| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Ascaroside activity in Caenorhabditis elegans is highly dependent on chemical structure
|
Hollister, Kyle A.
|
|
2013
|
21 |
18 |
p. 5754-5769
16 p.
|
artikel
|
| 2 |
Bioorganic & Medicinal Chemistry Reviews and Perspectives
|
|
|
2013
|
21 |
18 |
p. I-IV
nvt p.
|
artikel
|
| 3 |
Biotransformation of ent-pimaradienoic acid by cell cultures of Aspergillus niger
|
Severiano, Marcela E.
|
|
2013
|
21 |
18 |
p. 5870-5875
6 p.
|
artikel
|
| 4 |
Chrysophaentins are competitive inhibitors of FtsZ and inhibit Z-ring formation in live bacteria
|
Keffer, Jessica L.
|
|
2013
|
21 |
18 |
p. 5673-5678
6 p.
|
artikel
|
| 5 |
Design, stereoselective synthesis, and biological evaluation of novel tri-cyclic compounds as inhibitor of apoptosis proteins (IAP) antagonists
|
Asano, Moriteru
|
|
2013
|
21 |
18 |
p. 5725-5737
13 p.
|
artikel
|
| 6 |
Development of a pharmacophore model for the catecholamine release-inhibitory peptide catestatin: Virtual screening and functional testing identify novel small molecule therapeutics of hypertension
|
Tsigelny, Igor F.
|
|
2013
|
21 |
18 |
p. 5855-5869
15 p.
|
artikel
|
| 7 |
Editorial board
|
|
|
2013
|
21 |
18 |
p. IFC-
1 p.
|
artikel
|
| 8 |
Exploration of N-(2-aminoethyl)piperidine-4-carboxamide as a potential scaffold for development of VEGFR-2, ERK-2 and Abl-1 multikinase inhibitor
|
Jin, Feng
|
|
2013
|
21 |
18 |
p. 5694-5706
13 p.
|
artikel
|
| 9 |
Fine tuning of the pH-dependent drug release rate from polyHPMA-ellipticinium conjugates
|
Sedláček, Ondřej
|
|
2013
|
21 |
18 |
p. 5669-5672
4 p.
|
artikel
|
| 10 |
Graphical contents list
|
|
|
2013
|
21 |
18 |
p. 5649-5656
8 p.
|
artikel
|
| 11 |
Identification of 2,3-disubstituted pyridines as potent, orally active PDE4 inhibitors
|
Kato, Yoshihiro
|
|
2013
|
21 |
18 |
p. 5851-5854
4 p.
|
artikel
|
| 12 |
Investigation of acyclic uridine amide and 5′-amido nucleoside analogues as potential inhibitors of the Plasmodium falciparum dUTPase
|
Hampton, Shahienaz E.
|
|
2013
|
21 |
18 |
p. 5876-5885
10 p.
|
artikel
|
| 13 |
Medicinal attributes of pyrazolo[3,4-d]pyrimidines: A review
|
Chauhan, Monika
|
|
2013
|
21 |
18 |
p. 5657-5668
12 p.
|
artikel
|
| 14 |
Metallo-β-lactamase inhibitory activity of 3-alkyloxy and 3-amino phthalic acid derivatives and their combination effect with carbapenem
|
Hiraiwa, Yukiko
|
|
2013
|
21 |
18 |
p. 5841-5850
10 p.
|
artikel
|
| 15 |
New potent and selective polyfluoroalkyl ketone inhibitors of GVIA calcium-independent phospholipase A2
|
Magrioti, Victoria
|
|
2013
|
21 |
18 |
p. 5823-5829
7 p.
|
artikel
|
| 16 |
N-Heteroarylmethyl-5-hydroxy-1,2,5,6-tetrahydropyridine-3-carboxylic acid a novel scaffold for the design of uncompetitive α-glucosidase inhibitors
|
Long, Sha
|
|
2013
|
21 |
18 |
p. 5811-5822
12 p.
