| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acetylcholinesterase inhibitors from the toadstool Cortinarius infractus
|
Geissler, Torsten
|
|
2010
|
18 |
6 |
p. 2173-2177
5 p.
|
artikel
|
| 2 |
A class of novel Schiff’s bases: Synthesis, therapeutic action for chronic pain, anti-inflammation and 3D QSAR analysis
|
Zhou, Yinjian
|
|
2010
|
18 |
6 |
p. 2165-2172
8 p.
|
artikel
|
| 3 |
Alstiphyllanines E–H, picraline and ajmaline-type alkaloids from Alstonia macrophylla inhibiting sodium glucose cotransporter
|
Arai, Hiroko
|
|
2010
|
18 |
6 |
p. 2152-2158
7 p.
|
artikel
|
| 4 |
2-Amino-5-benzoyl-4-phenylthiazoles: Development of potent and selective adenosine A1 receptor antagonists
|
Scheiff, Anja B.
|
|
2010
|
18 |
6 |
p. 2195-2203
9 p.
|
artikel
|
| 5 |
Carbonic anhydrase activators. The first activation study of a coral secretory isoform with amino acids and amines
|
Bertucci, Anthony
|
|
2010
|
18 |
6 |
p. 2300-2303
4 p.
|
artikel
|
| 6 |
Carbonic anhydrase inhibitors. Inhibition of mammalian isoforms I–XIV with a series of natural product polyphenols and phenolic acids
|
Innocenti, Alessio
|
|
2010
|
18 |
6 |
p. 2159-2164
6 p.
|
artikel
|
| 7 |
Chemical biology studies on norrisolide
|
Guizzunti, Gianni
|
|
2010
|
18 |
6 |
p. 2115-2122
8 p.
|
artikel
|
| 8 |
Corrigendum to “Inhibitors of human tyrosyl-DNA phospodiesterase (hTdp1) developed by virtual screening using ligand-based pharmacophores” [Bioorg. Med. Chem. 18 (2010) 182–189]
|
Weidlich, Iwona E.
|
|
2010
|
18 |
6 |
p. 2346-
1 p.
|
artikel
|
| 9 |
Cytotoxic 2-benzylidene-6-(nitrobenzylidene)cyclohexanones which display substantially greater toxicity for neoplasms than non-malignant cells
|
Das, Umashankar
|
|
2010
|
18 |
6 |
p. 2219-2224
6 p.
|
artikel
|
| 10 |
Design and synthesis of novel series of pyrrole based chemotypes and their evaluation as selective aldose reductase inhibitors. A case of bioisosterism between a carboxylic acid moiety and that of a tetrazole
|
Pegklidou, Kyriaki
|
|
2010
|
18 |
6 |
p. 2107-2114
8 p.
|
artikel
|
| 11 |
Design, synthesis and evaluation of (E)-α-benzylthio chalcones as novel inhibitors of BCR-ABL kinase
|
Reddy, M.V. Ramana
|
|
2010
|
18 |
6 |
p. 2317-2326
10 p.
|
artikel
|
| 12 |
Differential binding of phenothiazine urea derivatives to wild-type human cholinesterases and butyrylcholinesterase mutants
|
Darvesh, Sultan
|
|
2010
|
18 |
6 |
p. 2232-2244
13 p.
|
artikel
|
| 13 |
Editorial board
|
|
|
2010
|
18 |
6 |
p. IFC-
1 p.
|
artikel
|
| 14 |
Efflux-mediated bis-indole resistance in Staphylococcus aureus reveals differential substrate specificities for MepA and MepR
|
Opperman, Timothy J.
|
|
2010
|
18 |
6 |
p. 2123-2130
8 p.
|
artikel
|
| 15 |
Exploration of inhibitors for diaminopimelate aminotransferase
|
Fan, Chenguang
|
|
2010
|
18 |
6 |
p. 2141-2151
11 p.
|
artikel
|
| 16 |
Gentisides A and B, two new neuritogenic compounds from the traditional Chinese medicine Gentiana rigescens Franch
|
Gao, Lijuan
|
|
2010
|
18 |
6 |
p. 2131-2134
4 p.
|
artikel
|
| 17 |
Graphical contents list
|
|
|
2010
|
18 |
6 |
p. 2067-2075
9 p.
|
artikel
|
| 18 |
In silico search for multi-target anti-inflammatories in Chinese herbs and formulas
|
Ehrman, Thomas M.
|
|
2010
|
18 |
6 |
p. 2204-2218
15 p.
