| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel QSAR model for predicting induction of apoptosis by 4-aryl-4H-chromenes
|
Afantitis, Antreas
|
|
2006
|
14 |
19 |
p. 6686-6694
9 p.
|
artikel
|
| 2 |
Antitumor agents 251: Synthesis, cytotoxic evaluation, and structure–activity relationship studies of phenanthrene-based tylophorine derivatives (PBTs) as a new class of antitumor agents
|
Wei, Linyi
|
|
2006
|
14 |
19 |
p. 6560-6569
10 p.
|
artikel
|
| 3 |
Arylisothiocyanato selective androgen receptor modulators (SARMs) for prostate cancer
|
Hwang, Dong Jin
|
|
2006
|
14 |
19 |
p. 6525-6538
14 p.
|
artikel
|
| 4 |
Bioorganic & Medicinal Chemistry Reviews and Perspectives
|
|
|
2006
|
14 |
19 |
p. 6778-6780
3 p.
|
artikel
|
| 5 |
Comparative uptake, metabolism, and utilization of menaquinone-4 and phylloquinone in human cultured cell lines
|
Suhara, Yoshitomo
|
|
2006
|
14 |
19 |
p. 6601-6607
7 p.
|
artikel
|
| 6 |
Cysteine based novel noncompetitive inhibitors of urease(s)—Distinctive inhibition susceptibility of microbial and plant ureases
|
Amtul, Zareen
|
|
2006
|
14 |
19 |
p. 6737-6744
8 p.
|
artikel
|
| 7 |
2-(4,5-Dihydroimidazol-2-yl)benzimidazoles as highly selective imidazoline I2/adrenergic α2 receptor ligands
|
Sączewski, Francieszek
|
|
2006
|
14 |
19 |
p. 6679-6685
7 p.
|
artikel
|
| 8 |
Discovery of heteroaryl sulfonamides as new EP1 receptor selective antagonists
|
Naganawa, Atsushi
|
|
2006
|
14 |
19 |
p. 6628-6639
12 p.
|
artikel
|
| 9 |
Discovery of imidazolidine-2,4-dione-linked HIV protease inhibitors with activity against lopinavir-resistant mutant HIV
|
Flosi, William J.
|
|
2006
|
14 |
19 |
p. 6695-6712
18 p.
|
artikel
|
| 10 |
Editorial Board
|
|
|
2006
|
14 |
19 |
p. CO2-
1 p.
|
artikel
|
| 11 |
Enhancing effect of indirubin derivatives on 1,25-dihydroxyvitamin D3- and all-trans retinoic acid-induced differentiation of HL-60 leukemia cells
|
Kim, Seung Hyun
|
|
2006
|
14 |
19 |
p. 6752-6758
7 p.
|
artikel
|
| 12 |
Glycosidation of lupane-type triterpenoids as potent in vitro cytotoxic agents
|
Gauthier, Charles
|
|
2006
|
14 |
19 |
p. 6713-6725
13 p.
|
artikel
|
| 13 |
Graphical contents list
|
|
|
2006
|
14 |
19 |
p. 6457-6465
9 p.
|
artikel
|
| 14 |
Inhibition of type 2 isopentenyl diphosphate isomerase from Methanocaldococcus jannaschii by a mechanism-based inhibitor of type 1 isopentenyl diphosphate isomerase
|
Hoshino, Takeshi
|
|
2006
|
14 |
19 |
p. 6555-6559
5 p.
|
artikel
|
| 15 |
Instructions to contributors
|
|
|
2006
|
14 |
19 |
p. I-
1 p.
|
artikel
|
| 16 |
Membrane interaction of amphotericin B as single-length assembly examined by solid state NMR for uniformly 13C-enriched agent
|
Matsuoka, Shigeru
|
|
2006
|
14 |
19 |
p. 6608-6614
7 p.
|
artikel
|
| 17 |
New progesterone receptor antagonists: Phosphorus-containing 11β-aryl-substituted steroids
|
Jiang, Weiqin
|
|
2006
|
14 |
19 |
p. 6726-6732
7 p.
|
artikel
|
| 18 |
Novel ligands for the human histamine H1 receptor: Synthesis, pharmacology, and comparative molecular field analysis studies of 2-dimethylamino-5-(6)-phenyl-1,2,3,4-tetrahydronaphthalenes
|
Ghoneim, Ola M.
|
|
2006
|
14 |
19 |
p. 6640-6658
19 p.
|
artikel
|
| 19 |
Predicting antitrichomonal activity: A computational screening using atom-based bilinear indices and experimental proofs
|
Marrero-Ponce, Yovani
|
|
2006
|
14 |
19 |
p. 6502-6524
23 p.
