| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A concise synthesis and evaluation of new malonamide derivatives as potential α-glucosidase inhibitors
|
Islam, Mohammad Shahidul
|
|
2016
|
24 |
8 |
p. 1675-1682
8 p.
|
artikel
|
| 2 |
Antiretroviral (HIV-1) activity of azulene derivatives
|
Peet, Julia
|
|
2016
|
24 |
8 |
p. 1653-1657
5 p.
|
artikel
|
| 3 |
C-3 benzoic acid derivatives of C-3 deoxybetulinic acid and deoxybetulin as HIV-1 maturation inhibitors
|
Liu, Zheng
|
|
2016
|
24 |
8 |
p. 1757-1770
14 p.
|
artikel
|
| 4 |
Compound profiling and 3D-QSAR studies of hydrazone derivatives with activity against intracellular Trypanosoma cruzi
|
Costa, Lívia Bandeira
|
|
2016
|
24 |
8 |
p. 1608-1618
11 p.
|
artikel
|
| 5 |
Design and evaluation of novel glutaminase inhibitors
|
McDermott, Lee A.
|
|
2016
|
24 |
8 |
p. 1819-1839
21 p.
|
artikel
|
| 6 |
Design and synthesis of small molecule-sulfotyrosine mimetics that inhibit HIV-1 entry
|
Dogo-Isonagie, Cajetan
|
|
2016
|
24 |
8 |
p. 1718-1728
11 p.
|
artikel
|
| 7 |
Design and synthesis of thiourea derivatives with sulfur-containing heterocyclic scaffolds as potential tyrosinase inhibitors
|
Liu, Pingping
|
|
2016
|
24 |
8 |
p. 1866-1871
6 p.
|
artikel
|
| 8 |
Design, physico-chemical properties and biological evaluation of some new N-[(phenoxy)alkyl]- and N-{2-[2-(phenoxy)ethoxy]ethyl}aminoalkanols as anticonvulsant agents
|
Waszkielewicz, A.M.
|
|
2016
|
24 |
8 |
p. 1793-1810
18 p.
|
artikel
|
| 9 |
Design, synthesis and biological evaluation of N,N-3-phenyl-3-benzylaminopropanamide derivatives as novel cholesteryl ester transfer protein inhibitor
|
Zhao, Dongmei
|
|
2016
|
24 |
8 |
p. 1589-1597
9 p.
|
artikel
|
| 10 |
Design, synthesis, and evaluation of 2-piperidone derivatives for the inhibition of β-amyloid aggregation and inflammation mediated neurotoxicity
|
Li, Lei
|
|
2016
|
24 |
8 |
p. 1853-1865
13 p.
|
artikel
|
| 11 |
Design, synthesis of phenstatin/isocombretastatin-oxindole conjugates as antimitotic agents
|
Kumar, G. Bharath
|
|
2016
|
24 |
8 |
p. 1729-1740
12 p.
|
artikel
|
| 12 |
Design, synthesis, topoisomerase I & II inhibitory activity, antiproliferative activity, and structure–activity relationship study of pyrazoline derivatives: An ATP-competitive human topoisomerase IIα catalytic inhibitor
|
Ahmad, Pervez
|
|
2016
|
24 |
8 |
p. 1898-1908
11 p.
|
artikel
|
| 13 |
Development of a fluorescent cardiomyocyte specific binding probe
|
Pes, Lara
|
|
2016
|
24 |
8 |
p. 1706-1717
12 p.
|
artikel
|
| 14 |
Development of a potent 2-oxoamide inhibitor of secreted phospholipase A2 guided by molecular docking calculations and molecular dynamics simulations
|
Vasilakaki, Sofia
|
|
2016
|
24 |
8 |
p. 1683-1695
13 p.
|
artikel
|
| 15 |
Discovery of new low-molecular-weight p53–Mdmx disruptors and their anti-cancer activities
|
Uesato, Shinichi
|
|
2016
|
24 |
8 |
p. 1919-1926
8 p.
|
artikel
|
| 16 |
Discovery of novel N,N-3-phenyl-3-benzylaminopropionanilides as potent inhibitors of cholesteryl ester transfer protein in vivo
|
Xie, Honglei
|
|
2016
|
24 |
8 |
p. 1811-1818
8 p.
|
artikel
|
| 17 |
Donor substrate promiscuity of bacterial β1–3-N-acetylglucosaminyltransferases and acceptor substrate flexibility of β1–4-galactosyltransferases
|
Li, Yanhong
|
|
2016
|
24 |
8 |
p. 1696-1705
10 p.
|
artikel
|
| 18 |
Editorial board
|
|
|
2016
|
24 |
8 |
p. IFC-
1 p.
