| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acridones circumvent P-glycoprotein-associated multidrug resistance (MDR) in cancer cells
|
Gopinath, Vadiraj S.
|
|
2008
|
16 |
1 |
p. 474-487
14 p.
|
artikel
|
| 2 |
A fluorescence probe for assaying micro RNA maturation
|
Davies, Brian P.
|
|
2008
|
16 |
1 |
p. 49-55
7 p.
|
artikel
|
| 3 |
Amide bond direction modulates G-quadruplex recognition and telomerase inhibition by 2,6 and 2,7 bis-substituted anthracenedione derivatives
|
Zagotto, Giuseppe
|
|
2008
|
16 |
1 |
p. 354-361
8 p.
|
artikel
|
| 4 |
A new insight into solid-state conformation of macrolide antibiotics
|
Miroshnyk, Inna
|
|
2008
|
16 |
1 |
p. 232-239
8 p.
|
artikel
|
| 5 |
Anthracene based base-discriminating fluorescent oligonucleotide probes for SNPs typing: Synthesis and photophysical properties
|
Saito, Yoshio
|
|
2008
|
16 |
1 |
p. 107-113
7 p.
|
artikel
|
| 6 |
Bioorganic & Medicinal Chemistry Reviews and Perspectives
|
|
|
2008
|
16 |
1 |
p. 586-588
3 p.
|
artikel
|
| 7 |
Bis-pyrene-labeled molecular beacon: A monomer–excimer switching probe for the detection of DNA base alteration
|
Yamana, Kazushige
|
|
2008
|
16 |
1 |
p. 78-83
6 p.
|
artikel
|
| 8 |
5′-Carbamoyl derivatives of 2′-C-methyl-purine nucleosides as selective A1 adenosine receptor agonists: Affinity, efficacy, and selectivity for A1 receptor from different species
|
Cappellacci, Loredana
|
|
2008
|
16 |
1 |
p. 336-353
18 p.
|
artikel
|
| 9 |
Characterization of distamycin A binding to damaged DNA
|
Inase-Hashimoto, Aki
|
|
2008
|
16 |
1 |
p. 164-170
7 p.
|
artikel
|
| 10 |
Chemoenzymatic synthesis and antiviral evaluation of conformationally constrained and 3′-methyl-branched carbanucleosides using both enantiomers of the same building block
|
Aubin, Yoann
|
|
2008
|
16 |
1 |
p. 374-381
8 p.
|
artikel
|
| 11 |
Chemo-, regio-, and stereoselectivity of F-ring opening reactions in the cephalostatin series
|
Nawasreh, M.
|
|
2008
|
16 |
1 |
p. 255-265
11 p.
|
artikel
|
| 12 |
Chromen-based TNF-α converting enzyme (TACE) inhibitors: Design, synthesis, and biological evaluation
|
Chun, Kwangwoo
|
|
2008
|
16 |
1 |
p. 530-535
6 p.
|
artikel
|
| 13 |
Constituents of Brazilian red propolis and their preferential cytotoxic activity against human pancreatic PANC-1 cancer cell line in nutrient-deprived condition
|
Awale, Suresh
|
|
2008
|
16 |
1 |
p. 181-189
9 p.
|
artikel
|
| 14 |
Design and synthesis of diketopiperazine and acyclic analogs related to the caprazamycins and liposidomycins as potential antibacterial agents
|
Hirano, Shinpei
|
|
2008
|
16 |
1 |
p. 428-436
9 p.
|
artikel
|
| 15 |
Design of a pyrene-containing fluorescence probe for labeling of RNA poly(A) tracts
|
Tanaka, Kazuo
|
|
2008
|
16 |
1 |
p. 400-404
5 p.
|
artikel
|
| 16 |
Design, synthesis, and in vitro evaluation of new naphthylnitrobutadienes with potential antiproliferative activity: Toward a structure/activity correlation
|
Petrillo, Giovanni
|
|
2008
|
16 |
1 |
p. 240-247
8 p.
