| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Chemical and biological aspects of posaconazole as a classic antifungal agent with non-classical properties: highlighting a tetrahydrofuran-based drug toward generation of new drugs
|
Dadashpour, Sakineh
|
|
|
31 |
6 |
p. 833-850
|
artikel
|
| 2 |
Design, synthesis, and biological evaluation of novel 2-acetylphenol-rivastigmine hybrids as potential multifunctional agents for the treatment of Alzheimer’s disease
|
Deng, Cong
|
|
|
31 |
6 |
p. 1035-1048
|
artikel
|
| 3 |
Design, synthesis of amide derivatives of scutellarin and their antileukemia and neuroprotective activities
|
Han, Tong
|
|
|
31 |
6 |
p. 905-915
|
artikel
|
| 4 |
Discovery of novel donepezil-M30D hybrids with neuroprotective properties for Alzheimer’s disease treatment
|
Yepes, Andrés F.
|
|
|
31 |
6 |
p. 867-885
|
artikel
|
| 5 |
Dual HDAC–BRD4 inhibitors endowed with antitumor and antihyperalgesic activity
|
Maach, Soumia
|
|
|
31 |
6 |
p. 960-974
|
artikel
|
| 6 |
Evaluation of novel multifunctional organoselenium compounds as potential cholinesterase inhibitors against Alzheimer’s disease
|
Refaay, Dina A.
|
|
|
31 |
6 |
p. 894-904
|
artikel
|
| 7 |
Hybrid molecules of scutellarein and 3, 5, 6-trimethylpyrazine-2-formic acid linked with polar amino acid for ischemic stroke
|
Wu, Shuxia
|
|
|
31 |
6 |
p. 916-924
|
artikel
|
| 8 |
Isoindolone derivatives as novel potential anti-Alzheimer’s candidates: synthesis, in silico, and AChE inhibitory activity evaluation
|
Andrade-Jorge, Erik
|
|
|
31 |
6 |
p. 851-866
|
artikel
|
| 9 |
Microwave-assisted synthesis and evaluation of their antiproliferative, antimicrobial, activities and DNA Binding studies of (3-Methyl-7H-furo[2,3-f]chromen-2-yl)(aryl)methanones
|
Dharavath, Ravinder
|
|
|
31 |
6 |
p. 993-1002
|
artikel
|
| 10 |
Novel norsufentanil analogues containing triazole ring; synthesis, radioligand binding assay, and pharmacological evaluation
|
Nami, Majid
|
|
|
31 |
6 |
p. 886-893
|
artikel
|
| 11 |
Novel orthodiphenyl five-member N-heteroaromatic compounds as potent anticancer cell agents
|
Hu, Shijia
|
|
|
31 |
6 |
p. 936-948
|
artikel
|
| 12 |
N-Phosphorylation of daunorubicin—synthetic approaches and antiproliferative properties of the products
|
Moiseeva, Aleksandra A.
|
|
|
31 |
6 |
p. 1011-1025
|
artikel
|
| 13 |
N-Substituted 4-sulfamoylbenzoic acid derivatives as inhibitors of cytosolic phospholipase A2α
|
Borecki, Daniel
|
|
|
31 |
6 |
p. 975-992
|
artikel
|
| 14 |
Platanic acid derived amides are more cytotoxic than their corresponding oximes
|
Kozubek, Marie
|
|
|
31 |
6 |
p. 1049-1059
|
artikel
|
| 15 |
Synthesis and antimycobacterial evaluation of fluoroquinolones derivatives coupled with isoprenyl moiety at the C-7 position
|
Ribeiro, César A.
|
|
|
31 |
6 |
p. 949-959
|
artikel
|
| 16 |
Synthesis and evaluation of new sartan derivatives
|
Dalaijargal, Bertsetseg
|
|
|
31 |
6 |
p. 1003-1010
|
artikel
|
| 17 |
Synthesis, cytotoxicities, and carbonic anhydrase inhibition activities of pyrazoline–benzenesulfonamide derivatives harboring phenol/polyphenol moieties
|
Bilginer, Sinan
|
|
|
31 |
6 |
p. 925-935
|
artikel
|
| 18 |
Synthesis, in-vitro biological evaluation, and molecular docking study of novel spiro-β-lactam-isatin hybrids
|
Jarrahpour, Aliasghar
|
|
|
31 |
6 |
p. 1026-1034
|
artikel
|
Tijdschrift beschrijving