|
artikel
|
| 17 |
NMR determination of Electrophorus electricus acetylcholinesterase inhibition and reactivation by neutral oximes
|
da Cunha Xavier Soares, Sibelle Feitosa
|
|
2013
|
21 |
18 |
p. 5923-5930
8 p.
|
artikel
|
| 18 |
Prodrugs of N-dicarboximide derivatives of the rat selective toxicant norbormide
|
Rennison, David
|
|
2013
|
21 |
18 |
p. 5886-5899
14 p.
|
artikel
|
| 19 |
Spectroscopic, computational modeling and cytotoxicity of a series of meso-phenyl and meso-thienyl-BODIPYs
|
Gibbs, Jaime H.
|
|
2013
|
21 |
18 |
p. 5770-5781
12 p.
|
artikel
|
| 20 |
Structural studies of β-hairpin peptidomimetic antibiotics that target LptD in Pseudomonas sp.
|
Schmidt, Jasmin
|
|
2013
|
21 |
18 |
p. 5806-5810
5 p.
|
artikel
|
| 21 |
Synthesis and biological activity of (24E)- and (24Z)-26-hydroxydesmosterol
|
Saini, Ratni
|
|
2013
|
21 |
18 |
p. 5794-5798
5 p.
|
artikel
|
| 22 |
Synthesis and biological evaluation of 1,7,8,8a-tetrahydro-3H-oxazolo[3,4-a]pyrazin-6(5H)-ones as antitumoral agents
|
Chiacchio, Ugo
|
|
2013
|
21 |
18 |
p. 5748-5753
6 p.
|
artikel
|
| 23 |
Synthesis and biological evaluation of berberine–thiophenyl hybrids as multi-functional agents: Inhibition of acetylcholinesterase, butyrylcholinesterase, and Aβ aggregation and antioxidant activity
|
Su, Tao
|
|
2013
|
21 |
18 |
p. 5830-5840
11 p.
|
artikel
|
| 24 |
Synthesis and biological evaluation of furopyrimidine N,O-nucleosides
|
Romeo, Roberto
|
|
2013
|
21 |
18 |
p. 5688-5693
6 p.
|
artikel
|
| 25 |
Synthesis and biological evaluation of novel benzyl-substituted (S)-phenylalanine derivatives as potent dipeptidyl peptidase 4 inhibitors
|
Liu, Yang
|
|
2013
|
21 |
18 |
p. 5679-5687
9 p.
|
artikel
|
| 26 |
Synthesis and evaluation of heteroaryl substituted diazaspirocycles as scaffolds to probe the ATP-binding site of protein kinases
|
Allen, Charlotte E.
|
|
2013
|
21 |
18 |
p. 5707-5724
18 p.
|
artikel
|
| 27 |
Synthesis and evaluation of novel 3-(3,5-dimethylbenzyl)uracil analogs as potential anti-HIV-1 agents
|
Sakakibara, Norikazu
|
|
2013
|
21 |
18 |
p. 5900-5906
7 p.
|
artikel
|
| 28 |
Synthesis and optimization of novel (3S,5R)-5-(2,2-dimethyl-5-oxo-4-phenylpiperazin-1-yl)piperidine-3-carboxamides as orally active renin inhibitors
|
Mori, Yutaka
|
|
2013
|
21 |
18 |
p. 5907-5922
16 p.
|
artikel
|
| 29 |
Synthesis, enzyme kinetics and computational evaluation of N-(β-d-glucopyranosyl) oxadiazolecarboxamides as glycogen phosphorylase inhibitors
|
Polyák, Mária
|
|
2013
|
21 |
18 |
p. 5738-5747
10 p.
|
artikel
|
| 30 |
Synthesis of imine-pyrazolopyrimidinones and their mechanistic interventions on anticancer activity
|
Baviskar, Ashish T.
|
|
2013
|
21 |
18 |
p. 5782-5793
12 p.
|
artikel
|
| 31 |
Synthesis of novel acridine and bis acridine sulfonamides with effective inhibitory activity against the cytosolic carbonic anhydrase isoforms II and VII
|
Ulus, Ramazan
|
|
2013
|
21 |
18 |
p. 5799-5805
7 p.
|
artikel
|
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