no |
title |
author |
magazine |
year |
volume |
issue |
page(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. |
article |
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. |
article |
3 |
Arylisothiocyanato selective androgen receptor modulators (SARMs) for prostate cancer
|
Hwang, Dong Jin |
|
2006 |
14 |
19 |
p. 6525-6538 14 p. |
article |
4 |
Bioorganic & Medicinal Chemistry Reviews and Perspectives
|
|
|
2006 |
14 |
19 |
p. 6778-6780 3 p. |
article |
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. |
article |
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. |
article |
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. |
article |
8 |
Discovery of heteroaryl sulfonamides as new EP1 receptor selective antagonists
|
Naganawa, Atsushi |
|
2006 |
14 |
19 |
p. 6628-6639 12 p. |
article |
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. |
article |
10 |
Editorial Board
|
|
|
2006 |
14 |
19 |
p. CO2- 1 p. |
article |
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. |
article |
12 |
Glycosidation of lupane-type triterpenoids as potent in vitro cytotoxic agents
|
Gauthier, Charles |
|
2006 |
14 |
19 |
p. 6713-6725 13 p. |
article |
13 |
Graphical contents list
|
|
|
2006 |
14 |
19 |
p. 6457-6465 9 p. |
article |
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. |
article |
15 |
Instructions to contributors
|
|
|
2006 |
14 |
19 |
p. I- 1 p. |
article |
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. |
article |
17 |
New progesterone receptor antagonists: Phosphorus-containing 11β-aryl-substituted steroids
|
Jiang, Weiqin |
|
2006 |
14 |
19 |
p. 6726-6732 7 p. |
article |
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. |
article |
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. |
article |
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. |
article |
21 |
Role of small bioorganic molecules in stem cell differentiation to insulin-producing cells
|
Roche, Enrique |
|
2006 |
14 |
19 |
p. 6466-6474 9 p. |
article |
22 |
Secondary assembly of bile salts mediated by β-cyclodextrin–terbium(III) complex
|
Liu, Yu |
|
2006 |
14 |
19 |
p. 6615-6620 6 p. |
article |
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. |
article |
24 |
Structures of new amphidinols with truncated polyhydroxyl chain and their membrane-permeabilizing activities
|
Morsy, Nagy |
|
2006 |
14 |
19 |
p. 6548-6554 7 p. |
article |
25 |
Synthesis and biological evaluation of benzopyran analogues bearing class III antiarrhythmic pharmacophores
|
Koufaki, Maria |
|
2006 |
14 |
19 |
p. 6666-6678 13 p. |
article |
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. |
article |
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. |
article |
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. |
article |
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. |
article |
30 |
Synthesis and in vitro cytotoxicity of haloderivatives of noscapine
|
Verma, Akhilesh Kumar |
|
2006 |
14 |
19 |
p. 6733-6736 4 p. |
article |
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. |
article |
32 |
Synthesis of aromatic C-xylosides by position inversion of glucose
|
Malmberg, Jesper |
|
2006 |
14 |
19 |
p. 6659-6665 7 p. |
article |
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. |
article |
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. |
article |
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. |
article |
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. |
article |