| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
7-Azaindole-1-carboxamides as a new class of PARP-1 inhibitors
|
Cincinelli, Raffaella
|
|
2014
|
22 |
3 |
p. 1089-1103
15 p.
|
artikel
|
| 2 |
Binding ability of a thymine-functionalized oligolysine towards nucleic acids
|
Roviello, Giovanni N.
|
|
2014
|
22 |
3 |
p. 997-1002
6 p.
|
artikel
|
| 3 |
Carbamazepine derivatives with P2X4 receptor-blocking activity
|
Tian, Maoqun
|
|
2014
|
22 |
3 |
p. 1077-1088
12 p.
|
artikel
|
| 4 |
Chemoenzymatic synthesis of ADP-d-glycero-β-d-manno-heptose and study of the substrate specificity of HldE
|
Li, Tiehai
|
|
2014
|
22 |
3 |
p. 1139-1147
9 p.
|
artikel
|
| 5 |
Design, synthesis and ex-vivo release studies of colon-specific polyphosphazene–anticancer drug conjugates
|
Sharma, Rajiv
|
|
2014
|
22 |
3 |
p. 1104-1114
11 p.
|
artikel
|
| 6 |
Direct synthesis of C3-mono-functionalized oxindoles from N-unprotected 2-oxindole and their antileishmanial activity
|
Scala, Angela
|
|
2014
|
22 |
3 |
p. 1063-1069
7 p.
|
artikel
|
| 7 |
Editorial board
|
|
|
2014
|
22 |
3 |
p. IFC-
1 p.
|
artikel
|
| 8 |
Formosusin A, a novel specific inhibitor of mammalian DNA polymerase β from the fungus Paecilomyces formosus
|
Mizushina, Yoshiyuki
|
|
2014
|
22 |
3 |
p. 1070-1076
7 p.
|
artikel
|
| 9 |
Functional regulation of RNA-induced silencing complex by photoreactive oligonucleotides
|
Matsuyama, Yohei
|
|
2014
|
22 |
3 |
p. 1003-1007
5 p.
|
artikel
|
| 10 |
Glutathione-analogous peptidyl phosphorus esters as mechanism-based inhibitors of γ-glutamyl transpeptidase for probing cysteinyl-glycine binding site
|
Nakajima, Mado
|
|
2014
|
22 |
3 |
p. 1176-1194
19 p.
|
artikel
|
| 11 |
Graphical contents list
|
|
|
2014
|
22 |
3 |
p. 929-936
8 p.
|
artikel
|
| 12 |
Inhibition of tyrosinase activity by polyphenol compounds from Flemingia philippinensis roots
|
Wang, Yan
|
|
2014
|
22 |
3 |
p. 1115-1120
6 p.
|
artikel
|
| 13 |
Linear propargylic alcohol functionality attached to the indazole-7-carboxamide as a JAK1-specific linear probe group
|
Kim, Mi Kyoung
|
|
2014
|
22 |
3 |
p. 1156-1162
7 p.
|
artikel
|
| 14 |
Morpholylureas are a new class of potent and selective inhibitors of the type 5 17-β-hydroxysteroid dehydrogenase (AKR1C3)
|
Flanagan, Jack U.
|
|
2014
|
22 |
3 |
p. 967-977
11 p.
|
artikel
|
| 15 |
New chiral derivatives of xanthones: Synthesis and investigation of enantioselectivity as inhibitors of growth of human tumor cell lines
|
Fernandes, Carla
|
|
2014
|
22 |
3 |
p. 1049-1062
14 p.
|
artikel
|
| 16 |
New melatonin (MT1/MT2) ligands: Design and synthesis of (8,9-dihydro-7H-furo[3,2-f]chromen-1-yl) derivatives
|
Landagaray, Elodie
|
|
2014
|
22 |
3 |
p. 986-996
11 p.
|
artikel
|
| 17 |
Small molecule mimetics of an interferon-α receptor interacting domain
|
Bello, Angelica M.
