| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Abacavir sulfate
|
Huff, Joel R
|
|
1999
|
7 |
12 |
p. 2667-2669
3 p.
|
artikel
|
| 2 |
A comparative molecular field analysis and molecular modelling studies on pyridylimidazole type of angiotensin II antagonists
|
Yoo, Sung-eun
|
|
1999
|
7 |
12 |
p. 2971-2976
6 p.
|
artikel
|
| 3 |
A new convenient transformation of erythromycin a into clarithromycin
|
Allevi, Pietro
|
|
1999
|
7 |
12 |
p. 2749-2752
4 p.
|
artikel
|
| 4 |
Biosynthesis of 20-hydroxyecdysone in Ajuga hairy roots
|
Ohyama, Kiyoshi
|
|
1999
|
7 |
12 |
p. 2925-2930
6 p.
|
artikel
|
| 5 |
Carbonic anhydrase activators: amino acyl/dipeptidyl histamine derivatives bind with high affinity to isozymes I, II and IV and act as efficient activators
|
Supuran, Claudiu T.
|
|
1999
|
7 |
12 |
p. 2915-2923
9 p.
|
artikel
|
| 6 |
2-Carboxymethylendothal analogues as affinity probes for stabilized protein phosphatase 2A
|
Laidley, Charles W
|
|
1999
|
7 |
12 |
p. 2937-2944
8 p.
|
artikel
|
| 7 |
3-(1′,1′-Dimethylbutyl)-1-deoxy-Δ8-THC and related compounds: synthesis of selective ligands for the CB2 receptor
|
Huffman, John W.
|
|
1999
|
7 |
12 |
p. 2905-2914
10 p.
|
artikel
|
| 8 |
D-ring substituted rhazinilam analogues: semisynthesis and evaluation of antitubulin activity
|
Dupont, Christophe
|
|
1999
|
7 |
12 |
p. 2961-2969
9 p.
|
artikel
|
| 9 |
Enantioselective synthesis and biological evaluation of 5-o-carboranyl pyrimidine nucleosides
|
Mourier, Nicolas S.
|
|
1999
|
7 |
12 |
p. 2759-2766
8 p.
|
artikel
|
| 10 |
α-Galactose based neoglycopeptides. Inhibition of verotoxin binding to globotriosylceramide
|
Arya, Prabhat
|
|
1999
|
7 |
12 |
p. 2823-2833
11 p.
|
artikel
|
| 11 |
Helenanolide type sesquiterpene lactones. Part 5: The role of glutathione addition under physiological conditions
|
Schmidt, Thomas J
|
|
1999
|
7 |
12 |
p. 2849-2855
7 p.
|
artikel
|
| 12 |
1-[2-Hydroxy-3-octadecan-1′-oate]propyl-2″,2″,5″,5″-tetramethyl Pyrolidine-N-oxyl-3″-carboxylate as a potential spin probe for membrane structure studies
|
Katoch, Rita
|
|
1999
|
7 |
12 |
p. 2753-2758
6 p.
|
artikel
|
| 13 |
Mitomycin C linked to DNA minor groove binding agents: synthesis, reductive activation, DNA binding and cross-linking properties and in vitro antitumor activity
|
Paz, Manuel M
|
|
1999
|
7 |
12 |
p. 2713-2726
14 p.
|
artikel
|
| 14 |
Model studies on a synthetically facile series of N-substituted phenyl-N′-pyridin-3-yl ureas leading to 1-(3-pyridylcarbamoyl) indolines that are potent and selective 5-HT2C/2B receptor antagonists
|
Bromidge, Steven M.
|
|
1999
|
7 |
12 |
p. 2767-2773
7 p.
|
artikel
|
| 15 |
Molecular dynamics of NPY Y1 receptor activation
|
Sylte, I.
|
|
1999
|
7 |
12 |
p. 2737-2748
12 p.
|
artikel
|
| 16 |
Molecular recognition by acetylcholinesterase at the peripheral anionic site: structure–activity relationships for inhibitions by aryl carbamates
|
Lin, Gialih
|
|
1999
|
7 |
12 |
p. 2683-2689
7 p.
|
artikel
|
| 17 |
Nonpeptidic HIV protease inhibitors possessing excellent antiviral activities and therapeutic indices. PD 178390: a lead HIV protease inhibitor
|
Vara Prasad, J.V.N.
|
|
1999
|
7 |
12 |
p. 2775-2800
26 p.
|
artikel
|
| 18 |
Probing the hydrophobic pocket of farnesyltransferase: aromatic substitution of CAAX peptidomimetics leads to highly potent inhibitors
|
Qian, Yimin
|
|
1999
|
7 |
12 |
p. 3011-3024
14 p.
|
artikel
|
| 19 |
Pseudo-cyclic oligonucleotides: in vitro and in vivo properties
|
Jiang, Zhiwei
|
|
1999
|
7 |
12 |
p. 2727-2735
9 p.
|
artikel
|
| 20 |
Ring-substituted 11-oxo-11H-indeno[1,2-b]quinoline-6-carboxamides with similar patterns of cytotoxicity to the dual topo I/II inhibitor DACA
|
Deady, Leslie W.
|
|
1999
|
7 |
12 |
p. 2801-2809
9 p.
