| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
β-Amino acid substitutions and structure-based CoMFA modeling of hepatitis C virus NS3 protease inhibitors
|
Nurbo, Johanna
|
|
2008
|
16 |
10 |
p. 5590-5605
16 p.
|
artikel
|
| 2 |
An improved synthesis of arsenic–biotin conjugates
|
Heredia-Moya, Jorge
|
|
2008
|
16 |
10 |
p. 5743-5746
4 p.
|
artikel
|
| 3 |
Antiglioma action of xanthones from Gentiana kochiana: Mechanistic and structure–activity requirements
|
Isakovic, Aleksandra
|
|
2008
|
16 |
10 |
p. 5683-5694
12 p.
|
artikel
|
| 4 |
1-Aryl-2-dimethylaminomethyl-2-propen-1-one hydrochlorides and related adducts: A quest for selective cytotoxicity for malignant cells
|
Pati, Hari N.
|
|
2008
|
16 |
10 |
p. 5747-5753
7 p.
|
artikel
|
| 5 |
Cytotoxic constituents from Brazilian red propolis and their structure–activity relationship
|
Li, Feng
|
|
2008
|
16 |
10 |
p. 5434-5440
7 p.
|
artikel
|
| 6 |
Design, synthesis, and application of novel triclosan prodrugs as potential antimalarial and antibacterial agents
|
Mishra, Satyendra
|
|
2008
|
16 |
10 |
p. 5536-5546
11 p.
|
artikel
|
| 7 |
Design, synthesis and biological evaluation of substituted pyrrolo[2,3-d]pyrimidines as multiple receptor tyrosine kinase inhibitors and antiangiogenic agents
|
Gangjee, Aleem
|
|
2008
|
16 |
10 |
p. 5514-5528
15 p.
|
artikel
|
| 8 |
Design, synthesis, and biological evaluation of thiophene analogues of chalcones
|
Romagnoli, Romeo
|
|
2008
|
16 |
10 |
p. 5367-5376
10 p.
|
artikel
|
| 9 |
Design, synthesis and evaluation of novel sulfonyl pyrrolidine derivatives as matrix metalloproteinase inhibitors
|
Cheng, Xian-Chao
|
|
2008
|
16 |
10 |
p. 5398-5404
7 p.
|
artikel
|
| 10 |
Design, synthesis, and QSAR studies of novel lysine derives as amino-peptidase N/CD13 inhibitors
|
Wang, Qiang
|
|
2008
|
16 |
10 |
p. 5473-5481
9 p.
|
artikel
|
| 11 |
Development of novel water-soluble photocleavable protective group and its application for design of photoresponsive paclitaxel prodrugs
|
Noguchi, Mayo
|
|
2008
|
16 |
10 |
p. 5389-5397
9 p.
|
artikel
|
| 12 |
Editorial board
|
|
|
2008
|
16 |
10 |
p. IFC-
1 p.
|
artikel
|
| 13 |
Evaluation of the amino acid binding site of Mycobacterium tuberculosis glutamine synthetase for drug discovery
|
Nordqvist, Anneli
|
|
2008
|
16 |
10 |
p. 5501-5513
13 p.
|
artikel
|
| 14 |
Graphical contents list
|
|
|
2008
|
16 |
10 |
p. 5355-5366
12 p.
|
artikel
|
| 15 |
Halogenated derivatives QSAR model using spectral moments to predict haloacetic acids (HAA) mutagenicity
|
Pérez-Garrido, Alfonso
|
|
2008
|
16 |
10 |
p. 5720-5732
13 p.
|
artikel
|
| 16 |
Heteroaromatic ester inhibitors of hepatitis A virus 3C proteinase: Evaluation of mode of action
|
Huitema, Carly
|
|
2008
|
16 |
10 |
p. 5761-5777
17 p.
|
artikel
|
| 17 |
Instructions to contributors
|
|
|
2008
|
16 |
10 |
p. I-
1 p.
|
artikel
|
| 18 |
Muscarinic antagonists with multiple stereocenters: Synthesis, affinity profile and functional activity of isomeric 1-methyl-2-(2,2-alkylaryl-1,3-oxathiolan-5-yl)pyrrolidine sulfoxide derivatives
|
Dei, Silvia
|
|
2008
|
16 |
10 |
p. 5490-5500
11 p.