|
artikel
|
| 17 |
Design, synthesis, and preliminary evaluation of 4-(6-(3-nitroguanidino)hexanamido)pyrrolidine derivatives as potential iNOS inhibitors
|
Liu, Feng-Zhi
|
|
2008
|
16 |
1 |
p. 578-585
8 p.
|
artikel
|
| 18 |
Discovery and structure–activity relationship of N-phenyl-1H-pyrazolo[3,4-b]quinolin-4-amines as a new series of potent apoptosis inducers
|
Zhang, Han-Zhong
|
|
2008
|
16 |
1 |
p. 222-231
10 p.
|
artikel
|
| 19 |
Discovery of long-acting N-(cyanomethyl)-N-alkyl-l-prolinamide inhibitors of dipeptidyl peptidase IV
|
Kondo, Takashi
|
|
2008
|
16 |
1 |
p. 190-208
19 p.
|
artikel
|
| 20 |
Discovery of novel α-glucosidase inhibitors based on the virtual screening with the homology-modeled protein structure
|
Park, Hwangseo
|
|
2008
|
16 |
1 |
p. 284-292
9 p.
|
artikel
|
| 21 |
Editorial board
|
|
|
2008
|
16 |
1 |
p. IFC-
1 p.
|
artikel
|
| 22 |
Emerging trends in molecular recognition: Utility of weak aromatic interactions
|
Tewari, Ashish Kumar
|
|
2008
|
16 |
1 |
p. 126-143
18 p.
|
artikel
|
| 23 |
Facile preparation of new 4-phenylamino-3-quinolinecarbonitrile Src kinase inhibitors via 7-fluoro intermediates: Identification of potent 7-amino analogs
|
Boschelli, Diane H.
|
|
2008
|
16 |
1 |
p. 405-412
8 p.
|
artikel
|
| 24 |
Fluorescence-based detection of short DNA sequences under non-denaturing conditions
|
Smolina, Irina V.
|
|
2008
|
16 |
1 |
p. 84-93
10 p.
|
artikel
|
| 25 |
Functionalized chalcones as selective inhibitors of P-glycoprotein and breast cancer resistance protein
|
Liu, Xiao-Ling
|
|
2008
|
16 |
1 |
p. 171-180
10 p.
|
artikel
|
| 26 |
Graphical contents list
|
|
|
2008
|
16 |
1 |
p. 1-16
16 p.
|
artikel
|
| 27 |
Heteroallyl-containing 5-nitrofuranes as new anti-Trypanosoma cruzi agents with a dual mechanism of action
|
Gerpe, Alejandra
|
|
2008
|
16 |
1 |
p. 569-577
9 p.
|
artikel
|
| 28 |
Inducing the replacement of PNA in DNA·PNA duplexes by DNA
|
Grossmann, Tom N.
|
|
2008
|
16 |
1 |
p. 34-39
6 p.
|
artikel
|
| 29 |
Instructions to contributors
|
|
|
2008
|
16 |
1 |
p. I-
1 p.
|
artikel
|
| 30 |
Interaction of aliphatic cap group in inhibition of histone deacetylases by cyclic tetrapeptides
|
Nishino, Norikazu
|
|
2008
|
16 |
1 |
p. 437-445
9 p.
|
artikel
|
| 31 |
In vitro spermicidal activity of peptides from amphibian skin: Dermaseptin S4 and derivatives
|
Zairi, Amira
|
|
2008
|
16 |
1 |
p. 266-275
10 p.
|
artikel
|
| 32 |
2-Methylene 19-nor-25-dehydro-1α-hydroxyvitamin D3 26,23-lactones: Synthesis, biological activities and molecular basis of passive antagonism
|
Yoshimoto, Nobuko
|
|
2008
|
16 |
1 |
p. 457-473
17 p.
|
artikel
|
| 33 |
Molecular docking identifies the binding of 3-chloropyridine moieties specifically to the S1 pocket of SARS-CoV Mpro
|
Niu, Chunying
|
|
2008
|
16 |
1 |
p. 293-302
10 p.