|
artikel
|
| 21 |
Substrate/inhibition studies of bacteriophage T7 RNA polymerase with the 5′-triphosphate derivative of a ring-expanded (‘fat’) nucleoside possessing potent antiviral and anticancer activities
|
Bretner, Maria
|
|
1999
|
7 |
12 |
p. 2931-2936
6 p.
|
artikel
|
| 22 |
Syntheses and studies of multiwarhead siderophore-5-fluorouridine conjugates
|
Lu, Yong
|
|
1999
|
7 |
12 |
p. 3025-3038
14 p.
|
artikel
|
| 23 |
Synthesis and anti-HIV activity of 1,1,3-trioxo-2H,4H-thieno[3,4-e][1,2,4]thiadiazines (TTDs): a new family of HIV-1 specific non-nucleoside reverse transcriptase inhibitors
|
Arranz, Ma Esther
|
|
1999
|
7 |
12 |
p. 2811-2822
12 p.
|
artikel
|
| 24 |
Synthesis and antimalarial activity in vitro of potential metabolites of ferrochloroquine and related compounds
|
Biot, C.
|
|
1999
|
7 |
12 |
p. 2843-2847
5 p.
|
artikel
|
| 25 |
Synthesis and biological activity of 4-alkoxy chalcones: potential hydrophobic modulators of p-glycoprotein-mediated multidrug resistance
|
Bois, Frédéric
|
|
1999
|
7 |
12 |
p. 2691-2695
5 p.
|
artikel
|
| 26 |
Synthesis and biological activity of 22-iodo- and (E)-20(22)-dehydro analogues of 1α,25-dihydroxyvitamin D3
|
Sicinski, Rafal R.
|
|
1999
|
7 |
12 |
p. 2877-2889
13 p.
|
artikel
|
| 27 |
Synthesis and biological evaluation of a conformationally free seco-analogue of the immunosuppressant FR901483
|
Bonjoch, J.
|
|
1999
|
7 |
12 |
p. 2891-2897
7 p.
|
artikel
|
| 28 |
Synthesis and BZR affinity of pyrazolo[1,5-a]pyrimidine derivatives. part 1: study of the structural features for BZR recognition
|
Selleri, Silvia
|
|
1999
|
7 |
12 |
p. 2705-2711
7 p.
|
artikel
|
| 29 |
Synthesis and histamine H3 receptor activity of 4-(n-alkyl)-1H-imidazoles and 4-(ω-phenylalkyl)-1H-imidazoles
|
De Esch, Iwan J.P
|
|
1999
|
7 |
12 |
p. 3003-3009
7 p.
|
artikel
|
| 30 |
Synthesis and inotropic activity of hydroindene derivatives
|
Sevillano, Luis G.
|
|
1999
|
7 |
12 |
p. 2991-3001
11 p.
|
artikel
|
| 31 |
Synthesis and β-lactamase inhibitory activity of new 6β-cysteinesulfonamidopenicillanic acids
|
Changov, Lubomir S.
|
|
1999
|
7 |
12 |
p. 2899-2904
6 p.
|
artikel
|
| 32 |
Synthesis and monoamine oxidase B substrate properties of 1-methyl-4-heteroaryl-1,2,3,6-tetrahydropyridines
|
Yu, Jian
|
|
1999
|
7 |
12 |
p. 2835-2842
8 p.
|
artikel
|
| 33 |
Synthesis of novel unnatural amino acid as a building block and its incorporation into an antimicrobial peptide
|
Oh, Jong Eun
|
|
1999
|
7 |
12 |
p. 2985-2990
6 p.
|
artikel
|
| 34 |
Synthesis of oligonucleotides containing a new azobenzene fragment with efficient photoisomerizability
|
Yamana, Kazushige
|
|
1999
|
7 |
12 |
p. 2977-2983
7 p.
|
artikel
|
| 35 |
Synthesis of peptide aldehydes via enzymatic acylation of amino aldehyde derivatives
|
Voyushina, Tatiana L.
|
|
1999
|
7 |
12 |
p. 2953-2959
7 p.
|
artikel
|
| 36 |
Synthesis of β-Substituted Naphth-1-yl Ethylamido Derivatives as New Melatoninergic agonists
|
Mathé-Allainmat, Monique
|
|
1999
|
7 |
12 |
p. 2945-2952
8 p.
|
artikel
|
| 37 |
Synthesis of the Nanomolar Photoaffinity GABAB Receptor Ligand CGP 71872 Reveals Diversity in the Tissue Distribution of GABAB Receptor Forms
|
Belley, Michel
|
|
1999
|
7 |
12 |
p. 2697-2704
8 p.
|
artikel
|
| 38 |
The molecular structure of 2α-hydroxyneoanisatin and structure–activity relationships among convulsant sesquiterpenes of the seco-prezizaane and picrotoxane types
|
Schmidt, Thomas J
|
|
1999
|
7 |
12 |
p. 2857-2865
9 p.
|
artikel
|
| 39 |
The neurokinin-1 and neurokinin-2 receptor binding sites of MDL103,392 differ
|
Greenfeder, Scott
|
|
1999
|
7 |
12 |
p. 2867-2876
10 p.
|
artikel
|
| 40 |
Towards the development of novel antibiotics: synthesis and evaluation of a mechanism-based inhibitor of Kdo8P synthase
|
Du, Shoucheng
|
|
1999
|
7 |
12 |
p. 2671-2682
12 p.
|
artikel
|
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