|
artikel
|
| 19 |
New R/S-3,4-dihydro-2,2-dimethyl-6-halo-4-(phenylaminothiocarbonylamino)-2H-1-benzopyrans structurally related to (±)-cromakalim as tissue-selective pancreatic β-cell KATP channel openers
|
Sebille, Sophie
|
|
2008
|
16 |
10 |
p. 5704-5719
16 p.
|
artikel
|
| 20 |
Novel anti-inflammatory agents based on pyridazinone scaffold; design, synthesis and in vivo activity
|
Abouzid, Khaled
|
|
2008
|
16 |
10 |
p. 5547-5556
10 p.
|
artikel
|
| 21 |
Peptomeric analogues of trypsin inhibitor SFTI-1 isolated from sunflower seeds
|
Łęgowska, Anna
|
|
2008
|
16 |
10 |
p. 5644-5652
9 p.
|
artikel
|
| 22 |
Petiolins A–C, phloroglucinol derivatives from Hypericum pseudopetiolatum var. kiusianum
|
Tanaka, Naonobu
|
|
2008
|
16 |
10 |
p. 5619-5623
5 p.
|
artikel
|
| 23 |
Pharmacological and pharmacokinetic characterization of 2-piperazine-α-isopropyl benzylamine derivatives as melanocortin-4 receptor antagonists
|
Chen, Chen
|
|
2008
|
16 |
10 |
p. 5606-5618
13 p.
|
artikel
|
| 24 |
Podophyllotoxin directly binds a hinge domain in E2 of HPV and inhibits an E2/E7 interaction in vitro
|
Saitoh, Takeki
|
|
2008
|
16 |
10 |
p. 5815-5825
11 p.
|
artikel
|
| 25 |
Prediction of the aqueous solvation free energy of organic compounds by using autocorrelation of molecular electrostatic potential surface properties combined with response surface analysis
|
Michielan, Lisa
|
|
2008
|
16 |
10 |
p. 5733-5742
10 p.
|
artikel
|
| 26 |
Preparation of piperazine derivatives as 5-HT7 receptor antagonists
|
Yoon, Juhee
|
|
2008
|
16 |
10 |
p. 5405-5412
8 p.
|
artikel
|
| 27 |
Redefining the structure–activity relationships of 2,6-methano-3-benzazocines. Part 6: Opioid receptor binding properties of cyclic variants of 8-carboxamidocyclazocine
|
Wentland, Mark P.
|
|
2008
|
16 |
10 |
p. 5653-5664
12 p.
|
artikel
|
| 28 |
SAR and QSAR study on 2-aminothiazole derivatives, modulators of transcriptional repression in Huntington’s disease
|
Leone, Samantha
|
|
2008
|
16 |
10 |
p. 5695-5703
9 p.
|
artikel
|
| 29 |
Sensitization to p-amino aromatic compounds: Study of the covalent binding of 2,5-dimethyl-p-benzoquinonediimine to a model peptide by electrospray ionization tandem mass spectrometry
|
Eilstein, Joan
|
|
2008
|
16 |
10 |
p. 5482-5489
8 p.
|
artikel
|
| 30 |
Sulfadiazine/hydroxypropyl-β-cyclodextrin host–guest system: Characterization, phase-solubility and molecular modeling
|
de Araújo, Márcia Valéria Gaspar
|
|
2008
|
16 |
10 |
p. 5788-5794
7 p.
|
artikel
|
| 31 |
Synthesis and activity of tetrapeptidic HTLV-I protease inhibitors possessing different P3-cap moieties
|
Zhang, Meihui
|
|
2008
|
16 |
10 |
p. 5795-5802
8 p.
|
artikel
|
| 32 |
Synthesis and anti-platelet evaluation of 2-benzoylaminobenzoate analogs
|
Hsieh, Pei-Wen
|
|
2008
|
16 |
10 |
p. 5803-5814
12 p.
|
artikel
|
| 33 |
Synthesis and biochemical application of 2′-O-methyl-3′-thioguanosine as a probe to explore group I intron catalysis
|
Lu, Jun
|
|
2008
|
16 |
10 |
p. 5754-5760
7 p.
