| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Abscinazole-E2B, a practical and selective inhibitor of ABA 8′-hydroxylase CYP707A
|
Okazaki, Mariko
|
|
2012
|
20 |
10 |
p. 3162-3172
11 p.
|
artikel
|
| 2 |
A comparative study of backbone versus side chain peptide cyclization: Application for HIV-1 integrase inhibitors
|
Hayouka, Zvi
|
|
2012
|
20 |
10 |
p. 3317-3322
6 p.
|
artikel
|
| 3 |
A highly selective Hsp90 affinity chromatography resin with a cleavable linker
|
Hughes, Philip F.
|
|
2012
|
20 |
10 |
p. 3298-3305
8 p.
|
artikel
|
| 4 |
An efficient and convenient microwave-assisted chemical synthesis of (thio)xanthones with additional in vitro and in silico characterization
|
Verbanac, Donatella
|
|
2012
|
20 |
10 |
p. 3180-3185
6 p.
|
artikel
|
| 5 |
Bioorganic & Medicinal Chemistry Reviews and Perspectives
|
|
|
2012
|
20 |
10 |
p. I-III
nvt p.
|
artikel
|
| 6 |
Cellular uptake of covalent conjugates of oligonucleotide with membrane-modifying peptide, peptaibol
|
Wada, Shun-ichi
|
|
2012
|
20 |
10 |
p. 3219-3222
4 p.
|
artikel
|
| 7 |
COMPARE analysis of the toxicity of an iminoquinone derivative of the imidazo[5,4-f]benzimidazoles with NAD(P)H:quinone oxidoreductase 1 (NQO1) activity and computational docking of quinones as NQO1 substrates
|
Fagan, Vincent
|
|
2012
|
20 |
10 |
p. 3223-3232
10 p.
|
artikel
|
| 8 |
3-Deoxy-3,4-dehydro analogs of XM462. Preparation and activity on sphingolipid metabolism and cell fate
|
Camacho, Luz
|
|
2012
|
20 |
10 |
p. 3173-3179
7 p.
|
artikel
|
| 9 |
Design, synthesis and biological evaluation of novel chalcone derivatives as antitubulin agents
|
Zhang, Hui
|
|
2012
|
20 |
10 |
p. 3212-3218
7 p.
|
artikel
|
| 10 |
Discovery of Ipragliflozin (ASP1941): A novel C-glucoside with benzothiophene structure as a potent and selective sodium glucose co-transporter 2 (SGLT2) inhibitor for the treatment of type 2 diabetes mellitus
|
Imamura, Masakazu
|
|
2012
|
20 |
10 |
p. 3263-3279
17 p.
|
artikel
|
| 11 |
Discovery of potent and orally bioavailable 17β-hydroxysteroid dehydrogenase type 3 inhibitors
|
Harada, Koichiro
|
|
2012
|
20 |
10 |
p. 3242-3254
13 p.
|
artikel
|
| 12 |
Editorial board
|
|
|
2012
|
20 |
10 |
p. IFC-
1 p.
|
artikel
|
| 13 |
Evaluation of a synthetic C34 trimer of HIV-1 gp41 as AIDS vaccines
|
Hashimoto, Chie
|
|
2012
|
20 |
10 |
p. 3287-3291
5 p.
|
artikel
|
| 14 |
Graphical contents list
|
|
|
2012
|
20 |
10 |
p. 3143-3149
7 p.
|
artikel
|
| 15 |
Hepatitis C RNA-dependent RNA polymerase inhibitors: A review of structure–activity and resistance relationships; different scaffolds and mutations
|
Mayhoub, Abdelrahman S.
|
|
2012
|
20 |
10 |
p. 3150-3161
12 p.
|
artikel
|
| 16 |
Investigating the activity of quinine analogues versus chloroquine resistant Plasmodium falciparum
|
Dinio, Theresa
|
|
2012
|
20 |
10 |
p. 3292-3297
6 p.
|
artikel
|
| 17 |
In vitro growth inhibition of human cancer cells by novel honokiol analogs
|
Lin, Jyh Ming
|
|
2012
|
20 |
10 |
p. 3202-3211
10 p.
|
artikel
|
| 18 |
Paviosides A–H, eight new oleane type saponins from Aesculus pavia with cytotoxic activity
|
Lanzotti, Virginia
|
|
2012
|
20 |
10 |
p. 3280-3286
7 p.
|
artikel
|
| 19 |
Pharmacological evaluation of a novel cyclic phosphatidic acid derivative 3-S-cyclic phosphatidic acid (3-S-cPA)
|
Nozaki, Emi
|
|
2012
|
20 |
10 |
p. 3196-3201
6 p.
|
artikel
|
| 20 |
Screening a library of 1600 adamantyl ureas for anti-Mycobacterium tuberculosis activity in vitro and for better physical chemical properties for bioavailability
|
Scherman, Michael S.
|
|
2012
|
20 |
10 |
p. 3255-3262
8 p.
|
artikel
|
| 21 |
Structure–activity relationships and key structural feature of pyridyloxybenzene-acylsulfonamides as new, potent, and selective peroxisome proliferator-activated receptor (PPAR) γ Agonists
|
Rikimaru, Kentaro
|
|
2012
|
20 |
10 |
p. 3332-3358
27 p.
|
artikel
|
| 22 |
Synthesis and biological evaluation of a new class of glycoconjugated disulfides that exhibit potential anticancer properties
|
Bonaccorsi, Paola
|
|
2012
|
20 |
10 |
p. 3186-3195
10 p.
|
artikel
|
| 23 |
Synthesis, biological evaluation, and molecular docking studies of 2,6-dinitro-4-(trifluoromethyl)phenoxysalicylaldoxime derivatives as novel antitubulin agents
|
Zhao, Ting-Ting
|
|
2012
|
20 |
10 |
p. 3233-3241
9 p.
|
artikel
|
| 24 |
Synthesis, biological evaluation and molecular docking studies of 1,3,4-oxadiazole derivatives as potential immunosuppressive agents
|
Zhang, Zhi-Ming
|
|
2012
|
20 |
10 |
p. 3359-3367
9 p.
|
artikel
|
| 25 |
Synthesis, biological evaluation and molecular modeling study of pyrazole and pyrazoline derivatives as selective COX-2 inhibitors and anti-inflammatory agents. Part 2
|
El-Sayed, Magda A.-A.
|
|
2012
|
20 |
10 |
p. 3306-3316
11 p.
|
artikel
|
| 26 |
Synthesis, σ1, σ2-receptors binding affinity and antiproliferative action of new C1-substituted adamantanes
|
Riganas, Stefanos
|
|
2012
|
20 |
10 |
p. 3323-3331
9 p.
|
artikel
|
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