| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A new class of small molecule RNA polymerase inhibitors with activity against Rifampicin-resistant Staphylococcus aureus 1
|
Arhin, Francis
|
|
2006
|
14 |
17 |
p. 5812-5832
21 p.
|
artikel
|
| 2 |
Antioxidant and anticancer activities of novel p-alkylaminophenols and p-acylaminophenols (aminophenol analogues)
|
Takahashi, Noriko
|
|
2006
|
14 |
17 |
p. 6089-6096
8 p.
|
artikel
|
| 3 |
A study on the perturbation of model lipid membranes by phenoxazines
|
Hendrich, Andrzej B.
|
|
2006
|
14 |
17 |
p. 5948-5954
7 p.
|
artikel
|
| 4 |
CoMFA and CoMSIA investigations of dopamine D3 receptor ligands leading to the prediction, synthesis, and evaluation of rigidized FAUC 365 analogues
|
Salama, Ismail
|
|
2006
|
14 |
17 |
p. 5898-5912
15 p.
|
artikel
|
| 5 |
C19-Steroids as androgen receptor modulators: Design, discovery, and structure-activity relationship of new steroidal androgen receptor antagonists
|
Marwah, Padma
|
|
2006
|
14 |
17 |
p. 5933-5947
15 p.
|
artikel
|
| 6 |
Design, synthesis, and biological evaluation of 1,2,3-trisubstituted-1,4-dihydrobenzo[g]quinoxaline-5,10-diones and related compounds as antifungal and antibacterial agents
|
Tandon, Vishnu K.
|
|
2006
|
14 |
17 |
p. 6120-6126
7 p.
|
artikel
|
| 7 |
Design, synthesis and evaluation of naphthalene-2-carboxamides as reversal agents in MDR cancer
|
Lokhande, Tushar N.
|
|
2006
|
14 |
17 |
p. 6022-6026
5 p.
|
artikel
|
| 8 |
Editorial board
|
|
|
2006
|
14 |
17 |
p. CO2-
1 p.
|
artikel
|
| 9 |
Graphical contents list
|
|
|
2006
|
14 |
17 |
p. 5771-5780
10 p.
|
artikel
|
| 10 |
Homology model of RSK2 N-terminal kinase domain, structure-based identification of novel RSK2 inhibitors, and preliminary common pharmacophore
|
Nguyen, Tam Luong
|
|
2006
|
14 |
17 |
p. 6097-6105
9 p.
|
artikel
|
| 11 |
Influence of rhamnose substituents on the potency of SL0101, an inhibitor of the Ser/Thr kinase, RSK
|
Smith, Jeffrey A.
|
|
2006
|
14 |
17 |
p. 6034-6042
9 p.
|
artikel
|
| 12 |
Instructions to contributors
|
|
|
2006
|
14 |
17 |
p. I-
1 p.
|
artikel
|
| 13 |
Isothiazolidinone heterocycles as inhibitors of protein tyrosine phosphatases: Synthesis and structure–activity relationships of a peptide scaffold
|
Yue, Eddy W.
|
|
2006
|
14 |
17 |
p. 5833-5849
17 p.
|
artikel
|
| 14 |
Luminescent pyrimidine hydrazide oligomers with peptide affinity
|
Li, Xiaoqiang
|
|
2006
|
14 |
17 |
p. 6075-6084
10 p.
|
artikel
|
| 15 |
Lycopladines B–D and lyconadin B, new alkaloids from Lycopodium complanatum
|
Ishiuchi, Kan’ichiro
|
|
2006
|
14 |
17 |
p. 5995-6000
6 p.
|
artikel
|
| 16 |
Molecular docking study and development of an empirical binding free energy model for phosphodiesterase 4 inhibitors
|
Oliveira, Fernanda G.
|
|
2006
|
14 |
17 |
p. 6001-6011
11 p.
|
artikel
|
| 17 |
γ-(Monophenyl)phosphono glutamate analogues as mechanism-based inhibitors of γ-glutamyl transpeptidase
|
Han, Liyou
|
|
2006
|
14 |
17 |
p. 6043-6054
12 p.
|
artikel
|
| 18 |
Oxazolones: New tyrosinase inhibitors; synthesis and their structure–activity relationships
|
Khan, Khalid Mohammed
|
|
2006
|
14 |
17 |
p. 6027-6033
7 p.
|
artikel
|
| 19 |
QSAR analysis of antimicrobial and haemolytic effects of cyclic cationic antimicrobial peptides derived from protegrin-1
|
Frecer, Vladimir
|
|
2006
|
14 |
17 |
p. 6065-6074
10 p.
|
artikel
|
| 20 |
QSAR for non-nucleoside inhibitors of HIV-1 reverse transcriptase
|
Duchowicz, Pablo R.
