| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Bioorganic & Medicinal Chemistry Reviews and Perspectives
|
|
|
2011
|
19 |
16 |
p. I-III
nvt p.
|
artikel
|
| 2 |
Biotinylated quercetin as an intrinsic photoaffinity proteomics probe for the identification of quercetin target proteins
|
Wang, Rongsheng E.
|
|
2011
|
19 |
16 |
p. 4710-4720
11 p.
|
artikel
|
| 3 |
Bivalent ligand approach on N-{2-[(3-methoxyphenyl)methylamino]ethyl}acetamide: Synthesis, binding affinity and intrinsic activity for MT1 and MT2 melatonin receptors
|
Spadoni, Gilberto
|
|
2011
|
19 |
16 |
p. 4910-4916
7 p.
|
artikel
|
| 4 |
Design of HIV-1 integrase inhibitors targeting the catalytic domain as well as its interaction with LEDGF/p75: A scaffold hopping approach using salicylate and catechol groups
|
Fan, Xing
|
|
2011
|
19 |
16 |
p. 4935-4952
18 p.
|
artikel
|
| 5 |
Design, synthesis, and biological evaluation of abiotic, non-lactone modulators of LuxR-type quorum sensing
|
McInnis, Christine E.
|
|
2011
|
19 |
16 |
p. 4812-4819
8 p.
|
artikel
|
| 6 |
Editorial board
|
|
|
2011
|
19 |
16 |
p. IFC-
1 p.
|
artikel
|
| 7 |
Effects of β-glucosidase hydrolyzed products of harpagide and harpagoside on cyclooxygenase-2 (COX-2) in vitro
|
Zhang, Liuqiang
|
|
2011
|
19 |
16 |
p. 4882-4886
5 p.
|
artikel
|
| 8 |
Ethyl malonate amides: A diketo acid offspring fragment for HIV integrase inhibition
|
Serafin, Katarzyna
|
|
2011
|
19 |
16 |
p. 5000-5005
6 p.
|
artikel
|
| 9 |
Evaluation of influence of Ap4A analogues on Fhit-positive HEK293T cells; cytotoxicity and ability to induce apoptosis
|
Krakowiak, Agnieszka
|
|
2011
|
19 |
16 |
p. 5053-5060
8 p.
|
artikel
|
| 10 |
Graphical contents list
|
|
|
2011
|
19 |
16 |
p. 4679-4689
11 p.
|
artikel
|
| 11 |
Identification of 3-aminomethyl-1,2-dihydro-4-phenyl-1-isoquinolones: A new class of potent, selective, and orally active non-peptide dipeptidyl peptidase IV inhibitors that form a unique interaction with Lys554
|
Banno, Yoshihiro
|
|
2011
|
19 |
16 |
p. 4953-4970
18 p.
|
artikel
|
| 12 |
Inhibition of monoamine oxidase by C5-substituted phthalimide analogues
|
Manley-King, Clarina I.
|
|
2011
|
19 |
16 |
p. 4829-4840
12 p.
|
artikel
|
| 13 |
Inhibition studies of the β-carbonic anhydrases from the bacterial pathogen Salmonella enterica serovar Typhimurium with sulfonamides and sulfamates
|
Nishimori, Isao
|
|
2011
|
19 |
16 |
p. 5023-5030
8 p.
|
artikel
|
| 14 |
Intramolecular ion-pair prodrugs of zanamivir and guanidino-oseltamivir
|
Liu, Kung-Cheng
|
|
2011
|
19 |
16 |
p. 4796-4802
7 p.
|
artikel
|
| 15 |
In vitro cytotoxic activity of abietane diterpenes from Peltodon longipes as well as Salvia miltiorrhiza and Salvia sahendica
|
Fronza, M.
|
|
2011
|
19 |
16 |
p. 4876-4881
6 p.
|
artikel
|
| 16 |
Isoxazole substituted chromans against oxidative stress-induced neuronal damage
|
Koufaki, Maria
|
|
2011
|
19 |
16 |
p. 4841-4850
10 p.
|
artikel
|
| 17 |
Ligand-based modelling followed by synthetic exploration unveil novel glycogen phosphorylase inhibitory leads
|
Habash, Maha
|
|
2011
|
19 |
16 |
p. 4746-4771
26 p.
|
artikel
|
| 18 |
LuxR dependent quorum sensing inhibition by N,N′-disubstituted imidazolium salts
|
Sabbah, Mohamad
|
|
2011
|
19 |
16 |
p. 4868-4875
8 p.
|
artikel
|
| 19 |
N-alkylated cyclen cobalt(III) complexes of 1-(chloromethyl)-3-(5,6,7-trimethoxyindol-2-ylcarbonyl)-2,3-dihydro-1H-pyrrolo[3,2-f]quinolin-5-ol DNA alkylating agent as hypoxia-activated prodrugs
|
Lu, Guo-Liang
|
|
2011
|
19 |
16 |
p. 4861-4867
7 p.
|
artikel
|
| 20 |
Novel benzofuroxan derivatives against multidrug-resistant Staphylococcus aureus strains: Design using Topliss’ decision tree, synthesis and biological assay
|
Jorge, Salomão Dória
|
|
2011
|
19 |
16 |
p. 5031-5038
8 p.
|
artikel
|
| 21 |
Novel multienzyme oxidative biocatalyst for lignin bioprocessing
|
Crestini, Claudia
|
|
2011
|
19 |
16 |
p. 5071-5078
8 p.
|
artikel
|
| 22 |
Novel nonsecosteroidal vitamin D3 carboxylic acid analogs for osteoporosis, and SAR analysis
|
Kashiwagi, Hirotaka
|
|
2011
|
19 |
16 |
p. 4721-4729
9 p.