|
artikel
|
| 19 |
Melanogenesis inhibitors from the desert plant Anastatica hierochuntica in B16 melanoma cells
|
Nakashima, Souichi
|
|
2010
|
18 |
6 |
p. 2337-2345
9 p.
|
artikel
|
| 20 |
Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species
|
Prado-Prado, Francisco J.
|
|
2010
|
18 |
6 |
p. 2225-2231
7 p.
|
artikel
|
| 21 |
Novel C-aryl glucoside SGLT2 inhibitors as potential antidiabetic agents: 1,3,4-Thiadiazolylmethylphenyl glucoside congeners
|
Lee, Junwon
|
|
2010
|
18 |
6 |
p. 2178-2194
17 p.
|
artikel
|
| 22 |
Pharmacophore modeling, resistant mutant isolation, docking, and MM-PBSA analysis: Combined experimental/computer-assisted approaches to identify new inhibitors of the bovine viral diarrhea virus (BVDV)
|
Tonelli, Michele
|
|
2010
|
18 |
6 |
p. 2304-2316
13 p.
|
artikel
|
| 23 |
Potent DNA-directed alkylating agents: Synthesis and biological activity of phenyl N-mustard–quinoline conjugates having a urea or hydrazinecarboxamide linker
|
Kakadiya, Rajesh
|
|
2010
|
18 |
6 |
p. 2285-2299
15 p.
|
artikel
|
| 24 |
SAR and molecular mechanism study of novel acylhydrazone compounds targeting HIV-1 CA
|
Jin, Yinxue
|
|
2010
|
18 |
6 |
p. 2135-2140
6 p.
|
artikel
|
| 25 |
Structural-based design and synthesis of novel 9-deazaguanine derivatives having a phosphate mimic as multi-substrate analogue inhibitors for mammalian PNPs
|
Hikishima, Sadao
|
|
2010
|
18 |
6 |
p. 2275-2284
10 p.
|
artikel
|
| 26 |
Structural basis for the design of novel Schiff base metal chelate inhibitors of trypsin
|
Iyaguchi, Daisuke
|
|
2010
|
18 |
6 |
p. 2076-2080
5 p.
|
artikel
|
| 27 |
Synthesis and biological evaluation of 2′,5′-dimethoxychalcone derivatives as microtubule-targeted anticancer agents
|
Tu, Huang-Yao
|
|
2010
|
18 |
6 |
p. 2089-2098
10 p.
|
artikel
|
| 28 |
Synthesis and bradykinin inhibitory activity of novel non-peptide compounds, and evaluation of in vivo analgesic activity
|
Kam, Yoo Lim
|
|
2010
|
18 |
6 |
p. 2327-2336
10 p.
|
artikel
|
| 29 |
Synthesis and in vitro biological evaluation of carbon-11-labeled quinoline derivatives as new candidate PET radioligands for cannabinoid CB2 receptor imaging
|
Gao, Mingzhang
|
|
2010
|
18 |
6 |
p. 2099-2106
8 p.
|
artikel
|
| 30 |
Synthesis and kinetic analysis of some phosphonate analogs of cyclophostin as inhibitors of human acetylcholinesterase
|
Dutta, Supratik
|
|
2010
|
18 |
6 |
p. 2265-2274
10 p.
|
artikel
|
| 31 |
Synthesis of theophylline derivatives and study of their activity as antagonists at adenosine receptors
|
Hierrezuelo, Jesús
|
|
2010
|
18 |
6 |
p. 2081-2088
8 p.
|
artikel
|
| 32 |
Synthesis of 2-(thienyl-2-yl or -3-yl)-4-furyl-6-aryl pyridine derivatives and evaluation of their topoisomerase I and II inhibitory activity, cytotoxicity, and structure–activity relationship
|
Thapa, Pritam
|
|
2010
|
18 |
6 |
p. 2245-2254
10 p.
|
artikel
|
| 33 |
Synthesis, radiofluorination, and hypoxia-selective studies of FRAZ: A configurational and positional analogue of the clinical hypoxia marker, [18F]-FAZA
|
Kumar, Piyush
|
|
2010
|
18 |
6 |
p. 2255-2264
10 p.
|
artikel
|
| 34 |
Virtual screening using ligand-based pharmacophores for inhibitors of human tyrosyl-DNA phospodiesterase (hTdp1)
|
Weidlich, Iwona E.
|
|
2010
|
18 |
6 |
p. 2347-2355
9 p.
|
artikel
|
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