| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acid-sensitive polyethylene glycol conjugates of doxorubicin: preparation, in vitro efficacy and intracellular distribution
|
Rodrigues, Paula C.A.
|
|
1999
|
7 |
11 |
p. 2517-2524
|
artikel
|
| 2 |
Altering the specificity of subtilisin Bacillus lentus through the introduction of positive charge at single amino acid sites
|
Davis, Benjamin G.
|
|
1999
|
7 |
11 |
p. 2303-2311
|
artikel
|
| 3 |
Application of comparative molecular field analysis to dopamine d2 partial agonists
|
McGaughey, Georgia B
|
|
1999
|
7 |
11 |
p. 2453-2456
|
artikel
|
| 4 |
Aromatic carboxylic acids as farnesyl surrogates in farnesylpyrophosphate-based farnesyltransferase inhibitors
|
Schlitzer, Martin
|
|
1999
|
7 |
11 |
p. 2391-2395
|
artikel
|
| 5 |
Benzimidazole derivatives. Part 1: Synthesis and structure–activity relationships of new benzimidazole-4-carboxamides and carboxylates as potent and selective 5-HT4 receptor antagonists
|
López-Rodrı́guez, Marı́a L.
|
|
1999
|
7 |
11 |
p. 2271-2281
|
artikel
|
| 6 |
Biomimetic oxidation of ibuprofen with hydrogen peroxide catalysed by horseradish peroxidase (HRP) and 5,10,15,20- tetrakis-(2′,6′-dichloro-3′-sulphonatophenyl)porphyrinatoiron(III) and manganese(III) hydrates in AOT reverse micelles
|
Chauhan, S.M.S.
|
|
1999
|
7 |
11 |
p. 2629-2634
|
artikel
|
| 7 |
Carbonic anhydrase inhibitors
|
Borras, Joaquin
|
|
1999
|
7 |
11 |
p. 2397-2406
|
artikel
|
| 8 |
Cell binding, uptake and cytosolic partition of HIV anti-gag Phosphodiester oligonucleotides 3′-linked to cholesterol derivatives in macrophages
|
LeDoan, Trung
|
|
1999
|
7 |
11 |
p. 2263-2269
|
artikel
|
| 9 |
Cleavage of abasic sites in DNA by intercalator-amines
|
Steullet, Vera
|
|
1999
|
7 |
11 |
p. 2531-2540
|
artikel
|
| 10 |
Comparative molecular field analysis (CoMFA) and docking studies of non-nucleoside HIV-1 RT inhibitors (NNIs)
|
Barreca, M.L.
|
|
1999
|
7 |
11 |
p. 2283-2292
|
artikel
|
| 11 |
Comparative molecular field analysis of some pyridazinone-containing α1-Antagonists
|
Cinone, N.
|
|
1999
|
7 |
11 |
p. 2615-2620
|
artikel
|
| 12 |
Cross-linking of proteins by maillard processes: characterization and detection of lysine–arginine cross-links derived from glyoxal and methylglyoxal
|
Lederer, Markus O
|
|
1999
|
7 |
11 |
p. 2499-2507
|
artikel
|
| 13 |
C5-Substituted Derivatives of 5-OMe-BPAT: Synthesis and Interactions with Dopamine D2 and Serotonin 5-HT1A Receptors
|
Homan, Evert J.
|
|
1999
|
7 |
11 |
p. 2541-2548
|
artikel
|
| 14 |
Dual-site binding of bivalent 4-aminopyridine- and 4-aminoquinoline-based AChE inhibitors: contribution of the hydrophobic alkylene tether to monomer and dimer affinities
|
Han, Yi Fan
|
|
1999
|
7 |
11 |
p. 2569-2575
|
artikel
|
| 15 |
Evidences for adduct formation between intracellular non-protein thiols and nitroazoles possessing an α,β-unsaturated carbonyl side chain and the effects on radiosensitization of hypoxic cells
|
Zhou, Ling
|
|
1999
|
7 |
11 |
p. 2591-2598
|
artikel
|
| 16 |
Hydrophobic benzoic acids as inhibitors of influenza neuraminidase
|
Atigadda, Venkatram R.
|
|
1999
|
7 |
11 |
p. 2487-2497
|
artikel
|
| 17 |
Improved synthesis of the bifunctional chelating agent 1,4,7,10-tetraaza-N-(1-carboxy-3-(4-nitrophenyl)propyl)-N′,N″,N‴-tris(acetic acid)cyclododecane (PA-DOTA)
|
Chappell, Lara L.
|
|
1999
|
7 |
11 |
p. 2313-2320
|
artikel
|
| 18 |
Inhibition of transcription factor NF-κB by sesquiterpene lactones: a proposed molecular mechanism of action
|
Rüngeler, Peter
|
|
1999
|
7 |
11 |
p. 2343-2352
|
artikel
|
| 19 |
In search of new chemical entities with spermicidal and anti-HIV activities
|
Srivastava, Seema
|
|
1999
|
7 |
11 |
p. 2607-2613
|
artikel
|
| 20 |
J-104129, a novel muscarinic M3 receptor antagonist with high selectivity for M3 over M2 receptors
|
Mitsuya, Morihiro
|
|
1999
|
7 |
11 |
p. 2555-2567
|
artikel
|
| 21 |
Microbial models of drug metabolism: microbial transformations of trimegestone® (RU27987), a 3-Keto-Δ4,9(10)-19-norsteroid drug
|
Lacroix, Isabelle
|
|
1999
|
7 |
11 |
p. 2329-2341
|
artikel
|
| 22 |
Molecular recognition of tyrosinyl adenylate analogues by prokaryotic tyrosyl tRNA synthetases
|
Brown, Pamela
|
|
1999
|
7 |
11 |
p. 2473-2485
|
artikel
|
| 23 |
Quantitative structure–activity relationship studies on cyclic cyanoguanidines acting as HIV-1 protease inhibitors
|
Gupta, S.P.
