nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Adaptive neuro-fuzzy inference system (ANFIS): A new approach to predictive modeling in QSAR applications: A study of neuro-fuzzy modeling of PCP-based NMDA receptor antagonists
|
Buyukbingol, Erdem |
|
2007 |
15 |
12 |
p. 4265-4282 18 p. |
artikel |
2 |
A new class of nifuroxazide analogues: Synthesis of 5-nitrothiophene derivatives with antimicrobial activity against multidrug-resistant Staphylococcus aureus
|
Masunari, Andrea |
|
2007 |
15 |
12 |
p. 4229-4236 8 p. |
artikel |
3 |
Antimicrobial and cytotoxic activity of agelasine and agelasimine analogs
|
Vik, Anders |
|
2007 |
15 |
12 |
p. 4016-4037 22 p. |
artikel |
4 |
Assessing potency of c-Jun N-terminal kinase 3 (JNK3) inhibitors using 2D molecular descriptors and binary QSAR methodology
|
Ijjaali, Ismail |
|
2007 |
15 |
12 |
p. 4256-4264 9 p. |
artikel |
5 |
Binding of lectins to DNA micro-assemblies: Modification of nucleo-cages with lactose-conjugated psoralen
|
Kim, Kwonil |
|
2007 |
15 |
12 |
p. 4311-4317 7 p. |
artikel |
6 |
Double mode of inhibition-inducing interactions of 1,4-naphthoquinone with urease: Arylation versus oxidation of enzyme thiols
|
Krajewska, Barbara |
|
2007 |
15 |
12 |
p. 4144-4151 8 p. |
artikel |
7 |
Editorial board
|
|
|
2007 |
15 |
12 |
p. IFC- 1 p. |
artikel |
8 |
Evaluation of a diverse set of potential P1 carboxylic acid bioisosteres in hepatitis C virus NS3 protease inhibitors
|
Rönn, Robert |
|
2007 |
15 |
12 |
p. 4057-4068 12 p. |
artikel |
9 |
Fmoc-protected iminosugar modified asparagine derivatives as building blocks for glycomimetics-containing peptides
|
Nuti, Francesca |
|
2007 |
15 |
12 |
p. 3965-3973 9 p. |
artikel |
10 |
Graphical contents list
|
|
|
2007 |
15 |
12 |
p. 3955-3964 10 p. |
artikel |
11 |
Immunogens related to the synthetic tetrasaccharide side chain of the Bacillus anthracis exosporium
|
Saksena, Rina |
|
2007 |
15 |
12 |
p. 4283-4310 28 p. |
artikel |
12 |
Inhibitory effect of obovatal on the migration and invasion of HT1080 cells via the inhibition of MMP-2
|
Lee, Su-Kyung |
|
2007 |
15 |
12 |
p. 4085-4090 6 p. |
artikel |
13 |
Instructions to contributors
|
|
|
2007 |
15 |
12 |
p. I- 1 p. |
artikel |
14 |
In-vitro investigation of oxazol and urea analogues of morphinan at opioid receptors
|
Peng, Xuemei |
|
2007 |
15 |
12 |
p. 4106-4112 7 p. |
artikel |
15 |
Molecular modeling study for the binding of zonisamide and topiramate to the human mitochondrial carbonic anhydrase isoform VA
|
Vitale, Rosa Maria |
|
2007 |
15 |
12 |
p. 4152-4158 7 p. |
artikel |
16 |
Novel cationic lipophilic peptides for oligodeoxynucleotide delivery
|
Chan, Enoch |
|
2007 |
15 |
12 |
p. 4091-4097 7 p. |
artikel |
17 |
Oxidation of C4-hydroxyphenyl 1,4-dihydropyridines in dimethylsulfoxide and its reactivity towards alkylperoxyl radicals in aqueous medium
|
Núñez-Vergara, Luis J. |
|
2007 |
15 |
12 |
p. 4318-4326 9 p. |
artikel |
18 |
Probing the receptor interactions of an H5 avian influenza virus using a baculovirus expression system and functionalised poly(acrylic acid) ligands
|
Barclay, Wendy S. |
|
2007 |
15 |
12 |
p. 4038-4047 10 p. |
artikel |
19 |
Prodrug-based design, synthesis, and biological evaluation of N-benzenesulfonylpiperidine derivatives as novel, orally active factor Xa inhibitors
|
Ishihara, Tsukasa |
|
2007 |
15 |
12 |
p. 4175-4192 18 p. |
artikel |
20 |
Radioiodination of new EGFR inhibitors as potential SPECT agents for molecular imaging of breast cancer