|
artikel
|
| 20 |
Role of glutamine 148 of human 15-hydroxyprostaglandin dehydrogenase in catalytic oxidation of prostaglandin E2
|
Cho, Hoon
|
|
2006
|
14 |
19 |
p. 6486-6491
6 p.
|
artikel
|
| 21 |
Role of small bioorganic molecules in stem cell differentiation to insulin-producing cells
|
Roche, Enrique
|
|
2006
|
14 |
19 |
p. 6466-6474
9 p.
|
artikel
|
| 22 |
Secondary assembly of bile salts mediated by β-cyclodextrin–terbium(III) complex
|
Liu, Yu
|
|
2006
|
14 |
19 |
p. 6615-6620
6 p.
|
artikel
|
| 23 |
Structure–activity-relationship studies of conformationally restricted analogs of combretastatin A-4 derived from SU5416
|
Pandit, Bulbul
|
|
2006
|
14 |
19 |
p. 6492-6501
10 p.
|
artikel
|
| 24 |
Structures of new amphidinols with truncated polyhydroxyl chain and their membrane-permeabilizing activities
|
Morsy, Nagy
|
|
2006
|
14 |
19 |
p. 6548-6554
7 p.
|
artikel
|
| 25 |
Synthesis and biological evaluation of benzopyran analogues bearing class III antiarrhythmic pharmacophores
|
Koufaki, Maria
|
|
2006
|
14 |
19 |
p. 6666-6678
13 p.
|
artikel
|
| 26 |
Synthesis and DNA cleavage activities of mononuclear macrocyclic polyamine zinc(II), copper(II), cobalt(II) complexes which linked with uracil
|
Wang, Xiao-Yan
|
|
2006
|
14 |
19 |
p. 6745-6751
7 p.
|
artikel
|
| 27 |
Synthesis and evaluation of uterine relaxant activity for a novel series of substituted p-hydroxyphenylethanolamines
|
Viswanathan, C.L.
|
|
2006
|
14 |
19 |
p. 6581-6585
5 p.
|
artikel
|
| 28 |
Synthesis and in vitro antimicrobial studies of medicinally important novel N-alkyl and N-sulfonyl derivatives of 1-[bis(4-fluorophenyl)-methyl]piperazine
|
Narendra Sharath Chandra, J.N.
|
|
2006
|
14 |
19 |
p. 6621-6627
7 p.
|
artikel
|
| 29 |
Synthesis and in vitro antitumor evaluation of some indeno[1,2-c]pyrazol(in)es substituted with sulfonamide, sulfonylurea(-thiourea) pharmacophores, and some derived thiazole ring systems
|
Rostom, Sherif A.F.
|
|
2006
|
14 |
19 |
p. 6475-6485
11 p.
|
artikel
|
| 30 |
Synthesis and in vitro cytotoxicity of haloderivatives of noscapine
|
Verma, Akhilesh Kumar
|
|
2006
|
14 |
19 |
p. 6733-6736
4 p.
|
artikel
|
| 31 |
Synthesis and pharmacological studies of new hybrid derivatives of fentanyl active at the μ-opioid receptor and I2–imidazoline binding sites
|
Dardonville, Christophe
|
|
2006
|
14 |
19 |
p. 6570-6580
11 p.
|
artikel
|
| 32 |
Synthesis of aromatic C-xylosides by position inversion of glucose
|
Malmberg, Jesper
|
|
2006
|
14 |
19 |
p. 6659-6665
7 p.
|
artikel
|
| 33 |
Synthesis of benzenepropanamine analogues as non-detergent spermicides with antitrichomonas and anticandida activities
|
Kiran Kumar, S.T.V.S.
|
|
2006
|
14 |
19 |
p. 6593-6600
8 p.
|
artikel
|
| 34 |
Synthesis of lipid A monosaccharide analogues containing acidic amino acid: Exploring the structural basis for the endotoxic and antagonistic activities
|
Akamatsu, Masao
|
|
2006
|
14 |
19 |
p. 6759-6777
19 p.
|
artikel
|
| 35 |
The 5-substituted piperazine as a novel secondary pharmacophore greatly improving the physical properties of urea-based inhibitors of soluble epoxide hydrolase
|
Li, Hui-Yuan
|
|
2006
|
14 |
19 |
p. 6586-6592
7 p.
|
artikel
|
| 36 |
The synthesis of l-carvone and limonene derivatives with increased antiproliferative effect and activation of ERK pathway in prostate cancer cells
|
Chen, Jiaojiao
|
|
2006
|
14 |
19 |
p. 6539-6547
9 p.
|
artikel
|
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