|
|
2006
|
14 |
17 |
p. 5876-5889
14 p.
|
artikel
|
| 21 |
Reactive oxygen species scavenging activity of aminoderivatized chitosan with different degree of deacetylation
|
Je, Jae-Young
|
|
2006
|
14 |
17 |
p. 5989-5994
6 p.
|
artikel
|
| 22 |
Short pseudopeptides containing turn scaffolds with high AT2 receptor affinity
|
Georgsson, Jennie
|
|
2006
|
14 |
17 |
p. 5963-5972
10 p.
|
artikel
|
| 23 |
Side-chain and backbone amide bond requirements for glycopeptide stimulation of T-cells obtained in a mouse model for rheumatoid arthritis
|
Holm, Lotta
|
|
2006
|
14 |
17 |
p. 5921-5932
12 p.
|
artikel
|
| 24 |
Synthesis and anticancer evaluation of bis(benzimidazoles), bis(benzoxazoles), and benzothiazoles
|
Huang, Shu-Ting
|
|
2006
|
14 |
17 |
p. 6106-6119
14 p.
|
artikel
|
| 25 |
Synthesis and antimicrobial evaluation of new 2-substituted 5,7-di-tert-butylbenzoxazoles
|
Vinsova, Jarmila
|
|
2006
|
14 |
17 |
p. 5850-5865
16 p.
|
artikel
|
| 26 |
Synthesis and biological evaluation of 5-arylamino-1H-benzo[d]imidazole-4,7-diones as inhibitor of endothelial cell proliferation
|
Chung, Kwang-Hoe
|
|
2006
|
14 |
17 |
p. 5795-5801
7 p.
|
artikel
|
| 27 |
Synthesis and biological evaluation of carboacyclic nucleosides with (Z) and (E)-9-[4,4-bis(hydroxymethyl)]-2-butenyl side chain
|
Tang, Ye
|
|
2006
|
14 |
17 |
p. 5866-5875
10 p.
|
artikel
|
| 28 |
Synthesis and cellular studies of a carboranylchlorin for the PDT and BNCT of tumors
|
Luguya, Raymond
|
|
2006
|
14 |
17 |
p. 5890-5897
8 p.
|
artikel
|
| 29 |
Synthesis and evaluation of novel multimeric neurotensin(8–13) analogs
|
Hultsch, Christina
|
|
2006
|
14 |
17 |
p. 5913-5920
8 p.
|
artikel
|
| 30 |
Synthesis and NMDA-receptor affinity of 4-oxo-dexoxadrol derivatives
|
Sax, Michael
|
|
2006
|
14 |
17 |
p. 5955-5962
8 p.
|
artikel
|
| 31 |
Synthesis, characterization, and DNA-binding properties of the Ln(III) complexes with 6-hydroxy chromone-3-carbaldehyde-(2′-hydroxy) benzoyl hydrazone
|
Wang, Bao-dui
|
|
2006
|
14 |
17 |
p. 6012-6021
10 p.
|
artikel
|
| 32 |
Synthesis of 1-O-monoacyl or 12-O-monoacyl, 1-,12-O-diacyl-, and 11,12-dehydrated excisanin A 7,14-acetonides and their cytotoxic activity
|
Aoyagi, Yutaka
|
|
2006
|
14 |
17 |
p. 5802-5811
10 p.
|
artikel
|
| 33 |
Synthesis, receptor binding, and activation studies of N(1)-alkyl-l-histidine containing thyrotropin-releasing hormone (TRH) analogues
|
Kaur, Navneet
|
|
2006
|
14 |
17 |
p. 5981-5988
8 p.
|
artikel
|
| 34 |
Synthesis, SAR studies, and pharmacological evaluation of 3-anilino-4-(3-indolyl) maleimides with conformationally restricted structure as orally bioavailable PKCβ-selective inhibitors
|
Tanaka, Masahiro
|
|
2006
|
14 |
17 |
p. 5781-5794
14 p.
|
artikel
|
| 35 |
The binding of 3′-N-piperidine-4-carboxyl-3′-deoxy-ara-uridine to ribonuclease A in the crystal
|
Leonidas, Demetres D.
|
|
2006
|
14 |
17 |
p. 6055-6064
10 p.
|
artikel
|
| 36 |
Tyrosinase inhibition studies of cycloartane and cucurbitane glycosides and their structure–activity relationships
|
Hassan Khan, Mahmud Tareq
|
|
2006
|
14 |
17 |
p. 6085-6088
4 p.
|
artikel
|
| 37 |
Unify QSAR approach to antimicrobials. Part 1: Predicting antifungal activity against different species
|
González-Díaz, Humberto
|
|
2006
|
14 |
17 |
p. 5973-5980
8 p.
|
artikel
|
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