nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A biphenyl derivative from the twigs of Chaenomeles speciosa
|
Suh, Won Se |
|
2017 |
72 |
C |
p. 156-160 5 p. |
artikel |
2 |
A natural product from Cannabis sativa subsp. sativa inhibits homeodomain-interacting protein kinase 2 (HIPK2), attenuating MPP+-induced apoptosis in human neuroblastoma SH-SY5Y cells
|
Wang, Guan |
|
2017 |
72 |
C |
p. 64-73 10 p. |
artikel |
3 |
Aryl- or heteroaryl-based hydrazinylphthalazine derivatives as new potential antitrypanosomal agents
|
Romero, Angel H. |
|
2017 |
72 |
C |
p. 51-56 6 p. |
artikel |
4 |
5-Bromo-2-aryl benzimidazole derivatives as non-cytotoxic potential dual inhibitors of α-glucosidase and urease enzymes
|
Arshad, Tanzila |
|
2017 |
72 |
C |
p. 21-31 11 p. |
artikel |
5 |
Carbohydrazones as new class of carbonic anhydrase inhibitors: Synthesis, kinetics, and ligand docking studies
|
Iqbal, Sarosh |
|
2017 |
72 |
C |
p. 89-101 13 p. |
artikel |
6 |
Cytotoxic effects of a novel maleimide derivative on epithelial and tumor cells
|
Ali, Bakat |
|
2017 |
72 |
C |
p. 199-207 9 p. |
artikel |
7 |
Design, synthesis and anti-diabetic activity of triazolotriazine derivatives as dipeptidyl peptidase-4 (DPP-4) inhibitors
|
Patel, Bhumika D. |
|
2017 |
72 |
C |
p. 345-358 14 p. |
artikel |
8 |
Design, synthesis and biological activity of 3-oxoamino-benzenesulfonamides as selective and reversible LSD1 inhibitors
|
Xi, Jiayue |
|
2017 |
72 |
C |
p. 182-189 8 p. |
artikel |
9 |
Design, synthesis, docking studies and biological evaluation of novel chalcone derivatives as potential histone deacetylase inhibitors
|
Mohamed, Mamdouh F.A. |
|
2017 |
72 |
C |
p. 32-41 10 p. |
artikel |
10 |
Design & synthesis of novel oxazolone & triazinone derivatives and their biological evaluation as COX-2 inhibitors
|
Mohamed, Lamia W. |
|
2017 |
72 |
C |
p. 308-314 7 p. |
artikel |
11 |
Development of combretastatins as potent tubulin polymerization inhibitors
|
Bukhari, Syed Nasir Abbas |
|
2017 |
72 |
C |
p. 130-147 18 p. |
artikel |
12 |
Discovery of 3,3-di(indolyl)indolin-2-one as a novel scaffold for α-glucosidase inhibitors: In silico studies and SAR predictions
|
Wang, Guangcheng |
|
2017 |
72 |
C |
p. 228-233 6 p. |
artikel |
13 |
Discovery of novel 2-substituted-4-(2-fluorophenoxy) pyridine derivatives possessing pyrazolone and triazole moieties as dual c-Met/VEGFR-2 receptor tyrosine kinase inhibitors
|
Gu, Weijie |
|
2017 |
72 |
C |
p. 116-122 7 p. |
artikel |
14 |
DNA fluorescent labeling with naphtho[1,2,3-cd]indol-6(2H)-one for investigation of protein-DNA interactions
|
Vasilyeva, Svetlana V. |
|
2017 |
72 |
C |
p. 268-272 5 p. |
artikel |
15 |
Editorial Board
|
|
|
2017 |
72 |
C |
p. i- 1 p. |
artikel |
16 |
Efficient synthesis of novel dialkyl-3-cyanopropylphosphate derivatives and evaluation of their anticholinesterase activity
|
Aouani, Iyadh |
|
2017 |
72 |
C |
p. 301-307 7 p. |
artikel |
17 |
Ellagitannin and flavonoid constituents from Agrimonia pilosa Ledeb. with their protein tyrosine phosphatase and acetylcholinesterase inhibitory activities
|
Nguyen, Duc Hung |
|
2017 |
72 |
C |
p. 293-300 8 p. |
artikel |
18 |
Facile synthesis of fluoro, methoxy, and methyl substituted ferrocene-based urea complexes as potential therapeutic agents
|
Asghar, Faiza |
|
2017 |
72 |
C |
p. 215-227 13 p. |
artikel |
19 |
Fatty-monastrol derivatives and its cytotoxic effect against melanoma cell growth
|
de Moraes, Milene Medeiros |
|
2017 |
72 |
C |
p. 148-155 8 p. |
artikel |
20 |
Hydrolysis of the amide bond in histidine- and methionine-containing dipeptides promoted by pyrazine and pyridazine palladium(II)-aqua dimers: Comparative study with platinum(II) analogues
|
Živković, Marija D. |
|
2017 |
72 |
C |
p. 190-198 9 p. |
artikel |
21 |
Issue TOC
|
|
|
2017 |
72 |
C |
p. ii-xi nvt p. |
artikel |
22 |
New 1,2-diaryl-4-substituted-benzylidene-5-4H-imidazolone derivatives: Design, synthesis and biological evaluation as potential anti-inflammatory and analgesic agents