|
artikel
|
| 23 |
NSAID-derived γ-secretase modulation requires an acidic moiety on the carbazole scaffold
|
Zall, Andrea
|
|
2011
|
19 |
16 |
p. 4903-4909
7 p.
|
artikel
|
| 24 |
N-Substituted homopiperazine barbiturates as gelatinase inhibitors
|
Wang, Jun
|
|
2011
|
19 |
16 |
p. 4985-4999
15 p.
|
artikel
|
| 25 |
Oxadiazole derivatives containing 1,4-benzodioxan as potential immunosuppressive agents against RAW264.7 cells
|
Sun, Juan
|
|
2011
|
19 |
16 |
p. 4895-4902
8 p.
|
artikel
|
| 26 |
Polyfluorinated bipyridine cisplatins manipulate cytotoxicity through the induction of S-G2/M arrest and partial intercalation mechanism
|
Chang, Tzu Ting
|
|
2011
|
19 |
16 |
p. 4887-4894
8 p.
|
artikel
|
| 27 |
P2–P1′ macrocyclization of P2 phenylglycine based HCV NS3 protease inhibitors using ring-closing metathesis
|
Lampa, Anna
|
|
2011
|
19 |
16 |
p. 4917-4927
11 p.
|
artikel
|
| 28 |
Recent advances in drug discovery of benzothiadiazine and related analogs as HCV NS5B polymerase inhibitors
|
Das, Debasis
|
|
2011
|
19 |
16 |
p. 4690-4703
14 p.
|
artikel
|
| 29 |
Regulation of the Escherichia coli AtoSC two component system by synthetic biologically active 5;7;8-trimethyl-1;4-benzoxazine analogues
|
Filippou, Panagiota S.
|
|
2011
|
19 |
16 |
p. 5061-5070
10 p.
|
artikel
|
| 30 |
Semisynthetic analogues of the marine cembranoid sarcophine as prostate and breast cancer migration inhibitors
|
Hassan, Hossam M.
|
|
2011
|
19 |
16 |
p. 4928-4934
7 p.
|
artikel
|
| 31 |
Single step synthesis of strigolactone analogues from cyclic keto enols, germination stimulants for seeds of parasitic weeds
|
Mwakaboko, Alinanuswe S.
|
|
2011
|
19 |
16 |
p. 5006-5011
6 p.
|
artikel
|
| 32 |
Structural modifications of quinolone-3-carboxylic acids with anti-HIV activity
|
He, Qiu-Qin
|
|
2011
|
19 |
16 |
p. 5039-5045
7 p.
|
artikel
|
| 33 |
Synthesis and antiproliferative activity of novel 2-aryl-4-benzoyl-imidazole derivatives targeting tubulin polymerization
|
Chen, Jianjun
|
|
2011
|
19 |
16 |
p. 4782-4795
14 p.
|
artikel
|
| 34 |
Synthesis and biological evaluation of (±)-benzhydrol derivatives as potent non-nucleoside HIV-1 reverse transcriptase inhibitors
|
Ma, Xiao-Dong
|
|
2011
|
19 |
16 |
p. 4704-4709
6 p.
|
artikel
|
| 35 |
Synthesis and evaluation of novel 2-butyl-4-chloro-1-methylimidazole embedded chalcones and pyrazoles as angiotensin converting enzyme (ACE) inhibitors
|
Kantevari, Srinivas
|
|
2011
|
19 |
16 |
p. 4772-4781
10 p.
|
artikel
|
| 36 |
Synthesis and topoisomerase I inhibitory activity of a novel diazaindeno[2,1-b]phenanthrene analogue of Lamellarin D
|
Cananzi, Salvatore
|
|
2011
|
19 |
16 |
p. 4971-4984
14 p.
|
artikel
|
| 37 |
Synthesis, biological evaluation, and molecular modeling of cinnamic acyl sulfonamide derivatives as novel antitubulin agents
|
Luo, Yin
|
|
2011
|
19 |
16 |
p. 4730-4738
9 p.
|
artikel
|
| 38 |
Synthesis, gp120 binding and anti-HIV activity of fatty acid esters of 1,1-linked disaccharides
|
Bachan, Stewart
|
|
2011
|
19 |
16 |
p. 4803-4811
9 p.
|
artikel
|
| 39 |
The combination of 4-anilinoquinazoline and cinnamic acid: A novel mode of binding to the epidermal growth factor receptor tyrosine kinase
|
Li, Dong-Dong
|
|
2011
|
19 |
16 |
p. 5012-5022
11 p.
|
artikel
|
| 40 |
The effect of sulfonate leaving groups on the hypoxia-selective toxicity of nitro analogs of the duocarmycins
|
Ashoorzadeh, Amir
|
|
2011
|
19 |
16 |
p. 4851-4860
10 p.
|
artikel
|
| 41 |
Thermodynamic and biological evaluation of a thrombin binding aptamer modified with several unlocked nucleic acid (UNA) monomers and a 2′-C-piperazino-UNA monomer
|
Jensen, Troels B.
|
|
2011
|
19 |
16 |
p. 4739-4745
7 p.
|
artikel
|
| 42 |
Thiolactone modulators of quorum sensing revealed through library design and screening
|
McInnis, Christine E.
|
|
2011
|
19 |
16 |
p. 4820-4828
9 p.
|
artikel
|
| 43 |
Trimethoxy-chalcone derivatives inhibit growth of Leishmania braziliensis: Synthesis, biological evaluation, molecular modeling and structure–activity relationship (SAR)
|
Bello, Murilo Lamim
|
|
2011
|
19 |
16 |
p. 5046-5052
7 p.
|
artikel
|
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