| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A clickable psoralen to directly quantify DNA interstrand crosslinking and repair
|
Evison, Benjamin J.
|
|
2016
|
24 |
5 |
p. 1071-1078
8 p.
|
artikel
|
| 2 |
Anionic surfactants enhance click reaction-mediated protein conjugation with ubiquitin
|
Schneider, Daniel
|
|
2016
|
24 |
5 |
p. 995-1001
7 p.
|
artikel
|
| 3 |
A novel library of saccharin and acesulfame derivatives as potent and selective inhibitors of carbonic anhydrase IX and XII isoforms
|
Carradori, Simone
|
|
2016
|
24 |
5 |
p. 1095-1105
11 p.
|
artikel
|
| 4 |
A spectroscopic study of substituted anthranilic acids as sensitive environmental probes for detecting cancer cells
|
Culf, Adrian S.
|
|
2016
|
24 |
5 |
p. 929-937
9 p.
|
artikel
|
| 5 |
Assemblies of ionic zinc chlorins assisted by water-soluble polypeptides
|
Miyatake, Tomohiro
|
|
2016
|
24 |
5 |
p. 1155-1161
7 p.
|
artikel
|
| 6 |
Design, synthesis, and biological evaluation of water-soluble amino acid prodrug conjugates derived from combretastatin, dihydronaphthalene, and benzosuberene-based parent vascular disrupting agents
|
Devkota, Laxman
|
|
2016
|
24 |
5 |
p. 938-956
19 p.
|
artikel
|
| 7 |
Discovery of benzenesulfonamide derivatives as potent PI3K/mTOR dual inhibitors with in vivo efficacies against hepatocellular carcinoma
|
Chen, Ying
|
|
2016
|
24 |
5 |
p. 957-966
10 p.
|
artikel
|
| 8 |
Discovery of novel phenoxazinone derivatives as DKK1/LRP6 interaction inhibitors: Synthesis, biological evaluation and structure–activity relationships
|
Thysiadis, Savvas
|
|
2016
|
24 |
5 |
p. 1014-1022
9 p.
|
artikel
|
| 9 |
Discovery of potent anti-tuberculosis agents targeting leucyl-tRNA synthetase
|
Gudzera, Olga I.
|
|
2016
|
24 |
5 |
p. 1023-1031
9 p.
|
artikel
|
| 10 |
Editorial board
|
|
|
2016
|
24 |
5 |
p. IFC-
1 p.
|
artikel
|
| 11 |
Glycopeptide-functionalized gold nanoparticles for antibody induction against the tumor associated mucin-1 glycoprotein
|
Cai, Hui
|
|
2016
|
24 |
5 |
p. 1132-1135
4 p.
|
artikel
|
| 12 |
Heptapeptide ligands against receptor-binding sites of influenza hemagglutinin toward anti-influenza therapy
|
Matsubara, Teruhiko
|
|
2016
|
24 |
5 |
p. 1106-1114
9 p.
|
artikel
|
| 13 |
Incorporation of fluorophore–cholesterol conjugates into liposomal and mycobacterial membranes
|
Wercholuk, Ashley N.
|
|
2016
|
24 |
5 |
p. 1045-1049
5 p.
|
artikel
|
| 14 |
Insight to the binding mode of triazole RGD-peptidomimetics to integrin-rich cancer cells by NMR and molecular modeling
|
Vasile, Francesca
|
|
2016
|
24 |
5 |
p. 989-994
6 p.
|
artikel
|
| 15 |
In vitro interactions between anidulafungin and nonsteroidal anti-inflammatory drugs on biofilms of Candida spp.
|
Rosato, Antonio
|
|
2016
|
24 |
5 |
p. 1002-1005
4 p.
|
artikel
|
| 16 |
Kinetic and X-ray crystallographic investigations on carbonic anhydrase isoforms I, II, IX and XII of a thioureido analog of SLC-0111
|
Lomelino, Carrie L.
|
|
2016
|
24 |
5 |
p. 976-981
6 p.
|
artikel
|
| 17 |
Metal-based biologically active azoles and β-lactams derived from sulfa drugs
|
Ebrahimi, Hossein Pasha
|
|
2016
|
24 |
5 |
p. 1121-1131
11 p.
|
artikel
|
| 18 |
Novel naphtho[2,1-d]oxazole-4,5-diones as NQO1 substrates with improved aqueous solubility: Design, synthesis, and in vivo antitumor evaluation
|
Li, Xiang
|
|
2016
|
24 |
5 |
p. 1006-1013
8 p.
|
artikel
|
| 19 |
Overcoming multidrug resistance by targeting mitochondria with NO-donating doxorubicins
|
Gazzano, Elena
|
|
2016
|
24 |
5 |
p. 967-975
9 p.
|
artikel
|
| 20 |
Pyrazole antagonists of the CB1 receptor with reduced brain penetration
|
Fulp, Alan
|
|
2016
|
24 |
5 |
p. 1063-1070
8 p.
|
artikel
|
| 21 |
Structure–activity relationship study of 4-(thiazol-5-yl)benzoic acid derivatives as potent protein kinase CK2 inhibitors
|
Ohno, Hiroaki
|
|
2016
|
24 |
5 |
p. 1136-1141
6 p.
|
artikel
|
| 22 |
Sulfonamide inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae
|
Del Prete, Sonia
|
|
2016
|
24 |
5 |
p. 1115-1120
6 p.
|
artikel
|
| 23 |
Symmetric 4,4′-(piperidin-4-ylidenemethylene)bisphenol derivatives as novel tunable estrogen receptor (ER) modulators
|
Sato, Manabu
|
|
2016
|
24 |
5 |
p. 1089-1094
6 p.
|
artikel
|
| 24 |
Synthesis and biological evaluation of enantiomerically pure glyceric acid derivatives as LpxC inhibitors
|
Tangherlini, Giovanni
|
|
2016
|
24 |
5 |
p. 1032-1044
13 p.
|
artikel
|
| 25 |
Synthesis and cytotoxicity of thieno[2,3-b]quinoline-2-carboxamide and cycloalkyl[b]thieno[3,2-e]pyridine-2-carboxamide derivatives
|
Leung, Euphemia
|
|
2016
|
24 |
5 |
p. 1142-1154
13 p.
|
artikel
|
| 26 |
Synthesis and pharmacological evaluation of trifluoromethyl containing 4-(2-pyrimidinylamino)benzamides as Hedgehog signaling pathway inhibitors
|
Xin, Minhang
|
|
2016
|
24 |
5 |
p. 1079-1088
10 p.
|
artikel
|
| 27 |
Synthesis, molecular docking and biological evaluation of N,N-disubstituted 2-aminothiazolines as a new class of butyrylcholinesterase and carboxylesterase inhibitors
|
Makhaeva, Galina F.
|
|
2016
|
24 |
5 |
p. 1050-1062
13 p.
|
artikel
|
| 28 |
Synthesis of 4-sulfamoylphenyl-benzylamine derivatives with inhibitory activity against human carbonic anhydrase isoforms I, II, IX and XII
|
Durgun, Mustafa
|
|
2016
|
24 |
5 |
p. 982-988
7 p.
|
artikel
|
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