|
artikel
|
| 34 |
Synthesis and biological activity of stable and potent antitumor agents, aniline nitrogen mustards linked to 9-anilinoacridines via a urea linkage
|
Kapuriya, Naval
|
|
2008
|
16 |
10 |
p. 5413-5423
11 p.
|
artikel
|
| 35 |
Synthesis and DNA cleaving activity of water-soluble non-conjugated thienyl tetraynes
|
Torikai, Kohei
|
|
2008
|
16 |
10 |
p. 5441-5451
11 p.
|
artikel
|
| 36 |
Synthesis and in vitro PDT activity of miscellaneous porphyrins with amino acid and uracil
|
Weimin, Shi
|
|
2008
|
16 |
10 |
p. 5665-5671
7 p.
|
artikel
|
| 37 |
Synthesis and preliminary evaluation of some substituted coumarins as anticonvulsant agents
|
Amin, Kamelia M.
|
|
2008
|
16 |
10 |
p. 5377-5388
12 p.
|
artikel
|
| 38 |
Synthesis and receptor binding properties of 2β-alkynyl and 2β-(1,2,3-triazol)substituted 3β-(substituted phenyl)tropane derivatives
|
Jin, Chunyang
|
|
2008
|
16 |
10 |
p. 5529-5535
7 p.
|
artikel
|
| 39 |
Synthesis, cytostatic and anti-HIV evaluations of the new unsaturated acyclic C-5 pyrimidine nucleoside analogues
|
Gazivoda, Tatjana
|
|
2008
|
16 |
10 |
p. 5624-5634
11 p.
|
artikel
|
| 40 |
Synthesis, in vitro antibacterial and carbonic anhydrase II inhibitory activities of N-acylsulfonamides using silica sulfuric acid as an efficient catalyst under both solvent-free and heterogeneous conditions
|
Massah, Ahmad Reza
|
|
2008
|
16 |
10 |
p. 5465-5472
8 p.
|
artikel
|
| 41 |
Synthesis of 5-chloro-N-aryl-1H-indole-2-carboxamide derivatives as inhibitors of human liver glycogen phosphorylase a
|
Onda, Kenichi
|
|
2008
|
16 |
10 |
p. 5452-5464
13 p.
|
artikel
|
| 42 |
Synthesis of 5′-functionalized nucleosides: S-Adenosylhomocysteine analogues with the carbon-5′ and sulfur atoms replaced by a vinyl or halovinyl unit
|
Wnuk, Stanislaw F.
|
|
2008
|
16 |
10 |
p. 5424-5433
10 p.
|
artikel
|
| 43 |
Synthesis of indirubin-N′-glycosides and their anti-proliferative activity against human cancer cell lines
|
Libnow, Stefanie
|
|
2008
|
16 |
10 |
p. 5570-5583
14 p.
|
artikel
|
| 44 |
Synthesis of methyl 5-S-alkyl-5-thio-d-arabinofuranosides and evaluation of their antimycobacterial activity
|
Sanki, Aditya K.
|
|
2008
|
16 |
10 |
p. 5672-5682
11 p.
|
artikel
|
| 45 |
Synthesis of new heteroaryl and heteroannulated indoles from dehydrophenylalanines: Antitumor evaluation
|
Queiroz, Maria-João R.P.
|
|
2008
|
16 |
10 |
p. 5584-5589
6 p.
|
artikel
|
| 46 |
Synthetic methods for the preparation of ARQ 501 (β-Lapachone) human blood metabolites
|
Yang, Rui-Yang
|
|
2008
|
16 |
10 |
p. 5635-5643
9 p.
|
artikel
|
| 47 |
The pyridoxamine action on Amadori compounds: A reexamination of its scavenging capacity and chelating effect
|
Adrover, Miquel
|
|
2008
|
16 |
10 |
p. 5557-5569
13 p.
|
artikel
|
| 48 |
Thermodynamics and fluorescence studies of the interactions of cyclooctapeptides with Hg2+, Pb2+, and Cd2+
|
Ngu-Schwemlein, Maria
|
|
2008
|
16 |
10 |
p. 5778-5787
10 p.
|
artikel
|
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