|
artikel
|
| 34 |
Mono- and dialkyl isoprenoid bisphosphonates as geranylgeranyl diphosphate synthase inhibitors
|
Wiemer, Andrew J.
|
|
2008
|
16 |
1 |
p. 390-399
10 p.
|
artikel
|
| 35 |
New cyanine dyes as base surrogates in PNA: Forced intercalation probes (FIT-probes) for homogeneous SNP detection
|
Bethge, Lucas
|
|
2008
|
16 |
1 |
p. 114-125
12 p.
|
artikel
|
| 36 |
New, stronger nucleophiles for nucleic acid-templated chemistry: Synthesis and application in fluorescence detection of cellular RNA
|
Miller, Gregory P.
|
|
2008
|
16 |
1 |
p. 56-64
9 p.
|
artikel
|
| 37 |
Non-ATP competitive glycogen synthase kinase 3β (GSK-3β) inhibitors: Study of structural requirements for thiadiazolidinone derivatives
|
Castro, Ana
|
|
2008
|
16 |
1 |
p. 495-510
16 p.
|
artikel
|
| 38 |
Novel cholesterol biosynthesis inhibitors targeting human lanosterol 14α-demethylase (CYP51)
|
Korošec, Tina
|
|
2008
|
16 |
1 |
p. 209-221
13 p.
|
artikel
|
| 39 |
Novel imidazo[1,2-a]pyrazine derivatives as potent reversible inhibitors of the gastric H+/K+-ATPase
|
Zimmermann, Peter Jan
|
|
2008
|
16 |
1 |
p. 536-541
6 p.
|
artikel
|
| 40 |
N-Phenyl and N-phenylalkyl-maleimides acting against Candida spp.: Time-to-kill, stability, interaction with maleamic acids
|
Sortino, Maximiliano
|
|
2008
|
16 |
1 |
p. 560-568
9 p.
|
artikel
|
| 41 |
Nucleic acid modification for fluorescence-based technologies
|
Seitz, Oliver
|
|
2008
|
16 |
1 |
p. 17-18
2 p.
|
artikel
|
| 42 |
Pyrene-modified guanosine as fluorescent probe for DNA modulated by charge transfer
|
Wanninger-Weiß, Claudia
|
|
2008
|
16 |
1 |
p. 100-106
7 p.
|
artikel
|
| 43 |
Pyrene–perylene as a FRET pair coupled to the N2′-functionality of 2′-amino-LNA
|
Lindegaard, Dorthe
|
|
2008
|
16 |
1 |
p. 94-99
6 p.
|
artikel
|
| 44 |
Pyridazinone derivatives: Design, synthesis, and in vitro vasorelaxant activity
|
Abouzid, Khaled
|
|
2008
|
16 |
1 |
p. 382-389
8 p.
|
artikel
|
| 45 |
RNA as scaffold for pyrene excited complexes
|
Grünewald, Christian
|
|
2008
|
16 |
1 |
p. 19-26
8 p.
|
artikel
|
| 46 |
SAR of a series of anti-HSV-1 acridone derivatives, and a rational acridone-based design of a new anti-HSV-1 3H-benzo[b]pyrazolo[3,4-h]-1,6-naphthyridine series
|
Bernardino, Alice M.R.
|
|
2008
|
16 |
1 |
p. 313-321
9 p.
|
artikel
|
| 47 |
Sequence-specific Methyltransferase-Induced Labelling (SMILing) of plasmid DNA for studying cell transfection
|
Schmidt, Falk H.-G.
|
|
2008
|
16 |
1 |
p. 40-48
9 p.
|
artikel
|
| 48 |
Single nucleotide specific detection of DNA by native chemical ligation of fluorescence labeled PNA-probes
|
Dose, Christian
|
|
2008
|
16 |
1 |
p. 65-77
13 p.
|
artikel
|
| 49 |
Small P-gp modulating molecules: SAR studies on tetrahydroisoquinoline derivatives
|
Colabufo, Nicola Antonio
|
|
2008
|
16 |
1 |
p. 362-373
12 p.
