| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Actin-binding doliculide causes premature senescence in p53 wild type cells
|
Foerster, Florian
|
|
2016
|
24 |
2 |
p. 123-129
7 p.
|
artikel
|
| 2 |
α-Aryl-N-aryl nitrones: Synthesis and screening of a new scaffold for cellular protection against an oxidative toxic stimulus
|
Matias, A.C.
|
|
2016
|
24 |
2 |
p. 232-239
8 p.
|
artikel
|
| 3 |
9-Benzoyl 9-deazaguanines as potent xanthine oxidase inhibitors
|
Rodrigues, Marili V.N.
|
|
2016
|
24 |
2 |
p. 226-231
6 p.
|
artikel
|
| 4 |
Chlorophenoxy aminoalkyl derivatives as histamine H3R ligands and antiseizure agents
|
Kuder, Kamil
|
|
2016
|
24 |
2 |
p. 53-72
20 p.
|
artikel
|
| 5 |
Combination of 4-anilinoquinazoline, arylurea and tertiary amine moiety to discover novel anticancer agents
|
Zuo, Sai-Jie
|
|
2016
|
24 |
2 |
p. 179-190
12 p.
|
artikel
|
| 6 |
Corrigendum to “Aminopyrazolo[1,5-a]pyrimidines as potential inhibitors of Mycobacterium tuberculosis: Structure activity relationships and ADME characterization” [Bioorg. Med. Chem. 23 (2015) 7240–7250]
|
Soares de Melo, Candice
|
|
2016
|
24 |
2 |
p. 314-
1 p.
|
artikel
|
| 7 |
Design, synthesis and activity evaluation of novel peptide fusion inhibitors targeting HIV-1 gp41
|
Tan, Jianjun
|
|
2016
|
24 |
2 |
p. 201-206
6 p.
|
artikel
|
| 8 |
Design, synthesis and evaluation of acridine derivatives as multi-target Src and MEK kinase inhibitors for anti-tumor treatment
|
Cui, Zhishan
|
|
2016
|
24 |
2 |
p. 261-269
9 p.
|
artikel
|
| 9 |
Design, synthesis and evaluation of bitopic arylpiperazinephenyl-1,2,4-oxadiazoles as preferential dopamine D3 receptor ligands
|
Cao, Yongkai
|
|
2016
|
24 |
2 |
p. 191-200
10 p.
|
artikel
|
| 10 |
Design synthesis and structure–activity relationship of 5-substituted (tetrahydronaphthalen-2yl)methyl with N-phenyl-N-(piperidin-2-yl)propionamide derivatives as opioid ligands
|
Deekonda, Srinivas
|
|
2016
|
24 |
2 |
p. 85-91
7 p.
|
artikel
|
| 11 |
Discovery of (2-benzoylethen-1-ol)-containing 1,2-benzothiazine derivatives as novel 4-hydroxyphenylpyruvate dioxygenase (HPPD) inhibiting-based herbicide lead compounds
|
Lei, Kang
|
|
2016
|
24 |
2 |
p. 92-103
12 p.
|
artikel
|
| 12 |
Discovery of novel tetrahydroisoquinoline-containing pyrimidines as ALK inhibitors
|
Achary, Raghavendra
|
|
2016
|
24 |
2 |
p. 207-219
13 p.
|
artikel
|
| 13 |
Dissection of N,N-diethyl-N′-phenylpiperazines as α7 nicotinic receptor silent agonists
|
Quadri, Marta
|
|
2016
|
24 |
2 |
p. 286-293
8 p.
|
artikel
|
| 14 |
Editorial board
|
|
|
2016
|
24 |
2 |
p. IFC-
1 p.
|
artikel
|
| 15 |
Fluorescent sulfonamide carbonic anhydrase inhibitors incorporating 1,2,3-triazole moieties: Kinetic and X-ray crystallographic studies
|
Carta, Fabrizio
|
|
2016
|
24 |
2 |
p. 104-112
9 p.
|
artikel
|
| 16 |
Highly potent tyrosinase inhibitor, neorauflavane from Campylotropis hirtella and inhibitory mechanism with molecular docking
|
Tan, Xuefei
|
|
2016
|
24 |
2 |
p. 153-159
7 p.
|
artikel
|
| 17 |
8-Hydroxyquinoline-based inhibitors of the Rce1 protease disrupt Ras membrane localization in human cells
|
Mohammed, Idrees
|
|
2016
|
24 |
2 |
p. 160-178
19 p.
|
artikel
|
| 18 |
Indomethacin derivatives as tubulin stabilizers to inhibit cancer cell proliferation
|
Chennamaneni, Snigdha
|
|
2016
|
24 |
2 |
p. 277-285
9 p.
|
artikel
|
| 19 |
Molecular modeling studies, synthesis and biological evaluation of dabigatran analogues as thrombin inhibitors
|
Dong, Ming-Hui
|
|
2016
|
24 |
2 |
p. 73-84
12 p.
|
artikel
|
| 20 |
N-Alkylated arylsulfonamides of (aryloxy)ethyl piperidines: 5-HT7 receptor selectivity versus multireceptor profile
|
Canale, Vittorio
|
|
2016
|
24 |
2 |
p. 130-139
10 p.
|
artikel
|
| 21 |
Recombinant thermoactive phosphoenolpyruvate carboxylase (PEPC) from Thermosynechococcus elongatus and its coupling with mesophilic/thermophilic bacterial carbonic anhydrases (CAs) for the conversion of CO2 to oxaloacetate
|
Del Prete, Sonia
|
|
2016
|
24 |
2 |
p. 220-225
6 p.
|
artikel
|
| 22 |
Structural insights into mechanisms for inhibiting amyloid β42 aggregation by non-catechol-type flavonoids
|
Hanaki, Mizuho
|
|
2016
|
24 |
2 |
p. 304-313
10 p.
|
artikel
|
| 23 |
Synthesis and antiviral properties of novel indole-based thiosemicarbazides and 4-thiazolidinones
|
Cihan-Üstündağ, Gökçe
|
|
2016
|
24 |
2 |
p. 240-246
7 p.
|
artikel
|
| 24 |
Synthesis, biological studies and molecular dynamics of new anticancer RGD-based peptide conjugates for targeted drug delivery
|
Gilad, Y.
|
|
2016
|
24 |
2 |
p. 294-303
10 p.
|
artikel
|
| 25 |
Synthesis of 5-trifluoromethyl-2-sulfonylpyridine PPARβ/δ antagonists: Effects on the affinity and selectivity towards PPARβ/δ
|
Kaupang, Åsmund
|
|
2016
|
24 |
2 |
p. 247-260
14 p.
|
artikel
|
| 26 |
Synthesis, structures and urease inhibitory activity of cobalt(III) complexes with Schiff bases
|
Jing, Changling
|
|
2016
|
24 |
2 |
p. 270-276
7 p.
|
artikel
|
| 27 |
The indole alkaloid meleagrin, from the olive tree endophytic fungus Penicillium chrysogenum, as a novel lead for the control of c-Met-dependent breast cancer proliferation, migration and invasion
|
Mady, Mohamed S.
|
|
2016
|
24 |
2 |
p. 113-122
10 p.
|
artikel
|
| 28 |
Triazole-curcuminoids: A new class of derivatives for ‘tuning’ curcumin bioactivities?
|
Caprioglio, Diego
|
|
2016
|
24 |
2 |
p. 140-152
13 p.
|
artikel
|
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