|
Abdellatif, Khaled R.A. |
|
2017 |
72 |
C |
p. 123-129 7 p. |
artikel |
23 |
New hybrid molecules combining benzothiophene or benzofuran with rhodanine as dual COX-1/2 and 5-LOX inhibitors: Synthesis, biological evaluation and docking study
|
El-Miligy, Mostafa M.M. |
|
2017 |
72 |
C |
p. 102-115 14 p. |
artikel |
24 |
Novel multi-targeted agents for Alzheimer's disease: Synthesis, biological evaluation, and molecular modeling of novel 2-[4-(4-substitutedpiperazin-1-yl)phenyl]benzimidazoles
|
Ozadali-Sari, Keriman |
|
2017 |
72 |
C |
p. 208-214 7 p. |
artikel |
25 |
Novel quinuclidinone derivatives induced apoptosis in human breast cancer via targeting p53
|
Malki, Ahmed |
|
2017 |
72 |
C |
p. 57-63 7 p. |
artikel |
26 |
Protective effects of hepatocyte-specific glycyrrhetic derivatives against carbon tetrachloride-induced liver damage in mice
|
Yang, Yifei |
|
2017 |
72 |
C |
p. 42-50 9 p. |
artikel |
27 |
PTP1B inhibitors from Selaginella tamariscina (Beauv.) Spring and their kinetic properties and molecular docking simulation
|
Le, Duc Dat |
|
2017 |
72 |
C |
p. 273-281 9 p. |
artikel |
28 |
Rational design, synthesis, pharmacophore modeling, and docking studies for identification of novel potent DNA-PK inhibitors
|
Ihmaid, Saleh |
|
2017 |
72 |
C |
p. 234-247 14 p. |
artikel |
29 |
Synthesis and biological evaluation of benzimidazole derivatives as the G9a Histone Methyltransferase inhibitors that induce autophagy and apoptosis of breast cancer cells
|
Zhang, Jin |
|
2017 |
72 |
C |
p. 168-181 14 p. |
artikel |
30 |
Synthesis and hybridization properties of oligonucleotide analogues with novel acyclic triazole internucleotide linkages
|
Gładysz, Michał |
|
2017 |
72 |
C |
p. 161-167 7 p. |
artikel |
31 |
Synthesis and preliminary biological assay of uridine glycoconjugate derivatives containing amide and/or 1,2,3-triazole linkers
|
Pastuch-Gawolek, Gabriela |
|
2017 |
72 |
C |
p. 80-88 9 p. |
artikel |
32 |
Synthesis and study of anti-HIV-1 RT activity of 5-benzoyl-4-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepin-2-one derivatives
|
Chander, Subhash |
|
2017 |
72 |
C |
p. 74-79 6 p. |
artikel |
33 |
Synthesis, biological evaluation and molecular modeling study of new (1,2,4-triazole or 1,3,4-thiadiazole)-methylthio-derivatives of quinazolin-4(3H)-one as DHFR inhibitors
|
El-Gazzar, Yomna I. |
|
2017 |
72 |
C |
p. 282-292 11 p. |
artikel |
34 |
Synthesis, crystal structure determination, biological screening and docking studies of N1-substituted derivatives of 2,3-dihydroquinazolin-4(1H)-one as inhibitors of cholinesterases
|
Sultana, Nargis |
|
2017 |
72 |
C |
p. 256-267 12 p. |
artikel |
35 |
Synthesis, in vitro antiproliferative activity and kinase profile of new benzimidazole and benzotriazole derivatives
|
Chojnacki, Konrad |
|
2017 |
72 |
C |
p. 1-10 10 p. |
artikel |
36 |
Synthesis, in vitro evaluation and molecular docking studies of novel amide linked triazolyl glycoconjugates as new inhibitors of α-glucosidase
|
Gupta, Shyam Ji |
|
2017 |
72 |
C |
p. 11-20 10 p. |
artikel |
37 |
Synthesis of alpha amylase inhibitors based on privileged indole scaffold
|
Noreen, Tayyaba |
|
2017 |
72 |
C |
p. 248-255 8 p. |
artikel |
38 |
Synthesis of indole analogs as potent β-glucuronidase inhibitors
|
Baharudin, Mohd Syukri |
|
2017 |
72 |
C |
p. 323-332 10 p. |
artikel |
39 |
Synthesis of novel dibenzoxanthene derivatives and observation of apoptosis in human hepatocellular cancer cells
|
Yang, Hui-Hui |
|
2017 |
72 |
C |
p. 333-344 12 p. |
artikel |
40 |
Tetrahydroacridine derivatives with fluorobenzoic acid moiety as multifunctional agents for Alzheimer’s disease treatment
|
Czarnecka, Kamila |
|
2017 |
72 |
C |
p. 315-322 8 p. |
artikel |
41 |
The first synthesis of 4-phenylbutenone derivative bromophenols including natural products and their inhibition profiles for carbonic anhydrase, acetylcholinesterase and butyrylcholinesterase enzymes
|
Bayrak, Çetin |
|
2017 |
72 |
C |
p. 359-366 8 p. |
artikel |