|
|
2014
|
22 |
3 |
p. 978-985
8 p.
|
artikel
|
| 18 |
Structure–activity relationships of substituted oxyoxalamides as inhibitors of the human soluble epoxide hydrolase
|
Kim, In-Hae
|
|
2014
|
22 |
3 |
p. 1163-1175
13 p.
|
artikel
|
| 19 |
Structure–activity relationship studies on acremomannolipin A, the potent calcium signal modulator with a novel glycolipid structure 2: Role of the alditol side chain stereochemistry
|
Tsutsui, Nozomi
|
|
2014
|
22 |
3 |
p. 945-959
15 p.
|
artikel
|
| 20 |
Synthesis and anti-rhinovirus activity of novel 3-[2-(pyridinyl)vinyl]substituted -2H-chromenes and -4H-chromen-4-ones
|
Conti, Cinzia
|
|
2014
|
22 |
3 |
p. 1201-1207
7 p.
|
artikel
|
| 21 |
Synthesis and biological evaluation of novel oxadiazole derivatives: A new class of thymidine phosphorylase inhibitors as potential anti-tumor agents
|
Shahzad, Sohail Anjum
|
|
2014
|
22 |
3 |
p. 1008-1015
8 p.
|
artikel
|
| 22 |
Synthesis and evaluation of Strychnos alkaloids as MDR reversal agents for cancer cell eradication
|
Munagala, Surendrachary
|
|
2014
|
22 |
3 |
p. 1148-1155
8 p.
|
artikel
|
| 23 |
Synthesis, biological evaluation and molecular docking studies of benzyloxyacetohydroxamic acids as LpxC inhibitors
|
Szermerski, Marina
|
|
2014
|
22 |
3 |
p. 1016-1028
13 p.
|
artikel
|
| 24 |
Synthesis/biological evaluation of hydroxamic acids and their prodrugs as inhibitors for Botulinum neurotoxin A light chain
|
Seki, Hajime
|
|
2014
|
22 |
3 |
p. 1208-1217
10 p.
|
artikel
|
| 25 |
Synthesis, biophysical characterization and anti-HIV activity of d(TG3AG) Quadruplexes bearing hydrophobic tails at the 5′-end
|
Romanucci, Valeria
|
|
2014
|
22 |
3 |
p. 960-966
7 p.
|
artikel
|
| 26 |
Synthesis, in vitro antimalarial activity and cytotoxicity of novel 4-aminoquinolinyl-chalcone amides
|
Smit, Frans J.
|
|
2014
|
22 |
3 |
p. 1128-1138
11 p.
|
artikel
|
| 27 |
Synthesis, modelling and biological characterization of 3-substituted-1H-indoles as ligands of GluN2B-containing N-methyl-d-aspartate receptors
|
Gitto, Rosaria
|
|
2014
|
22 |
3 |
p. 1040-1048
9 p.
|
artikel
|
| 28 |
Synthesis of novel indenoquinoxaline derivatives as potent α-glucosidase inhibitors
|
Khan, Madiha Sahar
|
|
2014
|
22 |
3 |
p. 1195-1200
6 p.
|
artikel
|
| 29 |
Synthesis of quercetin glycosides and their melanogenesis stimulatory activity in B16 melanoma cells
|
Yamauchi, Kosei
|
|
2014
|
22 |
3 |
p. 937-944
8 p.
|
artikel
|
| 30 |
Targeting the Warburg Effect in cancer; relationships for 2-arylpyridazinones as inhibitors of the key glycolytic enzyme 6-phosphofructo-2-kinase/2,6-bisphosphatase 3 (PFKFB3)
|
Brooke, Darby G.
|
|
2014
|
22 |
3 |
p. 1029-1039
11 p.
|
artikel
|
| 31 |
Unsymmetrical 1,5-diaryl-3-oxo-1,4-pentadienyls and their evaluation as antiparasitic agents
|
Ud Din, Zia
|
|
2014
|
22 |
3 |
p. 1121-1127
7 p.
|
artikel
|
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