|
artikel
|
| 19 |
Evaluation of the anti-inflammatory action of curcumin analog (DM1): Effect on iNOS and COX-2 gene expression and autophagy pathways
|
Paulino, Niraldo
|
|
2016
|
24 |
8 |
p. 1927-1935
9 p.
|
artikel
|
| 20 |
Exploration of 2-benzylbenzimidazole scaffold as novel inhibitor of NF-κB
|
Boggu, PullaReddy
|
|
2016
|
24 |
8 |
p. 1872-1878
7 p.
|
artikel
|
| 21 |
Investigation of 4-amino-5-alkynylpyrimidine-2(1H)-ones as anti-mycobacterial agents
|
Garg, Gaurav
|
|
2016
|
24 |
8 |
p. 1771-1777
7 p.
|
artikel
|
| 22 |
In vivo phase II-enzymes inducers, as potential chemopreventive agents, based on the chalcone and furoxan skeletons
|
Cabrera, Mauricio
|
|
2016
|
24 |
8 |
p. 1665-1674
10 p.
|
artikel
|
| 23 |
Isatin analogs as novel inhibitors of Candida spp. β-carbonic anhydrase enzymes
|
Akdemir, Atilla
|
|
2016
|
24 |
8 |
p. 1648-1652
5 p.
|
artikel
|
| 24 |
Molecular simulation of cyclohexanyl nucleic acid (CNA) duplexes with CNA, DNA and RNA and CNA triloop and tetraloop hairpin structures
|
Froeyen, Matheus
|
|
2016
|
24 |
8 |
p. 1778-1785
8 p.
|
artikel
|
| 25 |
Novel indole-based melatonin analogues: Evaluation of antioxidant activity and protective effect against amyloid β-induced damage
|
Gurer-Orhan, Hande
|
|
2016
|
24 |
8 |
p. 1658-1664
7 p.
|
artikel
|
| 26 |
Novel nicotine analogues with potential anti-mycobacterial activity
|
Gandhi, Paresh T.
|
|
2016
|
24 |
8 |
p. 1637-1647
11 p.
|
artikel
|
| 27 |
Novel squaramides with in vitro liver stage antiplasmodial activity
|
Ribeiro, Carlos J.A.
|
|
2016
|
24 |
8 |
p. 1786-1792
7 p.
|
artikel
|
| 28 |
Novel tricyclic pyrazolo[1,5-d][1,4]benzoxazepin-5(6H)-one: Design, synthesis, model and use as hMAO-B inhibitors
|
Chen, Rui
|
|
2016
|
24 |
8 |
p. 1741-1748
8 p.
|
artikel
|
| 29 |
Quinoxalinone (Part II). Discovery of (Z)-3-(2-(pyridin-4-yl)vinyl)quinoxalinone derivates as potent VEGFR-2 kinase inhibitors
|
Shi, Leilei
|
|
2016
|
24 |
8 |
p. 1840-1852
13 p.
|
artikel
|
| 30 |
Rational design, synthesis and biological evaluation of 1,3,4-oxadiazole pyrimidine derivatives as novel pyruvate dehydrogenase complex E1 inhibitors
|
He, Haifeng
|
|
2016
|
24 |
8 |
p. 1879-1888
10 p.
|
artikel
|
| 31 |
Synthesis, and anticonvulsant activity of new amides derived from 3-methyl- or 3-ethyl-3-methyl-2,5-dioxo-pyrrolidin-1-yl-acetic acids
|
Obniska, Jolanta
|
|
2016
|
24 |
8 |
p. 1598-1607
10 p.
|
artikel
|
| 32 |
Synthesis and biological evaluation of quinoline derivatives as potential anti-prostate cancer agents and Pim-1 kinase inhibitors
|
Li, Kun
|
|
2016
|
24 |
8 |
p. 1889-1897
9 p.
|
artikel
|
| 33 |
Synthesis, and docking studies of phenylpyrimidine-carboxamide derivatives bearing 1H-pyrrolo[2,3-b]pyridine moiety as c-Met inhibitors
|
Zhu, Wufu
|
|
2016
|
24 |
8 |
p. 1749-1756
8 p.
|
artikel
|
| 34 |
Thiadiazole derivatives as New Class of β-glucuronidase inhibitors
|
Salar, Uzma
|
|
2016
|
24 |
8 |
p. 1909-1918
10 p.
|
artikel
|
| 35 |
1,2,4-Triazolyl octahydropyrrolo[2,3-b]pyrroles: A new series of potent and selective dopamine D3 receptor antagonists
|
Micheli, Fabrizio
|
|
2016
|
24 |
8 |
p. 1619-1636
18 p.
|
artikel
|
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