles as new potent and selective inhibitors of carbonic anhydrase isoforms hCA IX and XII
|
Kumar, Satish
|
|
2016
|
24 |
13 |
p. 2907-2913
7 p.
|
artikel
|
| 20 |
Stable and biocompatible cystine knot peptides from the marine sponge Asteropus sp.
|
Su, Mingzhi
|
|
2016
|
24 |
13 |
p. 2979-2987
9 p.
|
artikel
|
| 21 |
Synthesis and evaluation of raloxifene derivatives as a selective estrogen receptor down-regulator
|
Shoda, Takuji
|
|
2016
|
24 |
13 |
p. 2914-2919
6 p.
|
artikel
|
| 22 |
Synthesis and structure–activity relationships of novel hybrid ferrocenyl compounds based on a bicyclic core skeleton for breast cancer therapy
|
Li, Changhao
|
|
2016
|
24 |
13 |
p. 3062-3074
13 p.
|
artikel
|
| 23 |
Synthesis, biological evaluation, and physicochemical property assessment of 4-substituted 2-phenylaminoquinazolines as Mer tyrosine kinase inhibitors
|
Wang, Sheng-Biao
|
|
2016
|
24 |
13 |
p. 3083-3092
10 p.
|
artikel
|
| 24 |
Synthesis of 4-(thiazol-2-ylamino)-benzenesulfonamides with carbonic anhydrase I, II and IX inhibitory activity and cytotoxic effects against breast cancer cell lines
|
Abdel Gawad, Nagwa M.
|
|
2016
|
24 |
13 |
p. 3043-3051
9 p.
|
artikel
|
| 25 |
Systematic evaluation of methyl ester bioisosteres in the context of developing alkenyldiarylmethanes (ADAMs) as non-nucleoside reverse transcriptase inhibitors (NNRTIs) for anti-HIV-1 chemotherapy
|
Hoshi, Ayako
|
|
2016
|
24 |
13 |
p. 3006-3022
17 p.
|
artikel
|
| 26 |
2-(Thienothiazolylimino)-1,3-thiazolidin-4-ones inhibit cell division cycle 25 A phosphatase
|
Huber-Villaume, Sophie
|
|
2016
|
24 |
13 |
p. 2920-2928
9 p.
|
artikel
|
| 27 |
Triterpene sapogenin–polyarginine conjugates exhibit promising antibacterial activity against Gram-positive strains
|
Na, Heiya
|
|
2016
|
24 |
13 |
p. 2999-3005
7 p.
|
artikel
|
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