|
|
1999
|
7 |
11 |
p. 2549-2553
|
artikel
|
| 24 |
Reaction of dopamine with d-glyceraldehyde under biomimetic conditions: stereoselective formation of tetrahydroisoquinolines and rate-accelerating effects of transition metal ions
|
Manini, Paola
|
|
1999
|
7 |
11 |
p. 2525-2530
|
artikel
|
| 25 |
Relevance of theoretical molecular descriptors in quantitative structure–activity relationship analysis of α1-adrenergic receptor antagonists
|
Menziani, M.C.
|
|
1999
|
7 |
11 |
p. 2437-2451
|
artikel
|
| 26 |
Structure–activity studies on 4-substituted-2-anilinopyrimidine corticotropin releasing factor (CRF) antagonists
|
Gilligan, Paul J.
|
|
1999
|
7 |
11 |
p. 2321-2328
|
artikel
|
| 27 |
Studies on 6-Aminoquinolones: synthesis and antibacterial evaluation of 6-amino-8-ethyl- and 6-amino-8-methoxyquinolones
|
Cecchetti, Violetta
|
|
1999
|
7 |
11 |
p. 2465-2471
|
artikel
|
| 28 |
Studies on Anti-Helicobacter pylori Agents. Part 1: Benzyloxyisoquinoline Derivatives
|
Yoshida, Yoshiki
|
|
1999
|
7 |
11 |
p. 2647-2666
|
artikel
|
| 29 |
Studies on β-d-Gal f -(1→4)-α-l-Rha p octyl analogues as substrates for mycobacterial galactosyl transferase activity
|
Pathak, Ashish K.
|
|
1999
|
7 |
11 |
p. 2407-2413
|
artikel
|
| 30 |
Synthesis and anti-HIV activity of 1,3,4,5-tetrahydro-2H-1,4-benzodiazepin-2-one (TBO) derivatives. truncated 4,5,6,7-tetrahydro-5-methylimidazo[4,5,1-jk][1,4]benzodiazepin-2(1H)-ones (TIBO) analogues
|
Breslin, Henry J.
|
|
1999
|
7 |
11 |
p. 2427-2436
|
artikel
|
| 31 |
Synthesis and anti-HIV evaluation of 2′,3′-dideoxy imidazo- and ν-triazolo[4,5-d]pyridazine nucleosides
|
Bussolari, Jacqueline C.
|
|
1999
|
7 |
11 |
p. 2373-2379
|
artikel
|
| 32 |
synthesis and biological activity of 4-methyl-3,5-dioxane derivatives as thromboxane a2 receptor antagonists
|
Marusawa, Hiroshi
|
|
1999
|
7 |
11 |
p. 2635-2645
|
artikel
|
| 33 |
Synthesis, and cytotoxic activity of some novel indolo[2,3-b]quinoline derivatives
|
Kaczmarek, Łukasz
|
|
1999
|
7 |
11 |
p. 2457-2464
|
artikel
|
| 34 |
Synthesis, characterization and anticonvulsant activity of enaminones. Part 6: Synthesis of substituted vinylic benzamides as potential anticonvulsants
|
Foster, James E.
|
|
1999
|
7 |
11 |
p. 2415-2425
|
artikel
|
| 35 |
Synthesis of all possible regioisomers of scyllo-Inositol phosphate
|
Chung, Sung-Kee
|
|
1999
|
7 |
11 |
p. 2577-2589
|
artikel
|
| 36 |
The anticonvulsant activities of N-benzyl 3-methoxypropionamides
|
Andurkar, Shridhar V.
|
|
1999
|
7 |
11 |
p. 2381-2389
|
artikel
|
| 37 |
The comparison of characteristics between membrane-active antifungal peptide and its pseudopeptides
|
Oh, Jong Eun
|
|
1999
|
7 |
11 |
p. 2509-2515
|
artikel
|
| 38 |
The controlled introduction of multiple negative charge at single amino acid sites in subtilisin Bacillus lentus
|
Davis, Benjamin G.
|
|
1999
|
7 |
11 |
p. 2293-2301
|
artikel
|
| 39 |
Three-dimensional quantitative structure–activity studies of octopaminergic agonists responsible for the inhibition of sex-pheromone production in Hercoverpa armigera
|
Hirashima, Akinori
|
|
1999
|
7 |
11 |
p. 2621-2628
|
artikel
|
| 40 |
Thrombin receptor-activating peptides (TRAPs): Investigation of bioactive conformations via structure–activity, spectroscopic, and computational studies
|
Ceruso, Marco A.
|
|
1999
|
7 |
11 |
p. 2353-2371
|
artikel
|
| 41 |
Transition state analogue inhibitors of protozoan nucleoside hydrolases
|
Furneaux, Richard H.
|
|
1999
|
7 |
11 |
p. 2599-2606
|
artikel
|
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