|
Fernandes, Célia |
|
2007 |
15 |
12 |
p. 3974-3980 7 p. |
artikel |
21 |
Scaffold hopping, synthesis and structure–activity relationships of 5,6-diaryl-pyrazine-2-amide derivatives: A novel series of CB1 receptor antagonists
|
Boström, Jonas |
|
2007 |
15 |
12 |
p. 4077-4084 8 p. |
artikel |
22 |
Studies of interactions between platinum(II) complexes and some biologically relevant molecules
|
Petrović, Dejan |
|
2007 |
15 |
12 |
p. 4203-4211 9 p. |
artikel |
23 |
2,3,5-Substituted tetrahydrofurans as cancer chemopreventives. Part 1: Synthesis and anti-cancer activities of 5-hydroxymethyl-2,3-diaryl-tetrahydro-furan-3-ols
|
Singh, Palwinder |
|
2007 |
15 |
12 |
p. 3990-3996 7 p. |
artikel |
24 |
Synthesis and antifungal activities of 5-(3,4,5-trimethoxyphenyl)-2-sulfonyl-1,3,4-thiadiazole and 5-(3,4,5-trimethoxyphenyl)-2-sulfonyl-1,3,4-oxadiazole derivatives
|
Chen, Cai-Jun |
|
2007 |
15 |
12 |
p. 3981-3989 9 p. |
artikel |
25 |
Synthesis and anti-HIV activity of trivalent CD4-mimetic miniproteins
|
Li, Hengguang |
|
2007 |
15 |
12 |
p. 4220-4228 9 p. |
artikel |
26 |
Synthesis and biological evaluation of new 6-s-cis locked 1,2,25-trihydroxyprevitamin D3 analogues
|
Sánchez-Abella, Laura |
|
2007 |
15 |
12 |
p. 4193-4202 10 p. |
artikel |
27 |
Synthesis and biological evaluation of phosphino dipeptide isostere inhibitor of human β-secretase (BACE1)
|
Manzenrieder, Florian |
|
2007 |
15 |
12 |
p. 4136-4143 8 p. |
artikel |
28 |
Synthesis and evaluation of amino-threoses in d- and l-series: Are five membered ring amino-sugars more potent glycosidase inhibitors than the six membered ones?
|
Chevrier, Carine |
|
2007 |
15 |
12 |
p. 4125-4135 11 p. |
artikel |
29 |
Synthesis and glycogen phosphorylase inhibitor activity of 2,3-dihydrobenzo[1,4]dioxin derivatives
|
Juhász, László |
|
2007 |
15 |
12 |
p. 4048-4056 9 p. |
artikel |
30 |
Synthesis and pharmacological investigation of novel 4-benzyl-1-substituted-4H-[1,2,4]triazolo[4,3-a]quinazolin-5-ones as new class of H1-antihistaminic agents
|
Alagarsamy, V. |
|
2007 |
15 |
12 |
p. 4009-4015 7 p. |
artikel |
31 |
Synthesis and topoisomerase poisoning activity of A-ring and E-ring substituted luotonin A derivatives
|
Nacro, Kassoum |
|
2007 |
15 |
12 |
p. 4237-4246 10 p. |
artikel |
32 |
Synthesis, antimicrobial, and QSAR studies of substituted benzamides
|
Kumar, Anil |
|
2007 |
15 |
12 |
p. 4113-4124 12 p. |
artikel |
33 |
Synthesis, inhibition and binding of simple non-nitrogen inhibitors of monoamine transporters
|
Petersen, Mikkel Due |
|
2007 |
15 |
12 |
p. 4159-4174 16 p. |
artikel |
34 |
Synthesis of andrographolide derivatives: A new family of α-glucosidase inhibitors
|
Xu, Hai-Wei |
|
2007 |
15 |
12 |
p. 4247-4255 9 p. |
artikel |
35 |
Synthesis of 1,3-diphenyl-2-propen-1-one derivatives and evaluation of their biological activities
|
Jang, Soyong |
|
2007 |
15 |
12 |
p. 4098-4105 8 p. |
artikel |
36 |
Synthesis of new S-derivatives of clubbed triazolyl thiazole as anti-Mycobacterium tuberculosis agents
|
Shiradkar, Mahendra Ramesh |
|
2007 |
15 |
12 |
p. 3997-4008 12 p. |
artikel |
37 |
Synthesis of pH-sensitive amphotericin B–poly(ethylene glycol) conjugates and study of their controlled release in vitro
|
Sedlák, Miloš |
|
2007 |
15 |
12 |
p. 4069-4076 8 p. |
artikel |
38 |
Synthesis, structure, and structure–activity relationship analysis of enamines as potential antibacterials
|
Xiao, Zhu-Ping |
|
2007 |
15 |
12 |
p. 4212-4219 8 p. |
artikel |