|
artikel
|
| 50 |
Spectroscopic properties of pyrene-containing DNA mimics
|
Samain, Florent
|
|
2008
|
16 |
1 |
p. 27-33
7 p.
|
artikel
|
| 51 |
Studies toward the structural optimization of new brazilizone-related trypanocidal 1,3,4-thiadiazole-2-arylhydrazone derivatives
|
Carvalho, Samir A.
|
|
2008
|
16 |
1 |
p. 413-421
9 p.
|
artikel
|
| 52 |
Synthesis and anti-HIV evaluation of novel 1,3-disubstituted thieno[3,2-c][1,2,6]thiadiazin-4(3H)-one 2,2-dioxides(TTDDs)
|
Lin, Yongqiang
|
|
2008
|
16 |
1 |
p. 157-163
7 p.
|
artikel
|
| 53 |
Synthesis and antiviral activity of new dimeric inhibitors against HIV-1
|
Danel, Krzysztof
|
|
2008
|
16 |
1 |
p. 511-517
7 p.
|
artikel
|
| 54 |
Synthesis and biological evaluation of 2-trifluoromethyl/sulfonamido-5,6-diaryl substituted imidazo[2,1-b]-1,3,4-thiadiazoles: A novel class of cyclooxygenase-2 inhibitors
|
Gadad, Andanappa K.
|
|
2008
|
16 |
1 |
p. 276-283
8 p.
|
artikel
|
| 55 |
Synthesis and evaluation of cationic phthalocyanine derivatives as potential inhibitors of telomerase
|
Zhang, Lixia
|
|
2008
|
16 |
1 |
p. 303-312
10 p.
|
artikel
|
| 56 |
Synthesis and insecticidal evaluation of novel N′-tert-butyl-N′-substitutedbenzoyl-N-5-chloro-6-chromanecarbohydrazide derivatives
|
Mao, Chun-Hui
|
|
2008
|
16 |
1 |
p. 488-494
7 p.
|
artikel
|
| 57 |
Synthesis and pharmacological activity of aminoindanone dimers and related compounds
|
Sheridan, H.
|
|
2008
|
16 |
1 |
p. 248-254
7 p.
|
artikel
|
| 58 |
Synthesis and pharmacology of 1-deoxy analogs of CP-47,497 and CP-55,940
|
Huffman, John W.
|
|
2008
|
16 |
1 |
p. 322-335
14 p.
|
artikel
|
| 59 |
Synthesis and structure–activity relationships of N-{1-[(6-fluoro-2-naphthyl)methyl]piperidin-4-yl}benzamide derivatives as novel CCR3 antagonists
|
Sato, Ippei
|
|
2008
|
16 |
1 |
p. 144-156
13 p.
|
artikel
|
| 60 |
Synthesis, anti-Toxoplasma gondii and antimicrobial activities of benzaldehyde 4-phenyl-3-thiosemicarbazones and 2-[(phenylmethylene)hydrazono]-4-oxo-3-phenyl-5-thiazolidineacetic acids
|
de Aquino, Thiago M.
|
|
2008
|
16 |
1 |
p. 446-456
11 p.
|
artikel
|
| 61 |
Synthesis of 2′-O-modified adenosine building blocks and application for RNA interference
|
Odadzic, Dalibor
|
|
2008
|
16 |
1 |
p. 518-529
12 p.
|
artikel
|
| 62 |
Synthesis of 4,5,6,7-tetrahydrothieno[3,2-c]pyridines and comparison with their isosteric 1,2,3,4-tetrahydroisoquinolines as inhibitors of phenylethanolamine N-methyltransferase
|
Grunewald, Gary L.
|
|
2008
|
16 |
1 |
p. 542-559
18 p.
|
artikel
|
| 63 |
The use of ligand-based de novo design for scaffold hopping and sidechain optimization: Two case studies
|
Feher, Miklos
|
|
2008
|
16 |
1 |
p. 422-427
6 p.
|
artikel
|
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